| 注册
首页|期刊导航|色谱|高效液相色谱法测定猪组织中残留的咪唑苯脲

高效液相色谱法测定猪组织中残留的咪唑苯脲

于慧敏 黄显会 钟家林 杨刚 方秋华

色谱2011,Vol.29Issue(8):750-754,5.
色谱2011,Vol.29Issue(8):750-754,5.DOI:10.3724/SP.J.1123.2011.00750

高效液相色谱法测定猪组织中残留的咪唑苯脲

Determination of imidocarb residue in swine tissues by high performance liquid chromatography

于慧敏 1黄显会 1钟家林 1杨刚 1方秋华1

作者信息

  • 1. 华南农业大学国家兽药残留基准实验室,广东广州510642
  • 折叠

摘要

Abstract

A quantitive method for the determination of imidocarb residue in edible tissues of swine by high performance liquid chromatography (HPLC) was developed. The analyte was digested by j8-glucosidase first, and then extracted with 1 mol/L hydrochloric acid. The aqueous phase was back-extracted with the mixture of hexane-isoamyl alcohol (3:2, v/v) for the purification. The mobile phases were acetonitrile (phase A) and 0. 007 5 mol/L 1 -pentansulfonic acid sodium aqueous solution containing 0. 1% triethylamine, adjusted to pH 3. 0 with glacial acetic acid (phase B). The analyte was detected by ultraviolet absorption spectroscopy after the separation was achieved on a C18 RP column. The linear range was 10 - 10 000 μg/L, and the correlation coefficient was more than 0. 999. The limit of detection (LOD) was 10 μg/kg, and the limit of qualification (LOQ) was 20 μg/kg. The mean recoveries of imidocarb in swine tissues at the added levels of LOQ, MRL (maximum residue limit) and 2MRL ranged from 80.04% to 110. 32%, and the relative standard deviations (RSDs) of intra- and inter-day analyses ranged from 0. 82% to 10. 00%. The method is simple and sensitive for the quantification of imidocarb residue in swine tissues.

关键词

高效液相色谱法/咪唑苯脲/兽药残留//可食性组织

Key words

high performance liquid chromatography (HPLC)/ imidocarb j veterinary drug residue / swine/ edible tissues

分类

化学化工

引用本文复制引用

于慧敏,黄显会,钟家林,杨刚,方秋华..高效液相色谱法测定猪组织中残留的咪唑苯脲[J].色谱,2011,29(8):750-754,5.

基金项目

2009年农业行业标准制定和修订计划项目 ()

色谱

OA北大核心CSCDCSTPCDMEDLINE

1000-8713

访问量0
|
下载量0
段落导航相关论文