Flue gas condensate cytotoxicity determination method based on cell electronic sensor
An electronic sensor and flue gas condensation technology, applied in biochemical equipment and methods, microbial measurement/inspection, etc., to achieve high sensitivity, simple operation steps, and good repeatability
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example 1
[0044] 1. Reagents and instruments:
[0045] Dimethyl sulfoxide DMSO (biological reagent pure, purity higher than 99%), MTT dye. CHO-K1 Chinese hamster ovary cell substrain was purchased from the Cell Resource Center of Shanghai Institute of Biological Sciences, Chinese Academy of Sciences. The specific components of the CHO-K1 cell culture medium are 2 mM L-glutamine, 1.5 g / L sodium bicarbonate in F12K, 90%; fetal bovine serum, 10%. xCELLigence cell electronic sensor (Roche Applied Science and ACEA Biosciences), 96-well cell electronic sensor chip. AE163 electronic balance (sensitivity: 0.0001 g) (Mettler, Switzerland).
[0046] 2. Preparation of flue gas condensate stock solution
[0047] First, the cigarette sample A was balanced under ISO standard conditions, and the cigarette was smoked according to the FTC smoking mode, and the total particulate matter (TPM) in the mainstream smoke was collected through an electrostatic collection tube. The total particulate matter...
example 2
[0053] As described in Example 1, the IC of the smoke condensate of cigarette sample B and sample C was measured 50 The values were 94.7 μg / mL and 115.9 μg / mL, respectively.
[0054] At the same time, the neutral red absorption method recommended by CORESTA and the classic method MTT method were used to evaluate the cytotoxicity of the smoke condensate of cigarette samples A and B. The test results of the three methods are shown in Table 1. As can be seen from the table, the cell electron The cytotoxicity determination results of the sensor method are consistent with the neutral red method and MTT method, but it has the advantages of rapidity, accuracy, label-free, simple steps and good reproducibility.
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