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  • Spektralphotometrie  (35)
  • bioavailability
  • pheromone
  • Springer  (69)
  • American Association for the Advancement of Science
  • Cambridge University Press
  • 1975-1979  (69)
  • 1979  (69)
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Publisher
  • Springer  (69)
  • American Association for the Advancement of Science
  • Cambridge University Press
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  • 1975-1979  (69)
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 16 (1979), S. 211-215 
    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.
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  • 2
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    European journal of clinical pharmacology 16 (1979), S. 417-421 
    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.
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  • 3
    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.
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  • 4
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    European journal of clinical pharmacology 16 (1979), S. 31-38 
    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.
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  • 5
    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.
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  • 6
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    European journal of clinical pharmacology 16 (1979), S. 45-48 
    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.
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  • 7
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    European journal of clinical pharmacology 16 (1979), S. 335-340 
    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.
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  • 8
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    European journal of clinical pharmacology 15 (1979), S. 269-274 
    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.
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  • 9
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    European journal of clinical pharmacology 16 (1979), S. 107-112 
    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.
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  • 10
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    European journal of clinical pharmacology 16 (1979), S. 141-147 
    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).
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  • 11
    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.
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  • 12
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    European journal of clinical pharmacology 16 (1979), S. 405-410 
    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.
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  • 13
    ISSN: 1573-1561
    Keywords: Neodiprion sertifer ; Pine saw-fly ; Hymenoptera ; Diprionidae ; pheromone ; trans-perillenal ; monoterpene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Volatile constituents present in nanogram quantities in various body parts and glands of the males and females of the speciesNeodiprion sertifer Geoffr. (Hymenoptera: Diprionidae) have been investigated by GC-MS. A significant amount of a volatile constituent was detected in the lateral parts of the integument of abdominal segments II-III. The constituent was identified as the furanoid monoterpenetrans-perillenal (I) previously not known to occur in nature. The identification and synthesis of this compound is described.
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  • 14
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    Journal of chemical ecology 5 (1979), S. 353-361 
    ISSN: 1573-1561
    Keywords: Stable fly ; Stomoxys calcitrans (L) ; pheromone ; mating stimulants ; alkenes ; cuticular lipids ; copulatory behavior
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The cuticular alkenes of the female stable fly,Stomoxys calcitrans (L), which were responsible for inducing male fly copulatory behavior are (Z)-9-hentriacontene, (Z)-9-tritriacontene, 13-methyl-1-hen-triacontene and 13-methyl-1-tritriacontene. The identifications of the branched alkenes and the synthesis of these four compounds are described. Bioassays indicate that these materials in combination with previously described methyl branched alkanes are more active than the individual components.
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  • 15
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    Journal of chemical ecology 5 (1979), S. 565-574 
    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.
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  • 16
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    Journal of chemical ecology 5 (1979), S. 941-953 
    ISSN: 1573-1561
    Keywords: White peach scale ; Pseudaulacaspis pentagona ; pheromone ; attractant ; microtechniques ; enantiomer ; isomers ; (R,Z)-3 ; 9-dimethyl-6-isopropenyl-3 ; 9-decadien-1-ol propionate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Micro techniques were used to obtain spectroscopic and degradative information from less than 5μg of the sex attractant of female white peach scale,Pseudaulascaspis pentagons (Targioni-Tozzetti) isolated from airborne collections. The pheromone was identified as (Z)-3,9-dimethyl-6-isopropenyl-3,9-decadien-1-ol propionate. Both enantiomers of theZ isomer and also the enantiomers of theE isomer were prepared from (R)-or (S)-limonene. Bioassays of material with minimum enantiomeric purity of 95% showed that at extreme dilution only theR,Z isomer attracted male white peach scale; however activity of theS,Z enantiomer could not be completely excluded.
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  • 17
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    Fresenius' Zeitschrift für analytische Chemie 298 (1979), S. 367-372 
    ISSN: 1618-2650
    Keywords: Best. von Lanthaniden, Europium, Dysprosium, Erbium, Samarium in Uran ; Spektralphotometrie ; Atomabsorption ; Graphitofen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary Studies were conducted on the assay of Sm, Eu, Dy and Er separated from uranium using aqueous standards by electrothermal AAS with Massmann type graphite furnace. The working curves were found to be linear in the ranges Sm (1–10 μg/ml), Eu (0.05–0.6 μg/ml), Dy (0.1–0.8 μg/ml) and Er (0.1–1.0 μg/ml). The values obtained for synthetic samples agreed favourably with those obtained by emission spectrographic method. Experiments using pyrolytic carbon coated tubes with and without pretreatment by La, Ta and Y have shown an enhancement with treatment upto a maximum of 15% and improve the memory effect marginally. The effect of Ta treatment was found to be singularly useful in improving the general behaviour of Sm. The interference effects of lanthanides, other than the analyte, were found to be negligible. However, the presence of uranium was found to affect the absorbance. The absorbance of Eu was found to be nearly independent of uranium after an initial increase. On the other hand, the absorbance of other elements studied was found to drastically decrease after an initial enhancement. Detailed investigations of temperature dependence of absorbance were carried out using Eu, Dy and Er. The differences in the behaviour of these elements is attributed to probable differences in the modes of their atomization.
