Wu Zhi-Xiong, Hu Jiang-Tao, Zheng Wei-Dong, Sheng Yi, Chen Si, Yin Wen-Ya
Department of Nutrition and Food Hygiene, West China School of Public Health, Sichuan University, Chengdu 610041, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2010 May;41(3):523-6.
To develop a method for simultaneous determination of avermectin (AVM) and ivermectin (IVM) in swine muscular tissues using high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS).
The AVM and IVM were extracted with acetonitrile, cleaned with basic alumina solid phase extraction cartridges, separated through C8 column, and then detected by mass spectrometry in positive ion mode with multiple reaction monitoring (MRM) using an electrospray ionization interface, with quantitative ion pair of 890.4/305.3 and 892.5/307.3 for AVM and IVM, respectively.
The linear ranges for both AVM and IVM were between 5 microg/L and 100 microg/L, with a correlation coefficient of 0.9999. The detection limit was 2.0 microg/kg. The recoveries at the spiked concentration of 2 microg/kg, 10 microg/kg and 20 microg/kg ranged from 77.4% to 83.1% for AVM and 77.2% to 84.8% for IVM, with relative standard deviation (RSD) ranging from 8.7% to 11.7% for AVM and 6.3% to 10.3% for IVM, respectively. No AVM and IVM residues were detected in samples taken from Chengdu markets.
A HPLC-MS/MS method was successfully developed for determining AVM and IVM in swine muscular tissues, which is simple, sensitive and precise and can meet both domestic and international requirements.
建立一种利用高效液相色谱 - 串联质谱法(HPLC-MS/MS)同时测定猪肌肉组织中阿维菌素(AVM)和伊维菌素(IVM)的方法。
用乙腈提取AVM和IVM,经碱性氧化铝固相萃取小柱净化,通过C8柱分离,然后采用电喷雾电离接口,以正离子模式通过多反应监测(MRM)进行质谱检测,AVM和IVM的定量离子对分别为890.4/305.3和892.5/307.3。
AVM和IVM的线性范围均为5μg/L至100μg/L,相关系数为0.9999。检测限为2.0μg/kg。在2μg/kg、10μg/kg和20μg/kg加标浓度下,AVM的回收率为77.4%至83.1%,IVM的回收率为77.2%至84.8%,AVM的相对标准偏差(RSD)为8.7%至11.7%,IVM的相对标准偏差为6.3%至10.3%。从成都市场采集的样品中未检测到AVM和IVM残留。
成功建立了一种测定猪肌肉组织中AVM和IVM的HPLC-MS/MS方法,该方法简便、灵敏、准确,能满足国内外要求。