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Fabrication of Poly( L ‐lactide)‐ block ‐Poly(ethylene glycol)‐ block ‐Poly( L ‐lactide) Triblock Copolymer Thin Films with Nanochannels: An AFM Study
Author(s) -
Choi SungWook,
Kim Yongwoo,
Cheong In Woo,
Kim JungHyun
Publication year - 2008
Publication title -
macromolecular rapid communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 154
eISSN - 1521-3927
pISSN - 1022-1336
DOI - 10.1002/marc.200700564
Subject(s) - ethylene glycol , copolymer , lactide , materials science , peg ratio , polymer chemistry , chemical engineering , solvent , block (permutation group theory) , micelle , polymer , chemistry , composite material , organic chemistry , aqueous solution , finance , economics , engineering , geometry , mathematics
This paper aims to report the fabrication of biodegradable thin films with micro‐domains of cylindrical nanochannels through the solvent‐induced microphase separation of poly( L ‐lactide)‐ block ‐poly(ethylene glycol)‐ block ‐poly( L ‐lactide) (PLA‐ b ‐PEG‐ b ‐PLA) triblock copolymers with different block ratios. In our experimental scope, an increase in each of the block lengths of the PLA and PEG blocks led to both a variation in the average number density (146 to 32 per 100 µm 2 ) and the size of the micro‐domains (140 to 427 nm). Analyses by atomic force microscopy (AFM) and fluorescence microscopy indicated that the hydrophilic PEG nanochannels were dispersed in the PLA matrix of the PLA‐ b ‐PEG‐ b ‐PLA films. We demonstrated that the micro‐domain morphology could be controlled not only by the block length of PEG, but also by the solvent evaporation conditions.