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  • bioavailability  (65)
  • Lepidoptera
  • evolution
  • wheat
  • Springer  (140)
  • MDPI Publishing
  • Oxford, UK
  • Periodicals Archive Online (PAO)
  • 1975-1979  (140)
Collection
Keywords
Publisher
  • Springer  (140)
  • MDPI Publishing
  • Oxford, UK
  • Periodicals Archive Online (PAO)
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Insect lysozymes from three species of lepidoptera: Their structural relatedness to the c (chicken) type lysozyme (1979)
    Springer
    Journal of molecular evolution 14 (1979), S. 267-271 
    Details
    ISSN: 1432-1432
    Keywords: Lysozyme ; Insect ; Lepidoptera ; Evolution ; Sequence
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Sequence studies of the N-terminal halves of the lysozymes isolated fromBombyx mori, Galleria mellonella andSpodoptera littoralis (Lepidoptera) allow us to classify these enzymes among the c (chicken) type lysozymes.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01732494
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  • 2
    Electronic Resource
    Electronic Resource
    Seedling resistance of wheat to the powdery mildew fungus, Erysiphe graminis f. sp. tritici. I. Resistance of first leaves (1979)
    Springer
    Mycopathologia 68 (1979), S. 131-137 
    Details
    ISSN: 1573-0832
    Keywords: Erysiphe graminis f. sp.tritici ; powdery mildew fungus ; resistance ; wheat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract During primary infection by conidia ofErysiphe graminis f. sp.tritici, three mechanisms of resistance operate in first leaves of 8-day-old seedlings of both resistant and susceptible wheats. The first mechanism, operating at the penetration site, is responsible for the failure of penetrations attempted by primary germ tubes (PGT). The second mechanism is concerned with the abortion of haustoria in normal-appearing host cells. The third mechanism relates to the abortion of haustoria and the hypersensitivity of the penetrated host cells. With the inoculum-level of 19–24 conidia/mm2, the three mechanisms together prevented 89.3 % of the attempted penetrations by PGT from producing normal haustoria in resistant wheat Purdue 5752C1-7-5-1 and 37.4 % in the susceptible wheat Vermillion. The first mechanism accounted for the prevention of 73.3 % of the attempted PGT penetrations on Purdue 5752C1-7-5-1 and 36 % on Vermillion. The second mechanism was responsible for stopping 19 % of all the successful penetrations in Purdue 5752C1-7-5-1 and 0.8 % in Vermillion. The third mechanism accounted for the failure of 41 % of all the successful penetrations in Purdue 5752C1-7-5-1 and 1.4% in Vermillion. Thirty-six hours after inoculation, 10.7% of all the attempted PGT penetrations appeared to be developing normally in first leaves of 8-day-old seedlings of resistant wheat Purdue 5752C1-7-5-1 as compared to 62.6 % in the susceptible wheat Vermillion. This appears to be the first report showing the relative effectiveness of various mechanisms of resistance concerning any powdery mildew fungus.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00578520
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  • 3
    Electronic Resource
    Electronic Resource
    Über den Einfluß der Kulturdauer im larvalen Wirt auf die Entwicklungsleistungen implantierter männlicher Genitalimaginalscheiben vonEphestia, kuehniella Z. (1979)
    Springer
    Development genes and evolution 186 (1979), S. 309-331 
    Details
    ISSN: 1432-041X
    Keywords: Lepidoptera ; Male genital disk ; Implantation ; Regeneration ; Control of metamorphosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Complete and bisected male genital disks (HO) from full-grown (T9) larvae were transplanted either into larvae and pharate pupae of different age (T4, T7, T9 larvae, A1–A5 pharate pupae) or repeatedly transferred into full-grown larvae before being implanted into a final larval host. After metamorphosis of the hosts, most of the complete transplants and regenerated HO halves showed normal morphological features, but the implanted genitals from old pharate pupae (A4 and A5) were abnormally differentiated. Frequency of Regeneration. After transplanting both halves of the bisected HO into T9 hosts, three groups of results were observed: (1) each of the two halves regenerated into a complete genital organ; (2) only one half regenerated; (3) neither of the two halves regenerated. In the pharate pupae no regeneration of the implanted halves took place. If the lapse of time between the transplantation and, the onset of metamorphosis (=onset of pharate pupae phase) was long enough by transplanting into young larvae (T4) or by repeatedly transferring into old larvae and subsequent transplantation into a final larval host, all the implanted halves were able to regenerate. Size of the Implanted Genital Organs After prolonging the in vivo culture in larval hosts by implanting into young larvae or repeatedly transferring into old larvae, it was found that the regenerated genitalia grew to the same size as the complete transplants, but the size of the complete transplants increased, if at all, only insignificantly. Duration of Development of the Hosts. Regeneration of one HO half implanted into a full-grown larva caused an average delay of further development of about 2 days. An additional delay was recorded when both halves had regenerated. However, no delay was observed when HO halves implanted into young (T4) larvae regenerated, and no delay occurred in the final hosts when the repeatedly transferred halves had reached a certain stage of regeneration. The developmental capacities of the tranplanted disks and the control of metamorphosis by regenerating disks are discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00848456
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  • 4
    Electronic Resource
    Electronic Resource
    Influence of milk products on fluoride bioavailability in man (1979)
    Springer
    European journal of clinical pharmacology 16 (1979), S. 211-215 
    Details
    ISSN: 1432-1041
    Keywords: fluoride ; bioavailability ; calcium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The effect of milk products on the gastrointestinal absorption of fluoride from sodium fluoride tablets was studied in five healthy subjects. Two different diets were tested: (1) 250 ml standardized milk (3% fat) and (2) 500 ml of milk, 3 pieces of white bread with cheese and 150 ml of yoghurt. The 100% bioavailability of sodium fluoride tablets during fasting was greatly decreased by coadministration of milk products: with Diet 1 the absolute bioavailability calculated from combined plasma and urine data was in the range 50–79% and with Diet 2 it ranged from 50–71%. It is suggested that the decreased bioavailability produced by dairy products should be taken into account when establishing fluoride dosage regimens for prophylaxis of caries.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00562063
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  • 5
    Electronic Resource
    Electronic Resource
    Comparative bioavailability of a microcrystalline theophylline tablet and uncoated aminophylline tablets (1979)
    Springer
    European journal of clinical pharmacology 16 (1979), S. 417-421 
    Details
    ISSN: 1432-1041
    Keywords: theophylline ; aminophylline ; bioavailability ; rapidly dissolving tablet
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The bioavailability of a rapidly dissolving tablet of theophylline and three brands of standard aminophylline tablets was estimated in a four way cross-over study involving 8 healthy adult volunteers. The relative extent of bioavailability as assessed by the measurement of the total area under the plasma concentration time curves showed no difference between the products (P〉0.05). Computed estimates of the rate of drug absorption were similar for all 4 products tested. The results indicate that the rapidly dissolving tablet offers no advantage in respect to rate and extent of absorption over conventional aminophylline tablets.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00568203
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  • 6
    Electronic Resource
    Electronic Resource
    Absolute bioavailability of chlorthalidone in man: A cross-over study after intravenous and oral administration (1979)
    Springer
    European journal of clinical pharmacology 15 (1979), S. 35-50 
    Details
    ISSN: 1432-1041
    Keywords: chlorthalidone ; pharmacokinetics ; oral and i.v. doses ; bioavailability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Seven normal human volunteers each received a constant-rate infusion of chlorthalidone for 2 h, and the same (commonly 50 mg) single oral dose on separate occasions. The concentration of unchanged chlorthalidone was analyzed over a 100 to 220 h period in plasma, red blood cells, urine and faeces after both dosage forms. A three compartment model was required to describe the intravenous plasma concentrations in five of the subjects. A two compartment model sufficed to account for the decay of the oral plasma concentrations in all seven subjects. The mean plasma t1/2 after i.v. dosing was 36.5 h (±10.5 SD), and the mean plasma t1/2 after oral doses was 44.1 h (±9.6 SD). The mean red blood cell concentration t1/2 after i.v. doses was 46.4 h (±9.9 SD), and the mean red blood cell t1/2 after the oral doses was 52.7 h (±9.0 SD). The shorter i.v. half-live was not equally manifest in all subjects, being mainly apparent in three of them. In all cases the urinary excretion rate plots were parallel to the plasma concentration curves. As the faster decay after i.v. administration was not accompanied by increased renal clearance, the difference must have been due to non-renal mechanism. The mean total of 65.4 (±8.6 SD) % of the intravenous dose was excreted in urine over infinite time, whereas the mean total excretion after the oral dose was 43.8 (±8.5 SD) %. Faecal excretion ranged from 1.3–8.5% of dose in the i.v. study to 17.5–31.2% of dose in the oral study. The sum of the amounts present in urine plus faeces pointed strongly to an important metabolic route of elimination of chlorthalidone. Bioavailability estimates (F) from three sets of data were — a mean F of 0.61 from plasma concentrations, 0.67 from urinary excretion measurements and 0.72 from the erythrocyte concentrations. Simulations with a non-linear model indicated lesser validity of the estimate from erythrocyte concentrations. It was concluded that the average of plasma and urine data, F=0.64, yielded the best estimate of the oral availability of chlorthalidone 50 mg in man.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00563556
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  • 7
    Electronic Resource
    Electronic Resource
    Disposition pharmacokinetics of bezafibrate in man (1979)
    Springer
    European journal of clinical pharmacology 16 (1979), S. 31-38 
    Details
    ISSN: 1432-1041
    Keywords: bezafibrate ; hyperlipoproteinemia ; bioavailability ; pharmacokinetics ; GC-MS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The disposition kinetics of bezafibrate, a newly developed drug of great lipid-lowering potency, were investigated in normal male subjects. Five male volunteers received14C-labelled bezafibrate orally in solution, and a further 10 were given the same dose (300 mg) of un-labelled drug as tablets. The concentration of bezafibrate in serum and urine from the latter was determined by GC, and in the former total radioactivity in serum, urine and feces was followed for 48 h, and urinary excretion products were analysed by TLC and GC-MS. Rapid absorption from the gastrointestinal tract led to peak serum levels 30 min and 2 h after administration of solution and tablets, respectively. Since approximately 95% of the administered14C-bezafibrate was excreted in urine within 48 h, and almost all the remainder was detected in feces, absorption can be regarded as complete after administration in solution. The relative optimal bioavailability from the tablets was also complete, since in both cases approximately 50% of the administered dose was detected as unchanged bezafibrate in urine within 24 h by GC in the tablet study, and by TLC in the solution study. Of the decomposition products, more than 20% of the dose was present as glucuronides and the remainder consisted of several more polar compounds, one of which was identified as a hydroxyderivative of bezafibrate. Since the apparent halflife of bezafibrate in serum was 2.1 h, this new drug possesses favourable pharmacokinetic features: rapid and complete absorption, even from tablets, combined with a conveniently short half-life, and clearance which is half renal (56 ml/min) and half metabolic (43 ml/min), giving a total clearance of 99 ml/min.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00644963
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  • 8
    Electronic Resource
    Electronic Resource
    Pharmacokinetic, bioavailability and pharmacodynamic study of indobufen (K 3920), an inhibitor of platelet aggregation, after a single dose in man (1979)
    Springer
    European journal of clinical pharmacology 15 (1979), S. 323-327 
    Details
    ISSN: 1432-1041
    Keywords: indobufen ; platelet aggregation ; single dose ; bioavailability ; pharmacodynamics ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Six healthy volunteers received single iv and oral doses of 2-[p-(1-oxo-2-isoindolinyl)phenyl] butyric acid 100 mg (indobufen; K 3920), an inhibitor of platelet aggregation. Plasma levels and urinary excretion of the drug were determined by GLC. Collagen-induced platelet aggregation was assessed turbidimetrically at various intervals after administration. The plasma half-life of the drug was 7–8 h and more than 70% of the administered dose was recovered within 48 h in urine, as unchanged drug and as the glucuronide of indobufen. After oral administration of tablets of two different formulations, the drug was completely absorbed, but one formulation showed faster absorption. The maximal inhibitory effect on platelet aggregation was observed 1 to 4 h after iv administration, and it had decreased by 8 h. After tablets, peak effect and the time of the peak were similar, but activity was significantly prolonged, in accordance with the higher plasma levels found at 8 h. The data suggest that the effect of indobufen on platelets is reversible, and that for this drug platelets behave as a compartment that slowly equilibrates with plasma.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00558435
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  • 9
    Electronic Resource
    Electronic Resource
    Absolute bioavailability of quinidine in two sustained release preparations (1979)
    Springer
    European journal of clinical pharmacology 16 (1979), S. 45-48 
    Details
    ISSN: 1432-1041
    Keywords: quinidine ; slow release formulation ; pharmacokinetics ; bioavailability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The bioavailability of quinidine in two sustained release preparations A and B has been compared in three females and three males with i.v. administration of quinidine. The initial rate of oral absorption did not differ between the two drug preparations; the peak concentration was observed after 4 h both for A and B, but was significantly higher after B. A slower decrease in plasma concentration was observed after preparation A than B. Absolute bioavailability did not differ significantly between A (median value 78.4%) and B (median 87.1%). Drug absorption in vivo was in good agreement with the results of in vitro dissolution tests on both preparations. The slower decrease in plasma concentration found for the new sustained release form of quinidine should be of clinical advantage.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00644965
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  • 10
    Electronic Resource
    Electronic Resource
    Bioavailability and pharmacokinetics of cimetidine (1979)
    Springer
    European journal of clinical pharmacology 16 (1979), S. 335-340 
    Details
    ISSN: 1432-1041
    Keywords: cimetidine ; enterohepatic circulation ; irregular absorption ; bioavailability ; pharmacokinetics ; volunteers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The bioavailability and pharmacokinetics of cimetidine have been studied in healthy volunteers after administration of single intravenous (100 mg) and oral doses (100, 400 and 800 mg). After i.v. administration, the kinetics of cimetidine could be described by a linear, two compartment open model. Substantial variation in half-life was observed between subjects, with a mean value of 2.1 h (range 0.9–4.7). Cimetidine had a low hepatic extraction ratio and a high total plasma clearance, due to extensive urinary excretion of unchanged drug. After oral administration, the plasma concentration vs time curves in most subjects exhibited two marked peaks, an observation that seemed to be constant within individuals and was independent of dose. Bioavailability, estimated as the area under the plasma concentration vs time curves (AUC), after oral doses as compared to the intravenous dose, in most cases exceeded 100%. There was no correlation between bioavailability estimated as AUC and as urinary excretion of unchanged drug. These observations may indicate an enterohepatic circulatory mechanism, predominantly after oral administration. Both unchanged drug and its sulphoxide metabolite appear to be excreted in bile. The latter was shown in vitro to be reduced to cimetidine by fecal bacteria.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00605632
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  • 11
    Electronic Resource
    Electronic Resource
    Influence of food on the absorption of phenytoin in man (1979)
    Springer
    European journal of clinical pharmacology 15 (1979), S. 269-274 
    Details
    ISSN: 1432-1041
    Keywords: phenytoin ; food-intake ; bioavailability ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The influence of food intake on the absorption of phenytoin was examined in eight healthy volunteers, by study of single-dose kinetics following ingestion of phenytoin 300 mg either with a standardized breakfast or on an empty stomach. Blood samples were collected at regular intervals from 0 to 48 h, and serum concentrations of unmetabolized phenytoin were determined by gas chromatography. Serum concentrations of the major metabolite of phenytoin, 4-hydroxyphenytoin, were measured by mass fragmentography. Concurrent intake of food and phenytoin appeared to accelerate absorption of the drug from the formulation used, and the peak concentrations were significantly higher (mean increase 40%) in the postprandial than in the preprandial state. As reflected by the AUC (area under the curve), the amount of drug absorbed was increased during postprandial conditions, although the difference only reached borderline significance. It is suggested that phenytoin should always be taken in a defined relation to meals.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00618516
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  • 12
    Electronic Resource
    Electronic Resource
    Absorption of quinidine from an enteric-coated preparation (1979)
    Springer
    European journal of clinical pharmacology 16 (1979), S. 107-112 
    Details
    ISSN: 1432-1041
    Keywords: quinidine ; enteric-coated tablets ; bioavailability ; gastric emptying ; pH
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The absorption of quinidine from single and multiple doses of an enteric-coated preparation (Systodin®) was studied in seven healthy subjects, and was compared with the pharmacokinetics of intravenously administered quinidine and the results of in vitro dissolution tests of the tablets. Absorption of quinidine began after a variable delay, 2–8 h (mean 4.8) after fasting and 3–10 h (mean 6.1) after food. The rate of absorption varied both in and between individuals. It appeared to be lower when the drug was administered after food. Multiple doses after food gave a pattern of plasma concentration-time curves similar to that found on administration of single doses after food. The delay prior to absorption was prolonged at night. The ratio between the maximum and minimum concentration of quinidine during a dose interval varied from 1.3 to 3.2 (mean 2.0). Bioavailability of quinidine in fasting subjects ranged from 69 to 95% (mean 83); variation was greater when doses were administered after food. The release of quinidine from the enteric-coated preparation was pH dependent and was sustained at low pHs as may be found in the intestines. The results indicate that the absorption of quinidine from the enteric-coated formulation was dependent on the highly variable rate of gastric emptying and the pH of intestinal fluid, and it varied greatly both within and between individuals.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00563116
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  • 13
    Electronic Resource
    Electronic Resource
    Pharmacokinetics of prazepam in man (1979)
    Springer
    European journal of clinical pharmacology 16 (1979), S. 141-147 
    Details
    ISSN: 1432-1041
    Keywords: prazepam ; N-desmethyldiazepam ; bioavailability ; pharmokinetics ; electron-capture gasliquid chromatography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary An original electron-capture gas chromatographic assay was developed for simultaneous measurement of plasma levels of the benzodiazepine derivative prazepam and of its principal unconjugated metabolite, N-desmethyldiazepam. The assay was used to study the pharmacokinetics of the drug and its comparative bioavailability from tablets and from a specially prepared solution. Nine healthy adult volunteers were studied. Each volunteer on one occasion took 30 mg of the drug in tablet form, and on another occasion 30 mg of the drug in solution. In all subjects, N-desmethyldiazepam appeared in plasma shortly after prazepam appeared and reached a peak within four hours of prazepam ingestion. Thereafter plasma N-desmethyldiazepam levels were much higher than plasma prazepam levels throughout. Prazepam became undetectable within six hours of intake, whereas its metabolite could still be measured in plasma fourteen days after dosage. Thus much of the pharmacological action of prazepam may be mediated through its metabolite, N-desmethyldiazepam. In five of the nine subjects, areas under the plasma level curves for the metabolite were not markedly different for the tablet and solution formulations studied. In the other four subjects the area under the curve for the tablets was 50% to 80% of the area under the curve for the solution. The time to reach peak plasma level for the metabolite was shorter after the solution formulation (mean 2.0±SD 1.2 h) than after the tablet formulation (mean 4.2±SD 1.7 h).
