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Physical Interaction Between Water-Soluble Poly(Acrylamide/Itaconic Acid) with Acriflavine and Procainamide Hydrochloride
Corresponding Author(s) : A.I. Kariper
Asian Journal of Chemistry,
Vol. 29 No. 2 (2017): Vol 29 Issue 2
Abstract
In this study, the water-soluble polymers, poly(itaconic acid acrylamide) (PAI) and poly(acrylamide) (PAAm), were synthesized through radical addition reactions. Structural characterization of poly(itaconic acids acrylamide) and poly(acrylamide) was performed by Fourier transform infrared and scanning electron microscope. Release and anti-release profile of the pharmaceutical active agents [acriflavine (AF) and procainamide hydrochloride (PH)] from the polymers (PAI and PAAm) were monitored by ultraviolet-visible spectrophotometry. It has been observed that the entire drug (1 mg procainamide hydrochloride), which was added to the solution with 1 g of polymer, was absorbed in around 3 h by poly(itaconic acids acrylamide). Also, 0.6 mg of acriflavine drug was absorbed in around 3 h. Thus, poly(itaconic acids acrylamide) and poly(acrylamide) polymers were tested for acriflavine and procainamide hydrochloride drugs. In the light of these results, the polymers that are suitable for the release of acriflavine and procainamide hydrochloride drugs were identified.
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- J. Zhu and R.E. Marchant, Rev. Med. Devices, 8, 607 (2011).
- M. Herring, J. Smith, M. Dalsing, J. Glover, R. Compton, K. Etchberger and T. Zollinger, J. Vasc. Surg., 20, 650 (1994).
- C. Gillis-Haegerstrand, S. Frebelius, A. Haegerstrand and J. Swedenborg, J. Vasc. Surg., 24, 226 (1996).
- U.M. Deogade, V.N. Deshmukh and D.M. Sakarkar, Int. J. Pharm. Tech. Res., 4, 799 (2012).
- E.A. Blackstone, J.P. Fuhr and S. Pociask, Am. Health Drug Benefits, 7, 216 (2014).
- W.H. De Jong and P.J.A. Borm, Int. J. Nanomedicine, 3, 133 (2008).
- E. Markovsky, H. Baabur-Cohen, A. Eldar-Boock, L. Omer, G. Tiram, S. Ferber, P. Ofek, D. Polyak, A. Scomparin and R. Satchi-Fainaro, J. Control. Rel., 161, 446 (2012).
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- E.M.S. Macoas, R. Fausto, J. Lundell, M. Pettersson, L. Khriachtchev and R. Rasanen, J. Phys. Chem. A, 105, 3922 (2001).
- R. Murugan, S. Mohan and A. Bigotto, J. Korean Phys. Soc., 32, 505 (1998).
- B. Marjanovic, G. Ciric-Marjanovic, A. Radulovic, I. Juranic and P. Holler, Mater. Sci. Forum, 555, 503 (2007).
- H. Mirhosseini and B.T. Amid, Chem. Cent. J., 7, 1 (2013).
- E. Gavini, V. Sanna, C. Juliano, M.C. Bonferoni and P. Giunchedi, AAPS PharmSci.Tech., 3, 32 (2002).
- H. Patel, D.A. Raval, D. Madamwar and S.R. Patel, Angew. Makromol. Chem., 263, 25 (1998).
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References
J. Zhu and R.E. Marchant, Rev. Med. Devices, 8, 607 (2011).
M. Herring, J. Smith, M. Dalsing, J. Glover, R. Compton, K. Etchberger and T. Zollinger, J. Vasc. Surg., 20, 650 (1994).
C. Gillis-Haegerstrand, S. Frebelius, A. Haegerstrand and J. Swedenborg, J. Vasc. Surg., 24, 226 (1996).
U.M. Deogade, V.N. Deshmukh and D.M. Sakarkar, Int. J. Pharm. Tech. Res., 4, 799 (2012).
E.A. Blackstone, J.P. Fuhr and S. Pociask, Am. Health Drug Benefits, 7, 216 (2014).
W.H. De Jong and P.J.A. Borm, Int. J. Nanomedicine, 3, 133 (2008).
E. Markovsky, H. Baabur-Cohen, A. Eldar-Boock, L. Omer, G. Tiram, S. Ferber, P. Ofek, D. Polyak, A. Scomparin and R. Satchi-Fainaro, J. Control. Rel., 161, 446 (2012).
A.S.G. Magalhaes, M.P. Almeida Neto, M.N. Bezerra, N.M.P.S. Ricardo and J.P.A. Feitosa, Quim. Nova, 35, 1464 (2012).
E.M.S. Macoas, R. Fausto, J. Lundell, M. Pettersson, L. Khriachtchev and R. Rasanen, J. Phys. Chem. A, 105, 3922 (2001).
R. Murugan, S. Mohan and A. Bigotto, J. Korean Phys. Soc., 32, 505 (1998).
B. Marjanovic, G. Ciric-Marjanovic, A. Radulovic, I. Juranic and P. Holler, Mater. Sci. Forum, 555, 503 (2007).
H. Mirhosseini and B.T. Amid, Chem. Cent. J., 7, 1 (2013).
E. Gavini, V. Sanna, C. Juliano, M.C. Bonferoni and P. Giunchedi, AAPS PharmSci.Tech., 3, 32 (2002).
H. Patel, D.A. Raval, D. Madamwar and S.R. Patel, Angew. Makromol. Chem., 263, 25 (1998).
N. Bolourtchian, F.S. Javid and S. Dadashzadeh, Iran. J. Pharm. Res., 4, 13 (2005).