Division of Animal Microbiology and Infectious Disease, State Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, China.
Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2009 Mar;26(3):314-25. doi: 10.1080/02652030802520860.
The use of sulfonamides, such as sulfamethazine (SM2), in pig production is recognized as a public health risk as it inevitably results in sulfamethazine residues in pork. This study is aimed at establishing rapid, simple, reliable methods, with both sensitivity and specificity, for detecting sulfamethazine residues. For this purpose, monoclonal antibodies against sulfamethazine were prepared and characterized. No cross-reaction of the monoclonal antibodies was identified with other sulfonamides or analytes. Based on the competitive immunoassay principle, an indirect competitive ELISA kit (SM2 kit) and a rapid detection strip for detecting sulfamethazine residues were developed using monoclonal antibodies and the colloidal gold technique. The indirect competitive ELISA kit and the strip assay could be performed within 2 h and 5-10 min, respectively. The results showed that the detection limits were 1 ng ml(-1) for the indirect competitive ELISA kit and 8 ng ml(-1) with the unaided eye and 1 ng ml(-1) with the strip reader for the rapid strip assay. Comparing the HPLC method with the SM2-kit or the strip in pig urine spiked with standards of SM2, the difference was <4.6% for SM2-kit and 4.3% for the strip. The two methods are suitable for the rapid screening of sulfamethazine residues in swine urine. Experimental data revealed that the two methods, especially the strip, proved to be sensitive, specific, rapid and easy to use for the quantitative, semi-quantitative or qualitative detection of SM2 residues in swine urine.
磺胺类药物(如磺胺二甲嘧啶(SM2))在猪生产中的使用被认为是公共卫生风险,因为它不可避免地导致猪肉中残留磺胺二甲嘧啶。本研究旨在建立快速、简单、可靠的方法,具有灵敏度和特异性,用于检测磺胺二甲嘧啶残留。为此,制备并表征了针对磺胺二甲嘧啶的单克隆抗体。单克隆抗体与其他磺胺类药物或分析物没有交叉反应。基于竞争免疫分析原理,使用单克隆抗体和胶体金技术开发了间接竞争 ELISA 试剂盒(SM2 试剂盒)和用于检测磺胺二甲嘧啶残留的快速检测条。间接竞争 ELISA 试剂盒和条带测定可在 2 小时和 5-10 分钟内分别进行。结果表明,间接竞争 ELISA 试剂盒的检测限为 1ng ml(-1),肉眼检测限为 8ng ml(-1),条带读数器检测限为 1ng ml(-1)。将 HPLC 方法与 SM2 试剂盒或标准品中 SM2 条带在猪尿中进行比较,SM2 试剂盒的差异<4.6%,条带的差异为 4.3%。这两种方法适用于猪尿中磺胺二甲嘧啶残留的快速筛选。实验数据表明,这两种方法,特别是条带,对于定量、半定量或定性检测猪尿中的 SM2 残留,具有灵敏度高、特异性强、快速、易于使用的特点。