Morris D M, Selinger K
Department of Clinical Pharmacology, Glaxo Inc. Research Institute, Research Triangle Park, NC 27709.
J Pharm Biomed Anal. 1994 Feb;12(2):255-64. doi: 10.1016/0731-7085(94)90037-x.
3TC (GR109714X) is a cytidine dideoxynucleoside analogue which has been shown to have in vitro activity against a variety of strains of HIV-1 and is currently being investigated in clinical trials as a treatment for HIV infection. An HPLC method for the determination of 3TC in human urine has been developed and validated. The method allows direct injection of urine (10 microliters) using HPLC column switching followed by UV detection. On-line extraction is performed using a Spherisorb-SCX (5 microns, 20 x 4.0 mm) eluted with deionized water at 1 ml min-1. 3TC is retained while the bulk of urine constituents are eluted to waste. The SCX column is then backflushed to a BDS-Hypersil-C18 (5 microns, 250 x 4.6 mm) and eluted with 100 mM acetate pH 4.5-methanol (95:5, v/v) for final separation. 3TC is detected by UV absorbance at lambda = 285. The quantitation range of the assay was 0.5-500 micrograms ml-1. The method has demonstrated sufficient ruggedness to be used in support of 3TC clinical trials. Application to other cytidine analogues including DDC has been demonstrated.
3TC(GR109714X)是一种双脱氧胞苷类似物,已显示出对多种HIV-1毒株具有体外活性,目前正在进行临床试验以研究其作为HIV感染的治疗方法。已开发并验证了一种用于测定人尿中3TC的高效液相色谱法。该方法允许使用高效液相色谱柱切换后直接进样尿液(10微升),随后进行紫外检测。在线萃取使用Spherisorb-SCX(5微米,20×4.0毫米)柱,以1毫升/分钟的流速用去离子水冲洗。3TC被保留,而大部分尿液成分被洗脱至废液。然后将SCX柱反冲至BDS-Hypersil-C18(5微米,250×4.6毫米)柱,并用100 mM pH 4.5的乙酸盐-甲醇(95:5,v/v)洗脱以进行最终分离。通过在λ = 285处的紫外吸光度检测3TC。该测定的定量范围为0.5 - 500微克/毫升。该方法已证明具有足够的耐用性,可用于支持3TC的临床试验。已证明该方法可应用于其他胞苷类似物,包括双脱氧胞苷(DDC)。