Augey V, Cociglio M, Galtier M, Yearoo R, Pinsani V, Bressolle F
Laboratoire de Pharmacocinétique, Hôpital Carémeau, Nimes, France.
J Pharm Biomed Anal. 1995 Aug;13(9):1173-8. doi: 10.1016/0731-7085(95)01544-u.
A reproducible, simple and sensitive high-performance liquid chromatographic method was described for the quantitative analysis of cis-diamminedichloroplatinum(II) (CDDP) in ultrafiltrate plasma in the presence of nickel chloride as internal standard. CDDP and the internal standard were chelated by exchange with diethyldithiocarbamate. After derivatization, the mixture was directly injected into the column. Chromatography was performed on an Ultrasphere column and the eluent measured spectrophotometrically at 260 nm for CDDP and at 250 nm for the internal standard. The peak area ratio of CDDP to the internal standard varied linearly with concentration over the range 0.05-10 micrograms ml-1. Precision and reproducibility were both excellent and the limit of quantification was 0.03 micrograms ml-1 using only 0.5 ml of ultrafiltrate. The present method, without extraction, should be entirely automated. This assay may be suitable for therapeutic drug monitoring in patients receiving CDDP.
描述了一种可重现、简单且灵敏的高效液相色谱法,用于在以氯化镍作为内标的情况下,对超滤血浆中的顺二氯二氨铂(II)(CDDP)进行定量分析。CDDP和内标通过与二乙基二硫代氨基甲酸盐交换进行螯合。衍生化后,将混合物直接注入色谱柱。在Ultrasphere柱上进行色谱分析,对CDDP在260 nm处、对内标在250 nm处进行分光光度法测定洗脱液。CDDP与内标的峰面积比在0.05 - 10微克/毫升范围内随浓度呈线性变化。精密度和重现性均极佳,仅使用0.5毫升超滤液时定量限为0.03微克/毫升。本方法无需萃取,应可完全自动化。该测定法可能适用于接受CDDP治疗的患者的治疗药物监测。