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Multi-Residue Determination of Non-Steroidal Anti-Inflammatory Drug Residues in Animal Serum and Plasma by HPLC and Photo-Diode Array Detection

机译:HPLC和光电二极管阵列检测技术对动物血清和血浆中非甾体类抗炎药残留进行多残留测定

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摘要

The European Union regulated the use of non-steroidal anti-inflammatory drugs (NSAIDs) in animal production and set the official analytical controls to detect their residues in plasma, serum, and milk within the frame of national monitoring programs in each member state. In this work, a multi-residue reversed-phase high-performance liquid chromatography with diode array detector (DAD) method is described for the simultaneous determination of 13 NSAIDs in serum and plasma of farm animals. Chromatographic separation by a C12 stationary phase column with a linear gradient is able to resolve all the compounds considered: salicylic acid, ketoprofen, flurbiprofen, phenylbutazone and its metabolite (oxyphenbutazone), carprofen, ibuprofen, naproxen, niflumic acid, suxibutazone, diclofenac, mefenamic acid, and tolfenamic acid. These compounds are chosen as the most representative of the different NSAID chemical sub-classes. The DAD analysis allows the confirmation of all drugs on the basis of their own UV-vis spectrum, according to the requirements of the European Council Decision 2002/657/EC. Moreover, the method is in-house validated, evaluating mean recoveries, specificity, repeatability, and within-laboratory reproducibility as the performance parameters required by the Decision. The results of this study indicate the method is specific and repeatable, with the mean percentage recoveries of the drugs ranging between 72.5% and 104.5%. Only salicylic acid has poor recovery, with results ranging between 36.3% and 54.9%.
机译:欧盟规范了在动物生产中使用非甾体类抗炎药(NSAID),并在每个成员国的国家监测计划框架内设置了官方分析控制措施,以检测血浆,血清和牛奶中的残留。在这项工作中,描述了使用二极管阵列检测器(DAD)方法的多残留反相高效液相色谱法,用于同时测定农场动物血清和血浆中的13种NSAID。通过C12固定相色谱柱进行线性梯度色谱分离,可以分离所有考虑的化合物:水杨酸,酮洛芬,氟比洛芬,苯基丁氮酮及其代谢产物(羟苯丁酮),卡洛芬,布洛芬,萘普生,尼氟米酸,舒巴他酮,双氯芬酸,甲芬那酸酸和甲苯磺酸。选择这些化合物作为不同NSAID化学亚类的最具代表性。 DAD分析允许根据欧洲理事会第2002/657 / EC号决定的要求,根据其自身的UV-可见光谱对所有药物进行确认。此外,该方法经过内部验证,评估平均回收率,特异性,可重复性和实验室内可重复性,作为该决策所需的性能参数。这项研究的结果表明该方法是特异性和可重复的,药物的平均回收率在72.5%至104.5%之间。只有水杨酸的回收率较差,结果介于36.3%和54.9%之间。

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