## Abstract Novel cholic acid functionalized branched oligo/poly(ε‐caprolactone)s were synthesized through the ring‐opening polymerization of ε‐caprolactone initiated by cholic acid with hydroxyl groups. The molecular weight of the branched polymers can be adjusted by controlling the feed ratio of
Novel cholic acid functionalized star oligo/poly(DL-lactide)s for biomedical applications
✍ Scribed by Tao Zou; Si-Xue Cheng; Xian-Zheng Zhang; Ren-Xi Zhuo
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 285 KB
- Volume
- 82B
- Category
- Article
- ISSN
- 1552-4973
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✦ Synopsis
Abstract
Novel cholic acid functionalized star oligo/poly(DL‐lactide)s with different molecular weights were synthesized through the ring‐opening polymerization of DL‐lactide initiated by cholic acid. Compared with poly(DL‐lactide), these star oligo/poly(DL‐lactide)s show faster hydrolytic degradation rates, and the degradation mechanism changes from bulk erosion to surface erosion with decreasing molecular weight. Based on the specific physicochemical properties of the novel star oligo/poly(DL‐lactide), the drug delivery system with submicron size was fabricated using a very convenient “ultrasonic dispersion method” which did not involve toxic organic solvents. The in vitro drug release was studied. © 2007 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2007
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