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Updated: Sep 17, 2026

Fabricating Superhydrophobic Polymeric Materials for Biomedical Applications
Published on: August 28, 2015
Enzymatic degradation of block copolymers prepared from epsilon-caprolactone and poly(ethylene glycol)
Suming Li1, Henri Garreau, Bernard Pauvert
1Centre de Recherche sur les Biopolymères Artificiels, Faculté de Pharmacie, 15 avenue Charles Flahault, 34060 Montpellier Cedex 2, France. lisuming@pharma.univ-montp1.fr
Abstract:
Block copolymers were prepared by ring-opening polymerization of epsilon-caprolactone in the presence of monohydroxyl or dihydroxyl poly(ethylene glycol) (PEG), using Zn powder as catalyst. The resulting poly(epsilon-caprolactone) (PCL)-PEG diblock and PCL-PEG-PCL triblock copolymers were characterized by various analytical techniques such as NMR, size-exclusion chromatography, differential scanning calorimetry, and X-ray diffraction. Both copolymers were semicrystalline polymers, the crystalline structure being of the PCL type. Films were prepared by casting dichloromethane solutions of the polymers on a glass plate. Square samples with dimensions of 10 x 10 mm were allowed to degrade in a pH = 7.0 phosphate buffer solution containing Pseudomonas lipase. Data showed that the introduction of PEG blocks did not decrease the degradation rate of poly(epsilon-caprolactone).
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