Zobrazeno 1 - 10
of 14
pro vyhledávání: '"David W.A. Bourne"'
Publikováno v:
Journal of Pharmaceutical Sciences. 63:865-868
The equilibrium between bisulfite ion and pyrosulfite ion in aqueous solutions of different ionic strengths was investigated spectrophotometrically. Values for the equilibrium constant at ionic strengths of 2.0, 0.9, 0.5, 0.1, and 0.01 M were found t
Autor:
David W.A. Bourne
Publikováno v:
Computer Methods and Programs in Biomedicine. 23:277-281
MULTI-FORTE is an expanded version of the MULTI non-linear fitting programs written by Yamaoka et al. The functions of the three original programs (including Gauss-Newton and Simplex fitting algorithms) have been combined and translated into FORTRAN
Publikováno v:
British Journal of Anaesthesia. 56:465-471
The pharmacokinetic behaviour of alcuronium was studied in three patients undergoing resection of an aortic aneurysm, and in another two patients undergoing total hip replacement (group I). A control group of five elderly patients undergoing relative
Publikováno v:
Journal of Chromatography B: Biomedical Sciences and Applications. 308:359-362
Autor:
Kwang‐IL Kwon, David W.A. Bourne
Publikováno v:
International Journal of Pharmaceutics. 37:219-226
A physiologically based pharmacokinetic model for tenoxicam distribution and excretion in the rat was developed. The drug concentrations in plasma and all the tissues except testis were simulated using flow-limited equations, while testis concentrati
Publikováno v:
Journal of veterinary pharmacology and therapeutics. 8(1)
Guerrini, V.H., Filippich, L.J., English, P.B., Cao, G.R. &: Bourne, D.W.A. Effect of probenecid on the pharmacokinetics of cefotaxime in sheep. J. vet. Pharmacol. Therap. 8, 38–46. The effect of probenecid given by intravenous (i.v.), intramuscula
Autor:
R.F. Bevill, Gary D. Koritz, David W.A. Bourne, Lewis W. Dittert, G. Rudawsky, M. Hayashi, C. H. Huang
Publikováno v:
Journal of pharmacokinetics and biopharmaceutics. 10(5)
Sulfadimethoxine was administered intravenously and orally to five swine. More than 75% of the dose was excreted into urine as the acetyl metabolite with 4-6% excreted unchanged. Plasma and urine data were not consistent when a linear pharmacokinetic
Publikováno v:
Journal of chromatography. 278(1)
Autor:
Kwang I. Kwon, David W.A. Bourne
Publikováno v:
Journal of pharmacokinetics and biopharmaceutics. 14(4)
Previous studies have shown that caffeine can affect drug kinetics by altering drug binding to plasma protein, drug absorption, or drug distribution. In this study, the effect of caffeine on the in vivo protein binding and the disposition of ceftriax
Autor:
Jenny Schneider, Lucio J. Filippich, G. R. Cao, V. H. Guerrini, David W.A. Bourne, P. B. English
Publikováno v:
Journal of veterinary pharmacology and therapeutics. 8(2)
Six Merino ewes were given 1 g (27 g/kg) probenecid by the intravenous (i.v.), intramuscular (i.m.) and subcutaneous (s.c.) routes. After i.v. injection, the biological half-life was 1.55 h and apparent volume of distribution at the steady state (Vds