화학공학소재연구정보센터
Polymer(Korea), Vol.37, No.6, 794-801, November, 2013
pH 감응성 NIPAM-co-MAA 고분자 마이크로젤의 제조 및 분석과 염 종류에 따른 부피상 변화
Preparation and Characterization of Novel Temperature and pH Sensitive (NIPAM-co-MAA) Polymer Microgels and Their Volume Phase Change with Various Salts
E-mail:
Novel microgels of N-isopropylacrylamide (NIPAM)-co-methacrylic acid (MAA) (NIPAM-co-MAA) with different contents of N,N-methylene bis acrylamide (MBA) were prepared by emulsion polymerization technique and were studied by Fourier transform infrared spectroscopy (FTIR), dynamic light scattering (DLS) and zeta potential measurement. Effect of pH, temperature and different salts concentration on the microgel particles was investigated. DLS results have shown that the hydrodynamic radius of the microgel increased upon increasing pH and decreased upon increasing temperature. The swelling/deswelling behaviors as determined by DLS showed the ionic repulsions of the carboxyl group of the methacrylic acid and hydrophobic interaction of NIPAM. The effect of various salts on volume phase transition temperature (VPTT) was also investigated. Upon increasing salt concentration, VPTT became broad and shifted to a lower temperature. Electrophoretic mobility measurements showed an increase with increasing pH and temperature at a constant ionic strength.
  1. Andrianov AK, Payne LG, Adv. Drug Deliv. Rev., 34, 155 (1998)
  2. Vinogradov SV, Bronich TK, Kabanov A, Adv. Drug Deliv. Rev., 54, 135 (2002)
  3. Peppas NA, Bures P, Leobandung W, Ichikawa H, Eur. J.Pharm. Biopharm., 50, 27 (2000)
  4. Bradley M, Ramos J, Vincent B, Langmuir, 21(4), 1209 (2005)
  5. Murray MJ, Snowden MJ, Adv. Colloid Interface Sci., 54, 73 (1995)
  6. Kiser PF, Wilson G, Needham D, Nature(London)., 394, 459 (1998)
  7. Weissman JM, Sunkara HB, Tse AS, Asher SA, Science, 274(5289), 959 (1996)
  8. Cussler EL, Stokar MR, Vararbert JE, AIChE J., 30, 578 (1984)
  9. Kratz K, Hellweg T, Eimer W, Colloid Surface A., 170, 137 (2000)
  10. Ostroha J, Pong M, Lowman A, Dan N, Biomaterials., 25, 4345 (2004)
  11. Brondsted H, Kopecek J, Biomaterials., 12, 584 (1991)
  12. Peppas NA, Mikos AG, Hydrogels in Medicine and Pharmacy, CRC Press, Boca Raton, FL, 01, 1 (1986)
  13. Zhang GZ, Jiang M, Zhu L, Wu C, Polymer, 42(1), 151 (2001)
  14. Pan YV, Wesley RA, Luginbuhl R, Denton DD, Ratner BD, Biomacromolecules, 2(1), 32 (2001)
  15. Nur H, Pinkrah VT, Mitchell JC, Benee LS, Snowden MJ, Adv. Colloid Interface Sci., 158, 15 (2010)
  16. Kim KS, Kim MH, Cho SH, J. Ind. Eng. Chem., 11(5), 736 (2005)
  17. Zhang Y, Liu T, Wang Q, Zhao J, Fang J, Shen W, Macromol. Res., 20(5), 484 (2012)
  18. Chan VC, Hoffmann AS, Nature., 373, 49 (1955)
  19. Tanaka T, Fillmore D, Sun S, Nishio I, Swislow G, Phys.Rev. Lett., 45, 1636 (1980)
  20. Sadeghi M, Ghasemi N, Indian J. Sci. Technol., 5, 1879 (2012)
  21. Sadeghi M, Hosseinzadeh H, Turk. J. Chem., 34, 739 (2010)
  22. Sadeghi M, Braz. J. Chem. Eng., 29, 295 (2012)
  23. Costa E, Lloyd MM, Chopko C, Aguiar-Ricardo A, Hammond PT, Langmuir, 28(26), 10082 (2012)
  24. Hoare T, Pelton R, Macromolecules, 37(7), 2544 (2004)