Issue
Korean Journal of Chemical Engineering,
Vol.30, No.1, 245-250, 2013
Photo-responsive microgels composed of polymeric β-cyclodextrin and Tween 20-coumarin conjugate
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 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.
[References]
  1. Szejtli J, Chem. Rev., 98(5), 1743, 1998
  2. Martin Del Valle EM, Process Biochem., 39, 1033, 2004
  3. Buschmann HJ, Schollmeter E, J. Cosmet. Sci., 53, 185, 2002
  4. Schneiderman E, Stalcup AM, J. Chromatogr B., 745, 83, 2000
  5. Hedges AR, Chem. Rev., 98(5), 2035, 1998
  6. Singh M, Sharma R, Banerjee UC, Biotechnol. Adv., 20, 341, 2002
  7. Brewster ME, Loftsson T, Adv. Drug Deliv. Rev., 59, 645, 2007
  8. Breslow R, Dong SD, Chem. Rev., 98(5), 1997, 1998
  9. Yang X, Kim JC, Int. J. Pharm., 388, 58, 2010
  10. Lee MS, Kim JC, Colloid. Polym. Sci., 289, 1177, 2011
  11. Lee MS, Kim JC, Polym. Adv. Technol., 23, 425, 2012
  12. Dai J, Kim JC, J. Disper. Sci. Technol., 33, 611, 2012
  13. Harada A, Acc. Chem. Res., 34, 456, 2001
  14. Renard E, Dertani A, Volet G, Sebille B, Eur. Polym. J., 33, 49, 1997
  15. Basappa C, Rao P, Rao DN, Divakar S, Int. J. Food. Sci. Technol., 33, 517, 1998
  16. Harris JM, Struck EC, Case MG, Paley MS, Yalpani M, Van Alstine JM, Brooks DE, J. Polym. Sci. Pol. Chem., 22, 341, 1984
  17. Tocco G, Carbonaro CM, Meli G, Podda G, Molecules., 14, 1044, 2009
  18. Jin Q, Liu XS, Liu GY, Ji J, Polymer, 51(6), 1311, 2010
  19. Dai J, Kim JC, Korean J. Chem. Eng., 29(3), 323, 2012
  20. Trenor SR, Shultz AR, Love BJ, Long TE, Chem. Rev., 104(6), 3059, 2004
  21. A-Lorenzo C, Bromberg L, Concheiro A, Photochem. Photobiol., 85, 848, 2009
  22. Raymo FM, Tomasulo M, J. Phys. Chem. A, 109(33), 7343, 2005