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00563121
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  • 14
    Electronic Resource
    Electronic Resource
    Systemic availability of ergotamine tartrate after three successive doses and during continuous medication (1979)
    Springer
    European journal of clinical pharmacology 16 (1979), S. 355-360 
    Details
    ISSN: 1432-1041
    Keywords: ergotamine ; migraine ; bioavailability ; radioimmunoassay ; plasma level ; CSF level ; continuous dosing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Plasma ergotamine concentrations were determined by radioimmunoassay in 10 healthy subjects after a 2 mg oral dose of ergotamine, administered at 24 h intervals on three consecutive days. After the first dose the mean peak plasma level of 0.35±0.05 (SEM) ng/ml was found 1–2 h after administration. In the samples obtained 2 h after the second and third doses, plasma ergotamine levels did not exceed the first peak value. On the other hand, after the third and last dose the plasma ergotamine began to rise slowly, reaching maximum of 0.70± 0.10 ng/ml on the 6th day after administration. This supports the concept of accumulation of the drug or of immunoreactive metabolites. CSF ergotamine was determined in 4 patients, who underwent lumbar puncture for other diagnostic purposes, 1 to 2 h after the 2 mg oral dose. A concentration of 0.40± 0.03 ng/ml was observed. In seven out of 18 migraine patients who were taking ergotamine preparations daily (mean 11.7 mg/week), ergotamine could not be detected in plasma 1 h after administration of the dose. In the remaining migraine patients, the pattern of plasma ergotamine after both the daily and the test doses was similar to that of the 10 healthy subjects. The results in volunteers and migraine patients suggest notable variation in bioavailability of the drug. It seems that in most subjects there is accumulation or tissue redistribution of ergotamine or its immunoreactive metabolites, although in a significant number of migraine patients who use the drug daily, ergotamine does not appear to be biologically available.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00605636
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  • 15
    Electronic Resource
    Electronic Resource
    The pharmacokinetics of diclofenac sodium following intravenous and oral administration (1979)
    Springer
    European journal of clinical pharmacology 16 (1979), S. 405-410 
    Details
    ISSN: 1432-1041
    Keywords: diclofenac ; plasma levels ; intravenous bolus administration ; oral administration ; enteric coating ; bioavailability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The pharmacokinetics of diclofenac were examined following single rapid intravenous injection and also following single oral doses to healthy female volunteers. After intravenous injection plasma levels of diclofenac fell rapidly and were below the limits of detection at 5.5 h postdosing. Individual drug profiles were described by a triexponential function and mean half-lives of the three exponential phases were 0.05, 0.26 and 1.1 h. After oral doses of enteric-coated tablets, the lag time between dosing and the appearance of drug in plasma varied between 1.0 and 4.5 h. However once drug absorption had commenced similar plasma drug profiles were obtained in different individuals. Peak plasma diclofenac levels ranged from 1.4 to 3.0 µg · ml−1. The mean terminal drug half-life in plasma was 1.8 h after oral doses. This value was not significantly greater than the value of 1.1 h following intravenous doses. Fifty percent of orally dosed diclofenac did not reach the systemic circulation due, predominantly, to first-pass metabolism.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00568201
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  • 16
    Electronic Resource
    Electronic Resource
    Maturation and senescence of an insect chemosensory response (1979)
    Springer
    Journal of chemical ecology 5 (1979), S. 587-594 
    Details
    ISSN: 1573-1561
    Keywords: Electroantennogram ; acceptors ; Pseudaletia unipuncta ; maturation ; senescence ; age ; benzaldehyde ; benzyl alcohol ; male pheromone ; Lepidoptera ; Noctuidae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Electroantennogram responses of male and femalePseudaletia unipuncta to the two major components of the presumed pheromone associated with the male anterior abdominal scent brushes vary with age. There is a postemergence period of maturation of responsiveness, followed by senescence. The age of maximum responsiveness differs according to the sex and to the compound tested.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00987843
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  • 17
    Electronic Resource
    Electronic Resource
    Specificity of trail markers of forest and eastern tent caterpillars (1979)
    Springer
    Journal of chemical ecology 5 (1979), S. 565-574 
    Details
    ISSN: 1573-1561
    Keywords: Lepidoptera ; Lasiocampidae ; Malacosoma americanum ; Malacosoma disstria ; Tortricidae ; Archips cerasivoranus ; trail marker ; pheromone ; interspecific response ; tent caterpillar
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Exploratory trails deposited on paper strips by the forest tent caterpillar (FTC),Malacosoma disstria Hubner, and the eastern tent caterpillar (ETC),M. americanum (Fabricius), as well as extracts of these trails, readily elicited interspecific trail-following behavior. In 2-choice tests involving simple Y mazes constructed from these paper strips, the caterpillars of both species preferred by approximately 3∶1 the trails of the FTC. Studies involving whole colonies of the ETC maintained under nearnatural conditions in the laboratory, however, indicated that the trails deposited by successful foragers of the ETC as they returned to their tent from feeding sites were more attractive than the exploratory trails of either the ETC or FTC. The pronounced interspecific response of these congeners to each other's trails suggests that they utilize either qualitatively similar or identical trail-marking chemicals. Both species preferred their own trails to those ofArchips cerasivoranus (Fitch) (Tortricidae), providing the first evidence that more distantly related lepidopterous larvae utilize distinct trails.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00987841
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  • 18
    Electronic Resource
    Electronic Resource
    Divergence in pharmacokinetic parameters of quinidine obtained by specific and nonspecific assay methods (1979)
    Springer
    Journal of pharmacokinetics and pharmacodynamics 7 (1979), S. 303-311 
    Details
    ISSN: 1573-8744
    Keywords: quinidine ; pharmacokinetic parameters ; assay methods ; assay specificity ; area under the plasma concentration-time curve ; bioavailability ; clearance ; therapeutic window
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Previously published estimates of pharmacokinetic characteristics of quinidine can be shown to be dependent on whether the investigators have used analytical methods which are specific for quinidine. Areas under the plasma concentration-time curve and peak plasma concentrations after administration of the drug were higher and clearance values consequently lower in studies utilizing nonspecific assays unable to distinguish quinidine from its metabolites. The error introduced is larger after oral administration as a result of marked first-pass metabolism of quinidine. The absolute oral bioavailabilities from pharmaceutical preparations might therefore be estimated higher in studies with assays including metabolites in the determination. Although the pharmacodynamic response to quinidine is related to the plasma concentration, the therapeutic window of drug concentrations has been defined only using nonspecific assays. In light of the availability of newly developed specific assays, redefinition of the range of therapeutic plasma concentrations is opportune.
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    Pharmacokinetics of ampicillin and its prodrugs bacampicillin and pivampicillin in man (1979)
    Springer
    Journal of pharmacokinetics and pharmacodynamics 7 (1979), S. 429-451 
    Details
    ISSN: 1573-8744
    Keywords: ampicillin ; bacampicillin ; pivampicillin ; prodrug ; bioavailability ; zero-order absorption ; two-compartment model ; renal clearance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Five healthy fasting male subjects were each given single doses of intravenous ampicillin (471 mg), oral ampicillin tablets (495 mg), oral bacampicillin hydrochloride tablets (562 mg ampicillin equivalent), and oral pivampicillin hydrochloride capsules (491 mg ampicillin equivalent) in a crossover experiment. The resulting concentrations of ampicillin were determined in plasma and urine. The pharmacokinetic analysis was made according to a two-compartment open model. The total distribution volume of unbound ampicillin during the disposition phase was 0.247 ± 0.045 (sd) liter/kg, which is only slightly more than the extracellular fluid, suggesting that tissue binding and intracellular distribution of ampicillin are limited. The bioavailability of the esters bacampicillin (86 ± 11%) and pivampicillin (92± 18%) was significantly greater than that of ampicillin (62 ± 17%); however, the difference between the esters was not statistically significant. The absorption for all drugs given orally proceeded at a constant rate, suggesting zero-order release rates from the products. The absorption rate was highest for bacampicillin (0.89 ± 0.39% of dose absorbed per minute), followed by pivampicillin (0.64 ± 0.19) and ampicillin (0.58 ± 0.16). Bacampicillin also had the shortest lag time for the start of absorption (7.0 ± 0.9 min) under the present conditions. Thus, in comparison with ampicillin, the esters have a higher bioavailability, which, in fact, is close to the theoretically highest possible value by clearance concepts. The higher bioavailability in connection with higher absorption rates may be clinically important in ampicillin treatment by the oral route.
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    URL: http://dx.doi.org/10.1007/BF01062386
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    Pharmacokinetics/pharmacodynamics of furosemide in man: A review (1979)
    Springer
    Journal of pharmacokinetics and pharmacodynamics 7 (1979), S. 1-27 
    Details
    ISSN: 1573-8744
    Keywords: furosemide ; renal failure ; congestive heart failure ; bioavailability ; diuretic effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The pharmacokinetics of furosemide and the attempt to correlate biological fluid measurements with diuretic response have been the subject of a large number of studies since the original reports of HajdÚ, Rupp, and coworkers in the mid-1960s. This article attempts to critically review these studies under seven different sections: furosemide pharmacokinetics in normal volunteers, furosemide pharmacokinetics in patients with decreased renal function, furosemide pharmacokinetics in patients with congestive heart failure, furosemide metabolism and assay methods, furosemide bioavailability, dose-response relationships, and the role of inhibitors and mediators on furosemide effects. The literature is reviewed through August 1978.
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    URL: http://dx.doi.org/10.1007/BF01059438
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    Bioavailability of imipramine tablets relative to a stable isotope-labeled internal standard: Increasing the power of bioavailability tests (1979)
    Springer
    Journal of pharmacokinetics and pharmacodynamics 7 (1979), S. 233-248 
    Details
    ISSN: 1573-8744
    Keywords: bioavailability ; confidence intervals ; hypothesis testing ; imipramine ; internal standard ; mass spectrometry ; power ; relative bioavailability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A new methodology for comparative bioavailability testing is described in which each drug formulation is compared with a stable isotope-labeled variant of the drug that is consumed orally in solution at the same time the tested formulation is ingested. The methodology is used to determine the comparative bioavailabilities of two commercially available brands of imipramine hydrochloride. The power of the new methodology to detect differences between drug formulations, when, in fact, such differences exist, is shown to be superior to that of conventional bioavailability tests.
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    Evolution of male sterility mechanisms in gynodioecious and dioecious species ofCirsium (Cynareae, Compositae) (1979)
    Springer
    Plant systematics and evolution 132 (1979), S. 327-332 
    Details
    ISSN: 1615-6110
    Keywords: Compositae ; Cynareae ; Cirsium ; Gynodioecy ; subdioecy ; dioecy ; male sterility ; sex ; evolution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The genusCirsium comprises both gynodioecious and dioecious species. The observation of microsporogenesis in female plants ofC. montanum, C. oleraceum, C. palustre andC. spinosissimum shows that the male sterility is due to a degeneration of the tapetum. This degeneration occurs more or less early according to the species and, in the light of these results, a scheme of evolution in the male sterility mechanism is proposed. Furthermore, the male sterility mechanism inC. montanum is very similar to that previously found in female plants of the dioecious speciesC. arvense. This fact enhances the possibility of evolution of the dioecy ofC. arvense from the gynodioecy found in other species. According to these results, a general scheme of evolution of sexes in the genusCirsium is proposed.
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    Selection for yield in wheat breeding (1979)
    Springer
    Euphytica 28 (1979), S. 37-40 
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    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; selection ; single seed descent ; early generation yield tests
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary If selection based on F3 yield tests is to be effective, the yield tests must be successful in discriminating among yield genotypes. The available literature indicates that simple tests with limited or no replication are not very effective, although more extensive, replicated tests may be. Data from an experiment comparing F3 yield tests with a single seed descent procedure showed that F3 selection based on a two-replicate test with single seed descent procedure did not justify the extra work involved.
