Kourti Dimitra, Angelopoulou Michailia, Petrou Panagiota, Kakabakos Sotirios
Immunoassays/Immunosensors Lab, Institute of Nuclear & Radiological Sciences & Technology, Energy & Safety, NCSR "Demokritos", 15341 Aghia Paraskevi, Greece.
Analytical Chemistry Lab, Department of Chemistry, University of Athens, Panepistimiopolis Zografou, 15771 Athens, Greece.
Toxins (Basel). 2024 Nov 29;16(12):515. doi: 10.3390/toxins16120515.
Aflatoxin M1 (AFM1) exposure through dairy products is associated with adverse health effects, including hepatotoxicity and carcinogenicity. Therefore, the AFM1 presence in milk and dairy products is strictly regulated. In this context, the current work focuses on the investigation of different competitive enzyme immunoassay configurations for the determination of AFM1 in milk with high sensitivity and short assay duration. Amongst the configurations tested, the one based on incubation of the anti-AFM1 specific antibody along with the calibrators/samples and a biotinylated conjugate of AFM1 with bovine serum albumin (BSA) in microwells coated with a secondary antibody provided a six-fold lower detection limit than the configuration involving immobilized AFM1-BSA conjugate and liquid phase antibody. The detection limit achieved was 5.0 pg/mL, with a dynamic range of up to 2.0 ng/mL. The assay was repeatable with intra- and inter-assay coefficients of variations lower than 3.2% and 6.5%, respectively, and accurate with recovery values from 87.5 to 108%. Moreover, the assay was completed in 1.5 h. The excellent analytical characteristics and short analysis time make the proposed assay suitable for use by the food industry. Furthermore, the proposed configuration could be employed to enhance the detection sensitivity of competitive immunoassays for other low-molecular-weight analytes.
通过乳制品接触黄曲霉毒素M1(AFM1)会对健康产生不良影响,包括肝毒性和致癌性。因此,牛奶和乳制品中AFM1的存在受到严格监管。在此背景下,当前工作聚焦于研究不同的竞争性酶免疫分析配置,以高灵敏度和短分析时间测定牛奶中的AFM1。在所测试的配置中,基于在包被有二抗的微孔中将抗AFM1特异性抗体与校准品/样品以及AFM1与牛血清白蛋白(BSA)的生物素化缀合物一起孵育的配置,其检测限比涉及固定化AFM1-BSA缀合物和液相抗体的配置低六倍。实现的检测限为5.0 pg/mL,动态范围高达2.0 ng/mL。该分析方法具有可重复性,批内和批间变异系数分别低于3.2%和6.5%,并且准确,回收率在87.5%至108%之间。此外,该分析在1.5小时内完成。出色的分析特性和短分析时间使得所提出的分析方法适用于食品行业。此外,所提出的配置可用于提高其他低分子量分析物竞争性免疫分析的检测灵敏度。