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Rapid screening of toxic salbutamol, ractopamine, and clenbuterol in pork sample by high-performance liquid chromatography-UV method

机译:通过高效液相色谱 - UV法快速筛选有毒沙丁胺醇,乳酰胺和Clenbuterol的猪肉样品

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A rapid and simple high-performance liquid chromatography-UV method was developed for the separation and quantification of salbutamol, ractopamine, and clenbuterol in pork. A mixture of acetonitrile formic acid ammonium acetate was used as the mobile phase to separate three beta-agonists on a C18 column with gradient. The effects of the addition of formic acid and ammonium acetate to mobile phases on the separation of beta-agonists were investigated. These additives can greatly improve the resolution and sensitivity. Under the optimized chromatographic condition, this separation does not need extra sample preparation. Complete baseline separation of three beta-agonists was achieved in 20 minutes; the linear range is 0.2-50 mu g/L with a correlation coefficient R-2 value of 0.99. Excellent method reproducibility was found by intra- and interday precisions with a relative standard deviation of 3%. The detection limit (S/N = 3) was found to be 0.05 mu g/L; this method can be used for routine screening of the beta-agonist residues in foods of animal origin before being identified by confirmatory methods. Copyright (C) 2016, Food and Drug Administration, Taiwan. Published by Elsevier Taiwan LLC. This is an open access article under the CC BY-NC-ND license.
机译:开发了一种快速简便的高效液相色谱 - UV方法,用于分离和定量猪肉中的萨丁莫醇,乳酰胺和亚丁甲醇。使用乙腈甲酸乙酸铵的混合物作为流动相,以将三个β-激动剂与梯度分离在C18柱上。研究了对β-激动剂分离的甲酸和醋酸铵加入乙酸铵与移动相的影响。这些添加剂可以大大提高分辨率和敏感性。在优化的色谱条件下,该分离不需要额外的样品制备。在&的完全基线分离三种β-激动剂20分钟;线性范围为0.2-50μmg/ l,具有相关系数R-2值& 0.99。通过具有相对标准偏差的间隔和间隔的精度发现优异的方法再现性。 3%。发现检测极限(S / N = 3)是<0.05μg/ l;该方法可用于通过确认方法鉴定在动物来源食品中的β-激动剂残留物中的常规筛选。版权所有(C)2016,食品和药物管理局,台湾。由elsevier taiwan llc发布。这是CC By-NC-ND许可下的开放式访问文章。

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