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奥芬达唑药物剂型分析:II. 马用糊剂中奥芬达唑和敌百虫的液相色谱法同时测定

Analysis of pharmaceutical dosage forms for oxfendazole: II. Simultaneous liquid chromatographic determination of oxfendazole and trichlorfon in equine paste.

作者信息

Fleitman J, Neu D, Benjamin E

出版信息

J Assoc Off Anal Chem. 1986 Jan-Feb;69(1):24-8.

PMID:3949692
Abstract

A reverse phase liquid chromatographic procedure is described for the simultaneous determination of oxfendazole [2-(methoxycarbonylamino)-5-phenylsulfinylbenzimidazole] and trichlorfon [(2,2,2-trichloro-1-hydroxyethyl)phosphonic acid dimethyl ester] in equine paste. The sample is extracted by sonication in methanol. Insoluble excipients are removed by centrifugation and an aliquot plus internal standard are diluted with dilution solvent (water-acetonitrile-phosphoric acid, 80 + 20 + 1). The samples are filtered and injected onto a Partisil-5 ODS-3 column with acetonitrile-0.01 M phosphate buffer pH 6.0 (20 + 80) as mobile phase. Method specificity is confirmed using an absorbance rationing technique. The method yields mean recoveries of 100.9 and 100.0% for trichlorfon and oxfendazole, respectively. Dependence of chromatographic performance characteristics on mobile phase organic content, pH, and buffer concentration is also reported.

摘要

本文描述了一种反相液相色谱法,用于同时测定马用膏剂中奥芬达唑[2-(甲氧基羰基氨基)-5-苯基亚磺酰基苯并咪唑]和敌百虫[(2,2,2-三氯-1-羟乙基)膦酸二甲酯]的含量。样品通过在甲醇中超声提取。不溶性辅料通过离心去除,取一份上清液加内标并用稀释溶剂(水-乙腈-磷酸,80 + 20 + 1)稀释。样品过滤后注入Partisil-5 ODS-3柱,以乙腈-0.01 M pH 6.0的磷酸盐缓冲液(20 + 80)作为流动相。使用吸光度比值技术确认了方法的特异性。该方法对敌百虫和奥芬达唑的平均回收率分别为100.9%和100.0%。还报道了色谱性能特征对流动相有机含量、pH值和缓冲液浓度的依赖性。

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