Laboratório de Resíduos de Medicamento Veterinários, Laboratório Nacional Agropecuário, Pedro Leopoldo, Brazil.
Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2012;29(4):535-40. doi: 10.1080/19440049.2011.627571. Epub 2011 Nov 7.
PremiTest, a microbial inhibition test for the screening of antimicrobial residues, was validated according to the criteria established by Decision 2002/657/EC. Sensitivity, detection capability (CCβ), specificity, selectivity, robustness and applicability were evaluated. The methodology involves the technique of solvent extraction, which increases the detection capability of the test for a wider range of antibiotics. The following CCβ values in poultry muscle were found: penicillin G ≤ 12.5 µg kg(-1), total sulfonamides ≤ 75 µg kg(-1), erythromycin 75 µg kg(-1) and lincomycin 50 µg kg(-1). The detection capability of chlortetracycline was equal to its maximum residue limit (100 µg kg(-1)) and the method did not detect gentamicin (1000 µg kg(-1)), for which no MRL is established in poultry muscle. Specificity evaluated in relation to different analytes and matrices did not detect any interferences in the tests results; whilst the robustness showed that the pH neutralisation point of the extract affects the analytical results and the kits' performance. Only the screening of tetracyclines requires the analysis of extracts without pH neutralisation. The results of the validation process showed that this method is acceptable for screening β-lactam, sulfonamide and macrolide antimicrobial groups in the National Residues and Contaminants Control Programme (PNCRC), and that for this it is fit for purpose.
PremiTest 是一种用于筛选抗菌药物残留的微生物抑制测试,根据欧盟委员会 2002/657/EC 号决定确定的标准进行了验证。评估了灵敏度、检测能力 (CCβ)、特异性、选择性、稳健性和适用性。该方法涉及溶剂提取技术,该技术提高了测试对更广泛抗生素的检测能力。在禽肉中发现以下 CCβ 值:青霉素 G ≤ 12.5 µg kg(-1)、总磺胺类药物 ≤ 75 µg kg(-1)、红霉素 75 µg kg(-1)和林可霉素 50 µg kg(-1)。金霉素的检测能力等于其最大残留限量 (100 µg kg(-1)),并且该方法未检测到庆大霉素 (1000 µg kg(-1)),因为在禽肉中没有为其建立最大残留限量。对不同分析物和基质的特异性评估未发现测试结果有任何干扰;而稳健性表明提取物的 pH 中和点会影响分析结果和试剂盒的性能。只有四环素的筛选需要分析未经 pH 中和的提取物。验证过程的结果表明,该方法可用于国家残留和污染物控制计划 (PNCRC) 筛选β-内酰胺类、磺胺类和大环内酯类抗菌药物组,并且符合目的。