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采用高效液相色谱法测定血浆和尿液中新型碳青霉烯衍生物DA-1131的含量。

Determination of a new carbapenem derivative, DA-1131, in plasma and urine by high-performance liquid chromatography.

作者信息

Kim S H, Kwon J W, Yang J, Lee M G

机构信息

College of Pharmacy, Seoul National University, South Korea.

出版信息

J Chromatogr B Biomed Sci Appl. 1997 Jan 10;688(1):95-9. doi: 10.1016/s0378-4347(97)88060-7.

Abstract

A high-performance liquid chromatographic method was developed for the determination of a new carbapenem, DA-1131 (I), in human plasma and urine and in rat blood and tissue homogenates. The method involved deproteinization of the biological samples with 1 volume each of 0.04 M Ba(OH)2 and ZnSO4 aqueous solution. A 50-microliters aliquot of the supernatant was injected onto a C18 reversed-phase column. The mobile phase employed was 0.015 M KH2PO4-acetonitrile (9:1, v/v) with a pH of 5.0. The flow-rate was 0.8 ml/min. The column effluent was monitored by a ultraviolet detector at 300 nm. The retention time of I was 8.0 min. The detection limits of I in human plasma and urine were 0.1 and 0.5 micrograms/ml, respectively. The coefficients of variation of the assay were generally low (below 8.39%) for human plasma and urine, and rat blood and tissue homogenates. No interferences from endogenous substances were observed.

摘要

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碳青霉烯类药物DA - 1131(I)的含量。该方法包括用等体积的0.04 M氢氧化钡和硫酸锌水溶液对生物样品进行去蛋白处理。取50微升上清液注入C18反相柱。所用流动相为0.015 M磷酸二氢钾 - 乙腈(9:1,v/v),pH值为5.0。流速为0.8毫升/分钟。柱流出物用紫外检测器在300纳米波长下进行监测。I的保留时间为8.0分钟。I在人血浆和尿液中的检测限分别为0.1微克/毫升和0.5微克/毫升。该测定方法在人血浆、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8.39%)。未观察到内源性物质的干扰。

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