Method for detecting 10 types of aromatic amines compounds in cigarette mainstream smoke by liquid chromatography-tandem mass spectrometry
A technology of cigarette mainstream smoke and tandem mass spectrometry, which is applied in the field of detection of 10 kinds of aromatic amine compounds in cigarette mainstream smoke by liquid chromatography-tandem mass spectrometry. Analysis efficiency, saving sample volume and effect of smoking experiment time
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Embodiment 1
[0037] The balanced and screened cigarettes were smoked according to the standard conditions stipulated in YC / T29-1996, and the particulate matter in the mainstream smoke of 5 cigarettes was collected with Cambridge filter, and collected in an absorption bottle filled with 25 mL of 5% HCl solution Gas phase.
[0038]Fold the Cambridge filter disc for trapping particulate matter into a 50 mL Erlenmeyer flask, pour into the 5% HCl solution in the absorption flask, add the mixed internal standard (D5-aniline, D7-1-aminonaphthalene and D9-4 -Aminobiphenyls were 50 ng / mL, 2.5 ng / mL, 0.5 ng / mL), ultrasonically extracted at room temperature for 30 min, the extraction solution was neutralized with NaOH solid to pH>13, and the 20 Load 1 mL of the extract onto an Agilent Oasis® HLB SPE cartridge that has been activated with 10 mL of methanol solution, allowing the extract to remain naturally by gravity, keeping the flow rate at about 1-1.5 mL / min. Then it was washed with 10 mL of water...
Embodiment 2
[0040] The Kentucky reference cigarette 3R4F was smoked according to the standard conditions stipulated in YC / T 29-1996. The particulate phase of 5 cigarettes was collected by the Cambridge filter, and the gas phase was collected by the absorption bottle filled with 25 mL of 5% HCl solution. Put the filter in the Erlenmeyer flask, pour into the 5% HCl solution in the absorption flask, add 50 ng / mL D5-aniline, 2.5 ng / mL D7-1-aminonaphthalene and 0.5 ng / mL D9-4-amino Biphenyl was mixed with the internal standard solution, and then the sample was purified and analyzed according to the steps described in Example 1. Five parallel experiments were carried out, and the relative standard deviation of the determination of each compound was between 3.23% and 9.46%, which indicated that the method had good reproducibility and stability.
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