Toraño J S, Vermes A, Guchelaar H J
Pharmaceutical and Clinical Toxicological Laboratory, Department of Clinical Pharmacy, Academic Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands.
Biomed Chromatogr. 2001 Apr;15(2):89-94. doi: 10.1002/bmc.38.
A validated, sensitive and precise reversed-phase high-performance liquid chromatographic method for the simultaneous determination of 5-flucytosine (5-FC) and 5-fluorouracil (5-FU) in human plasma is described. Two compounds, 5-methylcytosine (5-MC) and 5-chlorouracil (5-CU), were used as internal standards for the determination of 5-FC and 5-FU, respectively. Plasma samples were deproteinized with trichloroacetic acid and chromatographed on an octylsilica column, maintained at 30 degrees C during elution, using a 0.04 M phosphate buffer, pH 7.0, as eleunt. Spectrophotometric diode array detection was used at 266 nm. 5-FC, 5-FU, 5-MC and 5-CU were found to have retention times of 4.8, 5.8, 7.7 and 11.0 min respectively. Recoveries of 91-120% with reproducibility and repeatability coefficients of variation of 0.8-6% were obtained. Mean correlation coefficients of 0.99989 and 0.9995 were found for the linear calibration curves (n = 2) of 5-FC (4.816-192.6 mg/l) and 5-FU (0.05368-5.368 mg/l), respectively. The limits of quantitation were 0.3 mg/l for 5-FC and 0.05 mg/l for 5-FU.
本文描述了一种经过验证的、灵敏且精确的反相高效液相色谱法,用于同时测定人血浆中的5-氟胞嘧啶(5-FC)和5-氟尿嘧啶(5-FU)。分别使用两种化合物5-甲基胞嘧啶(5-MC)和5-氯尿嘧啶(5-CU)作为测定5-FC和5-FU的内标。血浆样品用三氯乙酸进行脱蛋白处理,然后在辛基硅胶柱上进行色谱分析,洗脱过程中柱温保持在30℃,以0.04M pH 7.0的磷酸盐缓冲液作为洗脱剂。采用分光光度二极管阵列检测,检测波长为266nm。发现5-FC、5-FU、5-MC和5-CU的保留时间分别为4.8、5.8、7.7和11.0分钟。回收率为91%-120%,重现性和重复性变异系数为0.8%-6%。5-FC(4.816-192.6mg/L)和5-FU(0.05368-5.368mg/L)的线性校准曲线(n = 2)的平均相关系数分别为0.99989和0.9995。5-FC的定量限为0.3mg/L,5-FU的定量限为0.05mg/L。