    Notes: Zusammenfassung Die Untersuchungen wurden mit Hilfe des Graphitrohrofens nach Maßmann durchgeführt. In folgenden Bereichen ergaben sich lineare Eichkurven: Sm 1–10 μg/ml, Eu 0,05–0,6 μg/ml, Dy 0,1–0,8 μg/ml, Er 0,1μ-1,0 μg/ml. Die aus synthetischen Proben erhaltenen Ergebnisse stimmten gut mit den durch Emissionsspektrographie erhaltenen überein. Versuche wurden mit Röhren mit pyrolytischen Kohlenstoffüberzug mit und ohne Vorbehandlung durch La, Ta und Y durchgeführt und ergaben eine bis 15%ige Steigerung durch die Behandlung sowie eine mäßige Besserung des Memoryeffektes. Eine Behandlung mit Ta war besonders für Sm vorteilhaft. Störungen durch andere Lanthanide waren vernachlässigbar. Uran beeinflußte jedoch die Absorption. Im Falle von Eu zeigte sich nach anfänglicher Zunahme fast eine Unabhängigkeit, während bei den anderen untersuchten Elementen nach anfänglicher Zunahme eine beträchtliche Abnahme auftrat. Mit Eu, Dy und Er wurde ebenfalls die Temperaturabhängigkeit der Absorption untersucht. Festgestellte Unterschiede im Verhalten werden auf unterschiedliche Atomisierung zurückgeführt.
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  • 18
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    Fresenius' Zeitschrift für analytische Chemie 294 (1979), S. 284-284 
    ISSN: 1618-2650
    Keywords: Best. von Uran(VI) mit Chlorphosphonazo III ; Spektralphotometrie ; Trioctylamin-Extraktion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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  • 19
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    Fresenius' Zeitschrift für analytische Chemie 294 (1979), S. 285-285 
    ISSN: 1618-2650
    Keywords: Best. von Phosphat in Ferrosilicium ; Spektralphotometrie ; Cer/Xylenolorange, indirekt
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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  • 20
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    Fresenius' Zeitschrift für analytische Chemie 294 (1979), S. 413-413 
    ISSN: 1618-2650
    Keywords: Best. von Kobalt mit Pyridin und Azid ; Spektralphotometrie ; Aussalzungsmittel, Mischkomplex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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  • 21
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    Fresenius' Zeitschrift für analytische Chemie 295 (1979), S. 270-270 
    ISSN: 1618-2650
    Keywords: Best. von Cer(IV) ; Spektralphotometrie ; indirekt, Fe(III)-Resacetophenonoximat-Komplex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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  • 22
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    Fresenius' Zeitschrift für analytische Chemie 299 (1979), S. 264-266 
    ISSN: 1618-2650
    Keywords: Best. von Kohlenhydraten in Huminsäuren ; Spektralphotometrie ; Anthronmethode
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Eine modifizierte Anthronmethode zur Bestimmung des Kohlenhydratgehaltes in Fraktionen von Huminsäure-Blei(II)-Chelatverbindungen, die mit chemischen und gelchromatographischen Methoden getrennt wurden, wird beschrieben. Um die Störung der Methode durch die Absorption der Huminsäuren, die mit abnehmender Wellenlänge ansteigt, gering zu halten, wird die Extinktion des Anthron-Kohlenhydrat-Reaktionsproduktes bei 620 nm gemessen. Die Huminsäurekonzentration darf 0,1 g/dl nicht überschreiten. Da die molare Extinktion des Anthron-Reaktionsproduktes von der Art des Kohlenhydrates abhängt, wird der Kohlenhydratgehalt auf das Hauptkohlenhydrat des Huminsäurehydrolysats berechnet (d.h. Glucose).
    Notes: Summary A modified anthrone method is described for the determination of carbohydrates in fractions of lead(II)-chelate compounds of humic acids separated with chemical as well as gel-chromatographic methods. To reduce the disturbance of the method by the absorption of humic acids increasing with the decrease of wavelength, the absorbance of the anthronecarbohydrate reaction products is measured at 620 nm and the humic acid concentration is not allowed to exceed 0.1 g/dl. Because the molar absorptivity of the anthrone reaction-products depends on the type of carbohydrate investigated, the content is calculated for the main carbohydrate of the humic-acid hydrolysate (i.e. glucose).
