Method for simultaneously determining DON toxin and NIV toxin
A toxin and retention time technology, applied in the field of detection, can solve the problems of complex experimental process, low efficiency of DON toxin and NIV toxin detection, inaccurate measurement results, etc., to achieve accurate results, excellent recovery rate and linear relationship, and convenient operation Effect
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[0044] Materials and Methods
[0045] 1.1 Main instruments and reagents
[0046] Table 1. Main instruments and reagents
[0047]
[0048]
[0049] 1.2 Standards and reagents
[0050] Table 2. Standards and reagents
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[0052] experimental method
[0053] 2.1 Pretreatment of test products
[0054] Accurately weigh 25g (accurate to 0.01g) of the sample and place it in a 250ml Erlenmeyer flask and add 100ml of acetonitrile:water solution (84 / 16, v / v). Then ultrasonically extract at 35°C for 30 min, and filter with quantitative filter paper after standing still.
[0055]Take 10ml of the above filtrate and transfer to Mycosep#227 or Mycosep#226 (romer) multifunctional purification column for processing. Take 4 ml of the treated effluent, place it in a glass tube, and dry it with a nitrogen blower at 55°C. Then take out the glass tube, add 1ml of mobile phase (water: acetonitrile: methanol = 90:5:5, v / v / v) to dissolve, and then filter through a 0.22um organic ...
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