College of Life Science, Northwest University, Xi'an, PR China.
Shaanxi Lifegen Co., Ltd, Xi'an, PR China.
J Food Drug Anal. 2016 Apr;24(2):277-283. doi: 10.1016/j.jfda.2015.12.002. Epub 2016 Feb 23.
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 β-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 β-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 β-agonists was achieved in < 20 minutes; the linear range is 0.2-50 μg/L with a correlation coefficient R 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 μg/L; this method can be used for routine screening of the β-agonist residues in foods of animal origin before being identified by confirmatory methods.
建立了一种快速、简单的高效液相色谱-紫外检测法,用于同时分离和检测猪肉中的沙丁胺醇、莱克多巴胺和克伦特罗。采用乙腈-甲酸-乙酸铵混合溶液作为流动相,在 C18 柱上进行梯度洗脱,可实现 3 种β-激动剂的分离。考察了向流动相中添加甲酸和乙酸铵对β-激动剂分离的影响。这两种添加剂可以极大地提高分离度和灵敏度。在优化的色谱条件下,该方法无需额外的样品前处理。3 种β-激动剂可在 20 分钟内完全基线分离,线性范围为 0.2-50μg/L,相关系数 R 值>0.99。日内和日间精密度的相对标准偏差均<3%,表明方法重现性良好。检测限(S/N=3)<0.05μg/L。该方法可用于在确证方法之前对动物源性食品中的β-激动剂残留进行常规筛选。