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Synthesis, Structure and Swelling Properties of Hydrogels Based on Polyacrylic Acid
Corresponding Author(s) : S.M. Mammadova
Asian Journal of Chemistry,
Vol. 29 No. 3 (2017): Vol 29 Issue 3
Abstract
In polar environment, net shaped polymers with ability of high swelling rate have been synthesized from crosslinking of 5, 10, 15 and 20 % ratio (by weight) of polyacrylic acid having an average molecular weight of 230 kDa with N,N-methylene-bis-acrylamide by using ultraviolet ray. The structure of gel has been studied and explained mechanism of the crosslinking process using infrared spectrometer, scanning electron microscopy and X-ray phase analysis methods. The swelling rate of crosslinked polymer, in polar, non-polar, acidic, neutral and alkali environments, as well as in different concentrations of sugar and physiological (0.9 % NaCl) solutions were also studied. It was determined that obtained polymer hydrogel, in the presence of 10 % (by weight) crosslink reagent in pH = 9-10, has maximum 680 % swelling rate within 4-5 days.
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- P.K. Prashant, B.R. Vivek, N.D. Deepashree and P.P. Pranav, Int. J. Pharm. Pharm. Sci., 4, 1 (2012).
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P.K. Prashant, B.R. Vivek, N.D. Deepashree and P.P. Pranav, Int. J. Pharm. Pharm. Sci., 4, 1 (2012).
N.A. Peppas, P. Bures, W. Leobandung and H. Ichikawa, Eur. J. Pharm. Biopharm., 50, 27 (2000).
M.P. Lutolf, Nat. Mater., 8, 451 (2009).
N. Das, T. Bera and A. Mukherjee, Int. J. Pharma Bio Sci., 3, 586 (2012).
J.K. Oh, Can. J. Chem., 88, 173 (2010).
B.V. Slaughter, S.S. Khurshid, O.Z. Fisher, A. Khademhosseini and N.A. Peppas, Adv. Mater., 21, 3307 (2009).
C.-C. Lin and K.S. Anseth, Pharm. Res., 26, 631 (2009).
N.C. Hunt and L.M. Grover, Biotechnol. Lett., 32, 733 (2010).
R.V. Ulijn, N. Bibi, V. Jayawarna, P.D. Thornton, S.J. Todd, R.J. Mart, A.M. Smith and J.E. Gough, Mater. Today, 10, 40 (2007).
Sh.Z. Tapdigov, S.M. Mammadova and N.A. Zeynalov, J. Chem. Chem. Eng., 8, 800 (2014).
F. Yang, C.G. Williams, D. Wang, H. Lee, P.N. Manson and J. Elisseeff, Biomaterials, 26, 5991 (2005).
N.A. Zeynalov, D.T. Babayeva, E.F. Nasiyyati and S.F. Humbatova, Am. J. Polym. Sci., 5, 18 (2015).
M. Minhas, M. Ahmad, L. Ali and M. Sohail, Daru, 21, 44 (2013).
S. Benamer, M. Mahlous, A. Boukrif, B. Mansouri and S.L. Youcef, Nucl. Instrum. Methods Phys. Res., 248, 284 (2006).
V. Thomas, M.M. Yallapu, B. Sreedhar and S.K. Bajpai, J. Colloid Interface Sci., 315, 389 (2007).
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E. Imamura, O. Sawatani, H. Koyanagi, Y. Noishiki and T. Miyata, J. Card. Surg., 4, 50 (1989).
B.K. Denizli, H.K. Can, Z.M.O. Rzaev and A. Guner, Polymer (Guildf.), 45, 6431 (2004).
R. López-Cebral, P. Paolicelli, V. Romero-Caamaño, B. Seijo, M.A. Casadei and A. Sanchez, J. Pharm. Sci., 102, 2632 (2013).
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H. Vihola, A. Laukkanen, L. Valtola, H. Tenhu and J. Hirvonen, Biomaterials, 26, 3055 (2005).
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E.S. Abdel-Halim and S.S. Al-Deyab, Carbohydr. Polym., 86, 1306 (2011).
K.T. Nguyen and J.L. West, Biomaterials, 23, 4307 (2002).
Z. Mohamadnia, M.J. Zohuriaan-Mehr, K. Kabiri, A. Jamshidi and H. Mobedi, J. Bioact. Compat. Polym., 22, 342 (2007).
M. Liu, H. Su and T. Tan, Carbohydr. Polym., 87, 2425 (2012).
S. Lu, M. Liu, B. Ni and C. Gao, J. Polym. Sci., B, Polym. Phys., 48, 1749 (2010).
P. Chivukula, K. Dusek, D. Wang, M. Duskova-Smrckova, P. Kopeckova and J. Kopecek, Biomaterials, 27, 1140 (2006).
E.C. Muniz and G. Geuskens, J. Mater. Sci. Mater. Med., 12, 879 (2001).
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T. Iizawa, H. Taketa, M. Maruta, T. Ishido, T. Gotoh and S. Sakohara, J. Appl. Polym. Sci., 104, 842 (2007).
T. Coviello, M. Grassi, R. Lapasin, A. Marino and F. Alhaique, Biomaterials, 24, 2789 (2003).
A.E. Sherr and A.M. Swift, J. Appl. Polym. Sci., 9, 3929 (1965).
Y.X. Zhang, F.P. Wu, M.Z. Li and E.J. Wang, Polymer, 46, 7695 (2005).
J.A. Beamish, J. Zhu, K. Kottke-Marchant and R.E. Marchant, J. Biomed. Mater. Res. A, 92, 441 (2010).