화학공학소재연구정보센터
Macromolecular Research, Vol.22, No.1, 32-41, January, 2014
Design and synthesis of dual-responsive hydrogels based on N,N-dimethylaminoethyl methacrylate by copolymerization with N-isopropylacrylamide
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Copolymeric hydrogels of N,N-dimethylaminoethyl methacrylate (DMAEMA) and N-isopropylacrylamide (NIPA) of various monomer ratios were evaluated as thermo-responsive and pH-responsive systems for the development of controlled-release and targeted-delivery devices. The swelling properties were investigated with different temperature, pH, and monomer feed ratios. The results show that the temperature-dependent and pH-dependent phase transition of poly(N,N-dimethylaminoethyl methacrylate-N-isopropylacrylamide) (P(DMAEMA-NIPA)) copolymeric hydrogels can be controlled by changing the amount of NIPA units in the network chains. In experiments to determine the temperature-dependent swelling of copolymeric hydrogels in water, it was found that the swelling ratio rapidly decreases as the temperature increases between 35 and 70°C. To characterize the network structure of the copolymeric hydrogels corresponding to effective cross-linking density and average network chain length, uniaxial compressive mechanical testing was carried both after the preparation of hydrogels and after their equilibrium swelling in water. The data obtained demonstrates that the resulting copolymeric hydrogels are promising as materials with tunable hydrophilicity-hydrophobicity and swelling behavior responsive to temperature and pH.
  1. Peppas NA, Bures P, Leobandung W, Ichikawa H, Eur. J. Pharm. Biopharm., 50, 27 (2000)
  2. Lin CC, Metters AT, Adv. Drug Deliv. Rev., 58, 1379 (2006)
  3. Eeckman F, Moes AJ, Amighi K, Eur. Polym. J., 40, 873 (2004)
  4. Priest JH, Murray SL, Nelson RJ, Hoffman AS, Russo PS, Eds., in Reversible Polymeric Gels and Related Systems, Am. Chem. Soc, Washington, DC, 1987, pp 254-264.
  5. Liu HY, Zhu XX, Polymer, 40(25), 6985 (1999)
  6. Shin BC, Kim SS, Ko JK, Jegal J, Lee BM, Eur. Polym. J., 39, 579 (2003)
  7. Brazel CS, Peppas NA, J. Control. Release, 39, 57 (1996)
  8. Cao ZQ, Liu WG, Gao P, Yao KD, Li HX, Wang GC, Polymer, 46(14), 5268 (2005)
  9. Liu XM, Wang LS, Wang L, Huang J, He C, Biomaterials, 25, 5659 (2004)
  10. Siegel RA, Firestone BA, Macromolecules, 21, 3254 (1988)
  11. Yalong Z, Ling X, Min Y, Maolin Z, Jianrui W, Hongfei H, Eur. Polym. J., 42, 2959 (2006)
  12. Cho SH, Jhon MS, Yuk SH, Lee HB, J. Polym. Sci. B: Polym. Phys., 35(4), 595 (1997)
  13. Lugo-Medina E, Licea-Claverie A, Cornejo-Bravo JM, Arndt KF, React. Funct. Polym., 67(1), 67 (2007)
  14. Zhang J, Xie R, Zhang SB, Cheng CJ, Ju XJ, Chu LY, Polymer, 50(11), 2516 (2009)
  15. Feil H, Bae YH, Feijen J, Kim SW, Macromolecules, 38, 5528 (1992)
  16. Emileh A, Farahani EV, Imani M, Eur. Polym. J., 43, 1986 (2007)
  17. Wang K, Xu X, Wang YJ, Guo G, Huang MJ, Luo F, Zhao X, Wei YQ, Qian ZY, Soft Mater., 8, 307 (2010)
  18. Qian ZY, Fu SZ, Feng SS, Nanomedicine, 8, 161 (2013)
  19. Orakdogen N, Polym. Bull., 67(7), 1347 (2011)
  20. Flory PJ, Principles of Polymer Chemistry, Cornell University Press, Ithaca, 1953.
  21. Treloar LRG, The Physics of Rubber Elasticity, University Press, Oxford, 1975.
  22. Lee WF, Yeh YC, Eur. Polym. J., 41, 2488 (2005)
  23. Inomato H, Goto S, Saito S, Macromolecules, 23, 4887 (1990)
  24. Tokuhiro T, Amiya T, Mamada A, Tanaka T, Macromolecules, 24, 2936 (1991)
  25. Otake K, Inomata H, Konno M, Saito S, Macromolecules, 23, 283 (1990)
  26. Feil H, Bae YH, Feijen J, Kim SW, Macromolecules, 26, 2496 (1993)
  27. Cho SH, Jhon MS, Yuk SH, Eur. Polym. J., 35, 1841 (1999)
  28. Yuk SH, Cho SH, Lee SH, Macromolecules, 30(22), 6856 (1997)