## Abstract Poly(ethylene glycol) (PEG) hydrogels are of great interest in tissue engineering because of their established biocompatibility, high permeability, and tunable material properties. However, rational design of PEG hydrogel scaffold properties has been inhibited by the interdependence of
Supramolecular Control of Ester Hydrolysis in Poly(ethylene glycol)-Interlocked Hydrogels
β Scribed by Takahiro Ichi; Tooru Ooya; Nobuhiko Yui
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 215 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1616-5187
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β¦ Synopsis
Abstract
Poly(ethylene glycol) (PEG)βinterlocked hydrogels were prepared by linking the PEG with Ξ±βcyclodextrins (Ξ±βCDs) threaded onto a PEG chain having ester linkages at the terminals (hydrolyzable polyrotaxane). These hydrogels were examined to clarify the effect of ionic strength of phosphate buffers, pH, and the addition of ethanol on erosion time in relation to inclusion states of Ξ±βCDs with the ester linkages. The most characteristic phenomenon of the hydrogel erosion was observed in an ethanol/PBS cosolvent system: the time to reach the complete erosion time was shortened with decreasing water content. NMR analysis revealed that the ester linkages were exposed to the aqueous environment due to the aggregation of Ξ±βCDs. These results suggest that the movement of Ξ±βCDs in the polyrotaxanes from the terminal ester region to the another region gives the ester linkages a chance to interact with water.
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