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    Stem solidness and its relationship to grain yield in 17 spring wheat crosses (1979)
    Springer
    Euphytica 28 (1979), S. 89-91 
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    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; stem solidness ; Cephus cinctus ; wheat stem sawfly resistance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Stem solidness in the wheat plant provides resistance to the wheat stem sawfly, a pest of wheat in Montana and North Dakota, but some agronomists have been concerned that stem solidness might be related to low grain yields. We evaluated 17 spring wheat crosses for stem solidness, grain yield, and other agronomic traits in F2 through F4 generations from 1972 to 1975. Highly significant correlation (0.735) and regression (0.731) coefficients between F2 and F3 generations verify previous studies showing that stem solidness is highly heritable and that selection in F2 should be successful. Solid-stemmed F4 composites yielded more than hollow stemmed composites at Bozeman and equal yields were obtained at Huntley, indicating that stem solidness is not a deterrent to high grain yield.
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    Morphology of the prothoracic defensive gland ofSchizura concinna (J.E. Smith) (Lepidoptera:Notodontidae) and the nature of its secretion (1979)
    Springer
    Journal of chemical ecology 5 (1979), S. 165-177 
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    ISSN: 1573-1561
    Keywords: Schizura concinna ; Lepidoptera ; Notodontidae ; prothoracic ; defensive gland ; allomone ; defensive secretion ; decyl acetate ; dodecyl acetate ; 2-tridecanone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The larval defensive gland ofSchizura concinna (J.E. Smith) is situated in the thorax and consists of two sacs joined by an interglandular neck. Its orifice opens into a transverse invagination of the integument at the cervical margin of the prosternite. The major component of the defensive secretion, formic acid, was identified as itsp-bromophenacyl ester. Ancillary components decyl acetate, dodecyl acetate, and 2-tridecanone from the anterior portion of the gland were identified by GLC and GS-MS.
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    Sex pheromone of the black cutworm moth,Agrotis ipsilon (1979)
    Springer
    Journal of chemical ecology 5 (1979), S. 439-457 
    Details
    ISSN: 1573-1561
    Keywords: Insect sex pheromone ; insect attractant ; Agrotis ipsilon ; Lepidoptera ; Noctuidae ; black cutworm moth ; Cucullia intermedia ; (Z)-7-dodecen-1-yl acetate ; (Z)-9-tetradecen-1-yl acetate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract (Z)-7-Dodecen-1-yl acetate (I) and (Z)-9-tetradecen-1-yl acetate (II) have been identified as sex pheromone components of the black cutworm moth,Agrotis ipsilon (Hufnagel). They are emitted by the female in approximately a 5∶1 ratio. Differential saturation studies with male antennae suggest that there are two different acceptor sites for the two pheromone components. The most effective lures found in field trapping tests were 30 μg of I plus 10 μg of II on a rubber septum, and a 3∶1 mixture of I and II dispensed from a 0.2-mm-ID glass capillary tube sealed at one end.
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    In vitro maintenance of the sex pheromone gland of the female Indian meal mothPlodia interpunctella (Hübner) (1979)
    Springer
    Journal of chemical ecology 5 (1979), S. 653-662 
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    ISSN: 1573-1561
    Keywords: Tissue culture ; sex pheromone gland ; Lepidoptera ; Pyralidae ; Plodia interpunctella ; Indian meal moth
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Sex pheromone glands ofPlodia interpunctella were isolated from surface-sterilized donors of different ages, freed of most of the attached gut, oviduct, and other tissues; rinsed in sterile medium; and cultured in 1 ml of culture medium. The sex pheromone gland cells that were cultured for 10 days in either chemically defined Grace's medium or modified Grace's medium appeared normal in histological examinations. Bioassays of extracted medium in which pheromone glands from mature females had been incubated showed that a greater percentage of the available pheromone was recovered from modified Grace's medium than from chemically defined Grace's medium.
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    Sex pheromone components of the obliquebanded leafroller moth,Choristoneura rosaceana (1979)
    Springer
    Journal of chemical ecology 5 (1979), S. 3-11 
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    ISSN: 1573-1561
    Keywords: Sex pheromone ; sex attractant ; Choristoneura rosaceana ; Lepidoptera ; Tortricidae ; obliquebanded leafroller ; (Z)-11-tetradecen-1-yl acetate ; (E)-11-tetradecen-1-yl acetate ; (Z)-11-tetradecen-1-ol ; (E)-11-− tetradecen-1-ol ; (Z)-11-tetradecenal
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Previously, (Z)-11-tetradecen-1-yl acetate was reported as the sex pheromone of the obliquebanded leafroller,Choristoneura rosaceana (Harris). A mixture of 92% (Z)-11-tetradecen-1-yl acetate and 8% (E)-tetradecen-1-yl acetate has been reported as an attractant for this insect. (E)-11-tetradecen-1-yl acetate and (Z)-11-tetradecen-1-ol have now been isolated and identified from female tip extracts and shown to be behaviorally active; in addition, there is some evidence for the presence of (E)-11-tetradecen-1-ol in these extracts. TheZ∶E ratio for both the acetates and the alcohols in these tip extracts was about 98∶2; the proportion of alcohols was rather variable, but the acetates always predominated. Maximum trap catches fn the field during the course of this study were obtained with 5 mg of 95∶5 (Z)∶(E)-11-tetradecen-1-yl acetates containing 0.5–10% (Z)-11-tetradecen-1-ol (approx. 1%Eisomer) in polyethylene caps. No evidence was found for the presence of (Z)-11-tetradecenal in female tip extracts, and this compound was found to be ineffective in increasing trap catches.
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    Components of the sex pheromone of the female spotted stalk borer,Chilo partellus (Swinhoe) (Lepidoptera: Pyralidae): Identification and preliminary field trials (1979)
    Springer
    Journal of chemical ecology 5 (1979), S. 153-163 
    Details
    ISSN: 1573-1561
    Keywords: Sex pheromone ; sex attractant ; Lepidoptera ; Pyralidae ; Chilo partellus ; spotted stalk borer ; electroantennography ; (Z)-11-hexadecenal ; (Z)-11-hexadecen-1-ol ; (Z)-9-tetradecenyl formate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract FemaleChilo partellus (Swinhoe) abdominal tip extracts were examined by gas-liquid chromatography (GLC) combined with simultaneous electroantennographic (EAG) recording from the male moth. Two olfactory stimulants were detected and identified as (Z)-11-hexadecenal (I) and (Z)-11-hexadecen-1-ol (II) by their GLC behavior, microchemical reactions, and comparison with synthetic materials. Both compounds were detected in volatiles emitted by the “calling” female moth. Synthetic (Z)-9-tetradecenyl formate, a structural analog of aldehyde (I), also elicited a significant EAG response from the male moth. Field trials carried out in India using synthetic (I) and (II) as bait in water traps showed that compound (I) was highly attractive to maleC. partellus; compound (II) was not attractive, and its addition to (I) significantly reduced trap catches.
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    Sex pheromone cross-attraction among four species of pine tip moths,Rhyacionia species (1979)
    Springer
    Journal of chemical ecology 5 (1979), S. 205-210 
    Details
    ISSN: 1573-1561
    Keywords: Rhyacionia spp. ; tip moths ; sex pheromones ; cross attraction ; pheromone specificity ; Lepidoptera ; Tortricidae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Field tests utilizing crude pheromone extracts fromRhyacionia frustrana, R. rigidana, R. subtropica, andR. buoliana showed thatR. subtropica andR. buoliana were mutually attractive.R. frustrana was attracted in low numbers to bothR. subtropica andR. buoliana, butR. subtropica andR. buoliana did not significantly respond toR. frustrana. R. rigidana did not respond to pheromone extracts from any otherRhyacionia spp., nor was it attractive to the others. Cross-attraction occurred among those species which were largely allopatric and shared few tree hosts.
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    (Z)-9-tetradecen-1-ol acetate (1979)
    Springer
    Journal of chemical ecology 5 (1979), S. 721-725 
    Details
    ISSN: 1573-1561
    Keywords: Fall armyworm ; Spodoptera frugiperda ; Lepidoptera ; Noctuidae ; pheromone ; sex attractant ; secondary sex pheromone ; (Z)-9-tetradecen-1-ol acetate ; (Z)-9-dodecen-1-ol acetate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract (Z)-9-Tetradecen-1-ol acetate [(Z)-9-TDA], identified originally as the sex pheromone of the fall armyworm,Spodoptera frugiperda (J.E. Smith), acted as a secondary sex pheromone when it was tested in sticky traps in field tests. Low-level synergism was obtained when 2 and 10% quantities of (Z)-9-TDA were added to 100 μg of (Z)-9-dodecen-1-ol acetate, which is now considered the primary sex pheromone.
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    Chemical conversion of 9-tetradecen-1-ol acetates to 3,13-octadecadien-1-ol acetates, sex attractants for male clearwing moths (Lepidoptera: Sesiidae) (1979)
    Springer
    Journal of chemical ecology 5 (1979), S. 759-766 
    Details
    ISSN: 1573-1561
    Keywords: Sex pheromone ; attractants ; 9-tetradecen-1-ol acetate ; 3,13-octadecadien-1-ol acetate ; clearwing moth ; Lepidoptera ; Sesiidae ; synthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Males of many species of clearwing moths are attracted by one of the geometrical isomers of 3,13-octadecadien-1-ol acetate or by a mixture of isomers. The synthesis of (E,Z)-, (E,E)-, and (Z,E)-3,13-octadecadien-1-ol acetate is described starting with the (Z)- and (E)-9-tetraceden-1-ol acetates, which are commercially obtainable.
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    Inheritance, heritability and breeding behaviour of three sources of resistance to Septoria tritici in wheat (1979)
    Springer
    Euphytica 28 (1979), S. 385-392 
    Details
    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; backcrosses ; breeding behaviour ; genetic correlation ; heritability ; heading date ; inheritance ; plant height ; Septoria tritici
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary We examined the inheritance, heritability, and breeding behaviour of resistance to Septoria tritict in the spring wheat cultivars Seabreeze, Veranopolis, and IAS-20 in crosses to the susceptible Australian spring cultivar Gamenya. Resistance in Seabreeze was higher than that in Veranopolis and IAS-20. Inheritance of resistance in Seabreeze seems to be determined by at least three recessive genes. Resistance in Veranopolis and IAS-20 might be due to a single gene. Similarity of inheritance patterns and breeding behaviour of the resistance from Veranopolis and IAS-20 and the common ancestry of these two cultivars suggest that they may carry the same gene. Standard unit heritabilities of Septoria scores, as measured by correlation of F2 plant with F3 family mean data, were high (57–68%). Parent offspring genetic correlations confirmed previously reported associations between resistance and lateness and resistance and tall plant height, but correlations were not sufficiently high to be a major obstacle to selection. Resistance in Veranopolis and IAS-20 were easily recovered in first backcrosses while that in Sea breeze was more difficult to recover.
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    An analysis of genes for resistance against Indian stem rust races in two bread wheat cultivars (1979)
    Springer
    Euphytica 28 (1979), S. 651-660 
    Details
    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; Puccinia graminis ; stem rust resistance ; inheritance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The genetic constitution of two bread wheat accessions from the International Spring Wheat Rust Nurseries (E 5883 and E 6032) has been studied for reaction to four Indian races of stem rust. Analysis of E 5883 has revealed that for each of the races 15C, 21 and 40 a single dominant gene operates for resistance. The dominant gene against race 15C was identified as Sr6. The dominant genes for resistance against races 21 and 40 were found to be different from the genes described so far. Resistance against race 122 is controlled by a single recessive gene producing characteristically a ‘2’ type of reaction. This gene was identified as Sr8. The resistance of E 6032 against each of the races 15C, 21 and 40 is controlled by two genes, one dominant and one recessive, which act independently. Dominant genes effective against 15C, 21 and 40 were conclusively identified as Sr6, Sr5 and Sr9b, respectively. From the correlated behaviour against races 15C and 40 as well as from the phenotypes of the resistance reactions rhe same recessive gene, undescribed so far, operates against the two races. The second recessive gene operating against race 21 was also observed to be different from those so far designated. E 6032 was, however, found to be susceptible to races 122. The presence of Sr6 both in E 5883 and E 6032 against race 15C was further confirmed through F2 and F3 segregation data.
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    Bioavailability of p-chlorophenoxyisobutyric acid (clofibrinic acid) after repeated doses of its calcium salt to humans (1978)
    Springer
    European journal of clinical pharmacology 13 (1978), S. 49-53 
    Details
    ISSN: 1432-1041
    Keywords: p-Chlorophenoxyisobutyric acid ; clofibrate ; steady-state plasma concentrations ; bioavailability ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Plasma concentrations and bioavailability of clofibrinic acid have been estimated under conditions approaching the steady-state during a ten-day period of administration as clofibrate or as a calcium clofibrinate-carbonate combination (1:1 w/w) at a dosage interval of 12 h. Formulation — related differences in bioavailability were not significant, and the 95% confidence limits of these differences were within −2% to +8% of the mean for the reference formulation of clofibrate. The mean steadystate plasma concentrations of clofibrinic acid measured on the tenth day of dosing were 116 µg/ml±22 S.D. and 119 µg/ml±23 S.D. after administration of 885 mg as clofibrate and the calcium clofibrinate-carbonate combination respectively. The peaks of mean plasma concentrations were 70 µg/ml±15 S.D., 119 µg/ml±32 S.D. and 131 µg/ml±26 S.D. on the first, fifth and tenth day of dosing with clofibrate, and 62 µg/ml±13 S.D., 127 µg/ml±S.D. and 143 µg/ml±25 S.D. on the corresponding days of dosing with the calcium clofibrinate-carbonate combination. After the last dose on the tenth day of dosing, the mean apparent half-lives of elimination of clofibrinic acid from plasma were 24.2 h±4.4 S.D. and 25.5 h±3.2 S.D. after administration of clofibrate and the calcium clofibrinate-carbonate combination respectively.
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    Gastrointestinal absorption of hydrochlorothiazide enhanced by concomitant intake of food (1978)
    Springer
    European journal of clinical pharmacology 13 (1978), S. 125-128 
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    ISSN: 1432-1041
    Keywords: bioavailability ; diuretics ; gastrointestinal absorption ; hydrochlorothiazide ; thiazides ; food effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Hydrochlorothiazide (hct) 75 mg was administered orally to eight healthy volunteers without (Study I) or together with a standardized meal (Study II), and plasma and urine concentrations of hct were analyzed by GLC. The plasma levels of hct were higher initially when the tablets were taken on an empty stomach, but after 5 h they were higher in Study II. There was no difference between the two studies in the area under plasma concentration time curves. The urinary recovery of hct totalled 55.6±4.9 mg when the drug was given with food and 47.4±6.0 when it was taken on an empty stomach. The difference is significant (p〈0.01). As the urinary recovery represents the uptake of hct, it appears that the gastrointestinal absorption of hct is enhanced when the drug is given with food.
