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A Molecular Imprinted Polymers with b-Cyclodextrin for Adsorption of Paeoniflorin
Corresponding Author(s) : W. Zhang
Asian Journal of Chemistry,
Vol. 27 No. 4 (2015): Vol 27 Issue 4
Abstract
b-Cyclodextrin and epichlorohydrin were respectively used as functional monomer and cross-linker to synthesize molecularly imprinted polymers microspheres (MIPs) by suspension polymerization, for adsorption of paeoniflorin (PF), named PF-MIPs. The experiment indicated the PF-MIPs have specific selectivity on paeoniflorin. The paeoniflorin binding site was found inside of PF-MIPs by Scatchard analysis, with Kd and Qmax of 0.46 mg/mL and 47.22 mg/g, respectively. The adsorption process was endothermic process, the adsorption of paeoniflorin on MIPs followed Freundlich adsorption model. The PF-MIPs can be re-used to isolation paeoniflorin at least 10 times.
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- G. Wulff, Angew. Chem. Int. Ed. Engl., 34, 1812 (1995); doi:10.1002/anie.199518121.
- J. Steinke, D.C. Sherrington and I.R. Dunkin, Adv. Polym. Sci., 123, 81 (1995); doi:10.1007/3-540-58908-2_3.
- T. Matsunaga, T.H. Hishiya and T. Takeuchi, Anal. Chim. Acta, 591, 63 (2007); doi:10.1016/j.aca.2007.02.072.
- C. Fang, L. Chen, W.M. Zhang and X.R. Zhou, J. Wuhan Univ., (Nat. Sci. Ed.), 49, 689 (2003).
- J. Matsui, L.A. Nicholls, I. Karube and K. Mosbach, J. Org. Chem., 61, 5414 (1996); doi:10.1021/jo9516805.
- Z.H. Meng, J.F. Wang, L.M. Zhou, Q.H. Wang and D.Q. Zhu, Chinese J. Chromatogr., 17, 323 (1999).
- M. Kaneda, Y. Iitaka and S. Shibata, Tetrahedron, 28, 4309 (1972); doi:10.1016/S0040-4020(01)88953-5.
- S. Shibata and M. Nakahara, Chem. Pharm. Bull. (Tokyo), 11, 372 (1963); doi:10.1248/cpb.11.372.
- Y.J. Tong, Y. Xin, H.L. Yang, L. Zhang, Y.R. Zhang, Y. Chen, X.L. Xia and W. Wang, Chromatographia, 74, 443 (2011); doi:10.1007/s10337-011-2089-0.
- M.H. Fan and S.Y. Xu, Sep. Purif. Technol., 61, 211 (2008); doi:10.1016/j.seppur.2007.07.046.
- Y.J. Fu, Y.G. Zu, W. Liu, C.L. Hou, L.Y. Chen, S.M. Li, X.G. Shi and M.H. Tong, J. Chromatogr. A, 1139, 206 (2007); doi:10.1016/j.chroma.2006.11.015.
- X.Z. Shi, A.B. Wu, G.R. Qu, R.X. Li and D.B. Zhang, Biomaterials, 28, 3741 (2007); doi:10.1016/j.biomaterials.2007.04.036.
- M.L. Yang and X.G. Chu, Anal. Lett., 43, 2390 (2010); doi:10.1080/00032711003717380.
- L.A. de Barros, I. Martins and S. Rath, Anal. Bioanal. Chem., 397, 1355 (2010); doi:10.1007/s00216-010-3629-4.
References
G. Wulff, Angew. Chem. Int. Ed. Engl., 34, 1812 (1995); doi:10.1002/anie.199518121.
J. Steinke, D.C. Sherrington and I.R. Dunkin, Adv. Polym. Sci., 123, 81 (1995); doi:10.1007/3-540-58908-2_3.
T. Matsunaga, T.H. Hishiya and T. Takeuchi, Anal. Chim. Acta, 591, 63 (2007); doi:10.1016/j.aca.2007.02.072.
C. Fang, L. Chen, W.M. Zhang and X.R. Zhou, J. Wuhan Univ., (Nat. Sci. Ed.), 49, 689 (2003).
J. Matsui, L.A. Nicholls, I. Karube and K. Mosbach, J. Org. Chem., 61, 5414 (1996); doi:10.1021/jo9516805.
Z.H. Meng, J.F. Wang, L.M. Zhou, Q.H. Wang and D.Q. Zhu, Chinese J. Chromatogr., 17, 323 (1999).
M. Kaneda, Y. Iitaka and S. Shibata, Tetrahedron, 28, 4309 (1972); doi:10.1016/S0040-4020(01)88953-5.
S. Shibata and M. Nakahara, Chem. Pharm. Bull. (Tokyo), 11, 372 (1963); doi:10.1248/cpb.11.372.
Y.J. Tong, Y. Xin, H.L. Yang, L. Zhang, Y.R. Zhang, Y. Chen, X.L. Xia and W. Wang, Chromatographia, 74, 443 (2011); doi:10.1007/s10337-011-2089-0.
M.H. Fan and S.Y. Xu, Sep. Purif. Technol., 61, 211 (2008); doi:10.1016/j.seppur.2007.07.046.
Y.J. Fu, Y.G. Zu, W. Liu, C.L. Hou, L.Y. Chen, S.M. Li, X.G. Shi and M.H. Tong, J. Chromatogr. A, 1139, 206 (2007); doi:10.1016/j.chroma.2006.11.015.
X.Z. Shi, A.B. Wu, G.R. Qu, R.X. Li and D.B. Zhang, Biomaterials, 28, 3741 (2007); doi:10.1016/j.biomaterials.2007.04.036.
M.L. Yang and X.G. Chu, Anal. Lett., 43, 2390 (2010); doi:10.1080/00032711003717380.
L.A. de Barros, I. Martins and S. Rath, Anal. Bioanal. Chem., 397, 1355 (2010); doi:10.1007/s00216-010-3629-4.