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作 者:单艺[1] 马微 王象欣[1] 鄂来明[1] 姜毓君[1]
机构地区:[1]东北农业大学黑龙江省乳品工业技术开发中心,黑龙江哈尔滨150086 [2]黑龙江出入境检验检疫局,黑龙江哈尔滨150001
出 处:《食品科学》2012年第20期171-175,共5页Food Science
摘 要:分别建立高效液相色谱-二极管阵列法(HPLC-PAD)、超高压液相色谱-串联质谱法(UPLC-MS/MS)测定乳及乳制品中三聚氰胺含量的方法。利用HPLC-PAD外标法进行样品中三聚氰胺的初筛,利用UPLC-MS/MS法进行确证,以13C315N3-三聚氰胺为同位素内标定量。乳制品经乙腈、乙酸锌、盐酸溶液提取,质谱检测时,样品再经MCX固相萃取柱富集净化。HPLC-PAD法的定量限为4mg/kg,UPLC-MS/MS的定量限为0.05mg/kg;HPLC-PAD的添加回收率为95.7%~102.3%,UPLC-MS/MS的添加回收率为91.3%~95.7%(基质匹配曲线校正),两种方法的相对标准偏差(RSD)分别为1.98%~4.51%,1.60%~3.27%。A method for the determination of melamine in milk and milk products was established by joint use of HPLC-PAD with external standard quantification and UPLC-MS/MS with internal standard quantification.Melamine content of samples was primarily analyzed by HPLC-PAD with external standard quantification,and then confirmed by UPLC-MS/MS and quantified by internal standard method using13C315N3.Samples were extracted with acetonitrile and then the extract was added with zinc acetate and hydrochloric acid and cleaned up using an MCX solid-phase extraction cartridge prior to UPLC-MS/MS analysis.The limit of quantification of the HPLC-PAD method was 4 mg/kg,while that of the UPLC-MS/MS method was 0.05 mg/kg.The average recovery rates of melamine from milk powder,liquid milk and milk cream across three spike levels as determined by the HPLCPAD and UPLC-MS/MS methods were 95.7%–102.3% and 91.3%–95.7%(matrix match calibration),respectively,and the relative standard deviations were 1.98%–4.51% and 1.60%–3.27%.
关 键 词:三聚氰胺 高效液相色谱 超高压液相色谱-串联质谱 内标法 乳制品
分 类 号:S853.74[农业科学—临床兽医学]
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