Fujitomo H, Nagaoka T, Nishino I, Umeda T
Shionogi Research Laboratories, Shionogi & Co., Ltd., Osaka, Japan.
J Chromatogr B Biomed Sci Appl. 1999 May 14;728(1):125-31. doi: 10.1016/s0378-4347(99)00093-6.
Direct injection high-performance liquid chromatographic (HPLC) methods with column switching and UV detection were developed for the rapid and accurate determination of S-1090 in human plasma and urine. An internal-surface reversed-phase pre-column and a C18 analytical column were used for the plasma assay. Two pre-columns packed with cyano and phenyl materials and a C18 analytical column were used for the urine assay. The calibration curves for plasma and urine assays were linear in the ranges 0.09-9 microg/ml and 0.5-100 microg/ml of S-1090, respectively. The relative standard deviations for plasma and urine assays were less than 6% with low relative errors. The established HPLC methods were demonstrated to be useful for clinical pharmacokinetic studies after oral administration of S-1090.
建立了具有柱切换和紫外检测功能的直接进样高效液相色谱(HPLC)方法,用于快速、准确地测定人血浆和尿液中的S-1090。血浆分析采用内表面反相预柱和C18分析柱。尿液分析采用两根分别填充氰基和苯基材料的预柱以及一根C18分析柱。血浆和尿液分析的校准曲线在S-1090浓度分别为0.09 - 9微克/毫升和0.5 - 100微克/毫升范围内呈线性。血浆和尿液分析的相对标准偏差小于6%,相对误差较低。所建立的HPLC方法被证明可用于口服S-1090后的临床药代动力学研究。