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首页> 外文期刊>Chromatographia >Simultaneous determination of furathiocarb and metabolites in biological tissues by high-performance liquid chromatography and post-column derivatization
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Simultaneous determination of furathiocarb and metabolites in biological tissues by high-performance liquid chromatography and post-column derivatization

机译:高效液相色谱和柱后衍生同时测定生物组织中的呋喃硫威和代谢物

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摘要

A new method to determine simultaneously the amount of furathiocarb and metabolites: carbofuran, 3-hydroxycarbofuran, and 3-ketocarbofuran in biological tissues such as liver and kidney is described. The method consists of extraction of samples with acetone, filtration, partition, purification of target analytes through a silica gel column and high-performance liquid chromatographic determination with post-column derivatization. Reasonable recoveries for routine analysis were obtained, and the limits of detection (LOD) with fluorescence detection were 0.2, 0.1, 0.1, and 0.2 mg L−1 for furathiocarb, carbofuran, 3-hydroxycarbofuran and 3-ketocarbofuran respectively, with a signal-to-noise ratio of 3. The present method was successfully applied to the dermal pharmacokinetic study of furathiocarb in Sprague-Dawley rats. Carbofuran and 3-hydroxycarbofuran were observed in liver while only carbofuran was detected in kidney.
机译:描述了一种同时测定呋喃硫威和代谢物(如呋喃呋喃,3-羟基呋喃呋喃和3-酮呋喃呋喃)的含量的新方法,该生物组织例如肝脏和肾脏。该方法包括用丙酮萃取样品,过滤,分配,通过硅胶柱纯化目标分析物,以及通过柱后衍生化进行高效液相色谱测定。获得了常规分析的合理回收率,并且使用呋喃硫脲,呋喃丹,3-呋喃呋喃,3-羟基呋喃呋喃和3-酮呋喃呋喃的荧光检出限(LOD)分别为0.2、0.1、0.1和0.2 mg L-1 ,信噪比为3。本方法成功应用于呋喃硫威在Sprague-Dawley大鼠中的皮肤药代动力学研究。在肝脏中观察到了呋喃丹和3-羟基呋喃呋喃,而在肾脏中仅检测到了呋喃丹。

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