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    Dose tolerance and pharmacokinetic studies of L (+) pseudoephedrine capsules in man (1978)
    Springer
    European journal of clinical pharmacology 14 (1978), S. 253-259 
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    ISSN: 1432-1041
    Keywords: Pseudoephedrine ; side effects ; bioavailability ; multiple oral dosing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Dose tolerance and pharmacokinetic studies of pseudoephedrine sustained action capsules were performed in thirty-three adult male subjects who received either 120 mg or 150 mg capsules every twelve hours for seven consecutive days in a double-blind parallel design study. Although only one subject in the 150 mg group was discontinued prematurely from this study, a large number of side effects typical of CNS stimulation were seen. A placebo effect might account for a portion of these complaints, however symtoms evaluated as being due to drug were significantly more severe and persistent in the 150 mg group. Pulse rates showed a persistent and significant increase while systolic and diastolic blood pressure fell from the baseline values in both groups. A pharmacokinetic analysis of the pseudoephedrine plasma concentration-time data provided estimates of half-life and the volume of distribution/availability ratio. The values obtained were in good agreement with values reported by others. Half-life was not influenced by urine pH probably as a result of the narrow range of urine pHs observed in the subjects. Calculations of relative bioavailability suggest that the 120 mg capsule formulation has a 30% greater bioavailability compared to the 150 mg capsule.
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    Absorption of oral and intramuscular chlordiazepoxide (1978)
    Springer
    European journal of clinical pharmacology 13 (1978), S. 267-274 
    Details
    ISSN: 1432-1041
    Keywords: Chlordiazepoxide ; benzodiazepines ; pharmacokinetics ; bioavailability ; intramuscular injection ; alcohol withdrawal
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The absorption of oral and intramuscular (i. m.) chlordiazepoxide hydrochloride (CDX · HCl) was compared in two pharmacokinetic studies. In Study One, single 50-mg doses of CDX · HCl were administered orally and by i. m. injection to 14 healthy volunteers using a crossover design. Whole-blood concentrations of chlordiazepoxide (CDX) and its first active metabolite, desmethylchlordiazepoxide (DMCDX), were determined in multiple samples drawn after the dose. Mean pharmacokinetic variables for CDX following oral and i. m. administration, respectively, were: highest measured blood concentration, 1.65 vs 0.87 µg/ml (p〈0.001); time of highest concentration, 2.3 vs 7.6 h after dosing (p〈0.001); apparent absorption half-life, 0.71 vs 3.39 h (p〈0.001). Biphasic absorption after i. m. injection, consistent with precipitation at the injection site, was observed in 9 of 14 subjects. Based upon comparison with previous intravenous data, the completeness of absorption was 100% for oral vs 86% for i. m. CDX · HCl (p〈0.1). In Study Two, 28 male chronic alcoholics with clinical manifestations of the acute alcohol withdrawal syndrome were randomly assigned to one of four treatment conditions: 50 or 100 mg doses of CDX · HCl, by mouth or by i. m. injection. Concentrations of CDX and DMCDX, determined in plasma samples drawn every 20 min for 5 h following the dose, were significantly higher after oral administration of a given dose than at corresponding points in time after i.m. injection after the same dose. Thus absorption of oral CDX is reasonably rapid and complete, whereas the absorption rate of i. m. CDX is slow.
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    Bioavailability of norethindrone in human subjects (1978)
    Springer
    European journal of clinical pharmacology 13 (1978), S. 35-39 
    Details
    ISSN: 1432-1041
    Keywords: Norethindrone ; bioavailability ; man ; competitive protein binding ; sex differences ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary A competitive protein binding assay for norethindrone was developed to measure plasma levels in human subjects. The plasma levels were considerably higher in women than in men, especially at low dose levels. The plasma levels were directly related to the dose in men; but greater variations in the plasma levels were observed in women. The plasma half-life was about 5 h in both sexes with single oral doses of 5 to 20 mg. A comparative bioavailability study with norethindrone from 2 different manufacturers, formulated in the same manner, showed no significant differences in absorption characteristics and provided sufficient data for pharmacokinetic analysis.
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    URL: http://dx.doi.org/10.1007/BF00606680
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    The pharmacokinetics of slow-release procainamide (1978)
    Springer
    European journal of clinical pharmacology 14 (1978), S. 261-265 
    Details
    ISSN: 1432-1041
    Keywords: Procainamide ; slow release formulations ; bioavailability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Procainamide was given to 20 patients with normal renal function as an i.v. bolus of 500 mg followed by 1.0 or 1.5 g eight-hourly by mouth in the form of a slow release preparation (Durules). 97.6±27.1 (SD)% of the oral procainamide was absorbed, the absorption half life being 1.54 h. The elimination half life following the oral formulation was 6.0±0.8 h, compared to a mean of 3.4±0.4 h following i.v. administration. Elimination half life following i.v. administration was slightly related to acetylator status, being 2.75±0.9 h in fast acetylators, and 4.4±2.4 h in slow acetylators. This dependence on acetylator status was not seen in half life following oral administration. Total body clearance, steady state plasma procainamide and N-acetylprocainamide were not significantly dependent on acetylator status, although a few patients who are slow acetylators had unexpectedly low clearance and high steady state procainamide concentrations when given the higher dose.
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    URL: http://dx.doi.org/10.1007/BF00560459
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    The comparative bioavailability of Lanoxin tablets and Lanoxicaps with and without sorbitol (1978)
    Springer
    European journal of clinical pharmacology 14 (1978), S. 357-360 
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    ISSN: 1432-1041
    Keywords: Lanoxin tablets ; Lanoxicaps ; sorbitol ; bioavailability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary (1) The mean cumulative urinary digoxin excretion over 8 days was compared in 8 healthy volunteers after single doses of digoxin administered as 3 Lanoxin tablets of 0.25 mg, 3 digoxin tablets of 0.2 mg, 12 Lanoxicaps without sorbitol of 0.05 mg, 6 Lanoxicaps without sorbitol of 0.1 mg digoxin, 3 Lanoxicaps without sorbitol of 0.2 mg and 3 Lanoxicaps with sorbitol of 0.2 mg. (2) There was no significant difference between the 8 day cumulative urinary excretion for any of the Lanoxicaps treatments. (3) Cumulative urinary excretion after 3 digoxin tablets of 0.2 mg was significantly (P〈0.05) lower than after all other treatments. (4) Cumulative urinary excretion after 3 Lanoxin tablets of 0.25 mg was not significantly different from that after any of the Lanoxicaps treatments except 0.1 mg Lanoxicaps without sorbitol, it was significantly (P〈0.05) lower after the latter. (5) Mean urinary excretion of digoxin was 60% of ingested dose for all Lanoxicaps treatments and was significantly (P〈0.05) higher than the mean value of 50% for both tablet treatments. (6) Enhanced absorption of digoxin from Lanoxicaps was confirmed and shown to be unrelated to the sorbitol content of the capsule shell.
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    Genetic aspects of wheat gliadin proteins (1978)
    Springer
    Biochemical genetics 16 (1978), S. 831-853 
    Details
    ISSN: 1573-4927
    Keywords: Triticum aestivum L. ; wheat ; storage proteins ; gliadins ; gel electrophoresis ; endosperm ; dominant genes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Inheritance of gliadin components unique to three different varieties of common wheat (Triticum aestivum L.) was studied in F1 and F2 seeds of intervarietal crosses using protein patterns obtained by polyacrylamide gel electrophoresis in aluminum lactate buffer (pH 3.2). The patterns of F1 seeds of the crosses Cheyenne × Justin and INIA 66R × Justin evidenced all the bands present in the patterns of the parents; band intensities reflected gene dosage levels dependent on whether the contributing parent was maternal or paternal in accordance with the triploid nature of endosperm tissue. Most of the gliadin components examined segregated in accordance with control by a single dominant gene, but in two instances single bands in the one-dimensional electrophoretic patterns segregated in the F2 as expected if controlled by two genes. A method of two-dimensional electrophoresis was developed that resolved these apparently single bands into two components each, which could segregate independently. Linkage analysis provided evidence of codominant alleles and closely linked genes coding for gliadin protein components in both coupling and repulsion situations. The gliadin protein components seem to be coded for by clusters of genes located on chromosomes of homoeologous groups 1 and 6 in hexaploid wheats.
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    URL: http://dx.doi.org/10.1007/BF00484739
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    Linear systems analysis in pharmacokinetics (1978)
    Springer
    Journal of pharmacokinetics and pharmacodynamics 6 (1978), S. 265-282 
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    ISSN: 1573-8744
    Keywords: pharmacokinetics ; linear systems analysis ; in vivo dissolution rates ; absorption rates ; metabolic rates ; bioavailability ; numerical desconvolution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The application of certain aspects of linear systems analysis to pharmacokinetic-problems is described. Topics covered include the evaluation of in vivodissolution rates, absorption rates, and metabolic rates, and the use of pharmacological data. Relevant numerical procedures are also discussed.
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    URL: http://dx.doi.org/10.1007/BF01312266
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    Dose-dependent bioavailability of tetracycline in man (1978)
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    Journal of pharmacokinetics and pharmacodynamics 6 (1978), S. 99-110 
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    ISSN: 1573-8744
    Keywords: bioavailability ; tetracycline HCl capsules ; dose dependency ; brand dependency ; water ingestion ; urinary excretion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Seven healthy male volunteers were administered, on different occasions, one, two, and three capsules of two commercially available brands (A and B) each containing 250 mg tetracycline HCl. Urinary excretion rates and cumulative amounts of drug excreted in the urine in 4 days were used to assess the bioavailability of the two brands at the different doses studied. The rate constants of absorption and elimination of tetracyline were similar at all dose levels. However, the extent of absorption (F)appears to be dependent on the brand, dose, and volume of water ingested with the drug. Fof Brand B was not significantly different than that of brand A at the 250-mg dose but was decreased by 23.3% (p〈0.01)at the 500-mg dose and by 19.7% (p 〈0.05) at the 750-mg dose. With respect to dose, Fof each brand at the 500-mg dose was not significantly different than its value at the 250-mg dose. However, Fof brand A at the 750-mg dose was reduced by 14.8% (p 〈0.05) and that of brand B by 21.1% (p 〈0.05) relative to their respective values at the single dose. Surprisingly, when the 750-mg dose of brand A was ingested with a small volume of water, Fwas increased by 18.9% (p 〈0.05) compared to the ingestion of the identical dose of the same brand under waterloading conditions.
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    Statistical moments in pharmacokinetics (1978)
    Springer
    Journal of pharmacokinetics and pharmacodynamics 6 (1978), S. 547-558 
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    ISSN: 1573-8744
    Keywords: statistical moments ; network theory ; pharmacokinetics ; bioavailability ; deconvolution ; plasma concentration-time curve ; urinary excretion rate-time curve ; compartment models
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Statistical moments are parameters that describe the characteristics of the time courses of plasma concentration (area, mean residence time, and variance of residence time) and of the urinary excretion rate that follow administration of a single dose of a drug. The relationship between the moments of a time-course curve and pharmacokinetic profiles of drug disposition, i.e., absorption, distribution, metabolism, and excretion, is described. The moments are related to the extent and rate of bioavailability, and it is shown that they can be effectively applied to the deconvolution operation.
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    Critical evaluation of the potential error in pharmacokinetic studies of using the linear trapezoidal rule method for the calculation of the area under the plasma level-time curve (1978)
    Springer
    Journal of pharmacokinetics and pharmacodynamics 6 (1978), S. 539-546 
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    ISSN: 1573-8744
    Keywords: trapezoidal rule ; area under the curve ; pharmacokinetics ; clearance ; bioavailability ; integration method ; sulfisoxazole
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The linear trapezoidal rule method is commonly used for the estimation of the area under the plasma level-time curve. Error analyses are performed when the method is used in first-order absorption and first-order elimination kinetics in the one-compartment system. It is found that significant underestimations and overestimations in area during the absorption phase and postabsorption phase, respectively, can occur when the method is improperly used. During the exponential postabsorption phase the relative error is only a function of the ratio (n)of the time interval over the half-life of the two plasma data points in the interval. The error from the linear trapezoidal rule method at n=0.5 is about 1%. The error increases to 15.5% and 57.1 % when nis increased to 2 and 4, respectively. It is recommended that for most absorption studies the linear trapezoidal method be used for prepeak and plateau plasma data and the logarithmic trapezoidal method for postpeak plasma data.
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    Absorption of oral tetracycline in patients with Billroth-II gastrectomy (1978)
    Springer
    Journal of pharmacokinetics and pharmacodynamics 6 (1978), S. 295-303 
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    ISSN: 1573-8744
    Keywords: tetracycline ; antibiotics ; Billroth-II gastrectomy ; gastrectomy ; pharmacokinetics ; bioavailability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The bioavailability of a single 250-mg oral dose of tetracycline hydroghloride was studied in seven patients following Billroth-II gastrectomy in comparison with seven control subjects matched for age and body weight. There were no significant differences between control subjects and gastrectomized patients in the apparent lag time prior to the start of absorption (23.6 vs. 22.8 min), peak serum tetracycline concentration (1.72 vs. 1.75 μg/ml), the time of attainment of peak concentrations (3.35 vs. 3.42 hr), the apparent first-order absorption half-life (1.8 vs. 1.4hr), or the apparent first-order elimination half-life (8.0 vs. 8.7hr). Completeness of tetracycline absorption, as judged by area under the 24-hr serum concentration curve, did not differ significantly between the two groups, nor did 24-hr urinary excretion of tetracycline. Thus the abnormalities of gastrointestinal structure and function produced by Billroth -II gastrectomy do not result in impairment of the rate and completeness of tetracycline absorption.
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    Genetic control of spikelet number per ear with particular reference to rate of spikelet initiation in hexaploid wheat, Triticum aestivum L.em.Thell.Thell. (1978)
    Springer
    Euphytica 27 (1978), S. 69-74 
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    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; spikelet number ; spikelet initiation ; development response ; quantitative inheritance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Inheritance of spikelet number per ear and rate of spikelet initiation in wheat (Triticum aestivum L. em. Thell.) was studied in the ‘land race’ spring wheats, 8–23 and 8–27 from Afghanistan, under controlled temperature and photoperiod. Spikelet number per ear was found to be under simple genetic control with dominance for high spikelet number. It is suggested that the gene determining spikelet number does so by determining the rate of spikelet initiation.
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    URL: http://dx.doi.org/10.1007/BF00039120
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    Inheritance of slow rusting to stem rust in wheat (1978)
    Springer
    Euphytica 27 (1978), S. 95-107 
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    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; Puccinia graminis ; wheat stem rust ; black rust resistance ; inheritance of slow rusting
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The inheritance of the slow rusting character was studied on F5 progenies from seven spring wheat cultivars (Triticum aestivum) crossed in all possible combinations without reciprocals. The cultivars and their progenies were evaluated for slow rusting in 1974 and 1975 in epidemics of Puccinia graminis f. sp. tritici, races 15 and 151, and traces of other races. Slow rusting varied significantly among the parents and among the F5 progeny of each cross. Transgressive segregation occurred in each cross, i.e. some progeny rusted more slowly than the parents and some faster. In crosses with both Idaed 59 and Kenya 58 the progeny distributions were skewed towards slow rust development but the distributions in the other crosses were normal. The genetic control of slow rusting was predominantly additive, and narrow sense heritability was approximately 80 percent. The number of segregating genes having an effect on slow rusting was estimated to be 2 to 12 pairs depending on the cross. Correlation between slow rusting and maturity was usually negative but in most crosses the relationship was small.
