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In relation to this article, we declare that there is no conflict of interest.
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Received May 3, 2012
Accepted August 14, 2012
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Photo-responsive microgels composed of polymeric β-cyclodextrin and Tween 20-coumarin conjugate

College of Biomedical Science and Institute of Bioscience and Biotechnology, Kangwon National University, 192-1, Hyoja-2dong, Chuncheon, Gangwon-do 200-701, Korea
jinkim@kangwon.ac.kr
Korean Journal of Chemical Engineering, January 2013, 30(1), 245-250(6), 10.1007/s11814-012-0136-7
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Abstract

Photo-responsive microgels were prepared by taking advantage of the interaction between Tween 20-coumarin conjugate (TCC) and polymeric β-cyclodextrin (PβCD). TCC was prepared by covalently attaching coumarin to the hydroxyl group of the head (PEO segment) of Tween 20. The molar ratio of coumarin residue and Tween 20 was 1 : 1, determined on the 1H NMR spectrum. PβCD was prepared by reacting epichlorohydrins (EPI) with the hydroxyl groups of βCDs. The primary hydroxyl groups participated in the polymerization reaction, evidenced by the 13C NMR spectrum. The CD content in PβCD, determined by a colorimetric method, was 37.4%. Microgels were prepared by adding TCC to the aqueous solution PβCD (20%, w/v) so the molar ratio of TCC to βCD residue was 0.72 : 1. The shape was spherical on SEM photo and optical microscopic photo, and the diameter, measured on light scattering equipment, was a few_x000D_ micrometers. The size dramatically decreased by the irradiation of λ at 365 nm, possibly due to the photo-dimerization of coumarin residue of TCC. Thr size of the photo-treated microgel markedly increased by the irradiation of λ at 254 nm, possibly due to the de-dimerization of the coumarin residue dimers.

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