Method for detecting tobacco specific nitrosamine by liquid phase chromatography and series mass spectrometry
A technology of tandem mass spectrometry and liquid chromatography, applied in the field of detection of N-nitrosamines, can solve the problems of low recovery rate and poor purification effect, and achieves simple operation, improved purification effect and recovery rate, and strong instrument versatility. Effect
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Embodiment 1
[0016] First add 1.0mL 300ng / mL trimethyl trimethyl to the 92mm diameter Cambridge filter disc that captured the smoke of 20 9mg 555 brand cigarettes 13 C 3 Mark the caffeine methanol solution, then add 30 mL each of citric acid-phosphate buffer solution at pH 4.3 containing 53 mmol / L citric acid and 20 mmol / L ascorbic acid and 30 mL of cyclohexane, and shake the filter for co-extraction. After separating the organic phase extract, N 2 Concentrate to about 1 mL under protection, then add 1 mL of 0.1 mol / L hydrochloric acid to it for acidification, and after phase separation, add 1 mol / L sodium hydroxide solution dropwise to the aqueous phase to pH 7.0. The obtained aqueous phase solution was quantitatively transferred to an Oasis HLB solid-phase extraction column from Waters, USA, which had been equilibrated successively with 3 mL of methanol and 3 mL of distilled water, then rinsed with 3 mL of 5% aqueous methanol, and eluted with 5 mL of methanol. The eluate was concentrat...
Embodiment 2
[0018] Using methanol as a solvent, configure a series of mixed standard sample solutions according to the concentration range in Table 1, wherein trimethyl 13 C 3 The labeled caffeine is 300ng / mL; then carry out LC / MS / MS analysis and detection under the above-mentioned experimental conditions, and the component peaks on the chromatogram and trimethyl 13 C 3 The area ratio of the marked caffeine peak is the response signal. According to the three parallel measurement results of the six mixed standard solutions, the standard curves of the four components of NNN, NNK, NAT and NAB were established, and the linear correlation coefficients of each standard curve were in order It is 0.9992, 0.9980, 0.9990 and 0.9992, showing that the response signal is significantly linearly correlated with the component concentration; 3 times of the standard deviation of the results of 5 parallel measurements of the lowest concentration mixed standard sample solution determines the method detectio...
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