Stereocomplexes of Triblock Poly(lactide- PEG2000-lactide) as Carrier of Drugs
Autor: | Abraham J. Domb, Hans R. Kricheldorf, Ashgan Bishara |
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Rok vydání: | 2005 |
Předmět: |
chemistry.chemical_classification
Lactide Materials science Polymers and Plastics Organic Chemistry technology industry and agriculture Polymer Condensed Matter Physics Ring-opening polymerization Controlled release chemistry.chemical_compound Polymer degradation chemistry Polymerization Chemical engineering Polymer chemistry Materials Chemistry Copolymer Drug carrier |
Zdroj: | Macromolecular Symposia. 225:17-30 |
ISSN: | 1521-3900 1022-1360 |
DOI: | 10.1002/masy.200550703 |
Popis: | Triblock copolymers of poly(lactide)-poly(ethylene-glycol)-poly(lactide) (ALA-PEG 2000 -PLA) were synthesized by ring-opening polymerization of lactide and PEG 2000 diol as co-catalyst. Stereocomplexes with particle sizes ranging from nanometers to microns were obtained by mixing acetonitrile solutions of pairs of enantiomeric homopoly(lactide) and the triblock copolymers. The stereocomplexes exhibited higher crystalline melting temperatures than the optically pure polymers. The ratio of PLA terminals in the copolymers had a significant effect on their stereocomplex degradation and drug release. These stereocomplexes were used for the encapsulation of dexamethasone for controlled release applications. Dexamethasone phosphate loading capacity, in vitro release, degradation and stability of polymers and formulation were investigated for one month. An increase in the dexamethsone phosphate content in the stereocomplex or a decrease in the PLA ratio in the copolymer resulted in a faster release of drug and polymer degradation. |
Databáze: | OpenAIRE |
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