啶虫脒
噻虫啉
生物素化
检出限
色谱法
花粉
化学
分析物
杀虫剂
生物
生物化学
植物
噻虫嗪
农学
益达胺
作者
Qingkui Fang,Quan Zu,Xiude Hua,Pei Lv,Wanwen Lin,Dahe Zhou,Zihan Xu,J. Z. Fan,Xiaohan Li,Haiqun Cao
出处
期刊:Molecules
[MDPI AG]
日期:2019-04-01
卷期号:24 (7): 1265-1265
被引量:20
标识
DOI:10.3390/molecules24071265
摘要
A sensitive biotinylated indirect competitive enzyme-linked immunosorbent assay (Bic-ELISA) was developed to detect acetamiprid pesticides in pollen, based on the heterogeneous coating antigen and biotinylated anti-acetamiprid monoclonal antibody. Under optimized experimental conditions, the detection limit for the Bic-ELISA was 0.17 ng/mL and the linear range was 0.25⁻25 ng/mL. The cross-reactivities could be regarded as negligible for the biotinylated antibodies with their analogues except for thiacloprid (1.66%). Analyte recoveries for extracts of spiked pollen (camellia pollen, lotus pollen, rape pollen) ranged from 81.1% to 108.0%, with intra-day relative standard deviations (RSDs) of 4.8% to 10.9%, and the average reproducibility was 85.4% to 110.9% with inter-assay and inter-assay RSDs of 6.1% to 11.7%. The results of Bic-ELISA methods for the Taobao's website samples were largely consistent with HPLC-MS/MS. Therefore, the established Bic-ELISA methods would be conducive to the monitoring of acetamiprid in pollen.
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