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作 者:朱浩嘉[1] 潘道东[1] 顾愿愿 李建龙[1] 赵紫微[1] 丁琳[1]
出 处:《中国食品学报》2015年第11期165-169,共5页Journal of Chinese Institute Of Food Science and Technology
基 金:国家支撑计划(2012BAK08B01);宁波市创新团队项目(2012B82017);宁波市人事局人才基金项目(ZX2012000380)
摘 要:将量子点标记技术与电化学检测技术相结合,基于竞争免疫分析,成功构建黄曲霉毒素B1(AFBl)检测新方法。以水相合成PbS量子点,通过TEM成像、XRD对其进行表征。随后以量子点标记AFB1单克隆抗体作为信号探针,基于酶标板表面AFB1人工抗原和样品中AFBI与量子点标记的AFBl单克隆抗体之间的竞争免疫结合,建立AFB1新型检测方法。在优化的条件下,方法线性范围0.1~30ng/mL,检测限0.03ng/mL。花生样品中加标回收试验结果表明,方法准确性良好,可用于实际样品的检测,为其它真菌毒素的检测提供参考。Combining Quantum dots labeled technique, electrochemical technology and competitive immunoassay technology, a new immune detection technology of aflatoxin B1(AFB1) was described. Primarily, the Pb S quantum dots was synthetized in aqueous phase and characterized by TEM, XRD. Then taked quantum dots labeled antibody as signal probes, the AFB1-BSA previously immobilised in the microtiter plate and AFB1 from the sample competitive conjugate signal probes, established a novel detection method for AFB1. Under the optimum conditions, the linear domain range was 0.1-30 ng/m L, the detection limit of 0.03 ng/m L. Results of recovery experiment in peanut sample showed that this method had a good accuracy and could be used for the detection of actual samples. The method could also be a valuable reference to other mycotoxins application.
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