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  • 23
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    Fresenius' Zeitschrift für analytische Chemie 295 (1979), S. 366-370 
    ISSN: 1618-2650
    Keywords: Best. von Quecksilber, Silber mit Formazanen ; Spektralphotometrie ; chelatbildende Ionenaustauscher
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Die Darstellung substituierter Formazane und ihre chemische Fixierung an Cellulose, amino- und chlormethyliertem Polystyrol wird beschrieben. Die Kapazitäten der Austauscher liegen zwischen 0,05 mÄq/g (Cellulose) und 0,6 mÄq/g (Polystyrol). In neutralem Medium zeigen sie eine besondere Affinität zu Hg(II), Pd(II) und Ag(I), aber keine Affinität zu Cu(II). Weiterhin wurde eine spektrophotometrische Bestimmung von Hg(II) und Ag(I) mit dem wasserlöslichen Formazan (FII)-NO2 ausgearbeitet [Hg(II): ɛ546=23 000 l Mol−1 cm−1, Ag(I): ɛ546 =38 000 l Mol−1 cm−1].
    Notes: Summary The preparation of substituted formazans and their fixation on cellulose, amino- and chloromethylated polystyrene is described. The capacities of the exchangers vary from 0.05 meq/g (cellulose) to 0.6 meq/g (polystyrene). They show in neutral medium greater affinity to Hg(II), Pd(II) and Ag(I), but no affinity to Cu(II). Further, a spectrophotometric determination of Hg(II) and Ag(I) with the watersoluble formazan (FII)-NO2 has been worked out. [Hg(II): ɛ546=23 000 l Mol−1 cm−1, Ag(I): ɛ546=38 000 l Mol−1 cm−1].
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  • 24
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    Fresenius' Zeitschrift für analytische Chemie 294 (1979), S. 356-360 
    ISSN: 1618-2650
    Keywords: Spektralphotometrie ; Mechanisierung, Prinzip, Optimierung
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Das Prinzip der Automatisierung der photometrischen Analyse mit kontinuierlichem Reagentienfluß und die speziellen Vorteile der Verwendung von Bausteinen der Flüssigkeits-Chromatographie werden ausführlich diskutiert. Die Optimierung folgender Parameter wird besprochen: Verweilzeit (Reaktionszeit), Einspritzmenge, Pumpgeschwindigkeit, Säulenabmessungen, Partikeldurchmesser.
    Notes: Summary The principle of automation of photometric analysis by the continuous flow method and the particular advantages of the use of component parts of liquid chromatography are discussed in detail. The optimization of the following parameters is pointed out: residence (reaction) time, injection volume, pumping rate, column dimensions and particle diameter.
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    Fresenius' Zeitschrift für analytische Chemie 295 (1979), S. 47-47 
    ISSN: 1618-2650
    Keywords: Best. von Vanadium in Stahl ; Spektralphotometrie ; Hydroxyphenyl-p-tolylbenzamidin
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    Fresenius' Zeitschrift für analytische Chemie 295 (1979), S. 393-397 
    ISSN: 1618-2650
    Keywords: Best. von Tensiden in Wasser ; Spektralphotometrie ; Aniontenside, Reinigungsstufen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Aniontenside werden an Feststoffen der Gewässer wie auch der Kläranlagen adsorbiert und teilweise angereichert. Ihre analytische Bestimmung erfordert eine mehrstufige Vorarbeit. Sie führt über die Extraktion des Probengutes, die Abtrennung der Tenside von Störstoffen durch Ausblasen (grobe Vorreinigung) und die chromatographische Reinigung der Rohfraktion auf Kieselgelschichten. Die Konzentration der reinen Tensidfraktion kann colorimetrisch oder IR-spektrometrisch bestimmt werden.
    Notes: Summary Anion tensides are adsorbed on solids in surface waters and sewage treatment plants and enriched to some extent. Their analytical determination requires multi-stage preparations, including sampling, separation of the tensides from disturbing material by air stripping (rough preliminary cleaning), and chromatographic cleaning of the raw fraction on silica gel. The concentration of the pure tenside fraction can be determined colorimetrically or by way of IR spectrometry.
