Interfacing boron doped diamond and biology: An insight on its use for bioanalytical applications

被引:32
作者
Fortin, E
Chane-Tune, J
Delabouglise, D
Bouvier, P
Livache, T
Mailley, P
Marcus, B
Mermoux, M
Petit, JP
Szunerits, S
Vieil, E
机构
[1] CEA, CNRS, UMR, Grp CRELAB,UJF 5819,DRFMC, F-38054 Grenoble, France
[2] Inst Natl Polytech Grenoble, ENSEEG, LEPMI, CNRS,UMR,INPG,UJF 5631, F-38042 St Martin Dheres, France
关键词
boron doped diamond; nucleoside oxidation; diamond functionalization; SECM;
D O I
10.1002/elan.200403190
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Boron doped diamond (BDD) films are promising materials for electroanalysis and bioelectroanalysis. This contribution gives a short review on BDD functionalization by chemical and biochemical entities and on the applications of BDD electrodes to electroanalysis of chemical compounds of biological interest. This review is illustrated by the developments on BDD interfaces in both these areas carried out in our group. BDD electrodes were prepared by means of microwave plasma-assisted CVD onto silicon substrate giving rise to H-terminated BDD films. Anodic polarization of BDD electrodes in aqueous media generates hydrophilic oxidized surfaces and extended electrochemical window in aqueous media. We took advantage of this enlarged electrochemical window together with the hydroxylated surface for the functionalization of BDD electrode surfaces with biomolecules and for bioelectroanalysis. We have designed a novel route of BDD functionalization using OH terminations of the anodized surface. The modification of the BDD surface with biotin groups will be presented here as biologically active model. Furthermore, as the anodic potential window of BDD increases upon electrochemical activation, 2'-deoxyguanosine (1.2 V vs. Ag/AgCl) and 2'-deoxyadenosine (1.5 V vs. Ag/AgCl) could be detected electrochemically with an acceptable signal to noise ratio. The electrochemical signature of each oxidizable base was assessed using differential pulse voltammetry (DPV). These experiments pointed towards adsorption of the oxidized products, which were investigated macroscopically by DPV and at the microscopic level by SECM (scanning electrochemical microscopy).
引用
收藏
页码:517 / 526
页数:10
相关论文
共 44 条
[21]   IN-SITU RAMAN MONITORING OF THE GROWTH OF DIAMOND FILMS IN PLASMA-ASSISTED CVD REACTORS [J].
MERMOUX, M ;
FAYETTE, L ;
MARCUS, B ;
ROSMAN, N ;
ABELLO, L ;
LUCAZEAU, G .
DIAMOND AND RELATED MATERIALS, 1995, 4 (5-6) :745-749
[22]   A confocal Raman imaging study of an optically transparent boron-doped diamond electrode [J].
Mermoux, M ;
Marcus, B ;
Swain, GM ;
Butler, JE .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (42) :10816-10827
[23]   Photochemical modification of diamond surfaces [J].
Miller, JB ;
Brown, DW .
LANGMUIR, 1996, 12 (24) :5809-5817
[24]   PROPERTIES OF PHOTOCHEMICALLY MODIFIED DIAMOND FILMS [J].
MILLER, JB ;
BROWN, DW .
DIAMOND AND RELATED MATERIALS, 1995, 4 (04) :435-440
[25]   Electrochemical oxidation of benzoic acid at boron-doped diamond electrodes [J].
Montilla, F ;
Michaud, PA ;
Morallón, E ;
Vázquez, JL ;
Comninellis, C .
ELECTROCHIMICA ACTA, 2002, 47 (21) :3509-3513
[26]   Platinum particles deposited on synthetic boron-doped diamond surfaces.: Application to methanol oxidation [J].
Montilla, F ;
Morallón, E ;
Duo, I ;
Comninellis, C ;
Vázquez, JL .
ELECTROCHIMICA ACTA, 2003, 48 (25-26) :3891-3897
[27]   Hydroxyl groups on boron-doped diamond electrodes and their modification with a silane coupling agent [J].
Notsu, H ;
Fukazawa, T ;
Tatsuma, T ;
Tryk, DA ;
Fujishima, A .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2001, 4 (03) :H1-H3
[28]   Surface carbonyl groups on oxidized diamond electrodes [J].
Notsu, H ;
Yagi, I ;
Tatsuma, T ;
Tryk, DA ;
Fujishima, A .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2000, 492 (01) :31-37
[29]   Surface functionalization of doped CVD diamond via covalent bond.: An XPS study on the formation of surface-bound quaternary pyridinium salt [J].
Ohtani, B ;
Kim, YH ;
Yano, T ;
Hashimoto, K ;
Fujishima, A ;
Uosaki, K .
CHEMISTRY LETTERS, 1998, (09) :953-954
[30]   Adsorption of guanine, guanosine, and adenine at electrodes studied by differential pulse voltammetry and electrochemical impedance [J].
Oliveira-Brett, AM ;
da Silva, LA ;
Brett, CMA .
LANGMUIR, 2002, 18 (06) :2326-2330