An application of E-10-hydroxy-2-decenoic acid in preparation of medicines or healthcare products for hepatic disease
A technique for liver disease, decenoic acid
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Embodiment 1
[0046] Example 1: Anti-HBV activity and cytotoxicity of royal jelly acid in vitro.
[0047] The inhibitory effect and cytotoxicity of the target compound HBV DNA were measured by Hep G2.2.15 cell in vitro assay.
[0048] experimental method
[0049] The inhibitory effect of the target compound on HBV DNA was determined by quantitative real-time fluorescent PCR: Hep G2.2.15 cells were cultured in DMEM medium containing 10% calf serum in 5% CO 2 Incubate in the incubator. Then the cells were seeded in 96-well plates, the number of cells was 3×10 4 , continue to cultivate, when the cell density reaches about 80%, discard the old culture solution, add new culture solution containing 1, 50, 100, 150, 200, 500nm concentration of the drug to be tested, set 3 parallel wells; every 2 days Replace the culture medium; on the 10th day after administration, take 100 μL of the supernatant, measure the content of HBV DNA by quantitative PCR, and calculate the 50% inhibitory concentration,...
Embodiment 2
[0053] Example 2: Determination of anti-hepatitis B virus activity in vivo.
[0054] The shelduck ducks with vertical transmission infection and positive DHBV DNA test were randomly divided into 8 ducks in each group. Water, entecavir and different doses of royal jelly acid were given by intragastric administration, once a day, for a total of 30 days. Venous blood was collected before administration, 15 days after administration, 30 days after administration and 15 days after drug withdrawal, and the content of DHBV DNA in serum was determined by external standard TaqMan real-time fluorescent PCR method.
[0055] The experimental results are shown in Table 2:
[0056]
Embodiment 3
[0057] Example 3: The effect of royal jelly acid in the treatment of liver disease models such as fatty liver.
[0058]Royal jelly acid regulates liver MDA, SOD, GSH-PX experiment:
[0059] Several healthy adult female SD rats of 250-300 g were selected, and carbon tetrachloride was used to make a fatty liver model. The experimental mice successfully modeled were randomly divided into a model control group and three test sample dosage groups, and the number of female mice in each group was 10-12; each group was treated with 14 mL / kg 56 degrees After intragastric administration of white wine to build the model, 30 minutes later, the royal jelly acid was dissolved in 0.1% DMSO (dimethyl sulfoxide), and adjusted to a concentration of 50 mg / L, 100 mg / L, and 200 mg / L, and 3 tablets were given orally. The test sample dosage group and the model control group were given the same volume of 0.1% DMSO solvent. The mice were sacrificed 1 hour after administration, blood was taken, and M...
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