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Combinatorial Chemistry & High Throughput Screening


ISSN (Print): 1386-2073
ISSN (Online): 1875-5402

Monoclonal Antibody-Based Fluorescence Polarization Immunoassay for High Throughput Screening of Furaltadone and its Metabolite AMOZ in Animal Feeds and Tissues

Author(s): Zhen-Lin Xu, Shi-Wei Zhang, Yuan-Ming Sun, Yu-Dong Shen, Hong-Tao Lei, Yue-Ming Jiang, Sergei A. Eremin, Jin-Yi Yang and Hong Wang

Volume 16, Issue 6, 2013

Page: [494 - 502] Pages: 9

DOI: 10.2174/1386207311316060010

Price: $65


A simple and fast homogeneous fluorescent polarization immunoassay (FPIA) was developed for the determination of furaltadone and its metabolite 3-amino-5-methylmorpholino-2-oxazolidinone (AMOZ). Monoclonal antibody with high cross-reactivity to furaltadone and the nitrophenyl derivative of AMOZ (NPAMOZ) were produced against a novel immunogen and the effects of several synthesized tracers on FPIA sensitivity studied. The proposed FPIA, using an optimum antibody and tracer pair, had an IC50 of 4.3µg L–1 and limit of detection at 0.6µg L–1 for furaltadone, and 2.7 µgL–1and0.3µg L–1 for NPAMOZ. Recoveries of furaltadone from animal feeds by FPIA ranged from 79.6 to 87.7%, while recoveries of AMOZ from animal tissues ranged from 72.9 to 83.1%. Good correlation (R>0.99) between the results of this FPIA and a standard analytical method was obtained. The FPIA does not require separation or washing steps and the total time required for equilibrium of the antibody-tracer interaction is only 10 min. These results indicated that the proposed FPIA offers great potential and utility for the high throughput screening of furaltadone residues in animal feed and its metabolite AMOZ residues in animal tissues.

Keywords: 3-amino-5-methylmorpholino-2-oxazolidinone, fluorescent polarization immunoassay, furaltadone, high throughput screening, monoclonal antibody, tracer.

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