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  • Articles  (601)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European journal of nutrition 24 (1985), S. 113-119 
    ISSN: 1436-6215
    Keywords: Chloramphenicol ; pharmacokinetics ; residue ; pig
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Medicine
    Description / Table of Contents: Summary Residues of Chloramphenicol (CAP) were examined in 24 pigs after intramuscular injection of 30 mg CAP/kg body weight. Two pigs were slaughtered after 3, 6, 12,18, 24, 36 hours, 2, 3, 6, 10, 21 and 30 days, respectively. CAP-concentrations were determined in muscle, blood, urine, liver, kidney, bile, and fat. Methods used were gas-liquid chromatography and radioimmunoassay. Detection limits reached were 1−5 ppb. The concentration-time curves obtained reflected a long elimination phase and allowed only calculation of this half-life. Elimination half-life was estimated to be for muscle, blood and urine 160–170 hours, for kidney 310 and for bile 250 hours. Significant correlations were found to exist between CAP-concentrations in plasma and muscle. It appears that blood would be a good body fluid for monitoring CAP-residues in tissue.
    Notes: Zusammenfassung Zur Untersuchung des Rückstandsverhaltens von Chloramphenicol (CAP) wurden 24 Mastschweine, 24–28 Wochen alt, intramuskulär mit 30 mg CAP/kg Körpergewicht behandelt und je 2 Tiere nach 3, 6, 12, 18, 24, 36 Stunden, 2, 3, 6, 10, 21 und 30 Tagen geschlachtet. Die CAP-Gehalte in Muskulatur, Blut, Urin, Leber, Niere, Galle und Fett wurden gaschromatographisch und radioimmunologisch bestimmt. Die Nachweisgrenze beider Methoden liegt in Abhängigkeit von der Matrix zwischen 1 und 5 ppb. Die erhaltenen Kinetiken weisen eine terminale Elimination auf, deren Halbwertszeiten für Muskulatur, Blut und Urin ca. 160–170 Stunden, für Niere 310 Stunden und für Galle 250 Stunden betragen. Die CAP-Konzentration in Muskulatur und Blut weisen eine signifikante, lineare Korrelation auf. Blutuntersuchungen könnten deshalb als Screening-Methode bei umfangreichen Rückstandskontrollen eingesetzt werden.
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  • 2
    ISSN: 1420-9071
    Keywords: Interferon ; immunomodulator ; catabolism ; pharmacokinetics ; administration routes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary When human recombinant interferon-α2 diluted in saline was injected s.c. into rabbits, the total amount recovered in thoracic lymph was less than 0.4%. Recoveries increased from 2- to 8-fold if interferon was injected in 4% albumin or with hyaluronidase, respectively. Albumin added to interferon acts as an interstitial fluid expander, thus favoring interferon absorption through lymphatics rather than blood capillaries. This strategy may increase the therapeutic index of interferon.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 16 (1974), S. 37-44 
    ISSN: 1432-0827
    Keywords: Human ; Dentine ; Glycosaminoglycan ; Chondroitin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Abstract The glycosaminoglycans of root dentine from permanent human teeth were studied. The tissue was digested with papain and the glycosaminoglycans were precipitated with cetylpyridinium chloride and recovered by centrifugation. A small quantity of keratan sulphate was recovered from the supernatant after fractionation on cetylpyridinium chloride and Ecteola-cellulose. The cetylpyridinium chloride-precipitated glycosaminoglycans were studied by infra-red spectrophotometry, cetylpyridinium chloride cellulose chromatography and electrophoresis on cellulose acetate. Individual hexosamines were determined on an autoanalyzer. The results indicate that chondroitin-4-sulphate is the major glycosaminoglycan and that chondroitin-6-sulphate, hyaluronic acid, dermatan sulphate and a nonsulphated galactosaminoglycan are also present in minor quantities.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 7 (1971), S. 175-190 
    ISSN: 1432-0827
    Keywords: Bone ; Human ; Age ; Glycosaminoglycans
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Description / Table of Contents: Résumé Les glycosaminoglycanes de l'os humain compact du fémur sont identifiés et leur concentration et distribution sont déterminées à partir de cas d'autopsie, d'âges variables, allant du nouveau-né à des sujets de 94 ans. L'absence d'altérations post-mortem des glycosaminoglycanes osseux est déterminée au niveau de l'os fémoral de chien, au bout de 72 heures. Le chondroitine-4-sulfate constitue le glycosaminoglycane majeur de l'os humain: de plus, une fraction mineure semble être constituée par l'acide hyaluronique. Les proportions de glycosaminoglycanes varient inversement en fonction, de l'âge chez des sujets en pleine croissance: mais aucun changement n'est observé plus tardivement. La distribution des glycosaminoglycanes est identique chez les sujets adultes. Seules de faibles différences, concernant cette distribution, sont relevées. Chez les sujets jeunes elles sont, peut-être, liées à des changements de poids moléculaire peu élevés ou au sulfate chondroitine sulfaté, peu élevé et, chez un sujet vieil à une proportion plus grande d'acide hyaluronique.
