A Nonenzymatic Biosensor Based on Gold Electrodes Modified with Peptide Self-Assemblies for Detecting Ammonia and Urea Oxidation

被引:57
作者
Bianchi, Roberta C. [1 ]
da Silva, Emerson Rodrigo [1 ]
Dall'Antonia, Luiz H. [2 ]
Ferreira, Fabio Furlan [1 ]
Alves, Wendel Andrade [1 ]
机构
[1] Univ Fed ABC, Ctr Ciencias Nat & Humanas, BR-09210580 Santo Andre, SP, Brazil
[2] Univ Estadual Londrina, Ctr Ciencias Exatas, Dept Quim, BR-86057970 Londrina, PR, Brazil
基金
巴西圣保罗研究基金会;
关键词
MOLECULAR RECOGNITION; NANOTUBES; DIPHENYLALANINE; NANOWIRES; WATER; GENERATION; SENSOR; IONS;
D O I
10.1021/la502315m
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have developed a nonenzymatic biosensor for the detection of ammonia and urea oxidation based on the deposition of peptide microstructures onto thiolated gold electrodes. FF-MNSs/MCP/Au assemblies were obtained by modifying gold substrates with 4-mercaptopyridine (MCP), followed by coating with l,l-diphenylalanine micro/nanostructures (FF-MNSs) grown in the solid-vapor phase. Benzene rings and amide groups with peptide micro/nanostructures interact with synthetic NH4(+) receptors through cation-? and hydrogen bonding. AuOH clusters on the Au surface provided the catalytic sites. The application of a predetermined concentration of analytes at the peptide interfaces activated the catalytic sites. We observed a relationship between the stability of films and the crystal structure of peptides, and we organized the FF-MNSs into an orthorhombic symmetry that was the most suitable assembly for creation of our biosensors. At 0.1 mol L(-1) NaOH, these FF-MNSs/MCP/Au electrodes have electrocatalytic properties regarding ammonia and urea oxidation that are comparable to those of enzyme-based architectures. Under optimal conditions, the electrocatalytic response is proportional to the ammonia and urea concentration in the range 0.1-1.0 mmol L(-1). The sensitivity was calculated as 2.83 and 81.3 ?A mmol L(-1) cm(-2) for ammonia and urea, respectively, at +0.40 V (vs SCE). Our detection method is easy to follow, does not require a mediator or enzyme, and has strong potential for detecting urea via nonenzymatic routes
引用
收藏
页码:11464 / 11473
页数:10
相关论文
共 60 条
[1]   Potentiometric urea biosensor based on multi-walled carbon nanotubes (MWCNTs)/silica composite material [J].
Ahuja, Tarushee ;
Kumar, D. ;
Singh, Nahar ;
Biradar, A. M. ;
Rajesh .
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, 2011, 31 (02) :90-94
[2]   Micro- and nano-sized peptidic assemblies prepared via solid-vapor approach: Morphological and spectroscopic aspects [J].
Amaral, H. R. ;
Kogikoski, S., Jr. ;
Silva, E. R. ;
Souza, J. A. ;
Alves, W. A. .
MATERIALS CHEMISTRY AND PHYSICS, 2012, 137 (02) :628-636
[3]   The effects of water molecules on the electronic and structural properties of peptide nanotubes [J].
Andrade-Filho, T. ;
Ferreira, Fabio Furlan ;
Alves, Wendel Andrade ;
Rocha, Alexandre Reily .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2013, 15 (20) :7555-7559
[4]   Carrier-based ion-selective electrodes and bulk optodes. 2. Ionophores for potentiometric and optical sensors [J].
Buhlmann, P ;
Pretsch, E ;
Bakker, E .
CHEMICAL REVIEWS, 1998, 98 (04) :1593-1687
[5]  
Burke LD, 2000, J SOLID STATE ELECTR, V4, P285
[6]   Interplay of metal ions and urease [J].
Carter, Eric L. ;
Flugga, Nicholas ;
Boer, Jodi L. ;
Mulrooney, Scott B. ;
Hausinger, Robert P. .
METALLOMICS, 2009, 1 (03) :207-221
[7]   Axial divergence in a conventional X-ray powder diffractometer. II. Realization and evaluation in a fundamental-parameter profile fitting procedure [J].
Cheary, RW ;
Coelho, AA .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1998, 31 (pt 6) :862-868
[8]   A FUNDAMENTAL PARAMETERS APPROACH TO X-RAY LINE-PROFILE FITTING [J].
CHEARY, RW ;
COELHO, A .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1992, 25 (pt 2) :109-121
[9]   Portable urea biosensor based on the extended-gate field effect transistor [J].
Chen, JC ;
Chou, JC ;
Sun, TP ;
Hsiung, SK .
SENSORS AND ACTUATORS B-CHEMICAL, 2003, 91 (1-3) :180-186
[10]   Spatial organization of peptide nanotubes for electrochemical devices [J].
Cipriano, T. C. ;
Takahashi, P. M. ;
de Lima, D. ;
Oliveira, V. X., Jr. ;
Souza, J. A. ;
Martinho, H. ;
Alves, W. A. .
JOURNAL OF MATERIALS SCIENCE, 2010, 45 (18) :5101-5108