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    Factors affecting genotypic and environmental variance for crude protein content in cereals (1978)
    Springer
    Euphytica 27 (1978), S. 117-126 
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    ISSN: 1573-5060
    Keywords: Hordeum vulgare ; barley ; Triticum aestivum ; Triticum durum ; wheat ; genotypic variance ; environmental variance ; protein content ; nitrogen fertilizer
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The effects of N fertilizer, irrigation and location on genotypic and environmental variances of barley and wheat varieties were studied in a series of trials. Genotypic variance for crude protein content, as well as for grain yield, tended to be higher under high N fertilizer rate (80 kg N/ha). The effect of N fertilizer rate on environmental variance varied with variety and location. Increase in crude protein content resulted in decrease in environmental variance for only a few of the varieties tested. The effect of quantity of irrigation water on genotypic and environmental variance for crude protein content was small.
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    URL: http://dx.doi.org/10.1007/BF00039126
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    The genomes of Arachis hypogaea. 1. Cytogenetic studies of putative genome donors (1978)
    Springer
    Euphytica 27 (1978), S. 665-675 
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    ISSN: 1573-5060
    Keywords: Arachis hypogaea ; groundnut ; peanut ; putative genome donors ; evolution ; origin ; karyotypes ; amphidiploidy ; chromosome pairing ; Arachis batizocoi ; Arachis cardenasii ; phytogeography
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Cytological studies of wild diploid Arachis species in the same section of the genus (sect. Arachis) as the cultivated peanut A. hypogaea L. show, with one exception, a karyotype characterized by the presence of 9 pairs of larger chromosomes and one pair of small (‘A’) chromosomes. The exceptional species A. batozocoi Krap. et Greg. has a more uniform karyotype. Interspecific hybrids between diploid species of similar karyotype have moderate to high pollen stainability, those involving A. batizocoi have zero pollen stainability and a very irregular PMC meiosis. Such infertile hybrids are the most likely to produce fertile, stable amphidiploids on doubling the chromosome complement. It is suggested that the cultivated peanut could have originated from such a sterile interspecific hybrid and on morphological and phytogeographic grounds the most likely genome donors are A. cardenasii (nomen nudum) and A. batizocoi of the species within section Arachis, which have been collected up to the present time.
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    Practical breeding for durable resistance to rust diseases in self-pollinating cereals (1978)
    Springer
    Euphytica 27 (1978), S. 529-540 
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    ISSN: 1573-5060
    Keywords: Self-pollinating cereals ; Triticum aestivum ; wheat ; differential resistance ; durable resistance ; genetic control ; horizontal resistance ; non-race-specific resistance ; partial resistance ; race-specific resistance ; slow rusting ; specific virulence ; uniform resistance ; vertical resistance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The rust pathogens of cereals exist as populations of races that differ in their ability to attack various varieties. Varieties that are resistant when first released often become susceptible later due to the spread of previously undetected races but the time taken for this to occur in very variable. It often occurs so rapidly as to curtail the commercial use of otherwise satisfactory varieties. Some varieties, however, are widely grown for many years and remain adequately resistant to the prevalent rust diseases. They may aptly be described as having durable resistance. This durable or long-lasting resistance can be detected without any assumptions about, or detailed knowledge of, whether durability depends on any particular mechanisms of resistance, on various degrees of racespecificity or on many or few genes. Cappelle-Desprez is given as an example of a wheat variety with durable resistance to yellow rust. The most powerful test for the detection of durable resistance occurs when a variety is widely grown commercially for several years. A much weaker test is obtained by growing varieties in small disease nursery plots even when the test is repeated for several years. Usually, resistance which is durable is also partial or incomplete. Often, however, partial resistance of wheat to yellow rust has not been durable. Thus the observation that resistance is partial is not, of itself, a satisfactory criterion for the detection of durable resistance. It is suggested that the most obvious sources of durable resistance for use in breeding programmes are varieties which have been widely grown and have displayed this character. The transfer of such resistance during breeding may be achieved if the creation or incorporation of higher levels of resistance that have not been tested for durability is avoided. It should then be possible to derive resistance from the durably. resistant parent. Methods of achieving this are discussed.
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    Genetics of resistance in the wheat cultivar chhoti lerma against stem rust race 122 (1978)
    Springer
    Euphytica 27 (1978), S. 461-464 
    Details
    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; Puccinia graminis ; stem rust ; resistance ; inheritance ; monsomic analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Genetics of rust resistance against stem rust race 122 in ‘Chhoti Lerma’ was studied both by conventional and aneuploid analysis. Observations on F1, F2 and F2 backcross progenies revealed the operation of two recessive genes, controlling resistance in ‘Chhoti Lerma’. Monosomic analysis confirmed the operation of two recessive genes conferring resistance to race 122 located on chromosomes 1D and 7D. A minor gene or modifier was also located on chromosome 1B. This was concluded from the fact that F2 of mono's x ‘Chhoti Lerma’ exhibited skewness in favour of resistant plants.
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    Effectiveness of genes for leaf rust resistance in international wheat rust nurseries, 1970–1975 (1978)
    Springer
    Euphytica 27 (1978), S. 511-519 
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    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; Puccinia recondita ; leaf rust ; resistance genes ; data base
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract Monogenic lines resistant to leaf rust of spring and winter wheats were grown in the world wheat-producing areas from 1970 through 1975. Lines containing the alleles Lr9 (Wi), Lr9 (Tc), and Lr19 (Tc) were more resistant to the leaf rust pathogen than those containing Lr1 (Tc), −1 (Wi), −1,3 (Wi), −2A (Tc), −2A (Wi), −2D (Tc), −3 (Tc), −3 (Wi), −10 (Tc), −16 (Tc), −17 (Tc), −18 (Tc), or −2D (Pld). Monogenic line Lr1 (Wi) possibly has more than one gene for resistance and resistance properties similar to cultivars with ‘field resistance’. A computer data base was created to produce the information used in this paper.
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    Date of heading and plant height of wheat varieties, as related to septoria leaf blotch damage (1978)
    Springer
    Euphytica 27 (1978), S. 577-580 
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    ISSN: 1573-5060
    Keywords: Truicum aestivum ; wheat ; Septoria tritici ; Septoria leaf bloth
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Septoria leaf blotch readings, date of heading and plant height appeared strongly correlated in six variety trials with 25 varieties each. Three trials were conducted in 1972 and three in 1976. The taller and later the cultivars, the lower its Septoria leaf blotch score tended to be. The yields also were less strongly reduced in taller and later cultivars, as calculated from another experiment.
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    Nitrogen uptake and nitrogen harvest index in durum wheat cultivars varying in their grain protein concentration (1978)
    Springer
    Euphytica 27 (1978), S. 561-566 
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    ISSN: 1573-5060
    Keywords: Triticum durum ; wheat ; durum wheat ; nitrogen harvest index ; harvest index ; grain protein
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary In a field experiment, plant (excluding roots) and grain nitrogen at harvest were estimated in 15 durum wheat cultivars varying in their grain protein concentration. They showed significant variation in grain yield, grain protein concentration, biological yield, total plant nitrogen at harvest and residual nitrogen in straw. Harvest index and nitrogen harvest index were calculated from this primary data. Nitrogen harvest index varied from 57 to 83%. Plant nitrogen showed significant positive correlation with biological yield, grain yield and grain protein yield, but the correlations with grain protein concentration, harvest index and nitrogen harvest index were not significant. Nitrogen harvest index was positively correlated with harvest index indicating that the distribution of N between straw and grain to a large extent, but not entirely, depends upon the partitioning of dry matter between the two. Grain protein concentration was neither correlated significantly to plant nitrogen nor to nitrogen harvest index.
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    Aneuploid analysis for protein content and tyrosinase activity in hexaploid wheat (Triticum aestivum L. em. Thell.) (1978)
    Springer
    Euphytica 27 (1978), S. 805-810 
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    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; kernel protein content ; tyrosinase enzyme ; aneuploid analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary A study was conducted to locate the genes responsible for the determination of kernel protein content and tyrosinase activity in a hexaploid wheat variety UP 301 using Pb. C591 monosomic series. Genes located on chromosomes 4B, 5B, 6B, 7B, 3D and 7D of UP 301 controlled protein content of UP 301. Of these the B genome chromosomes were found to have genes for increased protein content while the D genome chromosomes were found to carry genes for low protein content. A major gene coding for tyrosinase enzyme was detected on chromosome 6B of UP 301 and a modifier on chromosome 5B. This indicated the possibility of improving these quality characters through chromosome manipulation.
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    Effect of lidocaine on the absorption, disposition and tolerance of intramuscularly administered cefoxitin (1977)
    Springer
    European journal of clinical pharmacology 12 (1977), S. 273-279 
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    ISSN: 1432-1041
    Keywords: Cefoxitin ; lidocaine ; intramuscular ; bioavailability ; pain
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The use of lidocaine HCl solution at concentrations of 0.5 and 1.0% to reconstitute sodium cefoxitin relieves the pain associated with intramuscular injections of the antibiotic. Cefoxitin absorption by the intramuscular route is initially rapid and is virtually complete. Peak serum concentrations, corresponding to about one-half those of a comparable intravenous infusion, are achieved in 30 min. Continuing absorption tends to maintain higher serum concentrations for longer times. Renal clearance and serum half-life of cefoxitin do not appear to be affected by lidocaine at its effective anaesthetic concentrations.
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    Bioavailability of metronidazole in fasting and non-fasting healthy subjects and in patients with Crohn's disease (1977)
    Springer
    European journal of clinical pharmacology 12 (1977), S. 69-72 
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    ISSN: 1432-1041
    Keywords: Metronidazole ; serum concentration ; bioavailability ; food intake ; healthy subjects ; Crohn's disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The possible influence of food intake on the bioavailability of metronidazole was examined in ten healthy volunteers by administration of a single dose of metronidazole on an empty stomach, and with a standardized breakfast. Food intake did not significantly alter the bioavailability of metronidazole. The interindividual variation in bioavailability appeared to be slight. In nine patients with Crohn's disease, the absorption of metronidazole appeared to be reduced and to be more variable than in healthy subjects. In both groups there was a clear relationship between the amount absorbed and dose/kg body weight. Thus, from the pharmacokinetic point of view, metronidazole can safely be given either with or between meals. The dose should be related to body weight.
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    URL: http://dx.doi.org/10.1007/BF00561408
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    Bioavailability of three phenytoin preparations in healthy subjects and in epileptics (1977)
    Springer
    European journal of clinical pharmacology 12 (1977), S. 285-290 
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    ISSN: 1432-1041
    Keywords: Phenytoin acid ; phenytoin calcium ; bioavailability ; inequivalence of generics ; normal subjects ; volunteers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Serum phenytoin concentrations have been studied in epileptic patients and healthy subjects taking tablets of phenytoin calcium (Desitin), A, phenytoin acid (Desitin), B, and phenytoin acid (Nordmark), C. Retrospective data and prospective investigation of hospitalized patients on long-term phenytoin treatment showed that significantly higher serum concentrations of phenytoin were produced by the phenytoin acid preparations B and C than by the phenytoin calcium preparation A. In a cross over study six volunteers received 200 mg/day of preparations A, B, and C for three weeks. In this study, too, higher phenytoin serum concentrations were produced by B and C than by A, although the differences were not statistically significant. The reasons for the discrepancies between the studies in healthy and epileptic subjects are discussed.
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    Human pharmacokinetics and bioavailability of temazepam administered in soft gelatin capsules (1977)
    Springer
    European journal of clinical pharmacology 12 (1977), S. 383-386 
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    ISSN: 1432-1041
    Keywords: Benzodiazepine ; temazepam ; pharmacokinetics ; bioavailability ; hard and soft gelatine capsules
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Plasma levels of temazepam were determined in healthy subjects after single oral administration of soft and hard gelatin capsules, and after 7 consecutive night-time doses in soft capsules. Absorption from soft gelatin capsules was significantly faster and produced earlier and higher peak plasma levels. The two pharmaceutical forms did not show any significant difference in relative availability. The apparent half-life of temazepam after night-time administration was significantly shorter than after morning administration, but no change in half-life was observed between the first and seventh night-time doses.
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    Proscillaridin activity in portal and peripheral venous blood after oral administration to man (1977)
    Springer
    European journal of clinical pharmacology 11 (1977), S. 277-281 
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    ISSN: 1432-1041
    Keywords: Proscillaridin ; oral administration ; portal venous sample ; porto-peripheral concentration difference ; bioavailability ; 86Rb-uptake inhibition assay
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The absorption of proscillaridin A was studied in four patients undergoing catheterization of the portal vein for diagnostic purposes. Proscillaridin 1.5 mg was given as a single oral dose and plasma glycoside activity was analyzed by the86Rb-uptake inhibition technique. Proscillaridin appeared rapidly in the portal blood, peak activity being found after 15 min in three and after 30 min in one patient. In peripheral blood the peak activity occurred after approximately 35 min. Despite rapid passage across the gut wall, porto-peripheral differences in glycoside activity were small; they were zero after 4 h. The mean amount absorbed as active proscillaridin during the first 4 h after the dose was calculated to be only 7.1% of the given amount. Late porto-peripheral differences, probably due to enterohepatic recycling, appeared after 6 h in three patients. The results suggest that proscillaridin undergoes first pass inactivation in the gut wall. Enterohepatic recirculation may contribute to the amounts of active glycoside that reach the systemic circulation.
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    URL: http://dx.doi.org/10.1007/BF00607677
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    Plasma concentrations, bioavailability and dissolution of chlorpropamide (1977)
    Springer
    European journal of clinical pharmacology 11 (1977), S. 207-212 
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    ISSN: 1432-1041
    Keywords: Chlorpropamide ; hypoglycaemic agent ; bioavailability ; plasma concentrations ; bioequivalence ; dissolution tests
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The bioavailability of chlorpropamide from two new formulations (Melitase® tablets) has been compared to that from a reference formulation which is currently in clinical use as a hypoglycaemic agent. In both rate and extent of bioavailability, all three formulations may be considered equivalent, providing allowances are made for differences in drug content. With 95% confidence, the mean bioavailability of chlorpropamide from the new formulations was within about 16% of the mean from the reference formulation, and formulation-related differences were not statistically significant. Although all three formulations were shown to have similar dissolution profiles, dissolution of chlorpropamide was pH-dependent in vitro. Dissolution was almost complete during 30 min at pH 7.2, but only 40%–60% had dissolved during 90 min at pH 2.0. A peak mean concentration of 22.7 µg/ml was reached 3 h after administration of 2×100 mg tablets of the new formulation and peak mean concentrations of 26.8 µg/ml and 27.4 µg/ml were reached 3 h and 4 hours after administration of one 250 mg tablet of the new formulation and one 250 mg tablet of the reference formulation respectively. Formulation-related differences of mean plasma concentrations (after scaling for equal doses of 250 mg) were not significant and each formulation provided similar plasma concentrations at corresponding times after administration. Statistically significant subject-related differences in all the parameters of bioavailability were shown by analyses of variance.
