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高效液相色谱-串联质谱法同时测定牛奶中氯霉素、恩诺沙星和 29 种农药残留

Determination of chloramphenicol, enrofloxacin and 29 pesticides residues in bovine milk by liquid chromatography-tandem mass spectrometry.

机构信息

Analysis and Testing Center, Shenyang Agricultural University, Shenyang 110161, China.

出版信息

Chemosphere. 2011 Apr;83(3):349-55. doi: 10.1016/j.chemosphere.2010.12.016. Epub 2010 Dec 28.

Abstract

A sensitive method for determination of chloramphenicol, enrofloxacin and 29 pesticides residues in bovine milk by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was developed. Residues of the targets were extracted from milk with acetonitrile, cleaned up by C(18)-SPE cartridge, and then determined by HPLC-MS/MS. The MS detection was operated in positive or negative ionization mode, depending on the compounds. For confirmation of each target compound, two precursor ion>product ion transitions were selected by multi-reaction monitoring mode (MRM). The method showed good linearity for all the tested compounds over the studied concentration range with correlation coefficient higher than 0.9910. Recoveries for the studied compounds at three spiked levels (0.05, 0.10, 0.19mgkg(-1)) in bovine milk were in the range of 71-107% with RSDs not larger than 13.7%, except that recoveries of trifluralin ranged between 62% and 70% at the spiked levels. Limits of quantitation for the analytes were estimated to range between 0.03×10(-3) and 14.5×10(-3)mgkg(-1). The proposed method was applied for the determination of the analytes residues in real samples. The found levels of the analytes in milk samples were lower than maximum residues levels (MRL).

摘要

建立了一种高效液相色谱-串联质谱法(HPLC-MS/MS)测定牛奶中氯霉素、恩诺沙星和 29 种农药残留的灵敏方法。目标物的残留用乙腈从牛奶中提取,用 C(18)-SPE 小柱净化,然后用 HPLC-MS/MS 测定。MS 检测根据化合物的不同,采用正离子或负离子模式进行。对于每个目标化合物的确证,通过多反应监测模式(MRM)选择两个前体离子>产物离子跃迁。该方法在研究的浓度范围内对所有测试化合物均表现出良好的线性关系,相关系数均高于 0.9910。在牛奶中三个添加水平(0.05、0.10、0.19mgkg(-1))下,研究化合物的回收率在 71-107%之间,相对标准偏差(RSD)不大于 13.7%,除了三氟拉林的回收率在添加水平为 62%-70%之间。分析物的定量限估计在 0.03×10(-3)至 14.5×10(-3)mgkg(-1)之间。该方法应用于实际样品中分析物残留的测定。在牛奶样品中发现的分析物水平低于最大残留限量(MRL)。

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