Novel Pyridine Compounds
US-2024316020-A1 · Sep 26, 2024 · US
US9713593B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9713593-B2 |
| Application number | US-201514880755-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 12, 2015 |
| Priority date | Oct 23, 2014 |
| Publication date | Jul 25, 2017 |
| Grant date | Jul 25, 2017 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Provided is an alkyl cellulose excellent in formability when added even in a small amount and not causing marked delay in disintegration; a solid preparation including it; and a method for producing the solid preparation. More specifically, provided is an alkyl cellulose for use in tableting, the alkyl cellulose having a specific surface area of from 0.5 to 10.0 m 2 /g as measured by BET method and a solid preparation including the alkyl cellulose. Also provided is a method for producing the alkyl cellulose, including the steps of: bringing pulp into contact with an alkali metal hydroxide solution to obtain alkali cellulose, reacting the alkali cellulose with an etherifying agent to obtain a first alkyl cellulose, pulverizing the first alkyl cellulose, and depolymerizing the pulverized first alkyl cellulose through hydrolysis with an acid catalyst or through oxidative decomposition with an oxidant to obtain a second alkyl cellulose.
Opening claim text (preview).
The invention claimed is: 1. A method for producing a solid preparation comprising: bringing pulp into contact with an alkali metal hydroxide solution to obtain alkali cellulose, reacting the alkali cellulose with an etherifying agent to obtain a first methyl cellulose, pulverizing the first methyl cellulose, and depolymerizing the pulverized first methyl cellulose through hydrolysis in the presence of an acid catalyst or through oxidative decomposition in the presence of an oxidant to obtain a second methyl cellulose; pulverizing the second methyl cellulose, and a step of tableting a mixture or granulated product comprising an orally administrable drug and the pulverized second methyl cellulose for use in tableting by a dry direct tableting method or a dry granulation tableting method, to obtain the solid preparation, and wherein said second methyl cellulose is water-soluble. 2. The method according to claim 1 , wherein the acid catalyst comprises hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, or combinations thereof. 3. The method according to claim 1 , wherein a 2% by weight aqueous solution comprising the second methyl cellulose has a viscosity at 20° C. of from 1 to 15 mPa·s. 4. The method according to claim 1 , wherein the second methyl cellulose has an average particle size of from 1 to 120 μm. 5. The method according to claim 1 , wherein the second methyl cellulose having a loose bulk density of from 0.01 to 0.50 g/mL. 6. The method according to claim 1 , wherein the second methyl cellulose has a specific surface area that is from 1.2 to 2.0 m 2 /g as measured by BET method. 7. The method according to claim 1 , wherein the second methyl cellulose has a viscosity at 20° C. that is from 2.5 to 4.5 mPa·s. 8. The method according to claim 1 , wherein the second methyl cellulose has an average particle size is from 10 to 30 μm. 9. The method according to claim 1 , wherein the second methyl cellulose has a loose bulk density that is from 0.2 to 0.4 g/mL.
Alkyl or cycloalkyl ethers · CPC title
Post-etherification treatments of chemical or physical type, {e.g. mixed etherification in two steps}, including purification · CPC title
having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol · CPC title
Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose · CPC title
Tabletting processes · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.