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    Fresenius' Zeitschrift für analytische Chemie 297 (1979), S. 159-160 
    ISSN: 1618-2650
    Keywords: Best. von Vanadium(V) mit p-Hydroxybenzaldehyd und Hydroxyamidin ; Spektralphotometrie
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  • 28
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    Fresenius' Zeitschrift für analytische Chemie 298 (1979), S. 158-158 
    ISSN: 1618-2650
    Keywords: Best. von Palladium, Ruthenium ; Spektralphotometrie ; Isonitrosodibenzoylmethan
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    Fresenius' Zeitschrift für analytische Chemie 298 (1979), S. 160-160 
    ISSN: 1618-2650
    Keywords: Best. von Ruthenium(III) mit 3-Hydroxy-3-(p-dimethylaminophenyl)-1-phenyltriazen ; Spektralphotometrie
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    Fresenius' Zeitschrift für analytische Chemie 296 (1979), S. 45-45 
    ISSN: 1618-2650
    Keywords: Best. von o-Dichlorbenzol ; Spektralphotometrie ; UV
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    Fresenius' Zeitschrift für analytische Chemie 296 (1979), S. 46-46 
    ISSN: 1618-2650
    Keywords: Best. von p-Methylaminophenolsulfat, Metol ; Spektralphotometrie
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  • 32
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    Fresenius' Zeitschrift für analytische Chemie 296 (1979), S. 406-407 
    ISSN: 1618-2650
    Keywords: Best. von Ligninsulfonsäure, Huminsäure in Wasser ; Spektralphotometrie ; UV
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  • 33
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    Fresenius' Zeitschrift für analytische Chemie 296 (1979), S. 383-385 
    ISSN: 1618-2650
    Keywords: Best. von Bor in Silicaten ; Spektralphotometrie ; Pyrohydrolyse, Carminsäure
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    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary This simple method for the determination of boron takes a total time of 20 min. Samples are mixed with CaF2 suprapur in the ratio 3∶1 and pyrohydrolized in a Leco induction furnace for 15 min under steam of H2O. The BF3 liberated is collected in a NaOH-Na2CO3 solution (10 g NaOH +1 g Na2CO3 per liter). This solution is filled up to 200 ml with twice distilled water; 2 ml of this solution is mixed with conc. sulphuric acid and carminic acid solution and filled up to 50 ml. The absorption is measured by a Zeiss Elko II photometer with filter S 59. Analyses of four internations reference samples show excellent precision with a relative standard deviation of less than 5% (e.g. for a boron content of 2.1 ppm in granite G-2).
    Notes: Zusammenfassung Die Borbestimmung mit dieser schnellen und einfachen Methode benötigt ca. 20 min. Die Proben werden mit CaF2 Suprapur im Verhältnis 3∶1 vermischt und in einem Leco-Induktionsofen 15 min unter Einleitung von Wasserdampf pyrohydrolysiert. Das entstandene BF3 wird in einer NaOH-Na2CO3-Lösung(10 g NaOH+1 gNa2CO3pro Liter) aufgefangen. Diese Lösung wird mit zweifach destilliertem Wasser auf 200 ml aufgefüllt; 2 ml dieser Lösung werden mit konz. Schwefelsäure und Carminsäure-Lösung versetzt und auf 50 ml aufgefüllt, bevor ihre Absorption mit einem Zeiss — Elko II — Photometer mit Filter S 59 gemessen wird. Analysen von 4 internationalen Referenzproben zeigen eine hohe Präzision mit einer relativen Standardabweichung von weniger als 5% (z. B. für einen Gehalt von 2,1 ppm Bor im Granit G-2 des USGS).
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    Fresenius' Zeitschrift für analytische Chemie 296 (1979), S. 407-408 
    ISSN: 1618-2650
    Keywords: Best. von N-p-Tolylbenzohydroxamsäure ; Spektralphotometrie
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    Fresenius' Zeitschrift für analytische Chemie 296 (1979), S. 414-415 
    ISSN: 1618-2650
    Keywords: Best. von Quecksilber(II) mit 3-Methyl-5-pyrazolon-4-dithiocarbonsäure ; Spektralphotometrie
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  • 36
    ISSN: 1573-8744
    Keywords: quinidine ; pharmacokinetic parameters ; assay methods ; assay specificity ; area under the plasma concentration-time curve ; bioavailability ; clearance ; therapeutic window
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    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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  • 37
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    Journal of pharmacokinetics and pharmacodynamics 7 (1979), S. 429-451 
    ISSN: 1573-8744
    Keywords: ampicillin ; bacampicillin ; pivampicillin ; prodrug ; bioavailability ; zero-order absorption ; two-compartment model ; renal clearance
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    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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    Journal of pharmacokinetics and pharmacodynamics 7 (1979), S. 1-27 
    ISSN: 1573-8744
    Keywords: furosemide ; renal failure ; congestive heart failure ; bioavailability ; diuretic effects
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    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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  • 39
    ISSN: 1573-8744
    Keywords: bioavailability ; confidence intervals ; hypothesis testing ; imipramine ; internal standard ; mass spectrometry ; power ; relative bioavailability
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    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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  • 40
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    Journal of chemical ecology 5 (1979), S. 53-62 
    ISSN: 1573-1561
    Keywords: Coreidae ; Heteroptera ; Hemiptera ; sex attractant ; pheromone ; sexual selection ; n-octanol ; benzyl alcohol ; vanillin ; 2-phenyl-ethanol ; leaf-footed bugs ; chemotaxonomy ; allomome
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The 7–8th ventral abdominal gland secretions from 6 adult male leaf-footed bugs,Leptoglossus spp., and a related species,Euthochtha galeator, were chemically analyzed by GC-MS. Of the 11 volatile compounds identified, all but one of the compounds (n-octanol) were aromatic, including compounds with the familiar odors of cherries, vanilla, cinnamon, and roses. The preponderance of aromatics in the adult male ventral abdominal gland secretions contrasts sharply with the aliphatic compounds which comprise the metathoracic gland defensive secretions of adult males and females. Also, the male-specific secretions are species-specific, both qualitatively and quantitatively, whereas the metathoracic gland secretions of Coreoidea are only distinctive at the generic level. It is proposed that males were favored as the emitters of attractive signals by sexual selection, whereas the specificity of the signal is the result of natural selection against hybridization.
