Abstract
A molecularly imprinted solid-phase extraction (MISPE) method has been developed for the rapid analysis of wheat extracts for ochratoxin A (OTA). Molecularly imprinted polymer (MIP) particles were synthesized from N-phenylacrylamide (PAM) and slurry-packed into a micro-column for selective solid-phase extraction (SPE) of OTA. With water flowing at 0.5 mL min−1, a total binding capacity of 30 ng OTA was determined for the 20 mg of MIP particles. MISPE conditions were optimized using OTA in methanol/acetic acid (99:1 v/v). Nearly 100% binding could be achieved from one 20-μL injection of sample containing up to 30 ng of OTA. Pulsed elution (PE) using methanol/triethylamine (99:1 v/v) was good for the quantitative desorption of OTA. The MISPE–PE method, with fluorescence detection at λ ex=385 nm and λ em=445 nm, afforded a detection limit of 5.0 ng mL−1 (or 0.1 ng in 20 μL of sample injected) for OTA. Recovery of OTA from wheat extracts was 103±3%. Each MISPE–PE analysis required less than 5 min to complete.
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Acknowledgments
Financial support of the Natural Sciences and Engineering Research Council (NSERC) Canada is gratefully acknowledged. The authors thank Tom Nowicki and Mike Roscoe, Winnipeg Food Inspection Agency, for the wheat extracts and helpful discussions.
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Zhou, S.N., Lai, E.P.C. & Miller, J.D. Analysis of wheat extracts for ochratoxin A by molecularly imprinted solid-phase extraction and pulsed elution. Anal Bioanal Chem 378, 1903–1906 (2004). https://doi.org/10.1007/s00216-003-2409-9
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DOI: https://doi.org/10.1007/s00216-003-2409-9