Toussaint B, Chedin M, Bordin G, Rodriguez A R
Institute for Reference Materials and Measurements, Joint Research Center, European Commission (EC-JRC-IRMM), Geel, Belgium.
J Chromatogr A. 2005 Sep 23;1088(1-2):32-9. doi: 10.1016/j.chroma.2005.02.057.
A new LC-MS/MS method has been developed for the multiresidue determination of 11 (fluoro)quinolone antibiotics (FQs), including acidic and amphoteric species, around their maximum residue level (MRL) in pig kidney. The procedure involves a common sample preparation by solid-phase extraction on disposable extraction cartridges followed by a fast reversed-phase liquid chromatography-tandem mass spectrometry analysis. The method was validated according to the Commission Decision 2002/657/CE. The accuracy of the method was satisfactory with recoveries included in the interval 80-100%. The precision results showed mean repeatability and reproducibility coefficients of 7.4% and 11.8%, respectively. Limits of quantification much lower than the MRLs could be obtained.
已开发出一种新的液相色谱-串联质谱法,用于多残留测定猪肾中11种(氟)喹诺酮类抗生素(FQs),包括酸性和两性物质,测定浓度接近其最大残留限量(MRL)。该方法包括通过一次性萃取柱进行固相萃取的常规样品前处理,随后进行快速反相液相色谱-串联质谱分析。该方法根据委员会第2002/657/CE号决定进行了验证。该方法的准确度令人满意,回收率在80%-100%之间。精密度结果显示,平均重复性和再现性系数分别为7.4%和11.8%。可获得远低于最大残留限量的定量限。