Reprint

Application of LC-MS/MS in the Mycotoxins Studies

Edited by
June 2020
302 pages
  • ISBN978-3-03936-206-6 (Paperback)
  • ISBN978-3-03936-207-3 (PDF)

This book is a reprint of the Special Issue Application of LC-MS/MS in the Mycotoxins Studies that was published in

Biology & Life Sciences
Medicine & Pharmacology
Public Health & Healthcare
Summary
Mycotoxins are secondary metabolites produced by the fungi of different species (mainly Aspergillus, Fusarium, and Penicillium), with toxic effects for humans and animals. These mycotoxins can contaminate food and feed. The European Union (EU) has established the maximum permitted or recommended levels for well-known mycotoxins in different foodstuffs. However, there are other mycotoxins that are not included in the regulations: the “emerging mycotoxins” (whose toxicity is still not clear), and the “modified or masked mycotoxins” (produced as a consequence of a detoxification strategy of the host plant of the fungus or during food processing). These mycotoxins could pose a risk and should also be taken into account. In order to assure consumers’ health, analytical methods for the accurate determination of mycotoxins in different food matrices and feeds are required. In this sense, liquid chromatography tandem mass spectrometry (LC–MS/MS) is a powerful tool for their unique identification and quantification. Moreover, the use of high-resolution mass spectrometry (HRMS) allows one to identify novel mycotoxins and targeted/untargeted approaches for study. This Special Issue compiles recent applications of LC–MS/MS in mycotoxin studies, as well as the development and validation of new analytical methods for their identification and quantification in different food matrices and feed, occurrence studies, and the biomonitoring of mycotoxins and their metabolites in biological fluids.
Format
  • Paperback
License
© 2020 by the authors; CC BY-NC-ND license
Keywords
cereals; mycotoxigenic fungi; phylogeny; deoxynivalenol; zearalenone; Sub-Saharan Africa; aflatoxins; mycotoxins; total diet study; food contaminants; LC-MS/MS; Alternaria toxins; grape; modified QuEChERS; UHPLC-MS/MS; n/a; traditional sorghum malts; mycotoxins; aflatoxins; Aspergillus; LC/MS/MS; Biomarkers; exposure; LC-MS/MS; LC-HRMS; pig; broiler chicken; multi-mycotoxin; mycotoxins; stability; malting; brewing; beer; feed; pig; mycotoxins; liquid chromatography; fluorescence detection; mass spectrometry; solid-liquid extraction; co-occurrence; mycotoxins; metabolism; high-resolution mass spectrometry (HRMS); microsomal incubation; glucuronidation; human; biomonitoring; mycotoxins; UPLC-MS/MS; rumen fluid; maize silage; matrix-matched; moniliformin; lanthanide complexes; LC-MS/MS; LC-UV; LC-MS/MS; mycotoxins; collaborative study; isotopic dilution; compliance; infant food; emergent mycotoxins; urine; dispersive solid-phase extraction; magnetic carbon nanotube composite; mycotoxins; pesticides; Q-Exactive Orbitrap; CBD capsule; nutraceutical; Fusarium; maize; masked mycotoxins; LC-MS/MS; agricultural regions; South Africa; Mycotoxins; cereals; UHPLC-MS/MS; exposure assessment; Algeria; Mycotoxins; mixed feed rations; QuEChERS; dispersive solid phase extraction; liquid chromatography; high-resolution mass spectrometry; data independent SWATH; n/a