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Amphiphilic PEG/alkyl‐grafted comb polylactides
Authors:Xuwei Jiang  Erin B Vogel  Milton R Smith III  Gregory L Baker
Institution:1. Department of Chemistry, Michigan State University, East Lansing, Michigan 48824;2. Department of Chemistry, Michigan State University, East Lansing, Michigan 48824Department of Chemistry, Michigan State University, East Lansing, Michigan 48824
Abstract:Amphiphilic polylactides (PLAs) with well‐defined architectures were synthesized by ring‐opening polymerization of AB monomers (glycolides) substituted with both a long chain alkyl group and a triethylene glycol segment terminated in either a methyl or benzyl group. The resulting amphiphilic PLAs had number average molecular weights >100,000 g/mol. DSC analysis revealed a first‐order phase transition at ~ 20 °C, reflecting the crystalline nature of the linear alkyl side chains. Polymeric micelles were prepared by the solvent displacement method in water. Dynamic light scattering measurements support formation of a mixture of 20‐nm‐diameter unimolecular micelles and 60‐nm particles comprised of an estimated 25 polymer molecules. UV–vis characterization of micelles formed from acetone–water solutions containing azobenzene confirmed encapsulation of the hydrophobic dye, suggesting their potential as new amphiphilic PLAs as drug delivery vehicles. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 5227–5236, 2007
Keywords:amphiphiles  biodegradable  drug delivery systems  polylactide  ring‐opening polymerization (ROP)  side‐chain crystallization
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