Compacted Hemostatic Cellulosic Aggregates
US-2024173457-A1 · May 30, 2024 · US
US2016251451A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016251451-A1 |
| Application number | US-201615147739-A |
| Country | US |
| Kind code | A1 |
| Filing date | May 5, 2016 |
| Priority date | Nov 24, 2006 |
| Publication date | Sep 1, 2016 |
| Grant date | — |
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.
The invention relates to a method for dissolving the components of gel forming materials suitable for use in wound care comprising the steps of admixing said components with an ionic liquid. The ionic liquid may be selected from the group of tertiary amine N-oxides, N,N-dimethyl formamide/nitrogen tetroxide mixtures, dimethyl sulphoxide/paraformaldehyde mixtures and solutions of limium chloride in N,N-dimethyl acetamide or N-methyl pyrrolidone.
Opening claim text (preview).
1 ) A method for dissolving the components of gel forming materials suitable for use in wound care comprising the steps of admixing said components with an ionic liquid. 2 ) A method as claimed in claim 1 wherein the gel forming material is a gel forming fibre. 3 ) A method as claimed in claim 2 wherein the gel forming fibre is a modified cellulose fibre. 4 ) A method as claimed in any preceding claim wherein the ionic liquid is selected from the group of tertiary amine N-oxides, N,N-dimethyl formamide/nitrogen tetroxide mixtures, dimethyl sulphoxide/paraformaldehyde mixtures and solutions of lithium chloride in N,N-dimethyl acetamide or N-methyl pyrrolidone. 5 ) A method as claimed in any preceding claim wherein the components of gel forming materials suitable for use in wound care are a carboxymethylcellulose powder. 6 ) A solution comprised of a chemically modified cellulose in an ionic liquid. 7 ) A solution as claimed in claim 6 wherein the ionic liquid is selected from the group of tertiary amine N-oxides, N,N-dimethyl formamide/nitrogen tetroxide mixtures, dimethyl sulphoxide/paraformaldehyde mixtures and solutions of lithium chloride in N,N-dimethyl acetamide or N-methyl pyrrolidone. 8 ) A solution as claimed in claims 6 and 7 wherein the chemically modified cellulose is carboxymethylcellulose powder. 9 ) A method for regeneration of chemically modified cellulose that comprises admixing a solution of chemically modified cellulose in an ionic liquid with a liquid non-solvent for the chemically modified cellulose that is miscible with said ionic liquid, said admixing causing the cellulose and ionic liquid to form solid and liquid phases. 10 ) A method for electrospinning a chemically modified cellulose that comprises spinning a solution of chemically modified cellulose in an ionic liquid into a bath of a liquid non-solvent for the chemically modified cellulose that is miscible with the ionic liquid, said spinning causing the cellulose and ionic liquid to form fibres and a liquid phase.
Wet spinning methods {(D01D5/0046 takes precedence)} · CPC title
substituted with acid radicals, e.g. carboxymethyl cellulose [CMC] (C08L1/282 takes precedence) · CPC title
the fibre formed by coagulation, i.e. wet electro-spinning · CPC title
Post-etherification treatments of chemical or physical type, {e.g. mixed etherification in two steps}, including purification · CPC title
Celluloses · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.