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作 者:邱元进[1] 杨方[1] 刘正才[1] 林永辉[1] 刘素珍[1]
出 处:《色谱》2012年第5期463-467,共5页Chinese Journal of Chromatography
基 金:福建省科技攻关重点项目(2010Y0001);国家质检总局科研项目(2009IK143)
摘 要:建立了畜禽产品中维吉尼亚霉素M1和S1药物残留检测的液相色谱-串联质谱分析方法。样品以甲醇-乙腈溶液(1∶1,v/v)提取,上清液经0.01 mol/L磷酸二氢铵溶液稀释后,Oasis HLB固相萃取小柱净化,Luna C18色谱柱分离,以乙腈和含0.1%(体积分数)甲酸的5 mmol/L乙酸铵水溶液作为流动相进行梯度洗脱,电喷雾正离子模式电离(ESI+),多反应监测(MRM)模式检测,外标法定量。该方法对两物质线性范围均为0.15~10.0μg/L,相关系数r2均大于0.999;定量下限均为0.25μg/kg。在不同基质中,0.25、0.50、2.5μg/kg 3个添加水平的平均回收率范围为71.2%~98.4%,精密度范围为3.6%~15.4%。该方法具有快速简便、灵敏度高、准确性强等特点,适用于畜禽产品中维吉尼亚霉素的检测。A liquid chromatography-tandem mass spectrometry method was established for the determination of virginiamycin M1 and S1 residues in livestock and poultry products.The sample was extracted by methanol-acetonitrile solution(1∶1,v/v).The supernatant was diluted with 0.01 mol/L ammonium dihydrogen phosphate solution,then purified and concentrated on an Oasis HLB cartridge.The separation of virginiamycin M1 and S1 was performed on a Luna C18 column with the mobile phases acetonitrile and 5 mmol/L ammonium acetate aqueous solution(containing 0.1%(v/v) formic acid) in a gradient elution mode.The identification and quantification of the drugs were carried out by positive electrospray ionization(ESI+) in the multiple reaction monitoring(MRM) mode using external standard method.The calibration curves showed good linearity in the range of 0.15-10.0 μg/L with correlation coefficients(r2) above 0.999.The limits of quantities(LOQs) were both 0.25 μg/kg.The average recoveries of the two drugs spiked at 0.25,0.5 and 2.5 μg/kg levels in different matrices were between 71.2% and 98.4%,and the relative standard deviations(RSDs) were between 3.6% and 15.4%.The method is simple,rapid,sensitive and accurate.It is suitable for the confirmation and quantification of virginiamycin M1 and S1 residues in livestock and poultry products.
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