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作 者:张水锋[1] 林珍珍[2] 陈小珍[1] 张东雷[1] 曹慧[1] 王立世[3]
机构地区:[1]浙江省质量检测科学研究院浙江省食品安全重点实验室,浙江杭州310013 [2]浙江工业大学化学工程与材料学院,浙江杭州310014 [3]华南理工大学化学与工程学院,广东广州510640
出 处:《分析测试学报》2012年第10期1229-1235,共7页Journal of Instrumental Analysis
基 金:浙江省质量技术监督局科技计划项目(20100206;20090208);浙江省分析测试研究项目(2009F70033)
摘 要:建立了超高效液相色谱-串联质谱(UPLC-MS/MS)测定肉制品中酸性橙Ⅱ、酸性橙Ⅲ、酸性橙AGT的快速分析方法。用含5%氨水的乙腈溶液对样品进行提取,采用弱阴离子交换柱富集净化,在ESI负离子源模式下采用多反应监测(MRM)模式进行检测。通过在流动相中加入离子对试剂乙酸二己基铵(DHAA),使目标物在C18色谱柱上实现了分离,并有效改善了目标组分的离子化效率,使监测离子对更加稳定,确保了检测结果的稳定性和灵敏度。该方法分析时间小于6 min,线性范围为5.0~300μg/L,相关系数(r)大于0.999,检出限(LOD,S/N=3)为20.0~50.0μg/kg,定量下限(LOQ,S/N=10)为70.0~170.0μg/kg,方法回收率为83%~89%,精密度RSD≤7.5%。该方法快速、灵敏,适用于肉制品中3种酸性橙污染物的检测与确证。A method based on ultra performance liquid chromatography - tandem mass spectrometry (UPLC - MS/MS) was developed for the simultaneous determination of three industrial acid dyes, namely acid orange Ⅱ, acid orangeⅢ and acid orange AGT, in meat products. The samples were extracted with acetonitrile ( containing 5% ammonia ), cleaned up and enriched with WAX solid phase extraction(SPE) cartridge, and then analyzed by UPLC -MS/MS under the multiple reaction monitoring(MRM) mode. All the analytes were successfully detected in negative ion mode by adding an ion-pair reagent of dihexylammonium acetate(DHAA) to the mobile phase in 6 min. The calibration curves were linear between 5.0 μg/L and 300 μg/L, and the correlation coefficients(r) were more than 0. 999. The limits of detection ( LOD, S/N = 3 ) and the limits of quantitation ( LOQ, S/N= 10) were in the range of 20. 0 -50. μg/kg and 70. 0 - 170μg/kg, respectively. The spiked recoveries were in the range of 83% - 89% , and relative standard deviations ( RSD, n = 3) were no morethan 7.5%. The method was simple, effective and sensitive, and was suitable in the determination and confirmation of three industrial acid orange dyes in the meat product samples.
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