Method for rapid determination of Flavobacterium farinofermentans toxin A in food poisoning sample
A technology for rapid determination of Flavobacterium, which is applied in the field of food safety biotoxin detection, can solve the problems of complex sample extraction, low detection sensitivity, and inability to accurately characterize, achieve high sensitivity, simplify extraction steps, and improve accuracy.
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[0040] 1 instrument
[0041] 1290 ultra-high performance liquid chromatography (Agilent) \ AB3200Q TRAP (AB SCIEX); Nanopure pure water machine (Barnstead company); FLUCA homogenizer; SIGMA high-capacity high-speed centrifuge; ).
[0042] 2 reagents
[0043] 6mol / L hydrochloric acid, 40g / L sodium bicarbonate, petroleum ether (boiling range 30°C-60°C), n-hexane (HPLC), methanol (HPLC), formic acid (HPLC), standard: Flavobacterium oryzae toxin
[0044] A 1 mg / ml Sigma.
[0045] 3 Chromatographic conditions: Waters BEH HILIC 1.7μm 2.1×100mm chromatographic column; injection volume 20μl; column temperature 30°C; mobile phase A is water (0.1% formic acid): B is methanol, mobile phase ratio A:B=30% : 70% isocratic elution for 3min, flow rate 300μl / min.
[0046] 4 Mass Spectrometry Conditions Ionization method: electrospray ionization source (ESI) negative ion mode; detection method: multiple ion reaction monitoring (MRM); collision gas (CAD): Midium; curtain gas (CUR): 25psi; at...
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