Qin Jin, Sun Xiaojie, Li Dongxia, Yan Guiqin
Shanxi Normal University Linfen Shanxi 041000 China
RSC Adv. 2019 Apr 25;9(22):12747-12754. doi: 10.1039/c9ra02141h. eCollection 2019 Apr 17.
A simple and sensitive Mn-ZnS quantum dot room-temperature phosphorescent immunosensor for detecting microcystin-LR was developed. This sensor adopted antigens and antibodies as recognition units and used Mn-ZnS RTP QDs as sensing materials to specifically bind with MC-LR. The structurally specific binding between the microcystin-LR antibody and MC-LR led to the aggregation of antibody-crosslinked QDs, and then the electrons of QDs would be transferred to the complex, leading to the phosphorescence quenching of QDs. The microcystin-LR antigen-antibody specific binding site was first analyzed. This phosphorescent immunosensor rapidly and sensitively detected microcystin-LR, with linear ranges of 0.2-1.5 μg L and 1.5-20 μg L and a detection limit of up to 0.024 μg L. Meanwhile, coexisting pollutants of microcystin-LR in water did not significantly interfere with microcystin-LR detection. The new sensor was applied to detect real water samples and showed high sensitivity and selectivity.
开发了一种用于检测微囊藻毒素-LR的简单灵敏的Mn-ZnS量子点室温磷光免疫传感器。该传感器采用抗原和抗体作为识别单元,并使用Mn-ZnS室温磷光量子点作为传感材料与微囊藻毒素-LR特异性结合。微囊藻毒素-LR抗体与微囊藻毒素-LR之间的结构特异性结合导致抗体交联量子点的聚集,然后量子点的电子会转移到复合物上,导致量子点的磷光猝灭。首次分析了微囊藻毒素-LR抗原-抗体特异性结合位点。这种磷光免疫传感器能快速灵敏地检测微囊藻毒素-LR,线性范围为0.2-1.5μg/L和1.5-20μg/L,检测限高达0.024μg/L。同时,水中微囊藻毒素-LR的共存污染物对微囊藻毒素-LR的检测没有显著干扰。该新型传感器应用于实际水样检测,具有高灵敏度和选择性。