Composition for improving liver function having lactic acid bacterium-fermented product of black radish and method for preparation of lactic acid bacterium-fermented product of black radish
A technology of lactic acid bacteria fermentation and manufacturing method, which is applied in the direction of medical preparations containing active ingredients, drug combinations, and functions of food ingredients, etc. It can solve the problems that active ingredients cannot be separated, black radish cannot be diversified, and it is not easy to ingest, etc. , to achieve excellent anti-oxidation effect, improve liver function improvement effect, and easy intake effect
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experiment example 1
[0082] Experimental Example 1 - Evaluation of Antioxidant Efficacy
[0083] In this experiment, in order to evaluate the antioxidant efficacy of lactic acid bacteria fermentation products of black radish, ABTS radical cation removal activity, total polyphenol and total flavonoid content were measured.
[0084] Pretreatment of lactic acid bacteria fermentation product of black radish
[0085]In order to evaluate the antioxidant efficacy of the samples in powder state, 10% DMSO was added, ultrasonic extraction was performed for 30 minutes, and then the supernatant was used for the experiment. As a control group for each experiment, 10% DMSO was used.
[0086] ABTS radical cation removal activity
[0087] This experimental method is a method of measuring the degree to which the color of the reagent becomes lighter by removing the ABTS radical cation from the sample. As ABTS reagent, 2.45mM potassium persulfate and 7mM 2,2`-Azino-bis(3-ethylbenzothiazoline-6-sulfonic acid)dia...
experiment example 2
[0099] Experimental Example 2 - Evaluation of Hepatocyte Protection Efficacy
[0100] In this experiment, in order to evaluate the liver function improvement effect of the lactic acid bacteria fermentation product of black radish, the cytotoxicity measurement for setting the appropriate concentration of the sample and the fat globule formation inhibitory effect on Hep G2 cells and on the cells after ethanol treatment were carried out Evaluation of the inhibitory efficacy of ALT and AST production.
[0101] Cytotoxicity measurement
[0102] Before performing the experiment, as an MTT reagent, Thizolyl blue tetrazolium bromide (Sigma, USA) was dissolved in 1xPBS to make a final concentration of 5 mg / ml, and then light was blocked for use. To measure cytotoxicity, make cells at 1 x 10 5 After culturing cells / ml on a 96-well plate for 24 hours, each sample dissolved in the medium was treated at each concentration (100ug / ml, 500ug / ml, 1000ug / ml) and cultured for 24 hours. After...
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