Competitive direct enzyme-linked immunosorbent screening assay for the detection of sulfamethazine contamination of animal feeds.

D E Dixon-Holland, S E Katz
Author Information
  1. D E Dixon-Holland: Rutgers University, Cook College, Department of Biochemistry and Microbiology, New Brunswick, NJ 08903-0231.

Abstract

A sensitive screening method has been developed for detecting sulfamethazine (SMZ) contamination of feeds by using either polyclonal or monoclonal antibodies and a direct competitive enzyme-linked immunosorbent screening assay (ELISA). Feed samples of 25.0 g are extracted with 0.5N HCl and centrifuged. The extract is adjusted to pH 7.0 with 3.0N NaOH and recentrifuged. This pH-adjusted extract is used in the ELISA. Levels as low as 0.004 micrograms SMZ/g feed were detected in supplemented extracts by polyclonal antibodies; levels of 0.4 micrograms SMZ/g feed were detected by a monoclonal antibody.

MeSH Term

Animal Feed
Animals
Antibodies, Monoclonal
Drug Residues
Enzyme-Linked Immunosorbent Assay
Food Contamination
Mice
Rabbits
Reproducibility of Results
Sensitivity and Specificity
Sulfamethazine
Time Factors

Chemicals

Antibodies, Monoclonal
Sulfamethazine

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