Modified GCE (modified + gce)

Distribution by Scientific Domains


Selected Abstracts


Selective Determination of Dopamine in the Presence of Ascorbic Acid at Porous-Carbon-Modified Glassy Carbon Electrodes

ELECTROANALYSIS, Issue 11 2008
Shuqing Song
Abstract Selective dopamine (DA) determinations using porous-carbon-modified glassy carbon electrodes (GCE) in the presence of ascorbic acid (AA) were studied. The effects of structure textures and surface functional groups of the porous carbons on the electrochemical behavior of DA was analyzed based on both cyclic voltammetry (CV) and differential pulse voltammetry (DPV) measurements. The differential pulse voltammetry of DA on the modified GCE was determined in the presence of 400-fold excess of AA, and the linear determination ranges of 0.05,0.99, 0.20,1.96, and 0.6,12.60,,M with the lowest detected concentrations of 4.5×10,3, 4.4×10,2, and 0.33,,M were obtained on the mesoporous carbon, mesoporous carbon with carboxylic and amino groups modified electrodes, respectively. [source]


Electrooxidation of DNA at Glassy Carbon Electrodes Modified with Multiwall Carbon Nanotubes Dispersed in Chitosan

ELECTROANALYSIS, Issue 7-8 2007
Soledad Bollo
Abstract We report on the analytical performance of glassy carbon (GCE) electrodes modified with a dispersion of multiwall carbon nanotubes (CNT) in chitosan (CHIT) for the quantification of DNA. The electroanalytical response of the resulting electrodes was evaluated using differential pulse voltammetry, while the electrochemical reactivity of the film surface was characterized using scanning electrochemical microscopy. Different treatments of the modified GCE were evaluated to improve the stability of the film and the accumulation of DNA. The guanine oxidation signal of double stranded calf-thymus DNA after 3-min accumulation was 20 times higher at GCE/CHIT-CNT cross-linked with glutaraldehyde (GTA) than at bare GCE, while the peak potential was around 45,mV less positive. The guanine oxidation signal demonstrated to be highly reproducible, with 3.4% RSD for 5 different electrodes. The treatment with sodium hydroxide demonstrated to be not effective since the resulting films were less stable and the guanine oxidation signal was ten times smaller compared to electrodes prepared with the GTA treated films. The effect of chitosan molecular weight used to prepare the dispersion and the amount of carbon nanotubes dispersed were evaluated. The response of single stranded DNA and oligo(dG)15 is also discussed. [source]


Adsorptive Stripping Voltammetric Detection of Single-Stranded DNA at Electrochemically Modified Glassy Carbon Electrode

ELECTROANALYSIS, Issue 23 2002
Huai-Sheng Wang
Abstract Electrochemically modified glassy carbon electrode (GCE) was used to study the electrochemical oxidation and detection of denatured single-stranded (ss) DNA by means of adsorptive stripping voltammetry. The modification of GCE, by electrochemical oxidation at +1.75,V (vs.SCE) for 10,min and cyclic sweep between +0.3,V and ,1.3,V for 20,cycles in pH,5.0 phosphate buffer, results in 100-fold improvement in sensitivity for ssDNA detection. We speculated that the modified GCE has a high affinity to single-stranded DNA through hydrogen bond (specific static adsorption). Single-stranded DNA can accumulate at the GCE surface at open circuit and produce a well-defined oxidation peak corresponding to the guanine residues at about +0.80,V in pH,5.0 phosphate buffer, while the native DNA gives no signal under the same condition. The peak currents are proportional to the ssDNA concentration in the range of 0,18.0,,g,mL,1. The detection limit of denatured ssDNA is ca. 0.2,,g mL,1 when the accumulation time is 8,min at open circuit. The accumulation mechanism of ssDNA on the modified GCE was discussed. [source]


Nucleic Acid Biosensor for Detection of Human Immunodeficiency Virus Using Aquabis(1,10-phenanthroline)copper(II) Perchlorate as Electrochemical Indicator

CHINESE JOURNAL OF CHEMISTRY, Issue 1 2008
Shu-Yan NIU
Abstract The electrochemical behavior of aquabis(1,10-phenanthroline)copper(II) perchlorate [Cu(H2O)(phen)2]·2ClO4, where phen=1,10-phenanthroline, on binding to DNA at a glassy carbon electrode (GCE) and in solution, was described. Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) results showed that [Cu(H2O)(phen)2]2+ had excellent electrochemical activity on the GCE with a couple of quasi-reversible redox peaks. The interaction mode between [Cu(H2O)(phen)2]2+ and double-strand DNA (dsDNA) was identified to be intercalative binding. An electrochemical DNA biosensor was developed with covalent immobilization of human immunodeficiency virus (HIV) probe for single-strand DNA (ssDNA) on the modified GCE. Numerous factors affecting the probe immobilization, target hybridization, and indicator binding reactions were optimized to maximize the sensitivity and speed of the assay. With this approach, a sequence of the HIV could be quantified over the range from 7.8×10,9 to 3.1×10,7 mol·L,1 with a linear correlation of ,=0.9987 and a detection limit of 1.3×10,9 mol·L,1. [source]