蔡增轩,胡玲玲,王军淋,柳家鹏,任一平.超高效液相色谱检测奶及奶制品中的 M族黄曲霉毒素[J].食品安全质量检测学报,2014,5(3):801-807
超高效液相色谱检测奶及奶制品中的 M族黄曲霉毒素
Determination of M aflatoxins in milk and milk products by ultra high performance liquid chromatography
投稿时间:2014-02-07  修订日期:2014-03-17
DOI:
中文关键词:  奶制品  黄曲霉毒素M1  黄曲霉毒素M2  超高效液相色谱法  大体积流通池
英文关键词:milk products  aflatoxin M1  aflatoxin M2  ultra high performance liquid chromatography  large volume flow cell
基金项目:国家重大科学仪器设备开发专项项目(2011YQ060084)、浙江省重点科技创新团队计划( 2011R50021)
作者单位
蔡增轩 浙江省疾病预防控制中心 
胡玲玲 浙江工业大学化学工程与材料学院 
王军淋 浙江省疾病预防控制中心 
柳家鹏 北京华安麦科生物技术有限公司 
任一平 浙江省疾病预防控制中心 
AuthorInstitution
CAI Zeng-Xuan Zhejiang Provincial Center for Disease Prevention and Control 
HU Ling-Ling College of Chemical Engineering Materials Science 
WANG Jun-Lin Zhejiang Provincial Center for Disease Prevention and Control 
LIU Jia-Peng Beijing Huaan Magnech Bio-Tech Co., Ltd. 
REN Yi-Ping Zhejiang Provincial Center for Disease Prevention and Control 
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中文摘要:
      目的 建立一种免疫亲和柱净化-超高效液相色谱法同时测定奶及奶制品中M族黄曲霉毒素的方法。方法 以乙腈为提取剂和蛋白沉淀剂, 采用涡旋混合及超声提取, 免疫亲和柱净化。结果 经Welch Ultimate XB-C18色谱柱(100 mm×2.1 mm, 1.8 μm)分离, 应用大体积流通池荧光检测, 流动相为水和乙腈/甲醇(1:1)。线性范围在0.01~5.00 ng/mL之间, 线性系数均大于0.999, 黄曲霉毒素M1、M2的检出限为0.003 μg/kg。免疫亲和柱对黄曲霉毒素M1、M2的回收率均在80%以上, 液态奶中添加0.05、0.2、1.0 μg/kg的回收率在85.6%~106.4%之间, 奶粉中添加0.5、2.0、10.0 μg/kg的回收率在81.5%~93.4%之间。结论 该方法可以适用于奶粉、液态奶中M族黄曲霉毒素检测。
英文摘要:
      Objectives To develop the method of simultaneous determination of M aflatoxins in milk and milk products by ultra high performance liquid chromatography (UPLC) coupled with immunoaffinity column (IAC) clean-up. Methods Samples were extracted with acetonitrile after vortex mixing and ultrasound, meanwhile, acetonitrile was used as an protein precipitant, then extraction solution was clean-up with IAC. Results The analytes were separated on Welch Ultimate XB-C18 (100 mm×2.1 mm, 1.8 μm), and eluted with a mobile phase consisting of (a) waters and (b) acetonitrile: methanol (50: 50, v/v). The separated compounds were detected with fluorescence detection (FLD) equipped with a large volume flow cell. Meanwhile, high correlation coefficient (R2>0.999) was obtained within linear range from 0.01 to 5.0 ng/mL, and the limits of determination (LOD) of M aflatoxins were 0.003 μg/kg. Reasonable recoveries (above 80%) were demonstrated for aflatoxin M1 and M2 with aflatoxin M1 immunoaffinity column, and recoveries (85.6%~106.4%) were in 3 spiked levels (0.05, 0.2, 1.0 μg/kg) for milk, and recoveries (81.5%~93.4%) were in 3 spiked levels (0.5, 2. 0, 10.0 μg/kg) for milk powder. Conclusion This quan-titative method can be applied to the determination and quantification of M aflatoxins in milk and milk products.
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