Hirai T, Matsumoto S, Kishi I
Medical Research Laboratories, Lederle (Japan) Ltd., Saitama, Japan.
J Chromatogr B Biomed Sci Appl. 1997 Mar 7;690(1-2):267-73. doi: 10.1016/s0378-4347(96)00371-4.
A practical and sensitive high-performance liquid chromatographic method using normal solid-phase extraction has been developed for the determination of methotrexate (MTX) and its main metabolite 7-hydroxymethotrexate (7-OH-MTX) in human urine. A urine specimen followed by the addition of pH 5.0 acetate buffer was purified by solid-phase extraction on a Sep-Pak silica cartridge. The analyte was chromatographed on a reversed-phase Inertsil ODS-2 column using phosphate buffer-acetonitrile at pH 5.3 as the mobile phase, and the effluent from the column was monitored at 303 nm. A good linear relationship between peak height and concentration was found for both of MTX and 7-OH-MTX in the range 5 to 1000 ng/ml of human urine. The inter-day coefficients of variation for the assay (n = 5) were 8.8% (5 ng/ml), 3.4% (50 ng/ml) and 2.0% (500 ng/ml) for MTX, and 7.2, 2.7 and 2.3% for 7-OH-MTX in urine, respectively. The present method should prove useful for the evaluation of urinary drug excretion in patients undergoing MTX low-dose therapy.
已开发出一种实用且灵敏的高效液相色谱法,采用常规固相萃取法测定人尿中的甲氨蝶呤(MTX)及其主要代谢物7 - 羟基甲氨蝶呤(7 - OH - MTX)。尿样加入pH 5.0的醋酸盐缓冲液后,通过Sep - Pak硅胶柱进行固相萃取纯化。分析物在反相Inertsil ODS - 2柱上进行色谱分析,以pH 5.3的磷酸盐缓冲液 - 乙腈为流动相,柱流出物在303 nm处进行监测。在人尿中MTX和7 - OH - MTX浓度为5至1000 ng/ml范围内,峰高与浓度之间均呈现良好的线性关系。该测定法的日间变异系数(n = 5),尿中MTX分别为8.8%(5 ng/ml)、3.4%(50 ng/ml)和2.0%(500 ng/ml),7 - OH - MTX分别为7.2%、2.7%和2.3%。本方法对于评估接受低剂量MTX治疗患者的尿药排泄应是有用的。