Good S S, Reynolds D J, de Miranda P
Experimental Therapy Department, Wellcome Research Laboratories, Research Triangle Park, NC 27709.
J Chromatogr. 1988 Sep 23;431(1):123-33. doi: 10.1016/s0378-4347(00)83075-3.
A sensitive high-performance liquid chromatography (HPLC) assay has been developed to simultaneously determine levels of the anti human immunodeficiency virus agent, zidovudine (AZT), and its major metabolite (the 5'-O-glucuronide) in serum. Samples were first mixed with an internal standard (a stereoisomer of AZT), then prepared for analysis using solid-phase extraction columns and chromatographed using a reversed-phase analytical column. Isocratic elution with a mobile phase of 15% acetonitrile, buffered to pH 2.70 with ammonium phosphate, gave good resolution of the three analytes and endogenous serum components. The HPLC analysis time required per sample was 34 min and analyte recoveries were reproducibly high (greater than 93%). Replicate analyses of prepared standards gave satisfactory precision and accuracy, with coefficients of variation less than 15% and deviations from expected concentrations less than 10%.
已开发出一种灵敏的高效液相色谱(HPLC)分析法,用于同时测定血清中抗人类免疫缺陷病毒药物齐多夫定(AZT)及其主要代谢物(5'-O-葡萄糖醛酸苷)的水平。样品首先与内标(AZT的立体异构体)混合,然后使用固相萃取柱进行分析制备,并使用反相分析柱进行色谱分析。用15%乙腈作为流动相进行等度洗脱,并用磷酸铵将其缓冲至pH 2.70,可使三种分析物和内源性血清成分得到良好分离。每个样品所需的HPLC分析时间为34分钟,分析物回收率可重复且很高(大于93%)。对制备好的标准品进行重复分析,得到了令人满意的精密度和准确度,变异系数小于15%,与预期浓度的偏差小于10%。