An analytical study based on extraction with acetonitrile-water, immunoaffinity column cleanup, and HPLC/fluorescence detection for separation and identification of ochratoxin A in coriander was carried out. Validation of the applied methodology was done through accuracy and precision studies. Homogenized samples of coriander were spiked in triplicate with ochratoxin A at 0.5, 1.0, 2.0, and 5.0 μg/kg levels. Recovery values were in the range of 98% for a fortification level at 0.5 μg/kg to 109.1% at 1.0 μg/kg. Application to coriander samples available in Portuguese markes showed no contamination with ochratoxin A.
CITATION STYLE
Lino, C. M., Baeta, L., Pena, A. S., & Silveira, I. N. (2006). Determination of ochratoxin a in coriander (Coriandrum sativum L.) by HPCL/fluorescence detection. Quimica Nova, 29(3), 436–439. https://doi.org/10.1590/S0100-40422006000300006
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