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    First pass hydroxylation of nortriptyline: Concentrations of parent drug and major metabolites in plasma (1977)
    Springer
    European journal of clinical pharmacology 11 (1977), S. 219-224 
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    ISSN: 1432-1041
    Keywords: Nortriptyline ; 10-OH-nortriptyline ; bioavailability ; plasma metabolites ; first pass metabolism ; oral dose ; intramuscular dose
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Nortriptyline was given orally and intramuscularly to six depressed patients. Plasma concentrations of parent drug and the unconjugated and conjugated principal metabolite, 10-hydroxynortriptyline, were determined by mass fragmentography. There was a significant decrease in the area under the nortriptyline plasma concentration — time curve after the oral route of administration, whilst the elimination rate was unchanged. With the oral dose, plasma concentrations of the metabolites were higher and peaked earlier than after intramuscular administration, whilst the opposite was true for the parent compound. This proves that the difference in bioavailability between the two routes of administration was due to first pass metabolism. As determined from the ratio between corresponding areas, the relative bioavailability of the oral dose was 66±21 S.D. per cent. This fraction is higher than that reported previously when intravenous nortriptyline was used as the reference dosage form.
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    Influence of nutritional status on plasma levels and relative bioavailability of tetracycline (1977)
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    European journal of clinical pharmacology 12 (1977), S. 281-284 
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    ISSN: 1432-1041
    Keywords: Tetracycline ; bioavailability ; plasma levels ; nutritional state ; man
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Relative bioavailability after oral administration of a single dose and Cmin levels of tetracycline in plasma after multiple doses were determined in groups of well-nourished and undernourished subjects. The relative bioavailability of tetracycline, assessed by the area under serum concentration time-curves, did not differ in undernourished and well-nourished patients. The plasma levels were not different in the two groups after the conventional dose of tetracycline HCl 250 mg at 6 hour intervals. However, in these studies undernourished subjects received a higher dose per kg body weight, which could have compensated for any effect of a shortened half life of the drug. When the dose per kg body weight was reduced, the Cmin levels were lower. On the other hand, with the same dose per kg body weight at more frequent intervals, the plasma concentrations were similar to those in well-nourished subjects. These studies indicate that the dosage regimen should be based both on body weight and on the nutritional status of the individual.
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    The effect of an antacid on the bioavailability of indomethacin (1977)
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    European journal of clinical pharmacology 12 (1977), S. 65-68 
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    ISSN: 1432-1041
    Keywords: Indomethacin ; antacids ; drug-drug interactions ; bioavailability ; drug combinations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The biovailability of indomethacin from two indomethacin-antacid (aluminum hydroxide magnesium carbonate and magnesium hydroxide) combinations was compared with the bioavailability of oral indomethacin. Relative bioavailability was estimated by three methods: comparison of plasma concentrations at various times, comparison of areas under plasma concentration time curves, and comparison of the amount of drug excreted unchanged in the urine. A double blind three-way crossover study was conducted in twelve healthy volunteers. The combination with the slightly smaller amount of antacid (preparation A) showed significantly decreased bioavailability by all three methods in comparison with indomethacin alone (preparation C). The combination with the larger amount of antacid (preparation B) was also less bioavailable than preparation C. This effect was significant only for the comparison of areas under curves and not for plasma levels, although the mean plasma levels produced by preparation B at all times were lower than those for preparation C. These findings suggest that aluminum hydroxide magnesium carbonate and magnesium hydroxide decrease the bioavailability of indomethacin.
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    Pharmacokinetics of tolmetin with and without concomitant administration of antacid in man (1977)
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    European journal of clinical pharmacology 12 (1977), S. 421-428 
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    ISSN: 1432-1041
    Keywords: Tolmetin ; pharmacokinetics ; bioavailability ; antacid ; oral dose
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The purpose of this study was to determine whether a concomitant single dose of antacid or multiple doses of antacid administered prior to, and with tolmetin, alter the pharmacokinetics of tolmetin when the drug was administered as a commercially available tablet containing tolmetin sodium. The possible effects of the antacid on plasma concentrations and urinary excretion of tolmetin and its major metabolite were evaluated following administration of: (a) tolmetin sodium alone; (b) antacid four time a day for three days prior to a single dose of tolmetin sodium, with continuation of the antacid during the day tolmetin was given; and (c) co-administration of single doses of tolmetin sodium and antacid. The twenty-four subject study was of the crossover type. There were no significant differences among treatment means for: (i) peak plasma concentrations of both tolmetin and metabolite, (ii) AUC 0–8 h and AUC 0-∞ for both tolmetin and metabolite, (iii) time to peak plasma concentration for both tolmetin and metabolite, (iv) plasma concentrations of both tolmetin and the metabolite at all sampling times (except for tolmetin at 2 h), (v) renal clearance of both tolmetin and its metabolite, and (vi) the amount of metabolite excreted in the 0–24 h urine. There were small, but significant, differences among amounts of tolmetin excreted in the 0–24 h urine. Semilogarithmic plots of both tolmetin and metabolite plasma concentrations past the peak concentrations were curved over the entire 8-h observation period; although the elimination half-life of tolmetin has been reported to be about one hour, the half-life most probably exceeds 2.6 h in most subjects. The results of this study indicate a lack of a significant drug-drug interaction between the non-steroidal anti-inflammatory agent, tolmetin sodium, and a commonly used antacid, which is a mixture of magnesium and aluminium hydroxides.
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    Pharmacokinetics of coumarin and its 7-hydroxy-metabolites upon intravenous and peroral administration of coumarin in man (1977)
    Springer
    European journal of clinical pharmacology 12 (1977), S. 457-461 
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    ISSN: 1432-1041
    Keywords: Coumarin ; 7-Hydroxycoumarin ; drug disposition ; first-pass effect ; bioavailability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The pharmacokinetics of coumarin (C) upon i.v. and p.o. administration and its metabolites 7-hydroxy-coumarin (7-HC) and 7-hydroxy-coumarin glucuronide (7-HCG) have been studied. Six healthy volunteers were involved in this investigation. Four of the volunteers participated in a crossover study. Coumarin was administered i.v. and p.o. in dose sizes of 0.25 mg/kg and 0.857 mg/kg, respectively. Coumarin is rapidly absorbed p.o., however the availability to systemic circulation is less than 4%. The rest of the dose appears quantitatively as 7-HC and 7-HCG in systemic circulation suggesting an extensive firstpass effect. Coumarin and 7-HCG are best fitted to an open two-compartment model, whereas 7-HC is best fitted to an open one-compartment model. The biological half-life of both C (0.80 vs. 1.02 h) and 7-HCG (1.47 vs. 1.15 h) was not significantly different for the two routes of administration. The large total clearance of C again suggests a first-pass effect; while that of 7-HCG, which is nearly exclusively eliminated into urine, indicates active tubular secretion of the glucuronide.
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    Location of chromosomal control of GA-induced enzyme release by distal half-grains of wheat (1977)
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    Biochemical genetics 15 (1977), S. 47-57 
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    ISSN: 1573-4927
    Keywords: wheat ; chromosomes ; gibberellin ; enzymes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The three enzymes, α-amylase, peroxidase, and acid phosphatase, are among those released by the aleurone of bread wheat, Triticum aestivum, as a direct response to gibberellins (GA) from the embryo during germination. Aneuploid genotypes are used to investigate the chromosomal location, nature, and extent of genetic control of the release of these enzymes in endosperms after induction by exogenous GA. Ditelosomics demonstrate the effect of removal of known chromosome arms, and tetrasomics show the effect of duplication of chromosome pairs. Quantitative analysis demonstrates complex control systems over and above those previously found using zymogram techniques. For α-amylase, chromosome arms with net promoter effects and chromosomes with net inhibitor effects were found. These effects were not chromosome-dosage responsive, unlike the promoter-inhibitor system found for acid phosphatase control. Peroxidase levels in the endosperms were generally high in both types of aneuploids. With one exception, all chromosomes showing involvement as ditelosomics showed a similar effect as tetrasomics, indicating that in the euploid a balanced state restricting, rather than promoting, peroxidase levels existed.
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    Serum esterase genetics in rabbits. IV. The prealbumin and β-globulin systems (1977)
    Springer
    Biochemical genetics 15 (1977), S. 989-1000 
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    ISSN: 1573-4927
    Keywords: genetics ; esterases ; evolution ; rabbit ; mouse
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Discontinuous starch gel electrophoresis revealed a fourth allele of rabbit prealbumin serum esterase at locus Est-2. This allele is designated Est-2 f and appears to be silent. In addition to the prealbumin serum esterases, another serum esterase system was studied in rabbits. This system is localized in the β-globulin region. Genetic analysis indicated that one locus with two codominant alleles controls the variation in this region. Linkage of this system with Est-1 and Est-2 of the prealbumin serum esterases was demonstrated. Comparison of the arrangement of these esterase loci on linkage group VI with the esterase loci on chromosome 8 of the mouse gives additional support for the theory of evolutionary conservation of chromosomal segments coding for mammalian esterases.
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    Ultrastructure of a scent scale organ with pressure discharge in male Caligo eurilochus brasiliensis (Fldr.) (Lepidoptera: Brassolidae) (1977)
    Springer
    Cell & tissue research 177 (1977), S. 87-103 
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    ISSN: 1432-0878
    Keywords: Scent scales ; Lepidoptera ; Secretion discharge ; Gland cells ; Insect cuticle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The abdominal scent apparatus of male Caligo eurilochus was examined at different ages by light, scanning and transmission electron microscopy. The glandular epithelium is covered with specialized scales and forms a pad on each side of the 4th to 6th abdominal segments. The pads are surrounded by smooth, elastic cuticle and can protrude toward the opposite hind wing hair pencil. The scales have a poreless cuticle with a fibrillar texture. They are impregnated by an oily, slowly volatile substance. The scales are elongated toward the base, forming hoods over the long coneshaped sockets. The scale pedicel is anchored tension-free by rootlets in the central socket base. The slightly asymmetric cuticular sockets are very elastic, due to their high water content. They are stabilized by internal epicuticular rods. The release of the secretions from the cell and a possibly active microvillar transport is discussed. Different secretions are found in the space between the microvillar surface of the gland cell and the socket floor. They are probably discharged from the supraglandular space into the scale lumen by means of pressure and bending of the sockets. A flowback might be prevented by capillary effect of a “ball” of vesicles, which lies exactly above the outlet of the scale pedicel.
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    Amounts of ribosomal DNA inAllium (Liliaceae) (1977)
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    Plant systematics and evolution 128 (1977), S. 201-208 
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    ISSN: 1615-6110
    Keywords: Liliaceae ; Allium (sect.Allium) ; Nucleolus organizers ; rRNA/DNA hybridization ; rRNA gene amounts ; evolution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Eight species ofAllium subgen.Allium sect.Allium have been studied at the cytological level by means of karyological analyses and at the biochemical level with regard to the proportions of ribosomal DNA. All the species have a basic genome of x = 8.A. sativum, A. commutatum, A. ampeloprasum, andA. vineale possess approximately 0.050% rDNA and two nucleolus organizer regions per basic chromosome set.A. sphaerocephalon andA. arvense have two nucleolus organizers, andA. amethystinum three nucleolus organizers per haploid (n = x) genome: the three species possess approximately 0.075% rDNA.A. acutiflorum has five nucleolus organizer regions per haploid genome and 0.121% rDNA. An attempt to relate these differences with functional and ecological characteristics indicates that evolutionary variation of rDNA proportions is not casual. Such data also can help to define systematic affinities and circumscribe infrageneric taxa.
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    Evolutionary implications of herbivory onVernonia (Compositae) (1977)
    Springer
    Plant systematics and evolution 128 (1977), S. 277-286 
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    ISSN: 1615-6110
    Keywords: Compositae ; Vernonieae ; Vernonia ; Lepidoptera ; Insect resistance ; antifeedant ; sesquiterpene lactones ; glaucolide-A
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A field insect feeding experiment was conducted with two species ofVernonia which produce the sesquiterpene lactone glaucolide-A, one species which does not contain this bitter compound, and two F1 hybrid combinations. Also, naturalVernonia populations were observed over a two year period for their degree of herbivory. Contrary to the pattern observed in laboratory feeding preference tests,Vernonia flaccidifolia, the species lacking sesquiterpene lactones, was consistently fed upon less by insects than wereV. gigantea andV. glauca. Even though glaucolide-A appears to adequately protect some Vernonias against herbivores, especially mammals,Vernonia flaccidifolia has lost this compound. ApparentlyV. flaccidifolia has evolved an alternative defensive mechanism which is more effective against insects but less effective against mammalian herbivores.
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    Bioavailability assessment: Methods to estimate total area (AUC 0-∞) and total amount excreted (A e ∞ ) and importance of blood and urine sampling scheme with application to digoxin (1977)
    Springer
    Journal of pharmacokinetics and pharmacodynamics 5 (1977), S. 533-557 
    Details
    ISSN: 1573-8744
    Keywords: accelerated convergence method to estimate AUC0-∞ and A e ∞ ; bioavailability ; estimation of total areas ; estimation of total amounts excreted ; blood sampling schemes for digoxin ; elimination half-life of digoxin ; intra- and interindividual variation of renal clearance of digoxin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Five methods are compared to estimate the total area under the digoxin plasma or serum concentrationtime curve (AUC0-∞) after a single dose of drug. To obtain accurate estimates of AUC0-∞, data required are concentrations at a sufficient number of sampling times to define adequately the concentration-time curve prior to the log-linear phase, and at least three, but preferably four or more equally spaced points in the terminal loglinear phase. One method (designated Method I) requires a digital computer; another (Method III) is the classical method (these two methods do not require equally spaced points in the loglinear phase). Method IIA is the accelerated convergence method of Amidon et al.; Methods IIB and IIC are modifications of this method, but incorporate usual and orthogonal least squares, respectively, which make them more accurate with real (noisy) data. Methods I and IICgave very comparable estimates of AUC0-∞. Results indicate that digoxin administered orally in aqueous solution was completely (100%) absorbed when bioavailability estimates were based on oral and intravenous AUC0-∞ estimates and the actual doses, whereas formerly only about 80% absorption was reported, based on areas, under plasma concentration curves which were truncated at 96 hr. It is shown that the sampling scheme of blood can produce biased apparent bioavailability estimates when areas under truncated curves are employed, but an appropriate sampling scheme and application of method IIyield accurate bioavailability estimates. This is important particularly in those bioavailability studies where one is attempting to determine the appropriate label dose for a new “fastrelease” digoxin preparation relative to the label dose and bioavailability of currently marketed tablets. It is shown that the magnitudes and variability of apparent elimination rate constants and halflives of digoxin, estimated from urinary excretion data by the σ− method, depend on which value of A e ∞ is used. The formerly reported greater interindividual variability of AUC data compared to At data for digoxin is explained in that the AUCs, but not the Ae,'s, involve the renal clearance, which exhibits considerable inter- and intraindividual variation.
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    Effect of antacids on aspirin dissolution and bioavailability (1977)
    Springer
    Journal of pharmacokinetics and pharmacodynamics 5 (1977), S. 597-613 
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    ISSN: 1573-8744
    Keywords: aspirin ; dissolution ; bioavailability ; effect of antacids ; acid ; capacity ; consuming ; in vivo ; buffering effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The in vitrodissolution profile, in vitroand in vivobuffering characteristics, and single-dose bioavailability of various buffered aspirin tablet formulations were studied. Buffering agents,such as magnesium and aluminum hydroxides (formulations B and C) or magnesium carbonate and aluminum glycinate (formulation D), significantly increased the rate of aspirin dissolution from solid dosage forms as compared to an unbuffered tablet (formulation A). The extent of aspirin absorption was equivalent with all formulations;however, the faster rate of dissolution (t50 and t90)with buffered formulations resulted in earlier and higher peak concentration of salicylate compared to that with unbuffered formulation, following a two-tablet dose in the fasting state. A comparison of the in vivobuffer capacity of a four-tablet dose of formulations B and D was performed in the postcibal state at the time of maximal meal-induced acid secretion, using a radiotelemetry procedure for determination of pH. Formulation B prolonged the interval of elevation of intragastric pH 〉 3 for 32 min as compared to 12 min for D.
