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Investigation of Adsorption of 5-Fluorouracil and 5-Bromouracil onto Sepiolite and Loughlinite: An IR Spectroscopic Study
Corresponding Author(s) : Sevim Akyuz
Asian Journal of Chemistry,
Vol. 26 No. 15 (2014): Vol 26 Issue 15
Abstract
The adsorption of 5-fluorouracil (5FU) and 5-bromouracil (5BrU) by sepiolite and loughlinite (natural Na-sepiolite) has been investigated using FT-IR spectrometry. The spectroscopic results indicate that 5-halogenouracils adsorbed on sepiolite and loughlinite are coordinated to surface hydroxyls and/or to Lewis acidic centers by hydrogen bonding interaction through the oxygen lone pairs. Some intensity and frequency changes in the OH stretching and deformation bands of surface hydroxyls (Si-OH) of the 5-fluorouracil and 5-bromouracil treated sepiolite and loughlinite were observed. Adsorption capacity of the sepiolite is found to be higher than loughlinite for 5-halogenuracils. Moreover adsorption capacity of clays were found to decrease in the order 5-fluorouracil > 5-bromouracil.
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References
B.G. Katsung, Basic and Clinical Pharmacology, Appleton and Lange, Lebanon, edn 4 (1989).
S.A. Schroeder, M.A. Krupp, L.M. Tierney Jr. and S.J. McPhee, Current Medical Diagnosis and Treatment, Appleton and Lange, Prentice-Hall London (1990).
J.P. Henderson, J. Byun, J. Takeshita and J.W. Heinecke, J. Biol. Chem., 278, 23522 (2003); doi:10.1074/jbc.M303928200.
Q. Jiang, B.C. Blount and B.N. Ames, J. Biol. Chem., 278, 32834 (2003); doi:10.1074/jbc.M304021200.
Serratosa, In Proceedings of International Clay Conference, 1978, edited by M.M. Mortland and V.C. Farmer, Elsevier, Amsterdam, p. 99 (1979).
J.J. Fahey, M. Ross and J.M. Axelrod, Am. Mineral., 45, 270 (1960).
Y. Asci and P. Berkan, Asian J. Chem., 22, 2319 (2010).
O. Isildak and A. Sari, Asian J. Chem., 20, 2099 (2008).
B. Engin, M. Guru and A. Alicilar, Asian J. Chem., 21, 2067 (2009).
M.C. Floody, B.K.G. Theng and M.L. Mora, Clay Miner., 44, 161 (2009); doi:10.1180/claymin.2009.044.2.161.
R.R. Pawar, B.D. Kevadiya, H. Brahmbhatt and H.C. Bajaj, Int. J. Pharm., 446, 145 (2013); doi:10.1016/j.ijpharm.2013.02.021.
S. Akyuz and T. Akyuz, Asian J. Chem., 20, 3767 (2008).
S. Akyuz and T. Akyuz, Asian J. Chem., 22, 546 (2010).
E. Akalin, S. Akyuz and T. Akyuz, J. Mol. Struct., 834-836, 477 (2007); doi:10.1016/j.molstruc.2006.11.061.
S. Akyuz and T. Akyuz, Asian J. Chem., 23, 3211 (2011).
M. Ogawa, T. Hashizume, K. Kuroda and C. Kato, Inorg. Chem., 30, 584 (1991); doi:10.1021/ic00003a050.
J. Madejova, Vib. Spectrosc., 31, 1 (2003); doi:10.1016/S0924-2031(02)00065-6.
M.A. Palafox, V.K. Rastogi, H. Kumar, I. Kostova and J.K. Vats, Spectrosc. Lett., 44, 300 (2011); doi:10.1080/00387010.2010.524963.
V.K. Rastogi and M.A. Palafox, Spectrochim. Acta A, 79, 970 (2011); doi:10.1016/j.saa.2011.04.008.
M. Graindourze, T. Grootaers, J. Smets, Th. Zeegers-Huyskens and G. Maes, J. Mol. Struct., 237, 389 (1990); doi:10.1016/0022-2860(90)80154-C.
M. Alcolea Palafox and V.K. Rastogi, Spectrochim. Acta A, 58, 411 (2002); doi:10.1016/S1386-1425(01)00509-1.
B. Blicharska and T. Kupka, J. Mol. Struct., 613, 153 (2002); doi:10.1016/S0022-2860(02)00171-0.
S. Akyuz and T. Akyuz, J. Mol. Struct., 744-747, 47 (2005); doi:10.1016/j.molstruc.2004.10.024.
K. Katti and D. Katti, Langmuir, 22, 532 (2006); doi:10.1021/la051533u.