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Stereoisomeric effect on reverse thermal gelation of poly(ethylene glycol)/poly(lactide) multiblock copolymer

Title
Stereoisomeric effect on reverse thermal gelation of poly(ethylene glycol)/poly(lactide) multiblock copolymer
Authors
Joo M.K.Sohn Y.S.Jeong B.
Ewha Authors
손연수정병문
SCOPUS Author ID
손연수scopus; 정병문scopus
Issue Date
2007
Journal Title
Macromolecules
ISSN
0024-9297JCR Link
Citation
vol. 40, no. 14, pp. 5111 - 5115
Indexed
SCI; SCIE; SCOPUS WOS scopus
Abstract
Aqueous solutions of both polyethylene glycol)/poly(DL-lactic acid) (PEG/PDLLA) and polyethylene glycol)/poly(L-lactic acid) (PEG/PLLA) multiblock copolymers underwent "clear sol-to-turbid gel-to-syneresis" transitions as the temperature increased. To investigate the stereoisomeric effect on the phase behavior, PEG/PDLLA and PEG/PLLA multiblock copolymers with a similar block length and total molecular weight were carefully synthesized. Compared with the PEG/PDLLA multiblock copolymer, the PEG/PLLA multiblock copolymer showed a lower critical gel concentration, a lower sol-to-gel transition temperature, and a wider gel window. In addition, the maximal gel modulus of the PEG/PLLA multiblock copolymer (11.0 wt % in water) was 2 times larger than that of the PEG/PDLLA multiblock copolymer. X-ray diffraction spectra, transmission electron microscopic images, and polarizing optical microscopic images suggested the amorphous state for both PEG/PDLLA and PEG/PLLA multiblock copolymer thermogels. 13C NMR spectroscopy, critical micelle concentrations, hydrophobic dye partition, and circular dichroism spectra suggested that the differences in the thermogel properties come from lower dynamic molecular motion and the higher aggregation tendency of the PLLA due to the isotactic localization of the hydrophobic methyl groups rather than crystallization of PLLA. © 2007 American Chemical Society.
DOI
10.1021/ma070008u
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자연과학대학 > 화학·나노과학전공 > Journal papers
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