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采用反相液相色谱法测定人血浆和尿液中的替卡西林。

Determination of ticarcillin in human plasma and in urine by reversed-phase LC.

作者信息

La Follette G, Jayewardene A L, Seneviratne A K, Lin E T, Gambertoglio J G

机构信息

Division of Clinical Pharmacy, School of Pharmacy, University of California, San Francisco 94143-0622, USA.

出版信息

J Pharm Biomed Anal. 1995 Feb;13(2):159-64. doi: 10.1016/0731-7085(94)00137-q.

Abstract

A liquid chromatographic assay for ticarcillin (ticar.) in plasma and urine is described. For analysis, the internal standard cefoperazone (cfp) is dissolved in acetonitrile, which is used for precipitating the protein. The supernatant is evaporated, reconstituted in running mobile phase and injected directly onto the reversed-phase C18 column, with detection at 205 nm. The mobile phase is composed of water-acetonitrile-o-phosphoric acid-tetramethylammonium chloride (TMA). Coefficients of variation for reproducibility were in the range of 2.2-15.5% for extra-low, low, medium and high controls. Limits of detection were 0.5 microgram ml-1 for plasma and 1 microgram ml-1 for urine. No interference from other cephalosporins or other antibiotics was noted. This liquid chromatographic assay is simple, accurate, requires no extraction and overcomes previous problems related to the drug's peak splitting due to isomerization.

摘要

本文描述了一种用于测定血浆和尿液中替卡西林(ticar.)的液相色谱分析方法。分析时,将内标头孢哌酮(cfp)溶解于用于沉淀蛋白质的乙腈中。将上清液蒸发,用流动相复溶后直接进样到反相C18柱上,于205nm处进行检测。流动相由水 - 乙腈 - 邻磷酸 - 四甲基氯化铵(TMA)组成。超低、低、中、高浓度对照品的重现性变异系数在2.2 - 15.5%范围内。血浆的检测限为0.5微克/毫升,尿液的检测限为1微克/毫升。未发现其他头孢菌素或其他抗生素的干扰。这种液相色谱分析方法简单、准确,无需萃取,并且克服了以往因异构化导致药物峰分裂的问题。

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