Polyhydroxyalkanoate Copolymers Prepared by Ring-Opening Polymerization and Related Compositions and Articles
US-2024392063-A1 · Nov 28, 2024 · US
US8927682B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-8927682-B2 |
| Application number | US-22954408-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 25, 2008 |
| Priority date | Aug 24, 2007 |
| Publication date | Jan 6, 2015 |
| Grant date | Jan 6, 2015 |
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Poly(glycolide) polymers are disclosed. The polymers generally include a polymerized alkynyl-substituted glycolide having a polymer backbone with one or more alkynyl groups appended thereto. The alkynyl groups provide reactive sites for further functionalization of the polymer, for example by reaction with azide derivatives (e.g., azide-substituted organic compounds). Alkynyl and azide groups react via the “click” chemistry mechanism to form functional groups covalently bonded to the polymer via a triazole link. The polymers are biodegradable and can be used to deliver drugs or other therapeutic substances (e.g., large biomolecules such as single strand RNA) at targeted locations in a patient's body and/or at controlled release rates.
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What is claimed is: 1. A poly(glycolide) polymer consisting of a polymerized alkynyl-substituted glycolide, the alkynyl-substituted glycolide comprising an alkynyl group. 2. The poly(glycolide) polymer of claim 1 , wherein the alkynyl group contains 3 to 12 carbon atoms. 3. The poly(glycolide) polymer of claim 2 , wherein the alkynyl group comprises a propargyl group having a terminal alkynyl group. 4. The poly(glycolide…
Chemistry & Metallurgy · mapped topic
Chemistry & Metallurgy · mapped topic
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