Abstract

This study compared four extraction procedures for the simultaneous determination of mycotoxins ochratoxin A and citrinin in samples of rice. Soares and Rodriguez-Amaya and Tanaka procedures and the extraction methods QuEChERS (Quick, Easy, Cheap, Effective, Rugged and Safe) and by ultrasound were compared in terms of residue generation, limit of detection, limit of quantification and simultaneous recovery of mycotoxins. Soares and Rodriguez-Amaya and the method by ultrasound presented the lowest recoveries, 83 and 55% for ochratoxin A (OTA) and 48 and 55% for citrinin (CIT), respectively. Tanaka procedure and QuEChERS method presented the highest recoveries, 98 and 105% for OTA and 64 and 78% for CIT, respectively. The latter enabled the simultaneous extraction of the two mycotoxins, with a reduction of up to 25 times of the amount of the involved solvent.

Highlights

  • Fungi produce a large variety of toxic secondary metabolites called mycotoxins.[1]

  • Aspergillus, Penicillium and Fusarium are among the fungal genera that occur in food and that have toxigenic species, such as Aspergillus ochraceus and Penicillium citrinum, the main producers of ochratoxin A and citrinin, respectively.[4,5]

  • This study aims at comparing the phase of extraction and purification of four methods regarding its ability to simultaneously extract ochratoxin A and citrinin in rice, by using high performance liquid chromatography with a photodiode array detector (HPLC-PDA)

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Summary

Introduction

Fungi produce a large variety of toxic secondary metabolites called mycotoxins.[1]. These compounds comprise several chemical structures including some relatively simple ones,[1] which occur in mycelium of filamentous fungi, normally after a period of balanced growth followed by stress conditions.[2,3] Aspergillus, Penicillium and Fusarium are among the fungal genera that occur in food and that have toxigenic species, such as Aspergillus ochraceus and Penicillium citrinum, the main producers of ochratoxin A and citrinin, respectively.[4,5]Ochratoxin A (OTA) (N-{[(3R)-5​ -chloro-8​ -hydroxy-3​ -methyl-1​ -oxo-3​ ,4​ -dihydro-1​ H-isochromen-7​ -yl]carbonyl}-L-phenylalanine, Figure 1) is classified by the InternationalAgency for Research on Cancer (IARC from World Health Organization (WHO)) as a probably carcinogenic agent for humans (Group 2B, IARC).[6]. Fungi produce a large variety of toxic secondary metabolites called mycotoxins.[1] These compounds comprise several chemical structures including some relatively simple ones,[1] which occur in mycelium of filamentous fungi, normally after a period of balanced growth followed by stress conditions.[2,3] Aspergillus, Penicillium and Fusarium are among the fungal genera that occur in food and that have toxigenic species, such as Aspergillus ochraceus and Penicillium citrinum, the main producers of ochratoxin A and citrinin, respectively.[4,5]. Ochratoxin A (OTA) (N-{[(3R)-5​ -chloro-8​ -hydroxy-3​ -methyl-1​ -oxo-3​ ,4​ -dihydro-1​ H-isochromen-7​ -yl]carbonyl}-L-phenylalanine, Figure 1) is classified by the International. Its presence was detected in many stored and dry foods,[8,9] such as corn, wheat, oats, beans, nuts, peanuts, rice, barley, sorghum, cotton seed, coffee beans, cocoa and spices.[10,11,12,13]

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