Development of an enzyme-linked immunosorbent assay for detection of clopidol residues in chicken tissues

• Published in: Journal of the science of food and agriculture Vol. 94; no. 11; pp. 2295 - 2300
• Main Authors: Jiang, Jin-qing, Zhang, Hai-tang, Zhang, Hui-hui, Wang, Zi-liang, Yang, Xue-feng, Fan, Guo-ying
• Format: Journal Article
• Language: English
• Published: Chichester, UK John Wiley & Sons, Ltd 01-08-2014; John Wiley and Sons, Limited
• Subjects: Animals; Antibodies, Monoclonal; Antigens; artificial antigen; Assaying; Biological; chicken tissues; Chickens; clopidol; Clopidol - analysis; Coccidiostats - analysis; Diagnostic systems; Diet; Drug Residues - analysis; Enzyme-Linked Immunosorbent Assay - standards; Enzymes; Female; Food Contamination - analysis; Haptens - immunology; Hybridomas; Immunoassay; Meat - analysis; Mice; Mice, Inbred BALB C; Monoclonal antibodies; monoclonal antibody; Muscles - chemistry; Poultry; Residues; Tissues; clopidol; artificial antigen; monoclonal antibody; chicken tissues; immunoassay
• ISSN: 0022-5142; 1097-0010
• DOI: 10.1002/jsfa.6557

BACKGROUND
Clopidol is mainly used for the prevention and treatment of coccidiosis, which poses a serious potential hazard to public health, in veterinary medicine. The aim of this study was to prepare monoclonal antibodies (mAbs) against clopidol (CLOP) and develop an immunoassay for detecting CLOP residues in chicken tissues. After derivation, CLOP hapten was conjugated to carrier proteins to synthesize the artificial antigen, and immunized Balb/C mice were employed to screen mAbs.
RESULTS
A sensitive hybridoma named C1G3 was screened out and two indirect competitive enzyme‐linked immunosorbent assay (icELISA) standard curves were established. For the traditional two‐step assay the linear range was from 0.06 to 98 ng mL−1, with half‐maximal inhibitory concentration (IC50) and limit of detection (LOD) values of 2.76 ng mL−1 and 0.03 ng mL−1 respectively, while the rapid one‐step icELISA had a working range from 0.08 to 102 ng mL−1, with IC50 and LOD values of 3.52 ng mL−1 and 0.03 ng mL−1 respectively. It was also indicated that a 10‐fold dilution in chicken muscles gave an inhibition curve almost the same as that obtained in phosphate‐buffered saline. When applied to spiking tests in chicken samples, the correlation coefficient (R2) between concentrations added and measured was 0.9534.
CONCLUSION
The results of this study suggest that the immunoassay described is a promising alternative for screening CLOP residues in biological matrices and is suitable for routine diagnostics. © 2014 Society of Chemical Industry