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    Bioavailability of 11 phenytoin products (1977)
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    Journal of pharmacokinetics and pharmacodynamics 5 (1977), S. 133-146 
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    ISSN: 1573-8744
    Keywords: bioavailability ; phenytoin sodium capsules ; plasma levels ; human studies
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Eleven single lots of 100-mg phenytoin sodium capsules were evaluated for their relative bioavailability in 12 normal human volunteers. These products were manufactured by eight different companies and met all compendial specifications. The products were evaluated with respect to plasma levels at various times up to 96 hr following administration of single 100-mg doses, times of peak level, peak plasma concentrations, and areas under the plasma level—time curve. Several of the products exhibited statistically significant differences in the various parameters studied.
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    Pharmacokinetics of propranolol in normal healthy volunteers (1977)
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    Journal of pharmacokinetics and pharmacodynamics 5 (1977), S. 183-192 
    Details
    ISSN: 1573-8744
    Keywords: propranolol ; kinetics ; volunteers ; bioavailability ; threshold dose
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The pharmacokinetics of propranolol in blood was studied in healthy volunteers, following intravenous administration of 0.1 mg/kg and increasing oral doses of 10,20, and 40 mg, using a specific and sensitive gas Chromatographie method. The systemic availability of orally administered propranolol varied from 9% to 38% between subjects, but it was constant within each subject. A linear relationship was found between the area under the blood concentration-time curve and the oral dose. At variance with literature data, we could not observe a threshold dose.
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    2n gametes in potato species and their function in sexual polyploidization (1977)
    Springer
    Euphytica 26 (1977), S. 585-600 
    Details
    ISSN: 1573-5060
    Keywords: Solanum ; potato ; polyploidy ; 2n gametes ; sexual polyploidization ; evolution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The extent and pattern of polyploidy in the tuber-bearing Solanums varies among the many taxanomic series that have been identified in this subsection of Solanum. While several series appear to be entirely diploid, others exhibit a range of ploidy levels from 2x to 6x, and some contain only polyploid species. In many diploid, triploid and tetraploid species 2n gametes (gametes or gametophytes with the sporophytic chromosome number) have been detected. Both 2n eggs and 2n pollen occur. 2n gametes provide the opportunity for unilateral and bilateral sexual polyploidization. The genetic determination and consequences of sexual polyploidization strongly suggest that 2n gametes have been the major instrument in the polyploid evolution of the tuber-bearing Solanums. Somatic doubling of species and interspecific hybrids appears to be of very limited importance. New evidence for the occurrence of 2n eggs and 2n pollen in many species is reported, and data from the literature are added to illustrate the widespread distribution of 2n gametes throughout the subsection. A very high correlation is found between polyploidy and 2n gametes, and its significance is discussed. Proof is presented for the occurrence of alleles governing 2n pollen production in the cultivated tetraploids, providing additional evidence for the hypothesis that 2n gametes have been involved in their origin. Multiple unilateral and bilateral sexual polyploidizations are proposed for the origin of the cultivated tetraploids: this accounts for the large variability encountered in this group, which closely resembles that of the related diploids. Similar evolutionary pathways are hypothesized for the other polyploid complexes in the subsection. A scheme is proposed in which participation of both 2n and n gametes link together all ploidy levels in the tuber-bearing Solanums, thus overcoming the ploidy barriers and providing for gene flow throughout the sympatric species of the subsection.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00021684
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    The association of genes for purple coleoptile with chromosomes of the wheat variety Mironovskaya 808 (1977)
    Springer
    Euphytica 26 (1977), S. 475-479 
    Details
    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; anthocyanins ; centromere ; chromosome mapping ; crossover units ; dominant genes ; monosomics ; partially dominant ; purple coleoptile ; suppressors ; telocentric chromosome
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The association of genes for purple pigment in the coleoptile with the chromosomes of the winter wheat variety Mironovskaya 808 was investigated using monosomic F2 analysis. The segregation ratio for F2 hybrids of Chinese Spring monosomics x Mironovskya 808 seems to indicate that the purple colour of the coleoptile is determined by two dominant genes, Rc3 and Rc4, which are located on the chromosomes 7D and 6B respectively, and which reinforce each other. Apart from these two genes, suppressors found on the chromosomes 2A, 2B, 2D, 4B and 6A also play a role in the intensity of the purple colour. With the aid of a Chinese Spring telocentric chromosome marker it was observed that the Rc3 gene is located on the chromosome arm 7DS, at a distance of 16±4.23 crossover units from the centromere.
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    URL: http://dx.doi.org/10.1007/BF00027010
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  • 80
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    Flag leaf area in five spring wheat crosses and the relationship to grain yield (1977)
    Springer
    Euphytica 26 (1977), S. 739-744 
    Details
    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; flag leaf area ; grain yield
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Five spring wheat crosses were evaluated over a 6-year period using comparisons between F2 and F3 data and between near-isogenic F4 populations selected for flag leaf area. Nonsignificant r values for F2 vs. F3 flag leaf measurements may be due to the effect of environment on flag leaf area, but are probably also an indication of low heritability for this plant character. Near-isogenic populations selected on the basis of flag leaf area showed little difference in grain yield, an indication that other plant parts must be more influential in determining grain yield. Flag leaf area, by itself, appears not to be a good index to plant performance.
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    URL: http://dx.doi.org/10.1007/BF00021700
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  • 81
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    Utilization of tom thumb source of pre-harvest sprouting tolerance in a wheat breeding programme (1977)
    Springer
    Euphytica 26 (1977), S. 565-572 
    Details
    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; pre-harvest sprouting ; Tom Thumb derivatives ; GA3 response index ; apparent α-amylase synthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Segŕegating populations of the cross Tordo (a spring white-grained Tom Thumb derivative) and Tr 454-16 (a spring white-grained Sonora-Gabo derivative) were studied for plant height, apparent α-amylase synthesis (AAS) and response to gibberellic acid. Means, variances and heritabilities for these characters were computed and their association was studied by computing correlation coefficients. Plant height showed high heritability while AAS and response to GA3 showed moderate heritability. Plant height was positively correlated with AAS and response to GA3. The results pointed out the importance of using Tom Thumb as a source of pre-harvest sprouting tolerance in a wheat breeding programme, particularly in areas where wheat breeding is restricted to evolving white-grained cultivars.
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    URL: http://dx.doi.org/10.1007/BF00021682
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    Genetic and environmental variability in wheat characteristics reported to be involved in morphological resistance to wheat stem rust (1977)
    Springer
    Euphytica 26 (1977), S. 123-128 
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    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; stem rust ; Puccinia graminis tritici ; generalized resistance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Four morphological characteristics of wheat peduncles were evaluated for genetic and environmental variability. The thickness of the epidermis and the amount and distribution of chlorenchyma tissue in the peduncle were measured. The genetic variability was estimated to be large, whereas the environmental variability was small. It was also concluded that cultivars could be screened for morphological characteristics of the peduncle that contributed to non-specific resistance to stem rust with a minimum sample size of about 10 plants per replication from a single location.
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    URL: http://dx.doi.org/10.1007/BF00032077
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    Adaptation of semidwarf wheat cultivars to rainfed conditions (1977)
    Springer
    Euphytica 26 (1977), S. 129-139 
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    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; grain yield ; tall plant ; semidwarf plant ; adaptation ; dryland ; regression analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary With a view to determining the comparative adaptation of semidwarf wheats to rainfed conditions, adaptation analyses were carried out on grain yield data of the 6th and 7th International Spring Wheat Yield Nurseries of the International Maize and Wheat Improvement Centre. Sites were chosen which had not received irrigation: across a combined total of 44 such sites, yield variation was closely related to growing seasonal rainfall. Using these sites, yields of thirty-three common cultivars. Norin 10-derived semidwarf cultivars plus tall ones, were regressed against site mean yield to give a regression slope (b) and deviations from the regression (sd 2) for each cultivar. Semidwarf cultivars generally showed higher mean yields and larger regression slopes (b 〉 0.9) than tall cultivars from lower latitudes. Tall cultivars from higher latitudes showed the lowest mean yields and the lowest b values (〈 0.7). No consistent trends in sd 2 were evident. Despite the greater regression slopes of semidwarf wheats, the best yields under all but the lowest yielding (driest) conditions were given by certain semidwarf cultivars; these had high mean yields and b values close to 1.0 (for example Tobari 66, Inia 66, Pato ArGentino and Sonalika). In contrast other semiwdarfs (notably Chenab 70) of similar mean yield, plant height and phenology, were not well adapted to the drier conditions as indicated by b values close to 1.3. The usefulness of the regression technique and the implications of these results for selection of semidwarf wheats adapted to drier conditions are discussed.
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    URL: http://dx.doi.org/10.1007/BF00032078
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    On the problem of pre-harvest sprouting of wheat (1977)
    Springer
    Euphytica 26 (1977), S. 299-308 
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    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; pre-harvest sprouting ; components of resistance to sprouting ; complex resistance (RCP) ; α-amylase synthesis ; GA3 response ; wheat endosperm
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The problem of pre-harvest sprouting in wheat is very intricate. New concepts in breeding for resistance to pre-harvest sprouting regard many components such as α-amylase production potential, response to gibberellic acid and inhibition in the bracts as important as dormancy. In the research work carried out at The University of Sydney's Plant Breeding Institute, we found varietal differences for each of these components. We also developed criteria for screening breeding material for these components. The implications of our findings in planning efficient breeding programmes to evolve varieties with multiple resistance to pre-harvest sprouting have been discussed briefly.
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    URL: http://dx.doi.org/10.1007/BF00026991
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    Breeding for resistance to cereal cyst nematode in wheat II. Use of test tube cultures in selection (1977)
    Springer
    Euphytica 26 (1977), S. 89-95 
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    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; Heterodera avenae ; cyst nematode ; resistance breeding
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary The use of soil. naturally infested with Heterodera avenae, to select resistant heterozygotes in backcross progenies of wheat, was tested for reliability. Selfed progenies from plants selected as resistant were cultured monoxenically in test tubes with nematodes hatched from single cysts, while backcross progenies from the same parent plants were grown in pots of naturally infested soil. Cyst counts were made after two months' growth. The results showed that over 50% of the backcross lines, screened in previous generations with naturally infested soil, had been erroneously selected as resistant. The test tube cultures clearly differentiated lines carrying resistance from those which were susceptible and corroborated results from pot tests.
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    URL: http://dx.doi.org/10.1007/BF00032073
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    Gametocidal properties of RH-531, RH-532, RH-2956, and RH-4667 on spring wheat (Triticum aestivum L.) (1977)
    Springer
    Euphytica 26 (1977), S. 103-112 
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    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; hybrid wheat ; male sterility ; cross pollination ; seed production
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Several chemicals were evaluated for their gametocidal properties to control pollination in hybrid wheat (Triticum aestivum L. em Thell.) seed production. In a preliminary study, four chemicals were applied to three cultivars of spring wheat at two application times. RH-532 was the most effective of the four gametocides, reducing fertility to a 0 10% level for all three cultivars. In a second experiment, RH-532 was applied to one cytoplasmic male-sterile and three normal spring wheats at four rates (0.56, 1.12, 2.24, and 4.48 kg/ha) and at two times of application. Alternate strips of pollinator were planted throughout the experiment. All treatments decreased fertility. plant height, and spike length of the three normal wheats. RH-532 did not inhibit spike emergence of two semidwarf cultivars or one of conventional height. Cultivars did not respond similarly to treatments. Yields of cross-pollinated seed were only 1 21% of the normal yield when fertility levels on treated plants reached 0 10%. Hybrid seed content of the harvested seed ranged from 2 55%. On the treated male-sterile line, yield was significantly reduced in comparison with the open-pollinated check. Inhibitory properties of this chemical suppressed the fertilization potential of the female as well as inducing male sterility. The differential response of genotypes to treatments indicates that cultivars should be screened for male and female sensitivity to this chemical. If differential sensitivity is found, breeding and selection to improve this trait may be possible. Different environmental conditions may alter the response of cultivars to this chemical, with less effect on the female structures.
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    URL: http://dx.doi.org/10.1007/BF00032075
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    The crossing of common wheat (Triticum aestivum L.) with cultivated rye (Secale cereale L.). II. Fertilization and early post-fertilization developments (1977)
    Springer
    Euphytica 26 (1977), S. 287-297 
    Details
    ISSN: 1573-5060
    Keywords: Triticum aestivum ; wheat ; Secale cereale ; rye ; intergeneric cross ; fertilization ; early post-fertilization developments
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Fertilization and early seed development was studied in the variety Chinese Spring of common wheat (Triticum aestivum L.) after pollination with rye (Secale cereale L.) and selfing, and in the common wheat variety Hope after selfing. In all three combinations the first pollen tube reached the micropyle in about 40 min after pollination. When pollinated with rye the migration of the sperm nuclei to the egg cell and the polar nuclei was delayed by about an hour. In the subsequent development until 72 hours after pollination the average cellular and nuclear doubling times of embryo and endosperm were about 16 and 8 hours for the interspecific combination. 18 and 9 hours for Chinese Spring selfed and 20 and 12 hours for Hope selfed.
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    Attraction and inhibition in moth species responding to sex-attractant lures containing Z-11-hexadecen-1-yl acetate (1977)
    Springer
    Journal of chemical ecology 3 (1977), S. 603-612 
    Details
    ISSN: 1573-1561
    Keywords: Eurois occulta ; Leucania commoides ; Scotogramma trifolii ; Crymodes devastator ; Mamestra configurata ; sex pheromones ; specificity ; Lepidoptera ; chemical communication
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Sex attractants for several sympatric noctuid moths required Z-11-hexadecen-1-yl acetate and additional olefinic compounds (coattractants) for effective, species-specific operation. In nearly all cases at least one of the coattractant compounds for each species functioned as a strong inhibitor of one or more of the other species in the group. It was concluded that species specificity in sex attractants can be achieved through conspecific coattractants which are at the same time transspecific inhibitors.
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    URL: http://dx.doi.org/10.1007/BF00989080
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    Skeleton weight allometry in aquatic and terrestrial vertebrates (1977)
    Springer
    Hydrobiologia 56 (1977), S. 35-37 
    Details
    ISSN: 1573-5117
    Keywords: allometry ; skeleton weight ; vertebrates ; whales ; fishes ; bones ; evolution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The relation of skeleton weight to body weight with increasing size is compared for aquatic and terrestrial vertebrates. Due to the buoyancy of water, the skeleton weights of aquatic vertebrates (fishes and whales) vary in nearly direct proportion (exponent 1.0) to body weight; while the skeletons of terrestrial vertebrates occupy an increasingly greater proportion of total body weight as size increases (exponent greater than i. i) due to the necessity of supporting their weight on land.
