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Stereocomplexes of Triblock Poly(lactide‐ PEG 2000 ‐lactide) as Carrier of Drugs
Author(s) -
Bishara Ashgan,
Kricheldorf Hans R.,
Domb Abraham J.
Publication year - 2005
Publication title -
macromolecular symposia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.257
H-Index - 76
eISSN - 1521-3900
pISSN - 1022-1360
DOI - 10.1002/masy.200550703
Subject(s) - copolymer , materials science , lactide , polymer , polyester , ethylene glycol , polymer chemistry , polymerization , peg ratio , chemical engineering , diol , composite material , finance , economics , engineering
Triblock copolymers of poly(lactide)‐poly(ethylene‐glycol)‐poly(lactide) (PLA‐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.