Hosotsubo H
Central Laboratory for Clinical Investigation, Osaka University Hospital, Japan.
J Chromatogr. 1989 Feb 24;487(2):421-7. doi: 10.1016/s0378-4347(00)83049-2.
A high-performance liquid chromatographic method has been developed for the quantitative analysis of vancomycin in plasma. The method involves protein precipitation with acetonitrile, followed by normal-phase chromatography on an aminopropyl column. The clear supernatant was injected after centrifugation, and the eluent was monitored at 240 nm. No interference was found either with endogenous substances or with many currently used drugs, indicating a good selectivity for the procedure. The standard curve was linear between 0.1 and 100 micrograms/ml, and the detection limit was 0.01 microgram/ml of plasma. The mean intra- and inter-assay coefficients of variation were 2.4 and 4.0%, respectively, in the 10-50 micrograms/ml range. Application of the method to the study of vancomycin pharmacokinetics in a rabbit after a single intravenous dose is also reported.
已开发出一种高效液相色谱法用于定量分析血浆中的万古霉素。该方法包括用乙腈进行蛋白沉淀,然后在氨丙基柱上进行正相色谱分析。离心后将澄清的上清液进样,洗脱液在240nm处进行监测。未发现内源性物质或许多目前使用的药物有干扰,表明该方法具有良好的选择性。标准曲线在0.1至100微克/毫升之间呈线性,血浆检测限为0.01微克/毫升。在10 - 50微克/毫升范围内,批内和批间变异系数的平均值分别为2.4%和4.0%。还报道了该方法在单次静脉给药后兔体内万古霉素药代动力学研究中的应用。