State Key Laboratory of Food Nutrition and Safety, Key Laboratory of Food Nutrition and Safety, Ministry of Education of China, College of Food Engineering and Biotechnology, Tianjin University of Science and Technology, Tianjin, 300457, China.
Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Technology & Business University (BTBU), Beijing, 100048, China.
Mikrochim Acta. 2019 Jul 24;186(8):564. doi: 10.1007/s00604-019-3667-3.
A high-sensitivity fluorescence immunoassay for atrazine was established. It is making use of hydrophilic NaYF:Yb/Er upconversion nanoparticles (UCNPs) conjugated to the anti-atrazine antibody as signal probe, and of polystyrene magnetic microspheres (PMMs) conjugated to the coating antigen as the capture probe. The coating antigen on the capture probe competes with atrazine for binding to the antibody on the signal probe to form the immuno complex. The complex is separated from the test system by magnetic action, and its green fluorescence is then measured at excitation/emission wavelengths of 980/552 nm using a fluorescence spectrophotometer equipped with an external 980 nm laser. The method was applied to the determination of atrazine in corn, rice, sugar cane juice, and river water. The immunoassay has a linear range that extends from 0.005 to 10 μg·L. The assay also recognizes propazine and prometryn, and it therefore can be applied to detect these three herbicides simultaneously. Sugar cane juice and river water samples can be analyzed directly without any pretreatment. The detection limits for atrazine are 2 ng·L in sugar cane juice and river water samples, and 20 ng·kg in corn and rice samples. The recoveries of spiked samples range from 84.7 to 113.6%. Graphical abstract A sensitive fluorescence immunoassay combining magnetic separation for the detection of atrazine in cereal, juice, and water samples using NaYF:Yb/Er upconversion nanoparticles as labels.
建立了一种高灵敏度的阿特拉津荧光免疫分析方法。该方法利用亲水 NaYF:Yb/Er 上转换纳米粒子(UCNPs)偶联到抗阿特拉津抗体作为信号探针,以及聚苯乙烯磁性微球(PMMs)偶联到包被抗原作为捕获探针。捕获探针上的包被抗原与阿特拉津竞争与信号探针上的抗体结合,形成免疫复合物。复合物通过磁作用从检测体系中分离出来,然后使用配备外部 980nm 激光的荧光分光光度计在 980/552nm 的激发/发射波长下测量其绿色荧光。该方法用于测定玉米、水稻、甘蔗汁和河水中的阿特拉津。免疫分析的线性范围从 0.005 到 10μg·L。该测定法还识别普马嗪和扑灭津,因此可用于同时检测这三种除草剂。甘蔗汁和河水样品无需预处理即可直接分析。阿特拉津在甘蔗汁和河水中的检测限为 2ng·L,在玉米和水稻样品中的检测限为 20ng·kg。加标样品的回收率范围为 84.7%至 113.6%。