LC-MS/MS multi-analyte method for mycotoxin determination in food supplements

被引:141
作者
Di Mavungu, Jose Diana [1 ]
Monbaliu, Sofie [1 ]
Scippo, Marie-Louise [2 ]
Maghuin-Rogister, Guy [2 ]
Schneider, Yves-Jacques [3 ,4 ]
Larondelle, Yvan [3 ,4 ]
Callebaut, Alfons [5 ]
Robbens, Johan [6 ]
Van Peteghem, Carlos [1 ]
De Saeger, Sarah [1 ]
机构
[1] Univ Ghent, Fac Pharmaceut Sci, Lab Food Anal, B-9000 Ghent, Belgium
[2] Univ Liege, Fac Vet Med, Lab Food Anal, CART, B-4000 Liege, Belgium
[3] Inst Sci Vie, Lab Biochim Cellulaire Nutr & Toxicol, B-1348 Louvain, Belgium
[4] Catholic Univ Louvain, B-1348 Louvain, Belgium
[5] CERVA CODA, B-3080 Tervuren, Belgium
[6] Univ Antwerp, Lab Ecophysiol Biochem & Toxicol, B-2020 Antwerp, Belgium
来源
FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT | 2009年 / 26卷 / 06期
关键词
mycotoxins; multi-target analysis; liquid chromatography; tandem mass spectrometry; food supplements; validation; standard addition; MASS-SPECTROMETRY METHOD; OF-THE-ART; LIQUID-CHROMATOGRAPHY; GAS-CHROMATOGRAPHY; TRICHOTHECENE MYCOTOXINS; FUMONISIN CONTAMINATION; FUSARIUM MYCOTOXINS; ALPHA-ZEARALENOL; B-TRICHOTHECENE; OCHRATOXIN-A;
D O I
10.1080/02652030902774649
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A multi-analyte method for the liquid chromatography-tandem mass spectrometric determination of mycotoxins in food supplements is presented. The analytes included A and B trichothecenes (nivalenol, deoxynivalenol, 3-acetyldeoxynivalenol, 15-acetyldeoxyvalenol, neosolaniol, fusarenon-X, diacetoxyscirpenol, HT-2 toxin and T-2 toxin), aflatoxins (aflatoxin-B-1, aflaxoin-G(1) and aflatoxin-G(2)). Alternaria toxins (alternariol, alternariol methyl ether and altenuene), fumonisins (fumonisin-B-1, fumonisin-B-2 and fumonisin-B-3), ochratoxin A, zearalenone, beauvericin and sterigmatocystin. Optimization of the stimulataneous extraction of these toxins and the sample pretreatment procedure, as well as method validation were performed on maca (Lepidium meyenii) food supplements. The results indicated that the solvent mixture ethyl acetate/formic acid (95:5, v/v) n-hexane was applied as partial clean-up step to remove excess of co-extracted non-polar components. Further clean-up was performed on Oasis HLB(TM) cartidges. Samples were analysed using an Acquity UPLC system coupled to a Micromass Quattro Micro triple quadrupole mass spectrometer equipped with an electrospray interface operated in the positive-ion mode. Limits of detection and quantification were in the range of 0.3-30 ng g(-1) and 1-100 ng g(-1), respectively. Recovery yields were above 60% for most of the analytes, except for different food supplements such as soy (Glycine max) isoflavones, St John's wort (Hypericum perforatum), garlic (Allium sativum), Ginkgo biloba, and black radish (Raphanus niger) demonstrated the general applicability of the method. Due to different matrix effects observed in different food supplement samples, the standard addition approach was applied to perform correct quantitative analysis. In 56 out of 62 samples analysed, none of the 23 mycotoxins investigated was detected. Positive samples contained at least one of the toxins fumonisin-B-1, fumonisin-B-2, fumonisin-B-3 and ochratoxin A.
引用
收藏
页码:885 / 895
页数:11
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