化学
益达胺
色谱法
啶虫脒
新烟碱
免疫分析
分析物
草药
噻虫胺
药用植物
杀虫剂
传统医学
噻虫嗪
医学
抗体
农学
免疫学
生物
作者
Zhanjiang Zhang,Qianpin Chen,Hao Huang,Kun Zhang,Longhua Bai,Guiyu Tan
标识
DOI:10.1080/00032719.2022.2148683
摘要
The safety of medicinal herbs is critical to human health, and the monitoring of pesticide residues in medicinal herbs is necessary. In the present study, a direct competitive enzyme-linked immunosorbent assay (dc-ELISA) was developed for the determination of imidacloprid in medicinal herbs. Using the optimal conditions, the 50% inhibiting concentration and detection range (20–80% inhibiting concentration) of the established dc-ELISA were 0.08 and 0.03–0.29 ng/mL, respectively. Except for clothianidin (4.64%) and acetamiprid (2.52%), the cross-reactivity with analyte analogs was negligible. In purple perilla, cordate houttuynia, water lily, bitter melon, and mung bean, the average imidacloprid recoveries were from 62.97 to 134.09%, with relative standard deviations between 0.21 and 14.58%. Furthermore, the immunoassay results correlated well with spiked samples analyzed by high-performance liquid chromatography – tandem mass spectrometry (HPLC-MS/MS). The established immunoassay is rapid, sensitive, and specific and suitable to monitor imidacloprid residues in medicinal herbs.
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