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Biomedical and Environmental Sciences ; (12): 449-457, 2012.
Article in English | WPRIM | ID: wpr-235518

ABSTRACT

<p><b>OBJECTIVE</b>To determine 3-amino-5-morpholinomethyl-2-oxazolidinone (AMOZ) residues released from protein bound AMOZ in animal tissues.</p><p><b>METHODS</b>Polyclonal and monoclonal antibodies were produced in this study. A rapid, sensitive, and specific competitive direct enzyme-linked immunosorbent assay (cdELISA) was developed.</p><p><b>RESULTS</b>Rabbit polyclonal antibodies were used in the optimized cdELISA method, and exhibited negligible cross-reactivity with other compounds structurally related to AMOZ. The IC(50) of the polyclonal antibody was 0.16 ng/mL. The method limit of detection in four different types of animal and fish tissues was less than 0.06 μg/kg. Recoveries ranged from 80% to 120% for fortified samples with the coefficient of variation values less than 15%. The results of the cdELISA method were in good agreement with the results from an established liquid chromatography-tandem mass spectrometry confirmatory method used for AMOZ residues.</p><p><b>CONCLUSION</b>The cdELISA method developed in the present study is a convenient practical tool for screening large numbers of animal and fish tissue samples for the the detection of released protein bound AMOZ residues.</p>


Subject(s)
Animals , Enzyme-Linked Immunosorbent Assay , Methods , Molecular Structure , Morpholines , Chemistry , Nitrofurans , Chemistry , Oxazolidinones , Chemistry
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