Low-Molecular-Weight Hydrogels as New Supramolecular Materials for Bioelectrochemical Interfaces

被引:23
作者
Jain, Deepak [1 ,2 ,3 ]
Karajic, Aleksandar [3 ,4 ,5 ]
Murawska, Magdalena [3 ,4 ,5 ]
Goudeau, Bertrand [3 ,5 ]
Bichon, Sabrina [3 ,4 ]
Gounel, Sebastien [3 ,4 ]
Mano, Nicolas [3 ,4 ]
Kuhn, Alexander [3 ,5 ]
Barthelemy, Philippe [1 ,2 ,3 ]
机构
[1] INSERM, U1212, F-33076 Bordeaux, France
[2] CNRS 5320, F-33076 Bordeaux, France
[3] Univ Bordeaux, 146 Rue Leo Saignat, F-33076 Bordeaux, France
[4] CNRS, CRPP, UPR 8641, F-33600 Pessac, France
[5] CNRS ENSCBP, Bordeaux INP UMR 5255, 16 Ave Pey Berland, F-33607 Pessac, France
关键词
low molecular weight gel; enzyme electrodes; bioelectrochemistry; porous electrodes; supramolecular assembly; fluorocarbon amphiphile; nucleoside; glycosyl; BIOFUEL CELLS; DRUG; MICROELECTRODES; NANOPARTICLES; GELS;
D O I
10.1021/acsami.6b12890
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Controlling the interface between biological tissues and electrodes remains an important challenge for the development of implantable,devices in terms of electroactivity, biocompatibility and long-term stability. To engineer such a biocompatible interface a low molecular weight gel (LMWG) based on a glycosylated nucleoside fluorocarbon amphiphile (GNF) was employed for the first time to,wrap gold electrodes via a noncovalent anchoring strategy, that, is, self-assembly of GNF at the electrode surface. Scanning electron microscopy (SEM) studies indicate that the gold surface is coated with the GNF hydrogels. Electrochemical measurements using cyclic voltammetry (CV) clearly show that the electrode properties, are not affected by the presence of the hydrogel. This coating layer of 1 to 2 mu m does not significantly slow down the mass transport through the hydrogel. Voltammetry experiments with gel coated macroporous enzyme electrodes reveal that during continuous use their current is improved by 100% compared to the noncoated electrode. This demonstrates he supramolecular hydrogel dramatically increases the stability of the bioelectrochemical interface. Therefore, such hybrid electrodes are promising candidates that will both offer the biocompatibility and stability needed for the development of more efficient biosensors and biofuel cells.
引用
收藏
页码:1093 / 1098
页数:6
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