    Abstract: Zusammenfassung Die Glykosaminoglykane aus menschlicher Compacta des Oberschenkels wurden charakterisiert und ihre Konzentrationen und Muster an Autopsien von Menschen verschiedenen Alters (Neugeborene bis 94jährige) festgelegt. Fällungen mit Cetylpyridin und Fraktionierungsmethoden wurden angewendet. Am Hundefemur konnte festgestellt werden, daß sich das Glykosaminoglykanmuster im Knochen bis zu 72 Std post mortem nicht veränderte. Als wichtigstes Glykosaminoglykan des menschlichen Knochens wurde das Chondroitin-4-sulfat identifiziert; dazu wurde ein kleiner Anteil versuchsweise als Hyaluronsäure eingestuft. Die Konzentrationen der Glykosaminoglykane standen in umgekehrtem Verhältnis zum Alter des im Wachstum stehenden Menschen, jedoch wurde nach dessen Abschluß keine Veränderung mehr beobachtet. Das Glykosaminoglykanmuster sieht für alle erwachsenen Menschen ähnlich aus. Nur kleine Abweichungen von diesem Muster konnten bei jungen Menschen festgestellt werden; möglicherweise sind sie auf eine leichte Änderung im Molekulargewicht oder auf eine schwache Sulfatierung des Chondroitinsulfates zurückzuführen. Dies gilt ebenso für einen alten Menschen, dessen Knochen einen höheren Anteil an Hyaluronsäure aufweisen.
    Notes: Abstract Glycosaminoglycans from human femoral compact bone were characterized and their concentrations and patterns were determined in autopsy cases of various ages, newborn to 94 years of age. Cetylpyridinium precipitation and fractionation methods were used. Absence of postmortem changes of bone glycosaminoglycan pattern for as long as 72 hours was checked on dog femoral bone. Chondroitin-4-sulphate was identified as the predominating glycosaminoglycan of human bone; in addition a minor part was tentatively identified as hyaluronic acid. Concentrations, of glycosaminoglycans were inversely related to age in growing subjects, but no change was noted later in life. The glycosaminoglycan pattern had a similar appearance for all of the adult subjects. Only small deviations from this pattern had a similar for young subjects, possibly due to low molecular weight change or low sulphated chondroitin sulphate; and for one old subjects to a higher proportion of hyaluronic acid.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Calcified tissue international 6 (1970), S. 260-264 
    ISSN: 1432-0827
    Keywords: Bone ; Human ; Tissue ; Histology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Description / Table of Contents: Résumé De l'os spongieux humain est utilisé pour déterminer la viabilité de cellules osseuses après exposition, pendant un temps déterminé, à l'air et au sérum physiologique. La réaction de Feulgen, ainsi que la culture de tissus sont utilisées pour déterminer la viabilité des cellules osseuses. Il apparait qu'aucun ostéocyte ne survit après 30 minutes d'exposition à l'air et au sérum physiologique. Les cellules de la moëlle ne survivent pas à 2 heures d'exposition ö l'air, ou 6 heures d'exposition au sérum physiologique. Le nombre de cellules qui survivent après action de l'air et du sérum physiologique diminue progressivement en fonction de l'augmentation du temps d'exposition.
