Immobilization of purine bases on a poly-4-aminophenol matrix

被引:31
作者
Brito-Madurro, Ana Graci
Ferreira, Lucas Franco
Vieira, Sabrina Nunes
Ariza, Rafael Goncalves
Goulart, Luiz Ricardo
Madurro, Joao Marcos
机构
[1] Univ Fed Uberlandia, Inst Quim, Lab Filmes Polimericos, BR-38400902 Uberlandia, MG, Brazil
[2] Univ Fed Uberlandia, Fac Engn Mecan, Lab Tribol Mat, BR-38400902 Uberlandia, MG, Brazil
[3] Univ Fed Uberlandia, Inst Genet & Bioquim, Mol Genet Lab, BR-38400902 Uberlandia, MG, Brazil
关键词
D O I
10.1007/s10853-006-0235-0
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Conducting polymers or semi-conductors have various features that make them excellent materials for the immobilization of biomolecules and the rapid transfer of electrons necessary for the production of biosensors. Conducting electroactive polymers of poly-4-aminophenol have been developed as sensors to detect the purine bases (adenosine triphosphate, ATP and guanosine triphosphate, GTP) of DNA. The electrooxidation of 4-aminophenol onto a graphite electrode in the presence of perchloric acid yielded thin polymer films. The conductivity was studied by cyclic voltammetry and surface morphology by optical microscopy and interferometry. The immobilization and detection of ATP and GTP on a graphite electrode or modified electrode coated with poly-4-aminophenol was studied by cyclic voltammetry. Systematic variation of the experimental conditions that influenced the electrode reaction, particularly the pH of the electrolytic solution, showed that the oxidation potentials of the immobilized ATP or GTP in the modified electrodes decreased with increasing pH of the electrolyte. When these conditions were optimized based on voltammetric measurements, modified electrodes coated with poly-4-aminophenol were found to be efficient in immobilizing purine bases, and increased the amplitude of the ATP and GTP signals by similar to 1.5 and similar to 24 times, respectively, when compared with non-coated graphite surfaces.
引用
收藏
页码:3238 / 3243
页数:6
相关论文
共 36 条
[21]   Electrochemical oxidation mechanism of guanine and adenine using a glassy carbon microelectrode [J].
Oliveira-Brett, AM ;
Diculescu, V ;
Piedade, JAP .
BIOELECTROCHEMISTRY, 2002, 55 (1-2) :61-62
[22]  
OSAMA O, 1992, ELECTR COMMUN JPN, V75, P1123
[23]   Detecting DNA hybridization and damage [J].
Palecek, E ;
Fojta, M .
ANALYTICAL CHEMISTRY, 2001, 73 (03) :74A-83A
[24]   AFM and electroanalytical studies of synthetic oligonucleotide hybridization [J].
Paquim, AMC ;
Diculescu, VC ;
Oretskaya, TS ;
Brett, AMO .
BIOSENSORS & BIOELECTRONICS, 2004, 20 (05) :933-944
[25]  
SVEDMYR N, 1985, EXCERPTA MED, P135
[26]   Polyaniline synthesis and its biosensor application [J].
Tahir, ZM ;
Alocilja, EC ;
Grooms, DL .
BIOSENSORS & BIOELECTRONICS, 2005, 20 (08) :1690-1695
[27]   DNA sensing on a DNA probe-modified electrode using ferrocenylnaphthalene diimide as the electrochemically active ligand [J].
Takenaka, S ;
Yamashita, K ;
Takagi, M ;
Uto, Y ;
Kondo, H .
ANALYTICAL CHEMISTRY, 2000, 72 (06) :1334-1341
[28]   Cutting out the middleman: DNA biosensors based on electrochemical oxidation [J].
Thorp, HH .
TRENDS IN BIOTECHNOLOGY, 1998, 16 (03) :117-121
[29]   A polytyramine film for covalent immobilization of oligonucleotides and hybridization [J].
Tran, LD ;
Piro, B ;
Pham, MC ;
Ledoan, T ;
Angiari, C ;
Dao, LH ;
Teston, F .
SYNTHETIC METALS, 2003, 139 (02) :251-262
[30]  
Trivedi D. C., 1997, HDB ORGANIC CONDUCTI, V2, P505