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A multiresidue liquid chromatographic/tandem mass spectrometric method for the detection and quantitation of 15 nonsteroidal anti-inflammatory drugs (NSAIDs) in bovine meat and milk

机译:一种多残留液相色谱/串联质谱法检测和定量分析牛肉和牛奶中的15种非甾体类抗炎药(NSAID)

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摘要

This study concerns a validated liquid chromatographic/tandem mass spectrometric (LC-MS/MS) multiresidue method for the simultaneous detection, identification, and quantitation of 15 nonsteroidal anti-inflammatory drugs (NSAIDs) in bovine meat and milk. The NSAIDs considered are carprofen, diclofenac, flufenamic acid, flunixin (5-hydroxyflunixin as marker metabolite in milk), ketoprofen, mefenamic acid, meloxicam, 4-methylaminoantipyrine (marker metabolite of metamizole in meat and milk), naproxen, niflumic acid, phenylbutazone (and metabolite oxyphenbutazone), ramifenazone, salicylic acid, and tolfenamic acid. These compounds were chosen as representatives of different chemical subclasses of NSAIDs. Flunixin-d(3), diclofenac-d(4), 4-aminoantipyrine-d(3), and phenylbutazone-d(10) were used as internal standards. Performance characteristics were validated according to the Commission Decision 2002/657/EC (Off J Eur Communities, L221: 8-36). Recovery percentages varied between 81 and 114 % for bovine meat and between 79 and 118 % for milk. Repeatability percentages were within the range of 1-12 % for meat and between 1 and 17 % for milk, whereas the intralaboratory reproducibility varied between 3 and 19 % for meat and between 3 and 23 % for milk. The decision limit and the detection capability for bovine meat were within the range of 0.5-579 mu g kg(-1)and 0.6-642 mu g kg(-1), respectively. Those for milk were within the range of 0.12-55 mu g kg(-1) and 0.14-61 mu g kg(-1), respectively. The methods developed were successfully applied for proficiency test samples and routine samples analyzed in the laboratory. The methodology concerns fast, user-friendly, and sensitive methods, which can be easily extended for other compounds and matrices. In general, such multiresidue methods contribute to the reduction of human exposure to these veterinary drug residues by consumption of contaminated bovine-derived products such as meat and milk.
机译:这项研究涉及一种经过验证的液相色谱/串联质谱(LC-MS / MS)多残留方法,该方法可同时检测,鉴定和定量牛肉和牛奶中的15种非甾体类抗炎药(NSAID)。认为的非甾体抗炎药为卡洛芬,双氯芬酸,氟芬那酸,氟尼辛(5-羟基氟尼辛作为牛奶中的标记代谢物),酮洛芬,美芬那酸,美洛昔康,4-甲基氨基安替比林(肉和牛奶中的咪唑的标记代谢物),萘普生,尼氟酸,苯基丁a (以及代谢产物oxyphenbutazone),ramifenazone,水杨酸和tolfenamic acid。选择这些化合物作为NSAIDs不同化学亚类的代表。 Flunixin-d(3),双氯芬酸-d(4),4-氨基安替比林-d(3)和苯基丁a-d(10​​)被用作内标。根据委员会决定2002/657 / EC(Off J Eur社区,L221:8-36)验证了性能特征。牛肉的回收率在81%至114%之间,牛奶的回收率在79%至118%之间。肉的重复性百分比在1-12%的范围内,牛奶的重复性百分比在1-17%的范围内,而肉类的实验室内部重复性在3%至19%之间,牛奶的3%至23%之间。牛肉的判定极限和检测能力分别在0.5-579μg kg(-1)和0.6-642μgkg(-1)范围内。牛奶的含量分别在0.12-55μg / kg(-1)和0.14-61μg/ kg(-1)范围内。所开发的方法已成功应用于实验室中的能力验证样品和常规样品分析。该方法论涉及快速,用户友好和敏感的方法,可以很容易地扩展到其他化合物和基质。通常,这种多残留方法通过食用受污染的牛衍生产品(例如肉和牛奶),有助于减少人类对这些兽药残留的接触。

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