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高效液相色谱法测定血浆和尿液中的头孢噻肟和去乙酰头孢噻肟

Determination of cefotaxime and desacetylcefotaxime in plasma and urine by high-performance liquid chromatography.

作者信息

Dell D, Chamberlain J, Coppin F

出版信息

J Chromatogr. 1981 Dec 11;226(2):431-40. doi: 10.1016/s0378-4347(00)86077-6.

Abstract

A high-performance liquid chromatographic method is described for the analysis of the anti-bacterial agent cefotaxime and desacetylcefotaxime in physiological fluids. Plasma or serum samples were mixed with chloroform--acetone to remove proteins and most lipid material. The aqueous phase was then freeze-dried, reconstituted in mobile phase and chromatographed on a reversed-phase column using UV detection at 262 nm. Urine was analysed directly after centrifugation to remove particulate matter. The detection limit was 0.5--1.0 micrograms/ml for serum and 5 micrograms/ml for urine. The method has been applied to the analyses of cefotaxime and desacetylcefotaxime in plasma, serum, urine, cerebrospinal fluid, saliva, and pus from infected wound secretions. Two additional metabolites, which are lactones in which the beta-lactam ring has been opened, could be separated by this method.

摘要

本文描述了一种高效液相色谱法,用于分析生理体液中的抗菌剂头孢噻肟和去乙酰头孢噻肟。血浆或血清样本与氯仿 - 丙酮混合以去除蛋白质和大部分脂质物质。然后将水相冷冻干燥,用流动相复溶,并在反相柱上进行色谱分析,使用262nm的紫外检测。尿液在离心去除颗粒物后直接进行分析。血清的检测限为0.5 - 1.0微克/毫升,尿液的检测限为5微克/毫升。该方法已应用于血浆、血清、尿液、脑脊液、唾液和感染伤口分泌物的脓液中头孢噻肟和去乙酰头孢噻肟的分析。另外两种代谢产物,即β-内酰胺环已打开的内酯,可以通过该方法分离。

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