Method for producing cordyceps sinensis Qisheng capsule preparation
A production method and technology of Cordyceps, which are applied in the directions of capsule delivery, pharmaceutical formulations, and medical preparations containing active ingredients, can solve the problems of easy rejection, single production method, loss of active ingredients, etc., and achieve a simple and feasible production method. The effect of reducing energy consumption and avoiding the loss of ingredients
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0021] The production method of Cordyceps Qishen Capsules, it comprises the steps:
[0022] 1) Weigh each raw material according to the weight part for later use: Cordyceps sinensis 80g, astragalus 1200g, salvia miltiorrhiza 600g, safflower 600g, jujube seed 320g;
[0023] 2) Take Cordyceps sinensis and crush it into fine powder;
[0024] 3) Take astragalus, crush it, pass through a 100-mesh sieve, put it in a container, add twice the weight of 85% (v / v) ethanol, stir and extract at 300rpm, control the microwave power to 500W during the extraction process, and the extraction time is 120min; Then place it at 4°C for 8 hours, filter, and filter the residue for later use; the filtrate is evaporated under reduced pressure to recover ethanol, and the filtrate is concentrated to extract A with a density of 1.2g / ml; the content of astragaloside IV in the extract A is tested by high performance liquid chromatography 1.31mg / ml;
[0025] Add twice the weight of water to the above filt...
Embodiment 2
[0040] Animal Toxicity Test
[0041] 40 healthy Kunming strain mice, half male and half female, body weight 18.6±2.1g, 40 mice were randomly divided into two groups, with half male and half male in each group, 20 of which were used as the control group and fed with normal water; the other 20 Only mouse is given the preparation of embodiment 1, dosage is 200mg / kg, every day three times, application mouse is carried out toxicity experiment and shows: compare with control group, after administration, mouse does not see obvious difference, and experiment observes continuously for two weeks, and mouse General condition, food intake, drinking water, and weight gain were all normal. On the day of administration and within two weeks after administration, no animal died, suggesting that the drug has low toxicity and is safe for clinical use.
Embodiment 3
[0043] Drug efficacy comparison test
[0044] Animals: 80 SD male rats, weighing 219±13g, healthy and clean, raised in the experimental animal center of our company.
[0045] Grouping treatment: 80 SD male rats, 20 were randomly selected as blank control group according to no significant difference in body weight, and the remaining 60 were prepared for doxorubicin nephropathy model. The model rats were randomly divided into model control group (gastric administration of normal saline, dose 100 mg / kg), Example 1 group (gastric administration of the preparation produced in Example 1, dose 100 mg / kg), control group 1 (gastric administration of control The preparation produced in Example 1, dose 100mg / kg), 20 rats in each group. Gastrointestinal administration once a day for one month in a row. The rats in each group were collected 24h urine volume at the beginning and end of the experiment to measure the 24h urine protein (sulfallic acid method).
[0046] Observation indicator...
PUM
Property | Measurement | Unit |
---|---|---|
Uv intensity | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com