用经验证的液相色谱-串联质谱法对孟加拉国禽肉中氯霉素残留的调查

Hosain Mz, Islam Sms, Kamal Mm
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引用次数: 0

摘要

氯霉素(CAP)是一种广泛应用于兽医实践的广谱抗生素。牲畜生产中持续使用CAP可能导致抗生素耐药性和与健康相关的危害。本研究建立了一种基于超高效液相色谱-串联质谱(UPLC-MS /MS)的快速、高灵敏度分析方法,用于检测和定量家禽肉中CAP对人类和动物安全的影响。从Dhaka省Tangail区的三个区,即Sadar、Mirzapur和Ghatail的不同家禽养殖场和禽肉销售商共收集了80份禽肉样本。试验分析采用基质匹配液相色谱-质谱法。在反相C18色谱柱上,采用二元梯度泵,在40℃温度下进行色谱分离,电喷雾方式采用LC-MS/MS进行定量。流动相成分为溶剂(a)去离子水和(b)乙腈。流速为0.35 mL/min,总运行时间为5 min。按照2021/808/EC指南对该方法进行了选择性、线性、回收率和精密度验证,所有病例均符合验收标准。基质匹配CAP标准品在0.25、0.50、0.75、1.0、2.0、5.0 μg/kg浓度下,精密度的相对标准偏差(RSD)为0.999,线性范围为0.0 ~ 5.0 μg/kg, R2 > 0.99。测定限(CC-a)和检测能力(cc - β)分别为0.29 μg/kg和0.31 μg/kg,回收率为94% ~ 100%。本研究检测的禽肉样品中CAP残留量均低于检测限。该方法总体参数符合验证标准,适用于禽肉样品中CAP残留的检测。因此,该方法可作为快速、常规分析禽肉中CA的一种精确、理想的分析方法,本研究获得的检测结果可作为可靠的数据,确保人类食用的不含氯霉素的禽肉安全。
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Investigation on Chloramphenicol Residues in Poultry Meat in Bangladesh Using a Validated Liquid Chromatography-Tandem Mass Spectrometry
Chloramphenicol (CAP) is a broad-spectrum antibiotic widely applied in veterinary practices. Continual use of CAP in livestock production may lead to antibiotic resistance and health-related hazards. In this study, a rapid and highly sensitive analytical method based on ultra-performance liquid chromatographytandem mass spectrometry (UPLC–MS/MS) was developed and validated to detect and quantify there is due of CAP in poultry meat regarding the safety of humans and animals. Total 80 samples of poultry meat were collected from different poultry farms, and poultry meat sellers in three upazilas namely- Sadar, Mirzapur and Ghatail of Tangail district in the Dhaka division. The test analysis was performed using matrix-matched liquid chromatography-mass spectrophotometry. The chromatographic separation of the CA Presidue was carried out at 40°C temperature on a reverse-phase C18 column using a binary gradient pump, and quantification was performed by LC-MS/MS in electrospray mode. Mobile phase constituents were solvent (a) deionized water, and (b) acetonitrile. The flow rate was 0.35 mL/min and the total run time was 5 min. The method was validated in terms of selectivity, linearity, recovery, and precision following the 2021/808/EC guidelines and acceptance criteria were met in all the cases. The relative standard deviation (RSD) for precision was <11%. The linearity of the calibration curves was excellent (R2 >0.999) at concentrations of 0.25, 0.50, 0.75, 1.0, 2.0, and 5.0 μg/kg for matrix-matched CAP standard, and the range of linearity of this method was 0.0-5.0 μg/kg with R2 value greater than 0.99. The decision limit (CC-a), and detection capability (CCβ) were 0.29 μg/ kg, and 0.31 μg/kg respectively, and the recovery percentages ranged from 94 to 100 %. In this study, the levels of CAP residue in tested poultry meat samples were found below the detection limit. The overall parameters of the proposed method met the validation criteria, and the method proved to be suitable for CAP residues determination in poultry meat samples. Thus, this method could be a precise and highly desirable analytical procedure for rapid and routine analysis of CA Presidues in poultry meat, and obtained tested results in this study could be an authentic data to ensure the chloramphenicol free safety poultry meat for human consumption.
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