Kim S H, Choi W S, Chang M S, Lee M G
College of Pharmacy, Seoul National University, South Korea.
Res Commun Mol Pathol Pharmacol. 1997 Jul;97(1):107-12.
A high-performance liquid chromatographic method was developed for the determination of a new antiulcer agent, YJA-20379-1, in human plasma and urine, and rat blood and tissue homogenates. 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 C18 reversed-phase column. The mobile phase employed was methanol--0.1 M Sørensen phosphate buffer of pH7.0--H2O (80:2:15, v/v/v), and was run at a flow-rate of 0.7 ml/min. The column effluent was monitored by ultraviolet detector at 254 nm. The retention time for YJA-20379-1 was approximately 6.3 min. The detection limits for YJA-20379-1 in human plasma and urine, and 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 9.44%) for the human plasma and urine, and rat blood and tissue homogenate. No interference from endogenous substances were found.
建立了一种高效液相色谱法,用于测定人血浆、尿液以及大鼠血液和组织匀浆中新型抗溃疡药物YJA - 20379 - 1的含量。样品制备方法简单:向生物样品中加入2.5倍体积的乙腈进行蛋白沉淀。取50微升上清液注入C18反相柱。所用流动相为甲醇 - pH7.0的0.1M索伦森磷酸盐缓冲液 - 水(80:2:15,v/v/v),流速为0.7毫升/分钟。柱流出物用紫外检测器在254纳米处进行监测。YJA - 20379 - 1的保留时间约为6.3分钟。YJA - 20379 - 1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纳克/毫升。该测定法(日内和日间)在人血浆、尿液以及大鼠血液和组织匀浆中的变异系数通常较低(低于9.44%)。未发现内源性物质的干扰。