Insulator semiconductor structures coated with biodegradable latexes as encapsulation matrix for urease

被引:18
作者
Barhoumi, H
Maaref, A
Rammah, A
Martelet, C [1 ]
Jaffrezic-Renault, N
Mousty, C
Cosnier, S
Perez, E
Rico-Lattes, I
机构
[1] Ecole Cent Lyon, CEGELY, CNRS, UMR 5005, F-69131 Ecully, France
[2] Lab Phys & Chim Interfaces, Fac Sci, Monastir, Tunisia
[3] Univ Grenoble 1, CNRS, Lab Electrochim Organ & Photochim Redox, UMR 56030 ICMG FR 2607, Grenoble, France
[4] Univ Toulouse 3, CNRS, UMR 5623, Lab IMRCP, F-31062 Toulouse, France
关键词
latex; urease; IS; clinical biosensor;
D O I
10.1016/j.bios.2004.10.010
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A new urea biosensor for clinical applications was obtained by immobilization of urease within different latex polymers functionalized by hydroxy, acetate and lactobionate groups. Responses of these biosensors based on pH-ion-selective field effect insulator-semiconductor (IS) systems to urea additions were evaluated by capacitance measurements. UV-visible spectroscopy was used to check the urease activity in various matrixes. A good retention of the catalytic urease activity in the case of the cationic polymers was observed. In addition, rotating disk electrode experiments were carried out to determine the matrix permeability characteristics. Under optimal conditions, i.e. buffer capacity corresponding to 5 mM phosphate buffer, the urea enzyme insulator semiconductor (ENIS) sensors showed a linear response for urea concentrations in the range 10(-1.5) to 10(-4) M. Furthermore, kinetic parameters for the immobilized urease were obtained from Lineweaver-Burk plot. Clearly, a fast response and a good adhesion for the urease-acetate polymer composite films, prepared without using glutaraldehyde as cross-linking agent was observed. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:2318 / 2323
页数:6
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