Theaflavin-containing pharmaceutical composition and application thereof in the aspect of lowering blood fat
A technology of theaflavin and composition, which is applied in the application field of treating hyperlipidemia and related diseases, can solve the problems of inconvenient quality control, drug efficacy, and inconvenient adverse reaction monitoring, so as to improve gastrointestinal microcirculation function, reduce Effect of drug oxidation failure and easy quality control
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0028] Weigh 6 g of EPA, 9.75 g of theaflavin (TF) and 10 g of commercially available microcrystalline cellulose, and pass through a 60-mesh sieve after mixing. Spray 6ml of 95% ethanol into the resulting mixture, stir and mix evenly and pass through a 30-mesh sieve again to obtain small particles, dry at 55°C for 1.5 hours and pack into No. 1 capsules to make hard capsules.
Embodiment 2
[0030] Weigh 7.5g of DHA, 8.5g of theaflavin (TF) and 2.5g of theaflavin (TF-3-G) respectively, add 15g of corn starch, 10g of microcrystalline cellulose, povidone K 30 3g, 7g of sodium carboxymethyl starch were mixed and passed through an 80-mesh sieve. Add 10ml of 95% ethanol to the resulting mixture, stir and mix evenly, pass through a 30-mesh sieve to prepare wet granules, then dry in an oven at 45°C for 1.5 hours, and turn the granules once every 30 minutes. After the dried granules are passed through a 20-mesh sieve for granulation, an appropriate amount of magnesium stearate is added, mixed evenly, and compressed to prepare tablets.
Embodiment 3
[0032] Weigh 7.5g of DHA, 3.5g of theaflavin (TF-3-G) and 4.5g of theaflavin (TFDG) respectively, add 10g of corn starch, 15g of microcrystalline cellulose, povidone K 30 3g, 7g of sodium carboxymethyl starch were mixed and passed through an 80-mesh sieve. Add 10ml of 95% ethanol to the resulting mixture, stir and mix evenly, pass through a 30-mesh sieve to prepare wet granules, then dry in an oven at 45°C for 1.5 hours, and turn the granules once every 30 minutes. After the dried granules are passed through a 20-mesh sieve for granulation, an appropriate amount of magnesium stearate is added, mixed evenly, and compressed to prepare tablets.
PUM
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