Zobrazeno 1 - 8
of 8
pro vyhledávání: '"S J, Roffey"'
Autor:
Anthony Harrison, Paul Morgan, John D. Davis, Katherine S. Fenner, Alison Betts, Pierre Comby, Kevin Beaumont, A Edgington, S. J. Roffey
Publikováno v:
Drug Metabolism and Disposition. 32:197-204
4-amino-5-(4-fluorophenyl)-6,7-dimethoxy-2-[4-(morpholinocarbonyl)-perhydro-1,4-diazepin-1-yl]quinoline (UK-294,315) is an antagonist of the human alpha1-adrenoceptor and exhibits nonlinear oral pharmacokinetics in humans. Superproportional increases
Publikováno v:
Clinical Infectious Diseases. 37:728-732
We characterized voriconazole concentrations in the cerebrospinal fluid (CSF) of immunocompetent guinea pigs and patients with invasive fungal infections. In animals, after receipt of oral doses of 4 or 10 mg/kg every 8 h, the mean ratios of CSF to p
Autor:
D. K. Walker, Dennis A. Smith, S. Cole, Pierre Comby, Angus N. R. Nedderman, S. J. Roffey, S. G. Jezequel, N. Wood, D. Gibson
Publikováno v:
Drug Metabolism and Disposition. 31:731-741
Voriconazole is a new triazole antifungal agent with potent, wide-spectrum activity. Its pharmacokinetics and metabolism have been studied in mouse, rat, rabbit, dog, guinea pig, and humans after single and multiple administration by both oral and in
Publikováno v:
Xenobiotica. 33:541-560
1. UK-240,455 ((+) 6,7-dichloro-5-[N-(2-hydroxyethyl)methanesulphonamido]-2,3 (1H,4H)-quinoxalinedione) is a potent, selective N-methyl D-aspartate (NMDA) glycine site antagonist that is being evaluated for the potential treatment of stroke. 2. UK-24
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 22:773-780
A selective method for the determination of sulphobutylether-beta-cyclodextrin (SBECD) in human plasma has been developed and validated over the range 4-200 microg ml(-1). SBECD is extracted from plasma using end-capped cyclohexyl solid phase extract
Publikováno v:
Drug metabolism reviews. 39(1)
Mass balance excretion studies in laboratory animals and humans using radiolabeled compounds represent a standard part of the development process for new drugs. From these studies, the total fate of drug-related material is obtained: mass balance, ro
Publikováno v:
Journal of pharmaceutical and biomedical analysis. 35(1)
The clinical pharmacokinetics of midazolam have been extensively studied, due to its high clearance by CYP3A4 and sensitivity to drug–drug interactions. In order to investigate the potential to model drug–drug interactions with midazolam in the d
Publikováno v:
International journal of clinical pharmacology and therapeutics. 36(2)