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反相高效液相色谱法快速简便测定反刍动物尿液中苯甲酸、苯乙酸及其甘氨酸共轭物的方法

Rapid and simple method for the determination of urinary benzoic and phenylacetic acids and their glycine conjugates in ruminants by reversed-phase high-performance liquid chromatography.

作者信息

Arín M J, Diez M T, Resines J A

机构信息

Departamento de Bioquímica y Biología Molecular, Facultad de Biología, Universidad de León, Spain.

出版信息

J Chromatogr. 1992 Nov 6;582(1-2):13-8. doi: 10.1016/0378-4347(92)80296-3.

Abstract

A simple, rapid and reproducible reversed-phase high-performance liquid chromatographic method for the simultaneous determination of benzoic acid (BA), phenylacetic acid (PAA) and their respective glycine conjugates hippuric acid (HA) and phenaceturic acid (PA) in sheep urine is described. The procedure involves only direct injection of a diluted urine sample, thus obviating the need for an extraction step or an internal standard. The compounds were separated on a Nova-Pak C18 column with isocratic elution with acetate buffer (25 mM, pH 4.5)-methanol (95:5). A flow-rate of 1.0 ml/min, a column temperature of 35 degrees C and detection at 230 nm were employed. These conditions were optimized by investigating the effects of pH, molarity, methanol concentration in the mobile phase and column temperature on the resolution of the metabolites. The total analysis time was less than 15 min per sample. At a signal-to-noise ratio of 3 the detection limits for ten-fold diluted urine were 1.0 microgram/ml for BA and HA and 5.0 micrograms/ml for PAA and PA with a 20-microliters injection.

摘要

本文描述了一种简单、快速且可重复的反相高效液相色谱法,用于同时测定绵羊尿液中的苯甲酸(BA)、苯乙酸(PAA)及其各自的甘氨酸共轭物马尿酸(HA)和苯乙酰尿酸(PA)。该方法仅需直接进样稀释后的尿液样品,从而无需萃取步骤或内标物。化合物在Nova-Pak C18柱上以乙酸盐缓冲液(25 mM,pH 4.5)-甲醇(95:5)等度洗脱进行分离。采用1.0 ml/min的流速、35℃的柱温以及在230 nm处检测。通过研究pH、摩尔浓度、流动相中甲醇浓度和柱温对代谢物分离度的影响,对这些条件进行了优化。每个样品的总分析时间少于15分钟。在信噪比为3时,对于十倍稀释的尿液,进样20微升时,BA和HA的检测限为1.0微克/毫升,PAA和PA的检测限为5.0微克/毫升。

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