Trapping method and cytotoxicity testing method for smoke aerosol of heating non-combustible cigarette
A heat-not-burn, cigarette smoke technology, applied in the preparation of test samples, the determination/inspection of microorganisms, biochemical equipment and methods, etc.
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Embodiment 1
[0031] Embodiment of the present embodiment is not heated cigarette smoke aerosol-combustion methods, which processes such as figure 1 As shown, including the following steps:
[0032] (1) linear smoking machine three heating the cigarette does not burn the test sample 1 using the suction mode of the suction depth of Canada (suction bell curve, the suction interval of 30s, each of capacity 55mL suction port, each port suction duration 2s), during suction diameter Cambridge filter capture 44mm total particulate matter smoke per puff by the time the gas was passed into Cambridge filter 15mL DMSO solution containing 4 5, the absorption bottle;
[0033] When the suction, each suction heat does not burn the cigarette 10, each of the Cambridge filter trap 4 total heating without burning cigarette smoke particle phase was prepared in a Cambridge filter 5 samples;
[0034] (2) after the trap, the five Cambridge filter was transferred to a conical flask 2 6, and the gas absorption bottle c...
Embodiment 2
[0040]In this example, the extracellular toxicity test is performed on the extravasation of the flue gas sol obtained in Example 1, and the trial cell is a 1549 cell line, and the CCK-8 kit test is used, and the specific test method is: 1) will be prepared. Cell suspension (15000 / well) in 56-well plates, cultured 24h; 2) Remove medium in the culture plate, adding a control medium and medium containing different concentrations of flue gas sol extract medium ( 100 μl / well), incubation under 37 ° C; 3) Remove the solution in the culture plate, add 100 μl of the configured CCK-8 solution to each well (10 μl of CCK-8 mother liquor per 100 μl), 37 ° C Incubation 0.5-2H; 4) Shake 5 min at room temperature, and the absorbing value was measured under 450 nm with an enzyme label. Cell survival rate = (experimental pore absorbance average / control pore absorbance average) × 100%. Test results figure 2 Indicated.
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Abstract
Description
Claims
Application Information
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