Li Peipei, Zhang Xiaojun, Zhang Juanmei, Yan Zhongyong, Zhang Shuai, Chen Si, Fang Yi
Marine Fishery Institute of Zhejiang Province, Zhoushan 316021, Zhejiang Province, China; Marine Sciences College, Ningbo University, Ningbo 315211, Zhejiang Province, China.
Marine Fishery Institute of Zhejiang Province, Zhoushan 316021, Zhejiang Province, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2018 Feb 1;1074-1075:39-45. doi: 10.1016/j.jchromb.2018.01.001. Epub 2018 Jan 3.
This paper described a reliable and simple method for the selective determination of MQCA in animal tissues using ultra high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). A highly targeted immunoaffinity column was used for sample purification after enzymatic hydrolysis. The purified extracts were analyzed by reversed-phase HPLC-MS/MS in positive ESI and multiple reaction monitoring mode. The calibration curves showed good linearity with correlation coefficient (r) larger than 0.995. The average recoveries at the spiked levels of 0.5, 2.0 and 20μgkg were 90.2% to 103.5% with intra-day and inter-day relatives standard deviations (RSD, n=6) ranging from 1.8% to 6.7% and 3.5% to 7.6% respectively. The limit of quantification (LOQ) was 0.5μgkg, which can fulfil the maximum residue level (MRL) of 4.0μgkg stipulated by the Agricultural Minister of China and the requirement of the confirmatory criteria according to the European Commission Decision 2002/657/EC. The method is sensitive, accurate, convenient and rapid, and has been successfully applied in real samples.
本文描述了一种使用超高效液相色谱-串联质谱法(UHPLC-MS/MS)选择性测定动物组织中MQCA的可靠且简单的方法。酶解后,使用高靶向免疫亲和柱对样品进行净化。纯化后的提取物采用反相HPLC-MS/MS在正离子电喷雾电离(ESI)和多反应监测模式下进行分析。校准曲线显示出良好的线性,相关系数(r)大于0.995。在0.5、2.0和20μg/kg的加标水平下,平均回收率为90.2%至103.5%,日内和日间相对标准偏差(RSD,n = 6)分别为1.8%至6.7%和3.5%至7.6%。定量限(LOQ)为0.5μg/kg,能够满足中国农业部长规定的4.0μg/kg的最大残留限量(MRL)以及欧盟委员会第2002/657/EC号决定中确证标准的要求。该方法灵敏、准确、方便且快速,已成功应用于实际样品分析。