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    Journal of chemical ecology 5 (1979), S. 125-130 
    ISSN: 1573-1561
    Keywords: Diptera ; Sarcophagidae ; flesh fly ; Sarcophaga bullata ; pheromone ; hexanal
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Hexanal, isolated from a whole animal extract of the flesh fly,Sarcophaga bullata, attracts over 65% of the females tested with no apparent effect on males.
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  • 42
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    Journal of chemical ecology 5 (1979), S. 109-123 
    ISSN: 1573-1561
    Keywords: Bark beetle ; Ips pini ; Coleoptera ; Scolytidae ; pheromone ; enantiomer ; olfaction ; single cell ; electrophysiology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Electrophysiological recordings inIps pini were made from single olfactory cells stimulated by six concentrations of eleven compounds—either pheromones or host constituents. The receptor cells were grouped according to their differential responses to these biologically significant compounds. Cells specialized to either ipsdienol or ipsenol (pheromones for severalIps species) appeared to be relatively uniform in their sensitivity to all compounds tested. Another group of cells specialized tocis- andtrans-verbenol were more variable in their sensitivities to the substances tested. The activation of separate groups of cells by the different pheromones and host compounds shows (by exclusion) that behaviorally expressed syner-gistic as well as inhibitory action mainly is due to an interaction in the central nervous system rather than an interaction of the compounds on the receptors. All “ipsdienol cells” responded to both enantiomers of ipsdienol. Although some differences between responses to the enantiomers by individual cells were observed, these did not form a consistent pattern, and no net differences could be found between the eastern and western populations ofI. pint.
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  • 43
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    Journal of chemical ecology 5 (1979), S. 237-249 
    ISSN: 1573-1561
    Keywords: Sawflies ; pheromone ; stereospecificity ; (−)-erythro configuration ; enantiomers ; chirality ; optical isomers ; Neodiprion lecontei
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The stereospecificity of the sawfly pheromone 3,7-dimethyl-2-pentadecanol acetate againstNeodiprion lecontei was studied. Twoerythro and a 1∶1 mixture ofthreo isomers (C-2 and C-3) were synthesized for this purpose. It was found that only one isomer with (−)-erythro configuration (2S, 3S) had biological activity. The potency of this synthetic pheromone was roughly identical to the one shown by the naturally occurring pheromone in this species.
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  • 44
    ISSN: 1573-1561
    Keywords: Dendroctonus brevicomis ; exo-brevicomin ; frontalin ; myrcene ; attractant ; pheromone ; pheromone production ; pest management ; bark beetle
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Three parameters are described for estimating the natural occurrence of chemically defined insect pheromones: (1) the rate and duration of release by the insect, (2) the density of the pheromone-emitting insect population in both time and space, and (3) dispersal and degradation rates of the chemicals. Each of these parameters, except dispersal, was estimated for a population ofDendroctonus brevicomis LeC, and its three component attractive pheromones. A single generation of 610,000 beetles, believed to comprise the entire population in a 65-km2 forest, was estimated to have released 0.78, 3.7, and 370.5 g of frontalin,exo-brevicomin, and myrcene, respectively, within a 30-day period.
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  • 45
    ISSN: 1573-1561
    Keywords: Grapholitha molesta ; Oriental fruit moth ; attractant ; pheromone ; (Z)-8-dodecenyl acetate ; (E)-8-dodecenyl acetate ; dodecyl acetate ; (Z)-8-dodecen-1-ol ; dodecanol
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The female-emitted pheromone ofGrapholitha molesta (Busck), the Oriental fruit moth, was collected by holding females in glass flasks during calling. Flask washes were found to contain four pheromone components: (Z)-8-dodecenyl acetate and (E)-8-dodecenyl acetate in a 100∶7 ratio, and (Z)-8-dodecen-1-ol and dodecanol in a 100∶20 ratio. The ratio of (Z)-8-acetate to (Z)-8-dodecen-1-ol was approx. 100∶30. Approximately 0.1–0.2 ng of pheromone was recovered per female per hour of calling.
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  • 46
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    Journal of chemical ecology 5 (1979), S. 415-422 
    ISSN: 1573-1561
    Keywords: Stable fly ; Stomoxys calcitrans (L.) ; pheromone ; sex pheromone ; polyene ; mating stimulant ; (Z,Z)-1,7,13-pentacosatriene
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The four geometrical isomers of 1,7,13-pentacosatriene were synthesized from 1,7-octadiyne. Two of the required isomers were synthesized using known methodology. Hydrogenation of acetylenic linkages were employed to produce predominantly cis alkenes, and alkali metal/amine reduction was used to produce a trans alkene. It was thus possible to produce the (Z,Z) and the (Z,E) isomers. Methods for olefin inversion were then employed to obtain the other two isomers.
