Synthesis and Erosion Properties of PEG‐Containing Polyanhydrides
Authors:
- 4 May 2007
- journal article
- research article
- Published by Wiley in Macromolecular Bioscience
- Vol. 7 (5) , 620-628
Abstract
To tailor the erosion rate of polyanhydrides while retaining their surface erosion characteristics, new three‐component polyanhydrides of sebacic acid, 1,3‐bis(p‐carboxyphenoxy)propane and poly(ethylene glycol) were synthesized. The hydrophilicity of the polymer increased and its mechanical strength decreased with increasing PEG content. Correspondingly, the erosion rate increases with increasing PEG content, whereas it decreases with increasing specimen thickness. This indicates that the incorporation of poly(ethylene glycol) into traditional two‐component polyanhydrides retains their surface erosion properties while making the erosion rate tunable. The new polyanhydrides hold potential for drug delivery applications. magnified imageKeywords
This publication has 26 references indexed in Scilit:
- Natural polymers for gene delivery and tissue engineering☆Advanced Drug Delivery Reviews, 2006
- Characterization of insulin protection properties of complexation hydrogels in gastric and intestinal enzyme fluidsJournal of Controlled Release, 2006
- Investigation into the erosion mechanism of salicylate‐based poly(anhydride‐esters)Journal of Biomedical Materials Research Part A, 2005
- Delivering DNA from photocrosslinked, surface eroding polyanhydridesJournal of Controlled Release, 2004
- Synthesis, characterization and drug release from three-arm poly(ε-caprolactone) maleic acid/poly(ethylene glycol) diacrylate hydrogelsJournal of Biomaterials Science, Polymer Edition, 2003
- Parathyroid Hormone An Anabolic Treatment for Osteoporosis.Current Pharmaceutical Design, 2001
- The influence of microstructure and monomer properties on the erosion mechanism of a class of polyanhydridesJournal of Polymer Science Part A: Polymer Chemistry, 1993
- Tooth-Colored Inlays and OnlaysThe Journal of the American Dental Association, 1992
- Polyanhydrides for controlled release of bioactive agentsBiomaterials, 1986
- Bioerodible polyanhydrides for controlled drug deliveryBiomaterials, 1983