Pharmacokinetics of the anti-human immunodeficiency virus nucleoside analog stavudine in cynomolgus monkeys.

Stavudine was administered (15 mg/kg of body weight) intravenously and orally to two monkeys in a randomized crossover study. Plasma and urine samples were analyzed for stavudine by high-performance liquid chromatography, and pharmacokinetic parameters were derived by a noncompartmental method. Tota...

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Pubblicato in:	Antimicrob Agents Chemother
Autori principali:	Kaul, S, Dandekar, K A
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	American Society for Microbiology (ASM) 1993
Soggetti:	Research Article
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC187922/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8390811/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/aac.37.5.1160
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