Han K S, Choi H C, Yoo J K, Lee J W, Lee M G
College of Pharmacy, Seoul National University, South Korea.
J Chromatogr B Biomed Sci Appl. 1997 Aug 29;696(2):312-6. doi: 10.1016/s0378-4347(97)00238-7.
A high-performance liquid chromatographic method was developed for the determination of a new proton pump inhibitor, YH1885 (I), in human plasma and urine, and rat blood and tissue homogenate using fenticonazole as an internal standard. The sample preparation was simple: a 2.5 volume of acetonitrile was added to the biological sample to deproteinize it. A 50-microliter aliquot of the supernatant was injected onto a C8 reversed-phase column. The mobile phase employed was methanol-0.005 M tetrabutylammonium dihydrogenphosphate (77:23, v/v), and it was run at a flow-rate of 1.0 ml/min. The column effluent was monitored using an ultraviolet detector at 270 nm. The retention times for I and the internal standard were 9.0 and 10.3 min, respectively. The detection limits for I in human plasma and urine, and in rat tissue homogenate (including blood) were 50, 100 and 100 ng/ml, respectively. The coefficients of variation of the assay (within- day and between-day) were generally low (below 8.84%) for human plasma and urine, and for rat tissue homogenate. No interferences from endogenous substances were found.
建立了一种高效液相色谱法,以芬替康唑为内标,用于测定人血浆、尿液以及大鼠血液和组织匀浆中的新型质子泵抑制剂YH1885(I)。样品制备简单:向生物样品中加入2.5倍体积的乙腈使其脱蛋白。取50微升上清液注入C8反相柱。所用流动相为甲醇-0.005 M磷酸二氢四丁铵(77:23,v/v),流速为1.0 ml/min。使用紫外检测器在270 nm处监测柱流出物。I和内标的保留时间分别为9.0和10.3分钟。I在人血浆、尿液以及大鼠组织匀浆(包括血液)中的检测限分别为50、100和100 ng/ml。该测定方法的变异系数(日内和日间)对于人血浆、尿液以及大鼠组织匀浆通常较低(低于8.84%)。未发现内源性物质的干扰。