Determination of Clenbuterol in Various Edible Parts of Livestock Products by LC-MS/MS and LC-MS/MS/MS Methods

Takako Hayashi, K. Hamase
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Abstract

The residual status of clenbuterol in various edible parts of livestock products was investigated using the LC-MS/MS and LC-MS/MS/MS methods. The target food products were the edible tissues of pig and cattle, and clenbuterol was extracted using acetonitrile containing anhydrous sodium sulfate and sodium chloride. Following the dispersive solid-phase extraction using C18 particles and purification with an anion-exchange solid-phase extraction cartridge, the resultant test sample solutions were subjected to the LC analysis. A C18 column was used as the analytical column, and the peak of clenbuterol was eluted at 4.8 min with the gradient elution from 5% acetonitrile to 99% acetonitrile in 10 min. As a result of the LC-MS/MS analysis, interfering peaks were detected around the retention time of clenbuterol. By using the LC-MS/MS/MS analysis, which was developed as a quantitative analysis method that reduces the influence of contaminants, most of the unknown peaks were removed, and it was confirmed that the food samples obtained in Kanagawa prefecture did not contain clenbuterol.
LC-MS/MS和LC-MS/MS法测定畜产品不同食用部位中的克伦特罗
采用LC-MS/MS和LC-MS/MS方法对瘦肉精在畜产品不同食用部位的残留状况进行了研究。目标食品是猪和牛的可食用组织,使用含有无水硫酸钠和氯化钠的乙腈提取瘦肉精。在使用C18颗粒进行分散固相萃取并使用阴离子交换固相萃取筒进行纯化之后,对所得测试样品溶液进行LC分析。使用C18柱作为分析柱,在4.8分钟洗脱克伦特罗的峰,在10分钟内从5%乙腈到99%乙腈进行梯度洗脱。作为LC-MS/MS分析的结果,在克伦特罗的保留时间附近检测到干扰峰。通过使用LC-MS/MS分析,这是一种减少污染物影响的定量分析方法,去除了大多数未知峰,并确认在神奈川县获得的食品样品不含瘦肉精。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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