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  • 47
    ISSN: 1573-1561
    Keywords: Pinus ponderosa ; Dendroctonus brevicomis ; western pine beetle ; attractant ; pheromone ; behavior ; traps ; Coleoptera ; Scolytidae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Western pine beetles were caught on unbaited sticky traps placed near a source ofexo-brevicomin, frontalin, and myrcene. Size of trap, distance and direction from the source of attractant, and height from the ground were varied. Significant differences in trap catch were observed in relation to each of the variables. Traps close to the source of attractant caught more beetles than traps farther from the source. Traps downwind of the source of attractant caught more beetles than did upwind traps. More males than females were trapped close to the source of attractant.
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    Journal of chemical ecology 5 (1979), S. 557-564 
    ISSN: 1573-1561
    Keywords: (Z)-9-tricosene ; muscalure ; housefly ; pheromone ; Musca domestica ; jojoba oil ; oleyl alcohol ; sex attractant ; Diptera
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract A four-step synthesis of (Z)-9-tricosene (“muscalure”), a component of the pheromone of the housefly, from jojoba oil (or three-step from oleyl alcohol) by 3-carbon (or 5-carbon) unit elongation was developed in overall high yield. The sequence of reactions and the purity of the products could be easily followed, with relatively good accuracy, by NMR technique.
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    Journal of chemical ecology 5 (1979), S. 35-52 
    ISSN: 1573-1561
    Keywords: Hymenoptera ; Formicidae ; Leptothorax ; Mychothorax ; Harpagoxenus americanus ; recruitment ; pheromone ; poison gland ; specificity ; comparative behavioral analysis
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Ants of the genusLeptothorax recruit to new nest sites and newly discovered food sources by tandem running. This involves one ant directly leading a nestmate to the target area. Pheromones from the poison gland have proved the most important signal employed during this recruitment behavior. Comparative behavioral analysis with 11 species ofLeptothorax demonstrated a subgenus specificity of the tandem calling pheromone between the subgeneraLeptothorax andMychothorax.
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    Journal of chemical ecology 5 (1979), S. 721-725 
    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
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    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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  • 51
    ISSN: 1573-1561
    Keywords: Trypodendron lineatum ; 4,6,6-lineatin ; 3,3,7-trimethyl-2,9-dioxatricyclo[3.3.1.04,7]nonane ; pheromone ; attractant ; tricyclic acetal ; Scolytidae ; aggregation pheromone ; ambrosia beetle
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    Notes: Abstract Authentic 4,6,6-lineatin (3,3,7-trimethyl-2,9-dioxatricyclo-[3.3.1.04,7]nonane) (I) was produced in low yield via three synthetic pathways. In field tests, microgram amounts of the product from all three syntheses attracted large numbers ofTrypodendron lineatum of both sexes. These results confirm that 4,6,6-lineatin (I) is a population aggregation pheromone forT. lineatum.
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    Journal of chemical ecology 5 (1979), S. 805-813 
    ISSN: 1573-1561
    Keywords: Dermestes maculatus ; Coleoptera ; Dermestidae ; pheromone ; behavior ; bioassay ; circadian rhythm
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    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Adults of the hide beetle,Dermestes maculatus (De Geer), were shown to have a female-produced sex pheromone which excited males. Male response was positively correlated with increasing age, but females produced a higher level of pheromone at 6–8 days of age than at younger or older ages. Extractable female pheromone and male response varied over the photophase with peak values that occurred during the latter hours. Quantitative bioassay indicated that the 50% male response level (RD50) would be elicited by a pheromone exposure of 0.01 female equivalents (FE). Females extracted 24 hr after mating had a lower level of extractable pheromone than did virgin females of the same age.
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    Journal of chemical ecology 5 (1979), S. 935-939 
    ISSN: 1573-1561
    Keywords: Lymantria dispar ; gypsy moth ; pheromone ; polymorphism ; disparlure ; enantiomer ; cis-7 ; 8-epoxy-2-methyloctadecane ; attractant
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Gyspy moth (Lymantria dispar L.) males atttracted to either (+)-cis-7,8-epoxy-2-methyloctadecane [(+)-disparlure] or its racemate [(±)-disparlure] do not represent distinct behavioral classes of individuals. Males attracted to within 2 cm of either (+)- or (+-)-disparlure dispensers on a tree trunk were caught, marked as to the lure visited, and then released into a 5×5 grid at ca. 20-m spacing of traps baited alternately with (+)-or (±)-disparlure. Males then reattracted to these lures showed no evident preference for the lures at which they were first captured, indicating that males attracted to either of these lures are not behavioral phenotypes.
