Eksborg S, Ehrsson H, Lindfors A
J Chromatogr. 1983 May 13;274:263-70. doi: 10.1016/s0378-4347(00)84429-1.
A method is given for the determination of the antineoplastic drug mitomycin C in plasma and urine samples. Mitomycin is isolated from the biological matrix with the aid of a Sep-Pak C18 extraction column and eluted with methanol. The methanol is evaporated and the residue is redissolved in the chromatographic mobile phase (methanolic phosphate buffer). Mitomycin C is separated from coextracted compounds by reversed-phase liquid chromatography on a LiChrosorb RP-8 column. A high detection sensitivity and selectivity was obtained by photometric measurements at 365 nm. The precision of the determinations was better than 6% relative standard deviation for plasma samples within the range 2-1000 ng/ml, and for urine samples within the range 0.5-4.4 micrograms/ml. The pH-dependent stability of mitomycin in buffer solutions has been studied.
给出了一种测定血浆和尿液样本中抗肿瘤药物丝裂霉素C的方法。借助Sep-Pak C18萃取柱从生物基质中分离出丝裂霉素,并用甲醇洗脱。蒸干甲醇,将残留物重新溶解于色谱流动相(甲醇磷酸盐缓冲液)中。在LiChrosorb RP-8柱上通过反相液相色谱法将丝裂霉素C与共萃取的化合物分离。通过在365nm处进行光度测量获得了高检测灵敏度和选择性。对于血浆样本,在2-1000ng/ml范围内以及对于尿液样本在0.5-4.4μg/ml范围内,测定的精密度优于6%相对标准偏差。研究了丝裂霉素在缓冲溶液中pH依赖性稳定性。