Application of antrodia camphorata in dispelling effects of alcohol and/or increasing alcohol metabolism
A technology of Antrodia cinnamomea and mycelium of Antrodia cinnamomea, applied in the field of hangover and/or increasing alcohol metabolism, Antrodia cinnamomea, can solve the problems of increasing the risk of metabolic syndrome, increasing uric acid and lactic acid content, and low mobility, etc., to achieve increased Effects on hangover efficiency, promotion of alcohol decomposition, and reduction of oxidative stress
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example 1
[0042] Example 1: Sample Preparation
[0043] Sample 1: Antrodia Antrodia water-soluble powder, wherein, Antrodia Antrodia water-soluble powder is a powdery extract obtained by emulsifying and drying the mycelia powder of Antrodia Antrodia through supercritical carbon dioxide extraction, and after testing, it is confirmed that it contains the same content as wild Antrodia Antrodia content of triterpenoids.
[0044] For example, the mycelium powder of Antrodia camphorata is subjected to supercritical carbon dioxide extraction, and then concentrated to obtain the super-extract of mycelium of Antrodia camphorata in paste form. The weight ratio of 1:6-7 is mixed at a temperature of 70° C. to obtain an oil phase solution of Antrodia camphorata. Prepare an aqueous phase solution, which contains water, dextrin fiber, and fatty acid sucrose lipid, and mixes them at a weight ratio of about 357-358:72:1. Antrodia camphorata oil phase solution and water phase solution are microemulsifi...
example 2
[0047] Example 2: Preliminary test
[0048] 3 groups of mice were administered intragastrically with 0.3mL / 20g, 0.35mL / 20g, 0.4mL / 20g alcohol solution (58% Jinmen sorghum) respectively, with 8 mice in each group, to observe whether the mice in each group appeared to turn over. Lost of righting reflex (LOR) and no amount of alcohol required for death of mice.
[0049] It was found that a small number of mice died when 0.4mL / 20g alcohol solution was given; no mice died when 0.35mL / 20g alcohol solution was given, the drunk rate was 100%, and the average drunk time was 794.0 ± 38.02 minutes; No mice died when the alcohol solution was 1 / 20g, and the drunk rate was 25%; therefore, in the follow-up hangover test, the mice were gavaged with 0.35mL / 20g alcohol solution.
example 3
[0050] Example 3: hangover test (1)
[0051] Mice were randomized into groups where:
[0052] The first group is the blank group, fed with equal volume of normal saline;
[0053] The second group is the low-dose group of Antrodia cinnamomea water-soluble powder, and the dosage is 16.3 mg / kg;
[0054] The third group is the medium-dose group of Antrodia antrodia water-soluble powder, and the dosage is 32.8mg / kg;
[0055] The fourth group is the high-dose Antrodia Cinnamomea water-soluble powder group, and the dosage is 49.2 mg / kg;
[0056] The fifth group is Hovenia dulcis Function Decoction group, and the dosage is 3.38g / kg;
[0057] The sixth group patent Hovenia dulcis fruit extract group, the dosage is 504.3mg / kg;
[0058] The seventh group was the mixed group, which was administered Hovenia dulcis Function Drink (dose 3.38g / kg) and Antrodia camphorata water-soluble powder (dose 16.3mg / kg) at the same time.
[0059] The mice in each group were fasted for 12 hours first...
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