Hou Xiao-Lin, Chen Guo, Zhu Li, Yang Ting, Zhao Jian, Wang Lei, Wu Yin-Liang
Beijing Key Laboratory of Traditional Chinese Veterinary Medicine, College of Animal Science and Technology, Beijing University of Agriculture, Beijing 102206, PR China.
Ningbo Academy of Agricultural Science, Ningbo 315040, PR China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Jul 1;962:20-29. doi: 10.1016/j.jchromb.2014.05.005. Epub 2014 May 14.
A simple, sensitive and reliable analytical method was developed for the simultaneous determination of 38 veterinary drugs (18 sulfonamides, 11 quinolones and 9 benzimidazoles) and 8 metabolites of benzimidazoles in bovine milk by ultra high performance liquid chromatography-positive electrospray ionization tandem mass spectrometry (UHPLC-ESI-MS/MS). Samples were extracted with acidified acetonitrile, cleaned up with Oasis(®) MCX cartridges, and analyzed by LC-MS/MS on an Acquity UPLC(®) BEH C18 column with gradient elution. The method allows such multi-analyte measurements within a 13min runtime while the specificity is ensured through the MRM acquisition mode. The method was validated according to the European Commission Decision 2002/657/EC determining specificity, decision limit (CCα), detection capability (CCβ), recovery, precision, linearity and stability. For compounds which have MRLs in bovine milk, the CCα values fall into a range from 11 to 115μg/kg, and the CCβ values fall within a range of 12-125μg/kg. For compounds which have not MRLs in bovine milk, the CCα values fall into a range from 0.01 to 0.08μg/kg, and the CCβ values fall within a range of 0.02-0.11μg/kg. The mean recoveries of the 46 analytes were between 87 and 119%. The calculated RSD values of repeatability and within-laboratory reproducibility experiments were below 11% and 15% for the 46 compounds, respectively. The method was demonstrated to be suitable for the simultaneous determination of sulfonamides, quinolones and benzimidazoles in bovine milk.
建立了一种简单、灵敏且可靠的分析方法,用于通过超高效液相色谱-正电喷雾电离串联质谱法(UHPLC-ESI-MS/MS)同时测定牛奶中的38种兽药(18种磺胺类药物、11种喹诺酮类药物和9种苯并咪唑类药物)以及8种苯并咪唑类药物的代谢物。样品用酸化乙腈萃取,通过Oasis(®) MCX柱净化,然后在Acquity UPLC(®) BEH C18柱上进行梯度洗脱的LC-MS/MS分析。该方法可在13分钟的运行时间内实现多分析物测量,同时通过多反应监测(MRM)采集模式确保特异性。该方法根据欧盟委员会第2002/657/EC号决定进行验证,确定了特异性、决策限(CCα)、检测能力(CCβ)、回收率、精密度、线性和稳定性。对于在牛奶中有最大残留限量(MRL)的化合物,CCα值在11至115μg/kg范围内,CCβ值在12至125μg/kg范围内。对于在牛奶中没有MRL的化合物,CCα值在0.01至0.08μg/kg范围内,CCβ值在0.02至0.11μg/kg范围内。46种分析物的平均回收率在87%至119%之间。46种化合物的重复性和实验室内再现性实验的计算相对标准偏差(RSD)值分别低于11%和15%。该方法被证明适用于同时测定牛奶中的磺胺类药物、喹诺酮类药物和苯并咪唑类药物。