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.

Additional Metadata
Keywords Molecularly imprinted polymer, Ochratoxin A, Pulsed elution, Rapid screening, Solid-phase extraction, Wheat extracts
Persistent URL dx.doi.org/10.1007/s00216-003-2409-9
Journal Analytical and Bioanalytical Chemistry
Zhou, S.N. (Simon N.), Lai, E. P, & Miller, JD. (2004). Analysis of wheat extracts for ochratoxin A by molecularly imprinted solid-phase extraction and pulsed elution. Analytical and Bioanalytical Chemistry, 378(8), 1903–1906. doi:10.1007/s00216-003-2409-9