Abstract

A reliable and practical multi-method was developed for the quantification of mycotoxins in plasma, urine, and feces of pigs, and plasma and excreta of broiler chickens using liquid chromatography–tandem mass spectrometry. The targeted mycotoxins belong to the regulated groups, i.e., aflatoxins, ochratoxin A and Fusarium mycotoxins, and to two groups of emerging mycotoxins, i.e., Alternaria mycotoxins and enniatins. In addition, the developed method was transferred to a LC-high resolution mass spectrometry instrument to qualitatively determine phase I and II metabolites, for which analytical standards are not always commercially available. Sample preparation of plasma was simple and generic and was accomplished by precipitation of proteins alone (pig) or in combination with removal of phospholipids (chicken). A more intensive sample clean-up of the other matrices was needed and consisted of a pH-dependent liquid–liquid extraction (LLE) using ethyl acetate (pig urine), methanol/ethyl acetate/formic acid (75/24/1, v/v/v) (pig feces) or acetonitrile (chicken excreta). For the extraction of pig feces, additionally a combination of LLE using acetone and filtration of the supernatant on a HybridSPE-phospholipid cartridge was applied. The LC-MS/MS method was in-house validated according to guidelines defined by the European and international community. Finally, the multi-methods were successfully applied in a specific toxicokinetic study and a screening study to monitor the exposure of individual animals.

Highlights

  • IntroductionThe worldwide contamination of feed with mycotoxins is of major agro-economic importance

  • The worldwide contamination of feed with mycotoxins is of major agro-economic importance.In addition to crop and feed loss and damage, these mycotoxins can have a large impact on animal health

  • The multi-methods were successfully applied in a specific toxicokinetic study and a screening study to monitor the exposure of individual animals

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Summary

Introduction

The worldwide contamination of feed with mycotoxins is of major agro-economic importance. In addition to crop and feed loss and damage, these mycotoxins can have a large impact on animal health. Surveys show that mycotoxins occur in more than 70% of the tested feed samples and 38% of Toxins 2019, 11, 171; doi:10.3390/toxins11030171 www.mdpi.com/journal/toxins. Toxins 2019, 11, 171 these samples contain multiple mycotoxins. Co-contamination of several mycotoxins can result in additive or synergistic effects. Multi-methods are an asset in mycotoxin analysis [1]. Aflatoxin B1 (AFB1), ochratoxin A (OTA), fumonisin B1 (FB1), T2-toxin (T2), zearalenone (ZEN) and deoxynivalenol (DON), as well as enniatins (ENN), beauvericin (BEA), alternariol (AOH) and tenuazonic acid (TeA) were included

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