Use of fargesin and its derivative in preparation of drugs for treating or preventing pulmonary hypertension
A technology for pulmonary arterial hypertension and octopylin, which is applied in the directions of drug combinations, active ingredients of heterocyclic compounds, cardiovascular system diseases, etc.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0031] Make magnolipin slow-release tablet according to the following formula (all used contents are weight percentages)
[0032]
[0033]
[0034] The preparation method is as follows:
[0035] (1) Mix magnolipin, lactose, hydroxypropyl methylcellulose, microcrystalline cellulose, and polyvinylpyrrolidone evenly, and granulate with absolute ethanol;
[0036] (2) Put the wet granules in a drying oven at about 50°C, and control the moisture content to about 2%;
[0037] (3) After the dried granules are sized through a 20-mesh sieve, magnesium stearate is added, mixed evenly, and pressed into tablets according to the specifications.
Embodiment 2
[0039] Make xinyisu tablet according to following formula (contents used are weight percentages)
[0040]
[0041] The preparation method is as follows:
[0042] (1) Pulverize magnoliatrin and lactose respectively, pass through a 100-mesh sieve, and directly pass the starch through a 100-mesh sieve for subsequent use;
[0043] (2) Take an appropriate amount of starch and add an aqueous solution to prepare a starch paste for use as a binder;
[0044] (3) Mix magnoliatin, lactose and the remaining amount of starch, add a binder to make a soft material, and pass through a 20-mesh sieve to granulate;
[0045] (4) Place the wet granules in a drying oven at about 50°C, and control the moisture content to about 2%;
[0046] (5) After the dry granules are sized through a 20-mesh sieve, magnesium stearate is added, mixed evenly, and pressed into tablets according to the specifications.
Embodiment 3
[0048] Make magnolipin dispersible tablet according to the following formula (all contents used are weight percentages)
[0049]
[0050]
[0051] The preparation method is as follows:
[0052] (1) By magnesia, microcrystalline cellulose, sodium carboxymethyl starch, aspartame, cross 80 mesh sieves, for subsequent use;
[0053] (2) Take the full amount of polyvinylpyrrolidone K30, make an aqueous solution with a concentration of 5%, stir until it is completely dissolved, and prepare it as an adhesive;
[0054] (3) Mix magnolipin, microcrystalline cellulose, sodium carboxymethyl starch, and aspartame evenly, make a soft material with a binder, and pass through a 20-mesh sieve to granulate;
[0055] (4) Dry the wet granules at about 60°C, and control the moisture to about 2%
[0056] (5) After the dried granules are sized through a 20-mesh sieve, add talcum powder and magnesium stearate, mix well, and press into tablets according to the specifications.
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