Method for simultaneously detecting five cannabinol compounds by using HPLC-MS/MS
A technology of cannabinol and compounds, applied in the field of simultaneous detection of 5 kinds of cannabinol compounds, to achieve the effect of alleviating difficulties, good recovery rate and easy operation
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[0052] 1) Sample pretreatment:
[0053] Weigh 0.5g of chocolate sample into a 10ml centrifuge tube, cover the lid, preheat in a water bath at 45°C for 5 minutes to melt, then add 2.5ml of methanol, vortex for 2min, centrifuge at 1000rmp for 5min, take the supernatant and pass through 0.22 μm organic filter membrane, ready for use.
[0054] 2) Detection:
[0055] The chromatographic conditions for HPLC separation are: a special column for cannabinol (4.6mm×250I.D., 5.0μm), and the column temperature is 30°C. The mobile phase A was 0.1% formic acid aqueous solution, the mobile phase B was acetonitrile, the flow rate was 1.0 mL / min, and the mobile phase was gradient eluted. The gradient elution program is: 0-15min, 70%-95%B; 15-15.1min, 95%-70%B; 15.1-25min, 70%B.
[0056] 3) Mass Spectrometry:
[0057] The mass spectrometry part adopts the multiple reaction monitoring mode (MRM), and the mass spectrometry parameters of the five cannabinoids are shown in the following table: ...
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