Broad-specificity monoclonal antibody against neonicotinoid insecticides via a multi-immunogen strategy and development of a highly sensitive GNP-based multi-residue immunoassay in ginseng and tomato

被引:8
|
作者
Zhang, Jing [1 ]
Ruan, Haonan [1 ]
Wang, Yunyun [1 ]
Wang, Yudan [1 ]
Ke, Tongwei [1 ]
Guo, Mengyue [1 ]
Tian, Jiao [1 ]
Huang, Ying [1 ]
Luo, Jiaoyang [1 ]
Yang, Meihua [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Inst Med Plant Dev, Minist Educ, Key Lab Bioact Subst & Resources Utilizat Chinese, Beijing 100193, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
Neonicotinoid insecticides; Multi-immunogen strategy; Broad-specificity monoclonal antibody; Molecular docking; Gold nanoparticle-based immunochromato; graphic assay; LINKED-IMMUNOSORBENT-ASSAY; LIQUID-CHROMATOGRAPHY; MICROCYSTINS; SAMPLES;
D O I
10.1016/j.foodchem.2023.136115
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Neonicotinoid insecticides (NNIs) are extensively used across the agricultural products and foods. In order to meet the rapid detection requirements, a novel broad-specificity monoclonal antibody against NNIs was developed for the first time using a multi-immunogen strategy. The antibody's high affinity and its ability to bind target molecules were verified by ic-ELISA. Furthermore, molecular docking was used to evaluate the pivotal forces affecting binding affinity and to determine binding sites. Subsequently, a highly sensitive gold nanoparticle-based immunochromatographic assay was established for the rapid detection of eight NNIs and the IC50 values were 0.03-1.61 ng/mL. The limits of detection for ginseng and tomato ranged from 0.76 to 30.19 mu g/ kg and 0.87 to 31.57 mu g/kg, respectively. The spiked recovery ranged from 72.04% to 120.74%, and the coefficient of variation were less than 9.0%. This study provides a new direction for the development of multiple NNIs residue immunoassays.
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页数:11
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