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    Zoogeography and the predator-prey ‘arms race:’ A comparison of eriphia and nerita species from three faunal regions (1977)
    Springer
    Hydrobiologia 56 (1977), S. 63-67 
    Details
    ISSN: 1573-5117
    Keywords: zoogeography ; predation ; evolution ; coevolution ; allometry ; Eriphia ; Nerita ; Gulf of California ; competition ; ecology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We measured maximum shell diameters and thicknesses of Nerita funiculata Menke and N. scabricosta Lamarck (Gastropoda: Neritidae), and claw sizes and carapace widths of the predatory crab Eriphia squamata Stimpson (Brachyura: Xanthidae), from the Gulf of California (Eastern Pacific). We also tested the ability of E. squamata to crush Nerita shells of various sizes. We compared this data on predator-prey counteradaptations with previously published data for congeneric species from the Western Atlantic and Indo-West Pacific regions. In relative abilities of the crabs to crush gastropod shells, and of the gastropod shells to resist such crushing, the Eastern Pacific species were ‘stronger’ than their counterparts in the Western Atlantic, but ‘weaker’ than their Indo-West Pacific congeners, indicative of an intermediate level of ‘faunal dominance’ or predator-prey ‘arms race’ escalation.
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    Innervation of heart and alary muscles in Sphinx ligustri L. (Lepidoptera) (1977)
    Springer
    Cell & tissue research 184 (1977), S. 467-486 
    Details
    ISSN: 1432-0878
    Keywords: Heart innervation ; Lepidoptera ; Neuromuscular junctions ; Perisynaptic reticulum ; Neurohaemal secretion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Description / Table of Contents: Zusammenfassung Ursprung und Verlauf der Herznerven bei Sphinx ligustri und Ephestia kuehniella wurden unter Verwendung von Präparationsunterlagen aus Bleiblech rasterelektronenmikroskopisch untersucht. Herz und Alarmuskeln von Sphinx ligustri wurden mit besonderer Berücksichtigung des caudalen Herzabschnitts im Transmissionselektronenmikroskop untersucht. Die Alarmuskeln bilden eine unvollständige Hülle um das Herz aus überwiegend längs orientierten Fasern, antagonistisch zum Faserverlauf im Herzmuskel. Herz und Alarmuskeln sind multiterminal über die transversalen Segmentalnerven innerviert, deren größte Zweige ein elektronentransparentes und mehrere neurosekretorische Axone enthalten. Verdickungen der Segmentalnerven enthalten möglicherweise Nervenzellen. Laterale Herznerven wurden nicht gefunden. Synaptische Axonendigungen nur eines Typs sind in den Alarmuskeln häufig, im Herzmuskel seltener. Sie werden nur von dem zentralen Axon aus gebildet. Die neuromuskulären Kontaktstellen sind von Gliazellen bedeckt, die über zahlreiche Ausläufer mit der Muskelzelle verzahnt sind und mit ihr ein “perisynaptisches Retikulum” bilden. Die Gliazellausläufer dringen in das T-System bis zu den Z-Banden vor. Exozytose von Neurosekret-Vesikeln in das perisynaptische Interzellularsystem wird angenommen. Neurohämale Abgabeorte finden sich entlang der Nervenäste und in speziellen Nervenendigungen auf der Höhe der Ostien. Der mögliche Einfluß der Innervierung auf die Herzaktivität wird diskutiert.
    Notes: Summary The origin and orientation of the heart nerves in Sphinx ligustri and Ephestia kuehniella were investigated by scanning electron microscopy using a special technique which involved pinning the dissected specimens on a stabilizing metal pad. The heart and alary muscles in Sphinx particularly their caudal extremity were also examined by transmission electron microscopy. The alary muscles form an incomplete sheath around the heart with a mainly longitudinal fibre orientation, e.i. antagonistically to the fibres of the heart itself. The heart and alary muscles are multiterminally innervated by branches of the transverse segmental nerves. All branches contain a single electron lucent axon; the thickest branches also possess several neurosecretory axons. Swellings of the segmental nerves may indicate the position of nerve cell bodies. There are no lateral heart nerves. Only one type of neuromuscular junction is abundant in the alary muscles but less frequently found in the heart. The terminals originate from the central axon only. They are capped by glial cells, which interdigitate with the muscle cells. They penetrate into the T-system toward the Z-discs and form a complex intercellular space system. Exocytosis of dense-cored vesicles into this “perisynaptic reticulum” seems likely. Sites of neurohaemal release are distributed along the nerve branches and special nerve endings occur at the level of the ostia. The possible nervous influence upon heart activity is discussed.
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    Bioavailability of tolamolol (1976)
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    European journal of clinical pharmacology 9 (1976), S. 315-317 
    Details
    ISSN: 1432-1041
    Keywords: Tolamolol ; bioavailability ; maximum exercise tachycardia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Bioavailability of capsule and tablet formulations of tolamolol were compared by measuring plasma concentration of tolamolol and reduction in maximum exercise heart rate over a period of twelve hours in eight healthy subjects in a two-way cross-over study. Tolamol was absorbed more rapidly from capsules than from tablets; this did not result in any significant difference in the reduction in maximum exercise heart rate between the two formulations. There was no significant difference between area under curve of reduction in exercise tachycardia and area under curve of plasma concentration of tolamolol for the two formulations. Reduction in maximum exercise heart rate was related to logarithm of plasma concentration of tolamolol between two and twelve hours after both formulations.
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    URL: http://dx.doi.org/10.1007/BF00561666
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    Bioavailability and pharmacokinetics of β- methyldigoxin after multiple oral and intravenous doses (1976)
    Springer
    European journal of clinical pharmacology 9 (1976), S. 373-379 
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    ISSN: 1432-1041
    Keywords: Methyldigoxin ; repetitive doses ; bioavailability ; deep compartments ; oral and i.v. dose ; volunteers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary To obtain true half lives, glycoside elimination from six healthy subjects was studied for 14 days after multiple intravenous doses or oral administration of a daily maintenance dose of β-methyldigoxin 0.3 mg. After oral or intravenous administration of β-methyldigoxin ceased, the plasma concentrations declined from the 14th to the 16th days with a half life of 1.7 days. From the 16th to the 20th day a change from a shorter to a longer half life of 2.8 and 2.9 days was observed. Similar half lives were found in urine: after the last dose the initial slope from the 14th to the 16th day had a half life of 1.8 days, and the terminal slope had one of 3.2 days. The results indicate release of the glycoside from slowly equilibrating tissues.
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    The pharmacokinetics of beta-methyl digoxin compared with digoxin tablets and capsules (1976)
    Springer
    European journal of clinical pharmacology 10 (1976), S. 231-236 
    Details
    ISSN: 1432-1041
    Keywords: Digoxin ; beta-methyl-digoxin ; capsules ; bioavailability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The intestinal absorption and urinary elimination rate of total cardioactive material was compared following digoxin and beta-methyldigoxin (BMD) administration to twelve healthy volunteers. Significantly more injected digoxin was recovered in urine. Urinary clearance was more rapid for digoxin, mean half-lives of elimination being 35 hours for digoxin and 40 hours for BMD. Calculated percentage intestinal absorption was lowest for digoxin tablets with a dissolution rate of 77% in one hour, intermediate for BMD tablets, and maximal for an experimental soft gelatin formulation of digoxin in solution. Respective mean values were 75%, 87% and 97%. Similar steady state plasma concentrations followed twice daily ingestion of the 0.25 mg digoxin tablets and 0.20 mg BMD tablets. Mean peak plasma concentration and percentage urinary recovery of ingested dose were higher during continued BMD administration. Between-subject variation in absorption was higher for the digoxin tablets. The comparative intestinal absorption of BMD and digoxin depends upon the formulation. Digoxin is virtually completely absorbed from a solution encapsulated in soft gelatin. Relatively more BMD is eliminated by nonrenal routes.
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    Clinical pharmacokinetics of sisomicin: Two-compartment model analysis of serum data after I.V. and I.M. administration (1976)
    Springer
    European journal of clinical pharmacology 10 (1976), S. 251-256 
    Details
    ISSN: 1432-1041
    Keywords: Sisomicin ; pharmacokinetics ; bioavailability ; two-compartment analysis ; man
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The pharmacokinetics of sisomicin, a new single component aminoglycoside antibiotic related to gentamicin c1a, were determined in four healthy volunteers after intravenous and intramuscular administration of a 1 mg/kg dose. The elimination profile of this antibiotic follows two-compartment model kinetics after I.V. administration. The fast (α) and slow (β) disposition rate constants averaged 0.072 and 0.004 min−1, respectively. The volume of distribution at the steady-state averaged 0.185 liters/kg which approximately corresponds to the volume of extracellular space. The physiological availability of an intramuscular dose appeared to be complete. A method of administration adapted to the kinetic properties of the drug is proposed.
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    Pharmacokinetics and bioavailability of indoprofen in man (1976)
    Springer
    European journal of clinical pharmacology 10 (1976), S. 257-262 
    Details
    ISSN: 1432-1041
    Keywords: Anti-inflammatory and analgesic drug ; indoprofen ; pharmacokinetics ; bioavailability ; man
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary In a pharmacokinetic study of the new analgesic and anti-inflammatory drug indoprofen, plasma levels and urinary excretion were determined in four healthy volunteers after 100 mg and 200 mg iv, and after 100 mg (capsules) and 200 mg (tablets) oral doses. After iv administration, the mean biological half-life (t1/2 β) was about 2 h (range 1.4 to 3.2 h). The apparent volume of distribution Vdβ ranged between 11 to 17 % of body weight, indicating its limited extravascular distribution. Most of the drug was excreted in urine as glucuronide and a smaller proportion as unchanged indoprofen: the 24 h urinary excretion of these compounds accounted for 67 to 95 % of an iv dose. Peak plasma levels occurred between 30 and 120 minutes after oral administration of 100 mg as capsules or 200 mg as tablets. The mean biological half-life was about 2 h, as after iv administration. The bioavailability of oral doses was assessed using both plasma levels and urinary excretion data. The absorption of capsules and tablets was practically complete, that of the former being faster.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00558338
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  • 97
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    Pharmacokinetics and pharmacodynamics of methyl proscillaridin in healthy man (1976)
    Springer
    European journal of clinical pharmacology 10 (1976), S. 101-108 
    Details
    ISSN: 1432-1041
    Keywords: Cardiac glycosides ; methyl proscillaridin ; plasma concentrations ; electrocardiogram ; bioavailability ; 86Rb-erythrocyte assay
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The aim of this study was to obtain data about the pharmacological properties of a new glycoside derivative in man. Plasma concentrations and ECG parameters were measured after oral and intravenous administration of a single dose of 1.2 mg methyl proscillaridin in 16 healthy volunteers, using a strictly randomized, two-period change-over design. Glycoside concentrations were measured using a modified86Rb-erythrocyte-assay. QT-duration, corrected for frequency (QTc), was the principal variable measured in the ECG. By either route, there was a maximum plasma level after 1 hour, which had decreased to a minimum at 3 hours, followed by a second peak at 4 to 10 hours (orally〉iv). From 10 to 72 hours the concentrations decreased with a median t 1/2 of 23.3 hours (iv) and 33.0 hours (orally). Comparison of the ratio of plasma concentrations following oral and iv administration resulted in a bioavailability of 69 % using the 48 hour plasma levels, and 59 % using the areas under the concentration-time curves. The mean QTc was maximally shortened to 28 msec at 1 hour after iv and to 19 msec at 10 hours after the oral dose. A distinct similarity between time-concentration and time-QTc curves was seen after the initial distribution phase, both after oral and intravenous administration. The new derivative shows a rapid elimination. Its bioavailability is reasonably high.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00609467
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  • 98
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    Studies on hydralazine (1976)
    Springer
    European journal of clinical pharmacology 10 (1976), S. 183-187 
    Details
    ISSN: 1432-1041
    Keywords: Hydralazine ; bioavailability ; pharmacogenetics ; first pass effect ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary After oral administration of a single 50 mg dose of hydralazine (Apresoline®), the serum half-life (T1/2) and bioavailability (AUC0−∞) were assessed in 16 healthy volunteers. The half-life was 2.57±0.14 h (S.E.) in 10 slow acetylators of sulphadimidine, and 2.18±0.15 h in 6 fast acetylators (difference not statistically significant). AUC0−∞ was significantly higher in slow acetylators, at 1.04±0.10 µg·hour·ml−1, compared to 0.66±0.12 µg·hour·ml−1 in the fast acetylators (p〈0.025). Treatment with Apresoline® 25 mg tid produced minimum serum concentrations at steady-state of 57.3±7.3 ng·ml−1 and 33.4±4.2 ng·ml−1 in 8 slow and 5 fast acetylators, respectively (p〈0.05). The corresponding maximum concentrations were 228.8±20.3 ng·ml−1 and 147.6±15.0 ng·ml−1 in slow and fast acetylators, respectively (p〈0.025). First-pass metabolism of hydralazine could explain the difference in bioavailability of the drug between fast and slow acetylators, without any corresponding difference in the elimination rate of the drug in the post-distributive phase.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00558327
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  • 99
    Electronic Resource
    Electronic Resource
    Studies on hydralazine (1976)
    Springer
    European journal of clinical pharmacology 10 (1976), S. 395-401 
    Details
    ISSN: 1432-1041
    Keywords: Hydralazine ; bioavailability ; polymorphic acetylation ; first-pass metabolism ; oral and intravenous dosing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The bioavailability of orally administered hydralazine was assessed in 4 healthy subjects after separate administration of a single oral or intravenous dose (0.3 mg·kg−1). Comparison of the areas under the serum concentration-time curves showed that 26 – 55 % of the oral dose was available to the systemic circulation as unchanged drug. The O - 24 h excretion of the drug in urine was rapid: 11.4 – 14.1 % of the dose after intravenous administration, and 2.0 – 3.6 % after an oral dose. Acetylation of hydralazine leads to formation of 3-methyl-s-triazolo-3,4,a-phthalazine (MTP) and a gas-liquid-chromatographic method for its measurement in urine was developed. After oral and intravenous administration, 0.8 – 1.2 % and 1.4 – 2.3 % of the dose, respectively, were recovered within 24 hours from urine as MTP. After oral administration there was a relative increase in the amount of MTP in every subject, which indicates route-dependent metabolism. The lower bioavailability of oral hydralazine could be explained in terms of first-pass metabolism.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00563075
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  • 100
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    Electronic Resource
    Bioavailability of various preparations and doses of penicillin V (1976)
    Springer
    European journal of clinical pharmacology 10 (1976), S. 55-58 
    Details
    ISSN: 1432-1041
    Keywords: Penicillin V ; bioavailability ; pharmacokinetics ; dose ranging
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary An absorption study was performed in ten healthy volunteers to test the bioavailability of various doses of two penicillin V-K preparations: Isocillin® (Hoechst AG, Federal Republic of Germany), — tablets of 600 000 and 1.2 Mega U; V-Cillin® (Eli Lilly, USA), — tablets of 200 000, 400 000 and 800 000 U. The serum concentrations and elimination of the active substance in urine were measured for six hours after administration. Independently of the source of the preparation, a strict linear relation between the dose and the area under the serum curve (AUC), or between the dose and the urinary elimination, was demonstrated by regression analysis. The dose-dependent increase in the AUC was highly significant (p〈0.01) in the range tested, i.e. between 200 000 and 1.2 Mega U. The relative elimination of active substance in urine lay within narrow limits for all doses (35.7–41.3%). Thus, both compounds proved to have the same bioavailability.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00561550
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