Abstract

Citrinin (CIT) deserves attention due to its known toxic effects in mammalian species and its widespread occurrence in food commodities, often along with ochratoxin A, another nephrotoxic mycotoxin. Human exposure, a key element in assessing risk related to food contaminants, depends upon mycotoxin contamination levels in food and on food consumption. Commercial supplements, commonly designated as red rice, usually used in daily diets in Asiatic countries due to their medicinal properties, may pose a health problem as a result of high CIT levels. In addition to the worldwide occurrence of CIT in foods and supplements, a wide range of several analytical and detection techniques with high sensitivity, used for evaluation of CIT, are reviewed and discussed in this manuscript. This review addresses the scientific literature regarding the presence of CIT in foods of either vegetable or animal origin, as well as in supplements. On what concerns analytical methodologies, sample extraction methods, such as shaking extraction and ultrasonic assisted extraction (UAE), clean-up methods, such as liquid-liquid extraction (LLE), solid phase extraction (SPE) and Quick, Easy, Cheap, Effective, Rugged and Safe (QuECHERS), and detection and quantification methods, such as thin layer chromatography (TLC), high performance liquid chromatography (HPLC), capillary electrophoresis (CE), biosensors, and ELISA, are also reviewed.

Highlights

  • Mycotoxins, toxic secondary metabolites, are produced by some fungal species, which readily colonize crops, contaminating them in the field or after harvest, and processed foods under certain favourable conditions of moisture, water activity, and temperature

  • In addition to CIT0 s worldwide occurrence in foods of either vegetable or animal origin and in supplements, this manuscript presents a review of extraction methods, such as shaking extraction and ultrasonic assisted extraction (UAE), clean-up procedures, such as liquid-liquid extraction (LLE), solid phase extraction (SPE), Quick, Easy, Cheap, Effective, Rugged and Safe (QuEChERS), and detection and quantification procedures, such as thin layer chromatography (TLC), high performance liquid chromatography (HPLC), and capillary electrophoresis (CE), and others such as biosensor-based techniques and still enzyme-linked immunoassays (ELISA)

  • The last report of the European Commission (2018) showed that about 96% of notifications of mycotoxins in the Rapid Alert System for Food and Feed (RASFF) concerned food, and notifications of citrinin are below 0.5% [33]

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Summary

Introduction

Mycotoxins, toxic secondary metabolites, are produced by some fungal species, which readily colonize crops, contaminating them in the field or after harvest, and processed foods under certain favourable conditions of moisture, water activity, and temperature. The most common toxins that attract notable attention in the contaminated agro-food products are aflatoxins (AFs), ochratoxin A (OTA), trichothecenes (deoxynivalenol (DON) and nivalenol (NIV)), fumonisins (FBs), zearalenone (ZEN), citrinin (CIT) and patulin (PAT) [1,2] They are produced by some species of toxigenic fungi such as Aspergillus, Penicillium, Fusarium, Alternaria and Monascus [3,4]. In addition to CIT0 s worldwide occurrence in foods of either vegetable or animal origin and in supplements, this manuscript presents a review of extraction methods, such as shaking extraction and ultrasonic assisted extraction (UAE), clean-up procedures, such as liquid-liquid extraction (LLE), solid phase extraction (SPE), Quick, Easy, Cheap, Effective, Rugged and Safe (QuEChERS), and detection and quantification procedures, such as thin layer chromatography (TLC), high performance liquid chromatography (HPLC), and capillary electrophoresis (CE), and others such as biosensor-based techniques and still enzyme-linked immunoassays (ELISA)

Physicochemical Properties
Degradation Products
Cereals and Derivatives
Derivatives
Olives
Apples
Spices
Cheese
Cured Meat
Legislation
Analytical Methods
Extraction
Clean-Up
Extraction Procedure
QuEChERS
Detection and Quantification
LC-FD and UPLC-FD
Immunoassays
Findings
Conclusions
Full Text
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