    Abstract: Zusammenfassung Poröser Knochen von Erwachsenen wurde zur Bestimmung der Überlebenszeit von Knochenzellen verwendet, nachdem er während bestimmter Zeiten der Luft oder physiologischer Kochsalzlösung ausgesetzt wurde. Um diese Überlebenszeit zu bestimmen, wurde die Feulgen-Reaktion gleichzeitig mit der Gewebekultur durchgeführt. Daraus läßt sich schließen, daß keine Osteocyten überleben, nachdem sie 30 min der Luft oder der Kochsalzlösung ausgesetzt waren. Markzellen überlebten nicht, wenn sie 2 Std der Luft oder 6 Std der Kochsalzlösung ausgesetzt waren. Die Anzahl überlebender Zellen nimmt ab, wenn die Dauer, während welcher sie der Luft oder der Kochsalzlösung ausgesetzt werden, zunimmt.
    Notes: Abstract Adult human cancellous bone was used to determine the viability of bone cells after timed exposure to air and saline. To determine the viability of the bone cells, the Feulgen reaction was used in conjunction with tissue culture. It is concluded that no osteocytes survived after 30 minutes exposure to air or saline. Marrow cells do not survive after 2 hours exposure to air, or 6 hours exposure to saline. The number of surviving cells after exposure to air or saline progressively diminishes as the time of exposure increases.
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  • 6
    ISSN: 1432-1211
    Keywords: Key words MHC class III region ; Mouse ; Human ; G7c ; Lung tumor susceptibility
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Immunogenetics 51 (2000), S. 487-488 
    ISSN: 1432-1211
    Keywords: Key words Immunoglobulin ; J segments ; IGKJ genes ; Alleles ; Human
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 32 (1987), S. 631-634 
    ISSN: 1432-1041
    Keywords: salbutamol ; albuterol ; pharmacokinetics ; bioavailability ; healthy volunteers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Salbutamol was administered to sixteen healthy male volunteers intravenously and by mouth in liquid, tablet, and capsule form using a Latin-Squares design. Pharmacokinetic parameters from intravenous data were similar to previously reported values obtained with oral administration, with a mean terminal half-life of 3.8 h and a mean clearance of 439 ml·min−1·1.73 m−2. Peak plasma concentrations of 10–20 ng·ml−1 were obtained 1–3 h following oral administration. The absolute bioavailability of each of the oral preparations was 44%. While statistically significant differences in lag time and time to peak concentration were noted among the various oral preparations, the drug is rapidly absorbed in all three dosage forms and the observed differences are unlikely to be of clinical significance.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 34 (1988), S. 179-186 
    ISSN: 1432-1041
    Keywords: ceftazidime ; pharmacokinetics ; elderly patients ; young volunteers ; acute infection
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The pharmacokinetics of ceftazidime have been investigated after single and multiple i.v. doses in 9 young healthy male volunteers and 15 elderly male patients with acute bacterial infections. All subjects had normal, age-correlated glomerular function. Distribution and elimination in young volunteers were unaffected by posture and were similar to what has been reported earlier. In contrast, elderly patients had longer t1/2β (3.1 vs 1.9 h), larger AUC (414.0 vs 276.6 h·mg/l), lower total and renal clearances, reduced urinary recovery over 12 h and enlarged Vss. Total serum clearance of ceftazidime was closely correlated with the51Cr-EDTA clearance. There was no significant change in51Cr-EDTA clearance after seven days of treatment. A reduction in the dose of betalactam antibiotics eliminated by the kidney is advisable in elderly patients with an acute bacterial infection.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 5 (1972), S. 44-52 
    ISSN: 1432-1041
    Keywords: alprenolol ; serum drug level ; exercise ; man ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The effects of alprenolol on heart rate and systolic blood pressure were studied in healthy subjects during standardized exercise on a bicycle ergometer. In one series of experiments, in which serum concentrations of alprenolol were also measured, the effects of single oral doses of 50, 100 and 200 mg of alprenolol and a placebo were compared by a double blind cross-over technique. In a second series of experiments 100 mg alprenolol was given four times in one day and the effect was followed for up to eighteen hours after the last dose. — Alprenolol diminished the expected increase in heart rate and systolic blood pressure during exercise. The reduction of exercise tachycardia in a given individual was linearly related to the logarithm of the dose or the serum concentration of alprenolol. The serum concentrations required for a given reduction of exercise tachycardia varied almost one hundred-fold amongst the subjects studied. The biological availability of alprenolol was dose-dependent, probably due to a limited capacity biotransformation of the drug before it entered the general circulation. After a single dose the serum level of alprenolol and its chronotropic effect diminished at a rate corresponding to an elimination half life of about two hours. This rate of elimination was consistent with that calculated from the results of the four dose study.
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