Suitability of a fully 13C isotope labeled internal standard for the determination of the mycotoxin deoxynivalenol by LC-MS/MS without clean up

被引:60
作者
Häubl, G [1 ]
Berthiller, F [1 ]
Krska, R [1 ]
Schuhmacher, R [1 ]
机构
[1] Univ Nat Resources & Appl Life Sci, Ctr Analyt Chem, IFA Tulln, Dept Agrobiotechnol,Christian Dopler Lab Mytoxin, A-3430 Tulln, Austria
关键词
deoxynivalenol; mass spectrometry; internal standard; stable isotope; wheat; maize;
D O I
10.1007/s00216-005-0218-z
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Very often, the accuracy of quantitative analytical methods for the determination of mycotoxins by liquid chromatography (LC)-mass spectrometry (MS) and LC-MS/MS is limited by matrix effects during the ionization process in the MS source. Stable isotope labeled standards are best suited to correct for matrix effects and to improve both the trueness and the precision of analytical methods employing LC-MS and LC-MS/MS. This paper describes the successful use of fully (13C) isotope labeled deoxynivalenol [(C-13(15))DON] as an internal standard (IS) for the accurate determination of DON in maize and wheat by LC electrospray ionization MS/MS. To show the full potential of (C-13(15))DON as IS, maize and wheat extracts were analyzed without further cleanup. Subsequent to calibration for the LC-MS end determination, DON was quantified in matrix reference materials (wheat and maize). Without consideration of the IS, apparent recoveries of DON were 29 +/- 6% (n=7) for wheat and 37 +/- 5% (n=7) for maize. However, the determination of DON in the reference materials yielded 95 +/- 3% (wheat) and 99 +/- 3% (maize) when (C-13(15))DON was used as an IS for data evaluation.
引用
收藏
页码:692 / 696
页数:5
相关论文
共 18 条
  • [1] Rapid simultaneous determination of major type A- and B-trichothecenes as well as zearalenone in maize by high performance liquid chromatography-tandem mass spectrometry
    Berthiller, F
    Schuhmacher, R
    Buttinger, G
    Krska, R
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2005, 1062 (02) : 209 - 216
  • [2] Biselli S, 2005, SPECTROSCOPY-US, V20, P20
  • [3] BOTTALICO B, 1998, J PLANT PATHOL, V80, P85
  • [4] Development of a multiresidue method for analysis of major Fusarium mycotoxins in corn meal using liquid chromatography/tandem mass spectrometry
    Cavaliere, C
    Foglia, P
    Pastorini, E
    Samperi, R
    Laganà, A
    [J]. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2005, 19 (14) : 2085 - 2093
  • [5] Simultaneous detection of type A and type B trichothecenes in cereals by liquid chromatography-electrospray ionization mass spectrometry using NaCl as cationization agent
    Dall'Asta, C
    Sforza, S
    Galaverna, G
    Dossena, A
    Marchelli, R
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2004, 1054 (1-2) : 389 - 395
  • [6] Rapid determination of fumonisin FB1 in corn products by high-performance liquid chromatography-electrospray mass spectrometry
    Hartl, M
    Herderich, M
    Humpf, HU
    [J]. EUROPEAN FOOD RESEARCH AND TECHNOLOGY, 1999, 209 (05) : 348 - 351
  • [7] Liquid chromatography/tandem mass spectrometry for the identification and determination of trichothecenes in maize
    Laganà, A
    Curini, R
    D'Ascenzo, G
    De Leva, I
    Faberi, A
    Pastorini, E
    [J]. RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2003, 17 (10) : 1037 - 1043
  • [8] Quantification of ochratoxin A in foods by a stable isotope dilution assay using high-performance liquid chromatography-tandem mass spectrometry
    Lindenmeier, M
    Schieberle, P
    Rychlik, M
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2004, 1023 (01) : 57 - 66
  • [9] MICHAUD DP, 1986, J LABELLED COMPD RAD, V25, P345
  • [10] Miller J.D., 1994, MYCOTOXINS GRAIN