Lefebvre I, Puy J-Y, Perrin C, Périgaud C
Institut des Biomolécules Max Mousseron (IBMM), UMR 5247 CNRS-UM1-UM2, Université Montpellier 2, case courrier 1705, place Eugène Bataillon, 34095 Montpellier Cédex 05, France.
J Chromatogr B Analyt Technol Biomed Life Sci. 2007 Oct 15;858(1-2):2-7. doi: 10.1016/j.jchromb.2007.07.028. Epub 2007 Jul 28.
A simple and rapid analytical method for the simultaneous quantification of zidovudine (AZT) and its monophosphate (AZTMP) in cell extracts has been developed using high-performance liquid chromatography (HPLC) with on-line solid-phase extraction and 2-aminoethyl-3'-azido-2',3'-dideoxythymidin-5'-yl phosphodiester sodium salt as internal standard (IS). The cell extract samples were directly injected on a short reversed-phase precolumn using an aqueous buffer containing an ion-pairing reagent as a mobile phase. Under these conditions, the analytes were retained on the precolumn whereas the proteins were discarded. The analytes were then transferred onto the analytical column by increasing the strength of the eluent. The calibration curve was linear over a concentration range of 0.5-100 microg/ml. Inter- and intra-day accuracy and precision results satisfied the accepted criteria for bioanalytical validation. This method was used to study the decomposition pathway of a model pronucleotide in an in vitro approach.
已开发出一种简单快速的分析方法,用于同时定量细胞提取物中的齐多夫定(AZT)及其单磷酸盐(AZTMP),该方法采用高效液相色谱(HPLC),并结合在线固相萃取,以内标(IS)2-氨基乙基-3'-叠氮基-2',3'-二脱氧胸苷-5'-基磷酸二酯钠盐进行分析。细胞提取物样品使用含有离子对试剂的水性缓冲液作为流动相,直接进样到短的反相预柱上。在这些条件下,分析物保留在预柱上,而蛋白质则被弃去。然后通过增加洗脱液强度将分析物转移到分析柱上。校准曲线在0.5 - 100μg/ml的浓度范围内呈线性。日间和日内准确度和精密度结果均符合生物分析验证的公认标准。该方法用于体外研究模型前药的分解途径。