Method for preparing a composition comprising perfluoropolyether having a carboxyl group at one terminal
US-9217059-B2 · Dec 22, 2015 · US
US9353217B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9353217-B2 |
| Application number | US-201113991495-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 9, 2011 |
| Priority date | Dec 9, 2010 |
| Publication date | May 31, 2016 |
| Grant date | May 31, 2016 |
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.
Spherical biodegradable particles have improved flexibility, cause less aggregation among particles, and have improved particle shape-recovering ability after passing through a catheter or the like. The biodegradable particles include a synthetic polymer chemically cross-linked to a polyvalent carboxylic acid, the biodegradable particles having a water content of 20 to 90% in a water-saturated state.
Opening claim text (preview).
The invention claimed is: 1. A method of producing biodegradable particles comprising: a dissolving step wherein a synthetic polymer, polyvalent carboxylic acid and condensing agent are dissolved in an aprotic polar organic solvent having a dielectric constant of 35 to 50, to obtain Solution A; a droplet-forming step wherein said Solution A is added dropwise to a poor solvent for said aprotic polar organic solvent, to obtain droplets of Solution A; and a chemical cross-linking step wherein a chemical cross-linking reaction of said synthetic polymer is allowed to proceed in said droplets, to obtain biodegradable particles. 2. The method according to claim 1 , wherein said synthetic polymer is: a homopolymer or block copolymer of a water-soluble polymer(s) selected from the group consisting of polyethylene glycol, polypropylene glycol, polyvinyl alcohol, polyacrylic acid, polyhydroxyethylacrylate, polyhydroxyethylmethacrylate, polyvinylpyrrolidone, carboxymethylcellulose, hydroxymethylcellulose and hydroxyethylcellulose; or a block copolymer of said water-soluble polymer(s) and a monomer(s) selected from the group consisting of α-hydroxy acids, cyclic dimers of α-hydroxy acids, hydroxydicarboxylic acids and cyclic esters. 3. The method according to claim 1 , wherein said condensing agent is a water-soluble carbodiimide. 4. The method according to claim 1 , wherein said aprotic polar organic solvent is selected from the group consisting of N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile and dimethylsulfoxide. 5. The method according to claim 1 , wherein said poor solvent comprises a natural oil selected from the group consisting of cottonseed oil, corn oil, coconut oil, olive oil, palm oil, rapeseed oil, safflower oil, sesame oil, soybean oil, sunflower oil, turpentine oil, almond oil, avocado oil, bergamot oil, castor oil, cedar wood oil, chlorophyll oil, clove oil, croton oil, eucalyptus oil, fennel oil, fusel oil, grape seed oil, jojoba oil, candlenut oil, lavender oil, lemon oil, linseed oil, macadamia nut oil, meadowfoam oil, orange oil, origanum oil, persic oil and rose hip oil. 6. The method according to claim 2 , wherein said condensing agent is a water-soluble carbodiimide. 7. The method according to claim 2 , wherein said aprotic polar organic solvent is selected from the group consisting of N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile and dimethylsulfoxide. 8. The method according to claim 3 , wherein said aprotic polar organic solvent is selected from the group consisting of N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile and dimethylsulfoxide.
Hydrogels or hydrocolloids · CPC title
Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule · CPC title
Materials at least partially resorbable by the body · CPC title
for embolization or occlusion, e.g. vaso-occlusive compositions or devices · CPC title
Crosslinking, e.g. vulcanising, of macromolecules (mechanical aspects B29C35/00; crosslinking agents C08K) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.