Imran Muhammad, Habib Fazal-E-, Majeed Saima, Tawab Abdul, Rauf Waqar, Rahman Moazur, Umer Muhammad, Iqbal Mazhar
a Health Biotechnology Division , National Institute for Biotechnology and Genetic Engineering (NIBGE) , Faisalabad 38000 , Pakistan.
b Department of Biotechnology NIBGE , Pakistan Institute of Engineering and Applied Sciences , Nilore 45650 , Islamabad , Pakistan .
Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2018 Aug;35(8):1530-1542. doi: 10.1080/19440049.2018.1463569. Epub 2018 Jun 1.
A simple, reliable and sensitive liquid chromatography-tandem mass spectrometry-based confirmatory method was redeveloped and validated for the simultaneous determination of chloramphenicol, thiamphenicol, florfenicol and florfenicol amine in chicken muscles. The analytes were extracted from minced chicken muscle with acetonitrile and ammoniated water mixture. A second extraction with ethyl acetate was followed by evaporation and dissolution of the residue in ammoniated methanol before defatting with n-hexane. Finally, the extract was further cleaned up by dispersive solid phase extraction using C-18 end-capped dispersive material. The validation protocol was adapted from the European Commission Decision 2002/657/EC and all the performance characteristics were successfully satisfied. The recoveries of all the analytes were found to be in the range of 86.4-108.1% and the precision values, within day and between days, ranged from 2.7% to 11% and 4.4% to 16.3%, respectively. The method was tested in various incurred samples and applied to analyse a wide range of random poultry market samples (n = 120) collected from three cities of the Punjab, Pakistan. Chloramphenicol and florfenicol residues were detected at low levels in less than 11% of the samples. Chloramphenicol was detected only in 4 samples with the concentration range of 0.17-0.477 µg kg, whereas the levels of florfenicol/florfenicol amine residues detected in 9 samples ranged from 8.7 to 32.8 µg kg. Moreover, most of the florfenicol residues were identified as tissue bound, extractable only after strong acid hydrolysis.
重新开发并验证了一种基于液相色谱 - 串联质谱的简单、可靠且灵敏的确证方法,用于同时测定鸡肉中氯霉素、甲砜霉素、氟苯尼考和氟苯尼考胺。将分析物从鸡肉碎末中用乙腈和氨水混合物提取。接着用乙酸乙酯进行二次提取,然后蒸发,将残渣溶解于氨化甲醇中,再用正己烷脱脂。最后,提取物通过使用C - 18封端分散材料的分散固相萃取进一步净化。验证方案依据欧盟委员会第2002/657/EC号决定制定,所有性能特征均成功满足要求。所有分析物的回收率在86.4% - 108.1%范围内,日内和日间精密度值分别在2.7%至11%和4.4%至16.3%之间。该方法在各种实际样品中进行了测试,并应用于分析从巴基斯坦旁遮普省三个城市收集的大量随机家禽市场样品(n = 120)。在不到11%的样品中检测到低水平的氯霉素和氟苯尼考残留。仅在4个样品中检测到氯霉素,浓度范围为0.17 - 0.477 μg/kg,而在9个样品中检测到的氟苯尼考/氟苯尼考胺残留水平在8.7至32.8 μg/kg之间。此外,大多数氟苯尼考残留被鉴定为与组织结合,仅在强酸水解后才可提取。