Literature DB >> 18348046

LC-MS/MS multi-method for mycotoxins after single extraction, with validation data for peanut, pistachio, wheat, maize, cornflakes, raisins and figs.

Martien C Spanjer1, Peter M Rensen, Jos M Scholten.   

Abstract

Mycotoxin analysis is usually carried out by high performance liquid chromatography after immunoaffinity column cleanup or in enzyme-linked immunosorbent assay tests. These methods normally involve determination of single compounds only. EU legislation already exists for the aflatoxins, ochratoxin A and patulin in food, and legislation will come into force for deoxynivalenol, zearalenone and the fumonisins in 2007. To enforce the various legal limits, it would be preferable to determine all mycotoxins by routine analysis in different types of matrices in one single extract. This would also be advantageous for HACCP control purposes. For this reason, a multi-method was developed with which 33 mycotoxins in various products could be analysed simultaneously. The mycotoxins were extracted with an acetonitrile/water mixture, diluted with water and then directly injected into a LC-MS/MS system. The mycotoxins were separated by reversed-phase HPLC and detected using an electrospray ionisation interface (ESI) and tandem MS, using MRM in the positive ion mode, to increase specificity for quality control. The following mycotoxins could be analysed in a single 30-min run: Aflatoxins B1, B2, G1 and G2, ochratoxin A, deoxynivalenol, zearalenone, T-2 toxin, HT-2 toxin, alpha-zearalenol, alpha-zearalanol, beta-zearalanol, sterigmatocystin, cyclopiazonic acid, penicillic acid, fumonisins B1, B2 and B3, diacetoxyscirpenol, 3- and 15-acetyl-deoxynivalenol, zearalanone, ergotamin, ergocornin, ergocristin, alpha-ergocryptin, citrinin, roquefortin C, fusarenone X, nivalenol, mycophenolic acid, alternariol and alternariol monomethyl ether. The limit of quantification for the aflatoxins and ochratoxin A was 1.0 microg kg(-1) and for deoxynivalenol 50 microg kg(-1). The quantification limits for the other mycotoxins were in the range 10-200 microg kg(-1). The matrix effect and validation data are presented for between 13 and 24 mycotoxins in peanuts, pistachios, wheat, maize, cornflakes, raisins and figs. The method has been compared with the official EU method for the determination of aflatoxins in food and relevant FAPAS rounds. The multi-mycotoxin method has been proven by the detection of more than one mycotoxin in maize, buckwheat, figs and nuts. The LC-MS/MS technique has also been applied to baby food, which is subject to lower limits for aflatoxin B1 and ochratoxin A, ergot alkaloids in naturally contaminated rye and freeze-dried silage samples.

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Year:  2008        PMID: 18348046     DOI: 10.1080/02652030701552964

Source DB:  PubMed          Journal:  Food Addit Contam Part A Chem Anal Control Expo Risk Assess        ISSN: 1944-0057


  43 in total

Review 1.  Occurrence, detection and detoxification of mycotoxins.

Authors:  Visenuo Aiko; Alka Mehta
Journal:  J Biosci       Date:  2015-12       Impact factor: 1.826

2.  Extracting fumonisins from maize: efficiency of different extraction solvents in multi-mycotoxin analytics.

Authors:  Stefanie Marschik; Julia Hepperle; Uwe Lauber; Renate Schnaufer; Susanne Maier; Caren Kühn; Gabriele Schwab-Bohnert
Journal:  Mycotoxin Res       Date:  2013-02-24       Impact factor: 3.833

3.  A new approach using micro HPLC-MS/MS for multi-mycotoxin analysis in maize samples.

Authors:  Sebastian Hickert; Johannes Gerding; Edson Ncube; Florian Hübner; Bradley Flett; Benedikt Cramer; Hans-Ulrich Humpf
Journal:  Mycotoxin Res       Date:  2015-03-12       Impact factor: 3.833

4.  Mycotoxin production by pure fungal isolates analysed by means of an uhplc-ms/ms multi-mycotoxin method with possible pitfalls and solutions for patulin-producing isolates.

Authors:  Els Van Pamel; Geertrui Vlaemynck; Marc Heyndrickx; Lieve Herman; Annemieke Verbeken; Els Daeseleire
Journal:  Mycotoxin Res       Date:  2010-11-05       Impact factor: 3.833

5.  Analysis of Fusarium toxins via HPLC-MS/MS multimethods: matrix effects and strategies for compensation.

Authors:  Anke Trebstein; Uwe Lauber; Hans-Ulrich Humpf
Journal:  Mycotoxin Res       Date:  2009-11-10       Impact factor: 3.833

6.  Production of (15)N-labeled α-amanitin in Galerina marginata.

Authors:  Hong Luo; Brandon DuBois; R Michael Sgambelluri; Evan R Angelos; Xuan Li; Daniel Holmes; Jonathan D Walton
Journal:  Toxicon       Date:  2015-06-19       Impact factor: 3.033

7.  Rapid determination of fumonisins B1 and B2 in corn by liquid chromatography-tandem mass spectrometry with ultrasonic extraction.

Authors:  Cun Li; Yin-Liang Wu; Ting Yang; Wei-Guo Huang-Fu
Journal:  J Chromatogr Sci       Date:  2012-01       Impact factor: 1.618

8.  OxaD: A Versatile Indolic Nitrone Synthase from the Marine-Derived Fungus Penicillium oxalicum F30.

Authors:  Sean A Newmister; Claire M Gober; Stelamar Romminger; Fengan Yu; Ashootosh Tripathi; Lizbeth Lorena L Parra; Robert M Williams; Roberto G S Berlinck; Madeleine M Joullié; David H Sherman
Journal:  J Am Chem Soc       Date:  2016-08-24       Impact factor: 15.419

9.  Isolation of alpaca anti-idiotypic heavy-chain single-domain antibody for the aflatoxin immunoassay.

Authors:  Yanru Wang; Peiwu Li; Zuzana Majkova; Candace R S Bever; Hee Joo Kim; Qi Zhang; Julie E Dechant; Shirley J Gee; Bruce D Hammock
Journal:  Anal Chem       Date:  2013-08-21       Impact factor: 6.986

10.  Precise determination of the Alternaria mycotoxins alternariol and alternariol monomethyl ether in cereal, fruit and vegetable products using stable isotope dilution assays.

Authors:  Stefan Asam; Katharina Konitzer; Michael Rychlik
Journal:  Mycotoxin Res       Date:  2010-11-11       Impact factor: 3.833

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