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    Fresenius' Zeitschrift für analytische Chemie 294 (1979), S. 286-286 
    ISSN: 1618-2650
    Keywords: Best. von Aminen mit Isothiocyanatodioxotolyldihydrobenzisochinolin ; Spektralphotometrie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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    Fresenius' Zeitschrift für analytische Chemie 294 (1979), S. 285-285 
    ISSN: 1618-2650
    Keywords: Best. von Eisen(III), Chrom(VI) mit Helasolviolett 4R ; Spektralphotometrie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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    Fresenius' Zeitschrift für analytische Chemie 295 (1979), S. 119-121 
    ISSN: 1618-2650
    Keywords: Best. von Wolfram(VI) mit Thioglykolsäure ; Spektralphotometrie ; Chelatbildung, Carbonsäuren
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung W(VI) bildet mit Thioglykolsäure und Glykolsäure mäßig stabile Fünfringchelate der Zusammensetzung WR2, mit Glycin ein sehr schwaches WR. Chelate mit den Sechsringbildnern 3-Mercaptopropionsäure und o-Mercaptobenzoesäure sind nicht nachweisbar. Das Thioglykolsäurechelat kristallisiert aus Methanol als gelbes Na-Salz WO2(SCH2COONa)2·2CH3OH und ist mit Di-phenylguanidin als Ionenpaar in Butanol extrahierbar. Die photometrische Wolframbestimmung mit Thioglykolsäure in wäßriger Lösung erreicht eine Bestimmungsgrenze von $$\underline c $$ = 0,92 ppm W (P=99,9%;M=2) und eine Standardabweichung vons=0,24 ppm W (f=21).
    Notes: Summary W(VI) forms moderately stable, five-membered ring chelates of the composition WR2 with thioglycolic and glycolic acid, and a very weak WR with glycine. Chelation with the six-ring forming 3-mercaptopropionic acid and o-mercaptobenzoic acid could not be detected. The chelate with thioglycolic acid crystallizes from methanol as the yellow sodium salt WO2(SCH2COONa)2·2CH3OH and can be extracted into butanol as an ion pair with diphenylguanidine. The photometric determination of tungsten with thioglycolic acid has a determination limit of $$\underline c $$ = 0.92 ppm W (P=99.9%;M=2) and a standard deviations=0.24 ppmW (f=21).
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    Fresenius' Zeitschrift für analytische Chemie 295 (1979), S. 122-124 
    ISSN: 1618-2650
    Keywords: Best. von Sulfat in Umweltmaterial ; Wasser ; Spektralphotometrie ; Durchflußsystem
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary Sulphate in various environmental samples was determined by measuring the optical absorbance upon reaction with the barium(II) dimethylsulphonazo(III) complex. The measurement took place in a flow-through system. Interferences from phosphate, metal ions and others were eliminated. The results of a turbidimetric measurement, a spectrophotometric measurement with thorin, an automatic titration and the proposed method are compared. The latter allows the determination of sulphate in the range of 1.4–60 μmol·l−1. The standard deviation is 0.3–0.6 μmol·l−1, depending on the type of sample (water) analysed. A determination takes 1.5min.
    Notes: Zusammenfassung Sulfat wurde in verschiedenen Umweltproben durch Messung der Extinktion nach Reaktion mit dem Barium(II)-dimethylsulfonazo(III)-komplex im Durchflußsystem bestimmt. Störungen von Phosphat, Metallionen, u.a. wurden beseitigt. Die Ergebnisse einer turbidimetrischen, einer photometrischen, einer automatischen Titration und der vorgeschlagenen Methode werden verglichen. Die Methode ermöglicht die Sulfatbestimmung im Bereich von 1,4–60 μmol·l−1. Die Standardabweichung beträgt 0,3–0,6 μmol· l−1 je nach Typ des Probematerials (Wasser). Eine Bestimmung erfordert 1,5min.
