Yamaguchi Takahiro, Kakimoto Kensaku, Nagayoshi Haruna, Yamaguchi Mizuka, Okihashi Masahiro, Kajimura Keiji, Yamamoto Yoshimasa
Osaka Prefectural Institute of Public Health.
Shokuhin Eiseigaku Zasshi. 2013;54(4):290-7. doi: 10.3358/shokueishi.54.290.
A method using dispersive and cartridge column solid-phase extraction (SPE) was developed for the simultaneous determination of veterinary drugs in livestock products by LC-MS/MS. The samples were extracted with 85% acetonitrile and cleaned up using dispersive and cartridge column SPE. Recoveries of 70 analytes fortified at the levels of 0.002 μg/g and 0.01 μg/g in cattle, swine and chicken muscles were examined. Among 70 analytes examined, 64 in cattle, 58 in swine and 49 in chicken satisfied the required Japanese validation guideline. The limit of quantitation values of the 70 analytes were 0.001 μg/g or 0.005 μg/g in three kinds of livestock products. This method is suitable to analyze 40 analytes in three kinds of livestock products at levels under the MRL.
建立了一种采用分散和柱式固相萃取(SPE)的方法,用于通过液相色谱-串联质谱法同时测定畜产品中的兽药。样品用85%乙腈提取,并使用分散和柱式固相萃取进行净化。考察了在牛、猪和鸡肉中添加水平为0.002 μg/g和0.01 μg/g的70种分析物的回收率。在所考察的70种分析物中,牛中的64种、猪中的58种和鸡中的49种符合日本规定的验证指南要求。70种分析物在三种畜产品中的定量限为0.001 μg/g或0.005 μg/g。该方法适用于分析三种畜产品中低于最大残留限量水平的40种分析物。