Kinetics and binding properties of cloramphenicol imprinted polymers

被引:31
作者
Corton, E.
Garcia-Calzon, J. A.
Diaz-Garcia, M. E.
机构
[1] Univ Oviedo, Dept Phys & Analyt Chem, E-33006 Oviedo, Spain
[2] Univ Buenos Aires, Dept Biol Chem, RA-1053 Buenos Aires, DF, Argentina
关键词
pharmaceuticals; polymers and organics; adsorption;
D O I
10.1016/j.jnoncrysol.2006.12.066
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Molecularly imprinted polymers (MIPs) are easily obtained by a non-covalent approach through the copolymerisation of suitable functional monomers and cross-linkers in the presence of the print molecule. Removal of the template leaves a polymer that selectively recognises it. However, experimental data have demonstrated that non-covalent molecularly imprinted polymers exhibit a heterogeneous binding sites distribution. In this work, two different imprinted polymers for chloramphenicol (CAP), obtained using different template concentrations, were evaluated for their kinetics and affinity binding properties against CAP in a batch approach. Experimental binding isotherms were fitted to Langmuir, Freundlich and Langmuir-Freundlich isotherms and the affinity distribution corresponding to the Freundlich isotherm was used to extract binding parameters. Parallel studies were performed for the binding of chloramphenicol diacetate to the CAP-imprinted polymers. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:974 / 980
页数:7
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