Bailey D G, Wilson T W, Johnson G E
J Chromatogr. 1975 Sep 3;111(2):305-11. doi: 10.1016/s0021-9673(00)99279-3.
A method is presented for the measurement of 6-mercaptopurine (6-MP) in serum. Serum samples containing the drug were treated with dithioerythritol and saturated with ammonium carbonate. 6-MP was then extracted from the serum with a mixture of isopropanol-ethyl acetate (1:1, v/v) containing 0.01% ethanethiol. The solvent was evaporated, the residue dissolved in dilute hydrocholoric acid, washed with chloroform, and extracted with ethyl acetate. 6-MP was derivatized with trimethylanilinium hydroxide and measured gas chromatographically. The sulfhydryl-protecting reagents, dithioerythritol and ethanethiol, were added to prevent the decomposition of 6-MP. The extraction and clean-up method recovered 78 +/- 2% (S.E.) of the 6-MP present. Tracer amounts of [8-14C]6-MP served as the internal standard during the extraction part of the method. Theophyline was used as the internal standard during the gas chromatographic analysis. The standard curve obtained from the gas chromatograph was linear between 0.5 and 20 mug/ml of 6-MP. Serum samples were stored in the freezer for two weeks without significant loss of drug. No interference was encountered from normal serum constituents or xanthines, such as caffeine or theophylline added to serum.
本文介绍了一种测定血清中6-巯基嘌呤(6-MP)的方法。含药血清样本用二硫苏糖醇处理,并用碳酸铵饱和。然后用含0.01%乙硫醇的异丙醇-乙酸乙酯(1:1,v/v)混合物从血清中提取6-MP。蒸发溶剂,将残留物溶于稀盐酸,用氯仿洗涤,再用乙酸乙酯萃取。6-MP用氢氧化三甲基苯胺衍生化,并用气相色谱法测定。加入巯基保护试剂二硫苏糖醇和乙硫醇以防止6-MP分解。该提取和净化方法回收了78±2%(标准误)的6-MP。在该方法的提取过程中,示踪量的[8-14C]6-MP用作内标。在气相色谱分析中,茶碱用作内标。气相色谱仪得到的标准曲线在6-MP浓度为0.5至20μg/ml之间呈线性。血清样本在冰箱中保存两周,药物无明显损失。正常血清成分或添加到血清中的黄嘌呤(如咖啡因或茶碱)未产生干扰。