首页> 外文期刊>Food Additives & Contaminants >Analytical strategy for the determination of non-steroidal anti-inflammatory drugs in plasma and improved analytical strategy for the determination of authorised and non-authorised non-steroidal anti-inflammatory drugs in milk by LC-MS/MS
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Analytical strategy for the determination of non-steroidal anti-inflammatory drugs in plasma and improved analytical strategy for the determination of authorised and non-authorised non-steroidal anti-inflammatory drugs in milk by LC-MS/MS

机译:LC-MS / MS测定血浆中非甾体类抗炎药的分析策略和测定授权和非授权牛奶中非甾体类抗炎药的改进分析策略

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摘要

A sensitive and selective method for the determination of six non-steroidal anti-inflammatory drugs (NSAIDs) in bovine plasma was developed. An improved method for the determination of authorised and non-authorised residues of 10 non-steroidal anti-inflammatory drugs in milk was developed. Analytes were separated and acquired by high performance liquid chromatography coupled with an electrospray ionisation tandem mass spectrometer (ESI-MS/MS). Target compounds were acidified in plasma, and plasma and milk samples were extracted with acetonitrile and both extracts were purified on an improved solid phase extraction procedure utilising Evolute? ABN cartridges. The accuracy of the methods for milk and plasma was between 73 and 109%. The precision of the method for authorised and non-authorised NSAIDs in milk and plasma expressed as % RSD, for the within lab reproducibility was less than 16%. The % RSD for authorised NSAIDs at their associated MRL(s) in milk was less than 10% for meloxicam, flunixin and tolfenamic acid and was less than 25% for hydroxy flunixin. The methods were validated according to Commission Decision 2002/657/EC.
机译:建立了一种灵敏且选择性的测定牛血浆中六种非甾体类抗炎药(NSAIDs)的方法。建立了一种测定牛奶中10种非甾体类抗炎药的许可和非许可残留物的改进方法。通过高效液相色谱和电喷雾电离串联质谱仪(ESI-MS / MS)进行分离和分析。目标化合物在血浆中酸化,血浆和牛奶样品用乙腈萃取,两种萃取物均采用Evolute?改进的固相萃取程序纯化。 ABN墨盒。牛奶和血浆方法的准确性在73%至109%之间。对于牛奶和血浆中授权和未经授权的NSAID的方法,其精密度以RSD%表示,因为实验室内的再现性小于16%。对于牛奶中的美洛昔康,氟尼辛和甲苯磺酸,授权的非甾体抗炎药在其相关最大残留限量的相对标准偏差百分比小于10%,对于羟基氟尼辛而言,小于20%。这些方法已根据委员会决定2002/657 / EC进行了验证。

著录项

  • 来源
    《Food Additives & Contaminants》 |2010年第7期|P.962-982|共21页
  • 作者单位

    The State Laboratory, Backweston Laboratory Complex, Young's Cross, Celbridge, Co. Kildare, Ireland;

    rnThe State Laboratory, Backweston Laboratory Complex, Young's Cross, Celbridge, Co. Kildare, Ireland;

    rnThe State Laboratory, Backweston Laboratory Complex, Young's Cross, Celbridge, Co. Kildare, Ireland;

    rnThe State Laboratory, Backweston Laboratory Complex, Young's Cross, Celbridge, Co. Kildare, Ireland;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    chromatography; LC/MS; veterinary drug residues; milk; animal;

    机译:色谱LC / MS;兽药残留;牛奶;动物;
  • 入库时间 2022-08-17 23:19:02

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