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. 2024 May 21;15:1356723. doi: 10.3389/fpls.2024.1356723

Table 2.

The parameters of quantitative analysis using in an Ultimate 3000 ultrahigh-performance liquid chromatography system coupled with a Q Exactive-Orbitrap High Resolution Mass Spectrometer (LC–MS/MS analysis) for DON, ZEN, NIV, 15ADON, 3ADON, and D3G contents.

Mycotoxinsx Molecular ion Precursor ion (m/z) RTz (min) Ion pairy (m/z) Collision energy (eV)
DON [DON-H]- 295.1171 3.19 265.1070*/247.0961 15
ZEN [ZEN-H]- 317.1380 7.90 175.0380*/273.1481 45
NIV [NIV+CH3COO]- 371.1331 2.13 281.1019*/311.1125 15
15ADON [15ADON+CH3COO]- 397.1485 5.88 337.1280*/150.0323 10
3ADON [3ADON-H]- 337.1279 5.87 307.1170*/173.0590 15
D3G [D3G+CH3COO]- 517.1895 3.01 427.1582*/457.1689 25

xDON, deoxynivalenol, its derivatives (D3G, DON-3-glucoside; 3ADON, 3-acetyldeoxynivalenol; 15ADON, 15-acetyldeoxynivalenol; and NIV, nivalenol); and ZEN, zearalenone. y *Quantitative ion. The detection limits of toxins in wheat were 10 µg/kg for DON and NIV, 10 µg/kg for 3ADON, 3 µg/kg for 15ADON, and 1 µg/kg for D3G, respectively. zRT = the retention time of chromatographic peaks.