CT-DNA were electrochemically immobilized on the surfaces of both nano-goldmodified glassy carbon electrode and bare glassy carbon electrode. The cyclic voltammetricbehavior of Co (phen)33+adsorbed on the immobilized ...CT-DNA were electrochemically immobilized on the surfaces of both nano-goldmodified glassy carbon electrode and bare glassy carbon electrode. The cyclic voltammetricbehavior of Co (phen)33+adsorbed on the immobilized DNA was studied. Increase in the peakcurrent of Co (phen)33+ redox reaction was obtained on nano-gold modified glassy carbon electrode.The result suggests that more DNA molecules were immobilized on this electrode and nano-goldmodification can enhance the heterogeneous electron transfer rate constant of the Co (phen)33+.展开更多
The electrochemical behaviors (cyclic voltammetry, CV and different pulse voltammetry, DPV) of dopamine (DA) were studied in this paper. The result indicated that the oxidation of dopamine was controlled by diffusion ...The electrochemical behaviors (cyclic voltammetry, CV and different pulse voltammetry, DPV) of dopamine (DA) were studied in this paper. The result indicated that the oxidation of dopamine was controlled by diffusion and adsorption simultaneously at nano-gold (NG) modified carbon fiber electrode (CFE). This modified electrode can separate the peak potentials of dopamine and ascorbic acid (AA). The peak current of DA in DPV curve was found to be linearly proportional to the concentration of DA at range of 2.0?0-6～1.5?0-5mol/L and 1.0?0-5～5.0?0-4mol/L, respectively.展开更多
Nano-gold (NG) modified glassy carbon electrodes (GCEs) were used for determination of epinephrine (EP) in the presence of high concentration ascorbic acid (AA) by cyclic voltammetry (CV). This modified electrode can...Nano-gold (NG) modified glassy carbon electrodes (GCEs) were used for determination of epinephrine (EP) in the presence of high concentration ascorbic acid (AA) by cyclic voltammetry (CV). This modified electrode can not only catalytically oxidize EP and AA, but also separate the catalytic peak potentials of EP and AA by about 183.5 mV. In pH = 7.0 ogisogate byffer solution, the linear range of epinephrine was 5 ′ 106 ~ 1 × 10-4 mol/L.展开更多
The assembling of a coating of time-resolved fluorescent chelator BSPDA (abbreviated for 4,7-bis(sulfhydrylphenyl)-1,10-phenanthroline-2,9-dicarboxylic acid) onto a nano-gold layer was demonstrated. First, BSPDA was s...The assembling of a coating of time-resolved fluorescent chelator BSPDA (abbreviated for 4,7-bis(sulfhydrylphenyl)-1,10-phenanthroline-2,9-dicarboxylic acid) onto a nano-gold layer was demonstrated. First, BSPDA was synthesized by simple procedures, and then an approach was developed to immobilize BSPDA onto the nano-gold layer deposited on a silane modified glass substrate, whereby europium ion (Ⅲ, Eu3+) was captured and released owing to the interactive process of complexation and dissociation between BSPDA functionalized coating and Eu3+ solution. The fluorescence spectra and related lifetimes were determined. Also, the BSPDA functionalized coating′s specific complexation with Eu3+ on the BSPDA assembly layer and the nonspecific adsorption of Eu3+ on the nano-gold layer were compared. These results allowed a selective complexation of Eu3+ by assembling a BSPDA chelating layer on the nano-gold layer; thus, a tunable time-resolved fluorescent layer was covalently attached. The results of the nanoparticle assembling and probing (or labeling) processes to specific bio-systems were very interesting and had significant implications to time-resolved-fluorescence-based detection on biosensor surfaces such as DNA chip and to arrayed light display devices.展开更多
文摘CT-DNA were electrochemically immobilized on the surfaces of both nano-goldmodified glassy carbon electrode and bare glassy carbon electrode. The cyclic voltammetricbehavior of Co (phen)33+adsorbed on the immobilized DNA was studied. Increase in the peakcurrent of Co (phen)33+ redox reaction was obtained on nano-gold modified glassy carbon electrode.The result suggests that more DNA molecules were immobilized on this electrode and nano-goldmodification can enhance the heterogeneous electron transfer rate constant of the Co (phen)33+.
基金The authors gratefully acknowledge financial support from the Natural Science Foundation of Anhui Provincethe Natural Science Foundation of Anhui Education Committee(2001kj185).
文摘The electrochemical behaviors (cyclic voltammetry, CV and different pulse voltammetry, DPV) of dopamine (DA) were studied in this paper. The result indicated that the oxidation of dopamine was controlled by diffusion and adsorption simultaneously at nano-gold (NG) modified carbon fiber electrode (CFE). This modified electrode can separate the peak potentials of dopamine and ascorbic acid (AA). The peak current of DA in DPV curve was found to be linearly proportional to the concentration of DA at range of 2.0?0-6～1.5?0-5mol/L and 1.0?0-5～5.0?0-4mol/L, respectively.
基金The authors gratefully acknowledge financial support from the Natural Science Foundation of Anhui Province and the Natural Science Foundation of Anhui Education Committee.
文摘Nano-gold (NG) modified glassy carbon electrodes (GCEs) were used for determination of epinephrine (EP) in the presence of high concentration ascorbic acid (AA) by cyclic voltammetry (CV). This modified electrode can not only catalytically oxidize EP and AA, but also separate the catalytic peak potentials of EP and AA by about 183.5 mV. In pH = 7.0 ogisogate byffer solution, the linear range of epinephrine was 5 ′ 106 ~ 1 × 10-4 mol/L.
基金Project supported by the National Natural Science Foundation of China (20505020) the Natural Science Foundation ofGuangdong Province (06300086) +2 种基金 China Postdoctoral Science Foundation (20060390202) Scientific Research Fund ofHunan Provincial Education Department (05C508) Skeleton Youth Faculty Programof Hunan Higher Educational School
文摘The assembling of a coating of time-resolved fluorescent chelator BSPDA (abbreviated for 4,7-bis(sulfhydrylphenyl)-1,10-phenanthroline-2,9-dicarboxylic acid) onto a nano-gold layer was demonstrated. First, BSPDA was synthesized by simple procedures, and then an approach was developed to immobilize BSPDA onto the nano-gold layer deposited on a silane modified glass substrate, whereby europium ion (Ⅲ, Eu3+) was captured and released owing to the interactive process of complexation and dissociation between BSPDA functionalized coating and Eu3+ solution. The fluorescence spectra and related lifetimes were determined. Also, the BSPDA functionalized coating′s specific complexation with Eu3+ on the BSPDA assembly layer and the nonspecific adsorption of Eu3+ on the nano-gold layer were compared. These results allowed a selective complexation of Eu3+ by assembling a BSPDA chelating layer on the nano-gold layer; thus, a tunable time-resolved fluorescent layer was covalently attached. The results of the nanoparticle assembling and probing (or labeling) processes to specific bio-systems were very interesting and had significant implications to time-resolved-fluorescence-based detection on biosensor surfaces such as DNA chip and to arrayed light display devices.
