Determination of stavudine in human plasma and urine by high-performance liquid chromatography using a reduced sample volume

被引:23
|
作者
Sarasa, M
Riba, N
Zamora, L
Carné, X
机构
[1] IDIBAPS, Hosp Clin, Clin Pharmacol Unit, Barcelona 08036, Spain
[2] Bristol Myers Squibb Co, Madrid 28040, Spain
关键词
stavudine;
D O I
10.1016/S0378-4347(00)00324-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Sensitive high-performance liquid chromatographic assays have been developed for the quantification of stavudine (2',3'-didehydro-3'-deoxythymidine, d4T) in human plasma and urine. The methods are linear over the concentration ranges 0.025-25 and 2-150 mu g/ml in plasma and urine, respectively. An aliquot of 200 yl of plasma was extracted with solid-phase extraction using Oasis(R) cartridges, while urine samples were simply diluted 1/100 with HPLC water. The analytical column, mobile phase, instrumentation and chromatographic conditions are the same for both methods. The methods have been validated separately, and stability tests under various conditions have been performed. The detection limit is 12 ng/ml in plasma for a sample size of 200 mu l. The bioanalytical assay has been used in a pharmacokinetic study of pregnant women and their newborns. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:183 / 189
页数:7
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