Yang Zong, Li Xiuqin, Wang Juan, Zhang Qinghe
National Institute of Metrology, Beijing 100013, China.
Se Pu. 2011 Sep;29(9):927-31.
An accurate method was described for the determination of chloramphenicol (CAP) in pork. The analyte was quantified by isotope dilution liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) operating in negative ion multiple reaction monitoring (MRM) mode. The sample was treated by liquid-liquid extraction with ethyl acetate followed by a clean-up step on an HLB solid-phase extraction cartridge. Chloramphenicol-D5 (CAP-D5) was added as an isotope internal standard. Under the optimized conditions, the calibration curve showed a good linearity in ranging from 0.01 to 0.5 ng/g CAP. The correlation coefficient r2 was 0.9998. The limit of detection and the limit of quantification were 0.004 and 0.02 ng/g, respectively. The average recoveries of CAP at 0.02 ng/g and 1.0 ng/g spiked levels ranged from 95.2%-109.1%, 99.7%-102.5%, respectively. The relative standard deviations (RSDs) of intra-day and inter-day were less than 2%. Meanwhile, matrix effect factors k of CAP and CAP-D5 were determined under different mobile phases and the sample solvent composition, the k was in the range of 0.950-1.015. The method can be used as a confirmed method for the determination of CAP in pork.
描述了一种测定猪肉中氯霉素(CAP)的准确方法。通过在负离子多反应监测(MRM)模式下运行的同位素稀释液相色谱 - 电喷雾电离串联质谱(LC - ESI - MS/MS)对分析物进行定量。样品先用乙酸乙酯进行液 - 液萃取,然后在HLB固相萃取柱上进行净化步骤。添加氯霉素 - D5(CAP - D5)作为同位素内标。在优化条件下,校准曲线在0.01至0.5 ng/g CAP范围内显示出良好的线性。相关系数r2为0.9998。检测限和定量限分别为0.004和0.02 ng/g。在0.02 ng/g和1.0 ng/g加标水平下,CAP的平均回收率分别为95.2% - 109.1%、99.7% - 102.5%。日内和日间的相对标准偏差(RSD)均小于2%。同时,在不同流动相和样品溶剂组成下测定了CAP和CAP - D5的基质效应因子k,k在0.950 - 1.015范围内。该方法可作为测定猪肉中CAP的确证方法。