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毛细管电泳-质谱法测定鸡肉和鱼肉中的喹诺酮残留量。

Determination of quinolone residues in chicken and fish by capillary electrophoresis-mass spectrometry.

作者信息

Juan-García Ana, Font Guillermina, Picó Yolanda

机构信息

Laboratori de Bromatologia i Toxicologia, Facultat de Farmàcia, Universitat de València, Burjassot, Spain.

出版信息

Electrophoresis. 2006 Jun;27(11):2240-9. doi: 10.1002/elps.200500868.

Abstract

A specific pressure-assisted CE-MS method is described for the analysis of five quinolone residues. MS using a single quadrupole is compared with multiple-stage MS using a quadrupole IT (QIT-MS(n)). The procedure involves a common sample preparation by SPE on disposable cartridges. The most suitable electrolyte is 60 mM (NH(4))(2)CO(3) at pH 9.2. Single quadrupole does not provide enough fragmentation to confirm identities according to the current legislation. However, QIT-MS(n) achieves selective fragmentation. Using this method, danofloxacin, enrofloxacin, flumequine, ofloxacin, and pipemidic acid are analyzed in fortified samples of chicken and fish. Recoveries at levels of 50 ng/g were 62-99%, except for flumequine, which gives recoveries > or =45%. RSDs are from 9 to 16% and the LOD is equal (20 ng/g) for the five analytes. Confirmation of the quinolones' identity is achieved using QIT-MS(3). Forty samples of chicken and fish taken from different local markets are analyzed. Enrofloxacin is also determined in incurred chicken muscle using this method.

摘要

本文描述了一种用于分析五种喹诺酮类药物残留的特定压力辅助毛细管电泳-质谱法。将使用单四极杆的质谱法与使用四极杆离子阱的多级质谱法(QIT-MS(n))进行了比较。该方法采用在一次性小柱上进行固相萃取的常规样品前处理。最合适的电解质是pH 9.2的60 mM碳酸铵。根据现行法规,单四极杆无法提供足够的碎片信息以确认身份。然而,QIT-MS(n)可实现选择性碎片分析。采用该方法对鸡肉和鱼肉加标样品中的达氟沙星、恩诺沙星、氟甲喹、氧氟沙星和吡哌酸进行了分析。除氟甲喹回收率≥45%外,50 ng/g添加水平下的回收率为62-99%。五种分析物的相对标准偏差为9-16%,检测限均为20 ng/g。使用QIT-MS(3)实现了喹诺酮类药物身份的确认。分析了从不同当地市场采集的40份鸡肉和鱼肉样品。还用该方法测定了鸡肉肌肉中恩诺沙星的实际残留量。

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