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Determination of 42 mycotoxins in oats using a mechanically assisted QuEChERS sample preparation and UHPLC-MS/MS detection.
De Colli, Lorenzo; Elliott, Christopher; Finnan, John; Grant, Jim; Arendt, Elke K; McCormick, Susan P; Danaher, Martin.
Affiliation
  • De Colli L; Institute for Global Food Security, Queen's University Belfast, Belfast, United Kingdom; Food Safety Department, Teagasc Food Research Centre, Ashtown, Dublin 15, Ireland. Electronic address: lorenzo.decolli@teagasc.ie.
  • Elliott C; Institute for Global Food Security, Queen's University Belfast, Belfast, United Kingdom.
  • Finnan J; Teagasc Crops Research Division, Oak Park, Carlow, Ireland.
  • Grant J; Teagasc Food Research Centre, Ashtown, Dublin 15, Ireland.
  • Arendt EK; School of Food and Nutritional Sciences, National University of Ireland, University College Cork, College Road, Cork, Co., Cork, Ireland.
  • McCormick SP; Mycotoxin Prevention and Applied Microbiology Research Unit, National Centre for Agricultural Utilization Research, U.S. Department of Agriculture, Peoria, IL 61604, United States.
  • Danaher M; Food Safety Department, Teagasc Food Research Centre, Ashtown, Dublin 15, Ireland.
Article in En | MEDLINE | ID: mdl-32473516
ABSTRACT
A method was developed and validated for the simultaneous determination of 42 mycotoxins in oats. The method includes all the mycotoxins listed under Commission Regulation 1881/2006 and Commission Recommendation 165/2013, the emerging mycotoxins (beauvericin, alternariol, alternariol-methyl-ether and enniatins), and two masked metabolites, namely deoxynivalenol-3-glucoside and T-2-glucoside. The method also focuses on a wide range of analytes of toxicological interest. The sample preparation involved extraction with an aqueous acetic acid solution and acetonitrile, followed by QuEChERS with mechanically assisted vibrational shaking. No further clean-up steps were employed, and analysis was performed using ultra-high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS). Trueness ranged between 78% and 158%, while precision ranged from 1.7% to 49.9% under within-laboratory reproducibility conditions. Beside the high degree of accuracy and sample throughput provided, the method can be applied to a large number of compounds currently not regulated, thus generating knowledge and for risk assessment purposes.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromatography, High Pressure Liquid / Avena / Tandem Mass Spectrometry / Mycotoxins Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: J Chromatogr B Analyt Technol Biomed Life Sci Journal subject: ENGENHARIA BIOMEDICA Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromatography, High Pressure Liquid / Avena / Tandem Mass Spectrometry / Mycotoxins Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Language: En Journal: J Chromatogr B Analyt Technol Biomed Life Sci Journal subject: ENGENHARIA BIOMEDICA Year: 2020 Document type: Article