Method for measuring content of mycotoxins in araliaceae plants by liquid chromatography-tandem mass spectrometry
A technology of mycotoxins and liquid chromatography, which is applied in the field of determination of mycotoxins in Araliaceae plants, can solve the problem that there is no simultaneous detection of multi-component residues, etc., and achieve the effects of good accuracy, strong specificity and high sensitivity
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[0030] 1. Materials and methods
[0031] 1.1 Main instruments and reagents
[0032] API 4000 tandem quadrupole mass spectrometer (Applied Biosystems, USA), ACQUITY Ultra Performance LC liquid chromatograph (Waters, USA), MIKRO 200R centrifuge (Hettich, Germany), ultrapure water machine (Millipore, USA).
[0033] Aflatoxin, deoxynivalenol, zearalenone, and T-2 toxin standard (SUPELCO, USA); acetonitrile, formic acid, and ammonium formate were all chromatographically pure. Mycosep 226 multifunctional purification column (Romer company). Ginseng was purchased from Shanghai Huayu Medicinal Materials Co., Ltd., place of origin: Jilin, batch number: 20040404.
[0034] 1.2 Experimental method
[0035] 1.2.1 Chromatographic conditions
[0036] ACQUITY UPLC BEH C18 (1.7μm, 2.1×100mm); 100% methanol as mobile phase A, 0.01% formic acid as mobile phase B, flow rate 0.3ml / min; gradient elution according to the following table:
[0037] Table 1. Mobile phase gradient
[0038]
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