Guo Jie-Biao, Cheng Jin-Sheng, Wei Tai-Long, Wu Fan-Min, Tang Gui-Hong, He Qing-Hua
Provincial Key Laboratory for Utilization and Conservation of Food and Medicinal Research in Northern Guangdong, Shaoguan University, No. 288 Daxue Road, Shaoguan 512005, China.
School of Innovation and Entrepreneurship, Shaoguan University, No. 288 Daxue Road, Shaoguan 512005, China.
Foods. 2022 Apr 15;11(8):1155. doi: 10.3390/foods11081155.
An immuno-separated assay for ochratoxin A detection coupled with a nano-affinity cleaning up for LC-confirmation was developed. Firstly, ochratoxin A was modified to quantum dot beads for immuno-fluorescent reporters. Secondly, FeO magnetic nanoparticles were conjugated with protein G for immuno-magnetic adsorbents. The immuno-separation of fluorescent reporters by magnetic adsorbents could be completed by ochratoxin A, so the fluorescent reporters released from the immune complex indicate a linear correlation with the concentration of ochratoxin A. Furthermore, the immuno-separated ochratoxin A can be eluted from magnetic adsorbent for LC-conformation. The optimized assay showed results as follows: the quantitative range of the immuno-separated assay was 0.03-100 ng mL of ochratoxin A. The recoveries for spiked samples ranged from 78.2% to 91.4%, with the relative standard deviation (RSD) being 11.9%~15.3%. Statistical analysis indicated no significant difference between the HPLC-FLD results based on commercial affinity column and by nano-affinity cleaning up.
开发了一种用于检测赭曲霉毒素A的免疫分离分析方法,并结合纳米亲和净化用于液相色谱确证。首先,将赭曲霉毒素A修饰为用于免疫荧光报告物的量子点珠。其次,将FeO磁性纳米颗粒与蛋白G偶联以制备免疫磁性吸附剂。磁性吸附剂对荧光报告物的免疫分离可由赭曲霉毒素A完成,因此从免疫复合物中释放的荧光报告物与赭曲霉毒素A的浓度呈线性相关。此外,免疫分离的赭曲霉毒素A可从磁性吸附剂上洗脱用于液相色谱确证。优化后的分析方法结果如下:免疫分离分析方法的定量范围为赭曲霉毒素A 0.03 - 100 ng/mL。加标样品的回收率在78.2%至91.4%之间,相对标准偏差(RSD)为11.9% - 15.3%。统计分析表明,基于商业亲和柱和纳米亲和净化的高效液相色谱 - 荧光检测结果之间无显著差异。