3'-叠氮-3'-脱氧胸腺嘧啶(AZT)的毒性分解产物-3'-氨基-3'-脱氧胸腺嘧啶(AMT)的竞争性ELISA测定。

B Ferrua, H Chakboub, C Roptin, R Garraffo, A Faraj, J Grassi, R Guedj, J P Sommadossi
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引用次数: 3

摘要

在本研究中,开发了一种竞争性ELISA技术来特异性定量3'-氨基-3'-脱氧胸腺嘧啶(AMT), AMT是AZT治疗患者血清中检测到的3'-叠氮-3'-脱氧胸腺嘧啶(AZT)的有毒分解产物。为了消除交叉反应的AZT,用乙酸乙酯提取血清样品,然后将AMT乙酰化(Ac-AMT)。用5′-半琥珀酸- amt -辣根过氧化物酶偶联物作为示踪剂,对5′-半琥珀酸- amt -牛血清白蛋白免疫原进行抗amt兔抗体培养。将抗兔IgG小鼠单克隆抗体不溶在微滴板上实现结合/自由分离。血清样品中Ac-AMT的定量限低至0.4 ng/ml。应用ELISA技术监测AZT治疗患者血浆AMT水平。AZT/AMT血浆浓度比的个体内和个体间变化强调了在研究这种有毒分解代谢物形成时需要这样一个特定的测试。
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Quantitation of 3'-amino-3'-deoxythymidine (AMT), a toxic catabolite of 3'-azido-3'-deoxythymidine (AZT), by competitive ELISA.

In the present study, a competitive ELISA technique was developed to specifically quantitate 3'-amino-3'-deoxythymidine (AMT), a toxic catabolite of 3'-azido-3'-deoxythymidine (AZT) detected in serum from AZT-treated patients. In order to eliminate cross-reacting AZT, serum sample was extracted with ethylacetate and then AMT was acetylated (Ac-AMT). A 5'-hemisuccinate-AMT-horseradish peroxidase conjugate was used as a tracer in the presence of anti-AMT rabbit antibodies which were raised against a 5' hemisuccinate-AMT-bovine serum albumin immunogen. Bound/free separation was achieved with an anti-rabbit IgG mouse monoclonal antibody insolubilized onto a microtiter plate. The limit of quantification of Ac-AMT was as low as 0.4 ng/ml in serum samples. This ELISA technique was applied for monitoring AMT plasma levels in patients receiving AZT therapy. The intra and inter-individual variations of the AZT/AMT plasma concentration ratios underlined the need for such a specific test in studying the formation of this toxic catabolite.

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