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采用柱切换高效液相色谱法同时测定生物样品中的氨苄西林和甲氧西林。

Simultaneous determination of ampicillin and metampicillin in biological fluids using high-performance liquid chromatography with column switching.

作者信息

Lee H, Lee J S, Lee H S

机构信息

Screening and Toxicology Center, Korea Research Institute of Chemical Technology, Taejeon.

出版信息

J Chromatogr B Biomed Appl. 1995 Feb 17;664(2):335-40. doi: 10.1016/0378-4347(94)00472-h.

Abstract

A new high-performance liquid chromatographic method with column switching has been developed for the simultaneous determination of metampicillin and its metabolite ampicillin in biological fluids. The plasma, urine and bile samples were injected onto a precolumn packed with LiChrosorb RP-8 (25-40 microns) after simple dilution with an internal standard solution in 0.05 M phosphate buffer (pH 7.0). The polar plasma components were washed out using 0.05 M phosphate buffer (pH 7.0). After valve switching, the concentrated drugs were eluted in the back-flush mode and separated by an Ultracarb 5 ODS-30 column with a gradient system of acetonitrile-0.02 M phosphate buffer (pH 7.0) as the mobile phase. The method showed excellent precision, accuracy and speed with a detection limit of 0.1 microgram/ml. The total analysis time per sample was less than 40 min and the coefficients of variation for intra- and inter-assay were less than 5.1%. This method has been successfully applied to plasma, urine and bile samples from rats after intravenous injection of metampicillin.

摘要

已开发出一种带柱切换的新型高效液相色谱法,用于同时测定生物流体中的美坦西林及其代谢产物氨苄西林。血浆、尿液和胆汁样品在用内标溶液于0.05 M磷酸盐缓冲液(pH 7.0)中简单稀释后,注入装有LiChrosorb RP - 8(25 - 40微米)的预柱。使用0.05 M磷酸盐缓冲液(pH 7.0)洗脱出极性血浆成分。阀切换后,浓缩的药物以反冲模式洗脱,并通过Ultracarb 5 ODS - 30柱进行分离,以乙腈 - 0.02 M磷酸盐缓冲液(pH 7.0)的梯度系统作为流动相。该方法具有出色的精密度、准确度和速度,检测限为0.1微克/毫升。每个样品的总分析时间少于40分钟,批内和批间变异系数均小于5.1%。该方法已成功应用于静脉注射美坦西林后大鼠的血浆、尿液和胆汁样品。

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