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    Fresenius' Zeitschrift für analytische Chemie 295 (1979), S. 271-271 
    ISSN: 1618-2650
    Keywords: Best. von Blei in Wasser, Abwasser, Staub ; Spektralphotometrie ; Dithizon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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    Fresenius' Zeitschrift für analytische Chemie 295 (1979), S. 413-413 
    ISSN: 1618-2650
    Keywords: Best. von Platin(IV) mit Chlorpromazin ; Spektralphotometrie
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    Topics: Chemistry and Pharmacology
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    Fresenius' Zeitschrift für analytische Chemie 297 (1979), S. 419-419 
    ISSN: 1618-2650
    Keywords: Spektralphotometrie ; Bouguer-Lambert-Beersches Gesetz, neues Konzept
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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    Fresenius' Zeitschrift für analytische Chemie 298 (1979), S. 160-160 
    ISSN: 1618-2650
    Keywords: Best. von Phenothiazinen ; Spektralphotometrie ; Silicowolframsäure
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    Topics: Chemistry and Pharmacology
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    Fresenius' Zeitschrift für analytische Chemie 294 (1979), S. 43-44 
    ISSN: 1618-2650
    Keywords: Best. von Salicylaldehyd ; Spektralphotometrie ; konz. Schwefelsäure
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    Fresenius' Zeitschrift für analytische Chemie 294 (1979), S. 46-46 
    ISSN: 1618-2650
    Keywords: Best. von Osmium mit N-Benzoyl-o-tolylhydroxylamin ; Spektralphotometrie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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    Fresenius' Zeitschrift für analytische Chemie 294 (1979), S. 415-416 
    ISSN: 1618-2650
    Keywords: Best. von Albumin in Serum ; Spektralphotometrie ; Isothiocyanatodioxo-tolyldihydro-benzisochinolin, Rinderserum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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    Fresenius' Zeitschrift für analytische Chemie 299 (1979), S. 128-128 
    ISSN: 1618-2650
    Keywords: Best. von Ruthenium mit 2-Methyl-1,4-naphtochinon-monoxim ; Spektralphotometrie ; Extraktion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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    Fresenius' Zeitschrift für analytische Chemie 295 (1979), S. 412-413 
    ISSN: 1618-2650
    Keywords: Best. von Palladium(II), Ruthenium(III) mit Isonitrosobenzoylacetone ; Spektralphotometrie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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    Fresenius' Zeitschrift für analytische Chemie 297 (1979), S. 384-387 
    ISSN: 1618-2650
    Keywords: Best. von Uran ; Spektralphotometrie ; Spuren, Extraktion mit Triphenylarsinoxid in Chloroform
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Es wurde eine einfache, vielseitig anwendbare spektralphotometrische Uranbestimmung für U6+-Mengen bis in den ng-Bereich ausgearbeitet, bei der über 60 Kationen und etwa 20 Anionen in weiten Grenzen nicht stören. Das mit Triphenylarsinoxid in CHCl3 aus der zu untersuchenden Lösung extrahierte Uran wird mit oxalsäurehaltiger 5,5 M HClO4 zurückextrahiert und in den Arsenazo III-Komplex überführt. Die mit diesem Schritt verbundene Aufkonzentrierung erlaubt noch bis zu 0,01 μg Uran in 200 ml Ausgangslösung spektralphotometrisch bei 655 nm zu bestimmen. Im günstigsten Arbeitsbereich beträgt die relative Standardabweichung ±1%. 4 Probelösungen können in 1 h analysiert werden.
    Notes: Summary A simple and versatile spectrophotometric method for the determination of uranium down to the μg range was worked out. About 60 cations and 20 anions were found not to cause interferences in a wide concentration range. U6+ is extracted with triphenylarsine oxide in chloroform, back-extracted with 5.5 M perchloric acid containing oxalic acid and converted to the arsenazo III-complex. The concentration step involved allows the spectrophotometric determination of 0.01 μg of uranium in 200 ml of original solution at 655 nm. A standard deviation of ±1 % can be achieved and it is possible to analyse about 4 solutions per hour.
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    Fresenius' Zeitschrift für analytische Chemie 298 (1979), S. 156-157 
    ISSN: 1618-2650
    Keywords: Best. von Sulfat in Wasser ; Spektralphotometrie ; Ionenaustausch, Dimethylsulfonazo(III)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
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    Fresenius' Zeitschrift für analytische Chemie 298 (1979), S. 150-154 
    ISSN: 1618-2650
    Keywords: Best. von Kupfer mit Fluoronen ; Spektralphotometrie ; Übersicht über die Fluorone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Fluorone, Verbindungen des 2,3,7-Trihydroxyisoxanthenons-(6), eignen sich als empfindliche Reagentien für die spektralphotometrische Analyse zahlreicher Metallionen im sichtbaren Teil des Spektrums. Neben einigen grundsätzlichen Anmerkungen zur Herstellung, zu den Eigenschaften und Reaktionen der Fluorone mit Metallionen wird die Verwendung des Cyclohexylfluorons (CHF) für die photometrische Bestimmung von Cu(II)-Ion beschrieben; hierbei ergibt sich ein molarer Extinktionskoeffizient von 191000 l/Mol · cm und eine Standardabweichung von ±0,2 ng/ml. Der Anwendungsbereich liegt bei 6–60 ng Cu/ml. Bi, Fe(II/III) und Sb müssen zuvor abgetrennt werden.
    Notes: Summary Fluorones, derivates of 2,3,7-trihydroxyisoxanthenone-(6), are sensitive reagents for the spectrophotometric determination of many metal ions in aqueous solution. Besides some principal remarks on the synthesis, properties and reactions of fluorones, the application of cyclohexylfluorone for the determination of Cu(II) ion is described in detail. This method is applicable in the concentration range 6–60 ng of Cu/ml. The molar absorptivity is 1910001/Mol · cm and the standard deviation is ±0.2 ng/ml. Bi, Fe(II, III) and Sb have to be separated prior to the determination.
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