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Received May 27, 2014
Accepted June 24, 2014
- This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Synthesis and adsorption properties of carbamazepine imprinted polymer by dispersion polymerization in supercritical carbon dioxide
Department of Chemical and Biomolecular Engineering, Chonnam National University, Yeosu, Jeonnam 550-749, Korea
Korean Journal of Chemical Engineering, December 2014, 31(12), 2266-2273(8), 10.1007/s11814-014-0178-0
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Abstract
We synthesized molecularly imprinted polymers (MIPs) which can selectively separate carbamazepine (CMZ) as a pharmaceutically active compound by using supercritical fluid technology in supercritical carbon dioxide (scCO2), and also evaluated the adsorption properties of the prepared CMZ imprinted polymers (CMZ-IPs). CMZIPs is prepared with methacrylic acid (MAA) as a functional monomer, CMZ as a template, and ethylene glycol dimethacrylate_x000D_
(EGDMA) as a crosslinking agent. The binding characteristics of CMZ-IPs are evaluated using equilibrium binding experiments. The adsorption ability in aqueous solution of CMZ-IPs was investigated by HPLC analysis, measuring the adsorbed amounts for the template and its structural analogue, the selectivity factor (α), and the imprintinginduced promotion of binding (IPB). The adsorption properties with the change of pH and temperature of aqueous solution_x000D_
were also examined. The results of the evaluation analysis indicate that the prepared CMZ-IPs have high selectivity (102, 94, 75 and 44 μmol/g) and separation abilities.
Keywords
References
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Pauling L, J. Amer. Chem. Soc., 62, 2643 (1940)
Polyakov MV, Kuleshina LP, Neimark IE, Zhurnal Fizicheskoi Khimii, 10, 100 (1937)
Dickey FH, Proceedings of the National Academy of Sciences of the United States of America, 35, 227 (1949)
Wulff G, Angew. Chem. Int. Ed., 34, 1812 (1995)
Mosbach K, Trends Biochem. Sci., 19, 9 (1994)
Shea KJ, Trends in Polymer Science, 2, 166 (1994)
Wulff G, Sarhan A, Zabrocki K, Tetrahedron Lett., 44, 4329 (1973)
Wulff G, Vesper R, Grobe-Einsler R, Sarhan A, Macromol. Chem. Phys., 178, 2799 (1977)
Jin Y, Choi DK, Row KH, Korean J. Chem. Eng., 25(4), 816 (2008)
Jin Y, Row KH, Korean J. Chem. Eng., 22(2), 264 (2005)
Wei S, Mizaikoff B, J. Sep. Sci., 30, 1794 (2007)
Hung CY, Huang YT, Huang HH, Hwang CC, J. Appl. Polym. Sci., 102(3), 2972 (2006)
Suedee R, Jantarat C, Lindner W, Viernstein H, Songkro S, Srichana T, J. Controlled Release, 142, 122 (2010)
Guan G, Liu B, Wang Z, Zhang Z, Sensors, 8, 8291 (2008)
Sellergren B, Angew. Chem. Int. Ed., 39, 1031 (2000)
Mosbach K, Ramstrom O, Nat. Biotechnol., 14, 163 (1996)
Yun YH, Shon HK, Yoon SD, J. Mater. Sci., 44(22), 6206 (2009)
Bernus I, Dickinson RG, Hooper WD, Eadie MJ, Epilepsy Research, 24, 163 (1996)
Nair R, Gonen S, Hoag SW, Int. J. Pharm., 240, 11 (2002)
Dai CM, Geissen SU, Zhang YL, Zhang YJ, Zhou XF, J. Hazard. Mater., 184(1-3), 156 (2010)
Beltran A, Caro E, Marce RM, Cormack PAG, Sherrington DC, Borrull F, Anal. Chim. Acta, 597, 6 (2007)
Beltran A, Marce RM, Cormack PAG, Borrull F, J. Chromatogr. A, 1216, 2248 (2009)
Sun SP, Zeng X, Lemley AT, J. Hazard. Mater., 252, 155 (2013)