Author/Authors :
Fang، نويسنده , , Qingkui and Wang، نويسنده , , Limin and Hua، نويسنده , , Xiude and Wang، نويسنده , , Yulong and Wang، نويسنده , , Suyan and Cheng، نويسنده , , Qi and Cai، نويسنده , , Jia and Liu، نويسنده , , Fengquan، نويسنده ,
Abstract :
In this study, four different haptens around the oxime moiety of Butocarboxim were designed and synthesised. Two of the haptens were conjugated with bovine serum albumin (BSA) to serve as the immunogen and all the haptens were conjugated with ovalbumin (OVA) for the coating antigen. The anti-Butocarboxim monoclonal antibody (Mab) was selected based on eight immunogen/coating antigen combinations. The first enzyme-linked chemiluminescent immunoassay (ELCIA) for determining Butocarboxim in agricultural products was developed. Under the optimised conditions, the detection limit for the ELCIA was 20 ng·mL−1 and the linear range was 27–2700 ng·mL−1. Analyte recoveries for extracts of spiked agricultural (apple and greengrocery) products and tap water ranged from 97.18% to 107.00%. The developed immunoassay has great potential to be developed as a test kit offering a simple and cost-effective approach (such as lateral flow test strip) for screening purposes and evaluating environmental exposure to Butocarboxim.
Keywords :
Butocarboxim , Oxime moiety , monoclonal antibody , Enzyme-linked chemiluminescent immunoassay