Poly-L-lysine(PLL) was first electrodeposited onto the surface of a glassy carbon(GC) electrode.The PLL modified electrode was used to immobilize chloroperoxidase(CPO) via 1-[(3-dimethylamino)propyl]-3-ethylcarbodiimi...Poly-L-lysine(PLL) was first electrodeposited onto the surface of a glassy carbon(GC) electrode.The PLL modified electrode was used to immobilize chloroperoxidase(CPO) via 1-[(3-dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride(EDC).The electrochemical behaviors of immobilized CPO on PLL/GC electrode were investigated by cyclic voltammetry(CV).The CV results obtained showed that CPO was successfully immobilized on the PLL/GC electrode and a fast direct electron transfer between CPO and PLL-GC electrod...展开更多
A voltammetric sensor based on the electropolymerization of cobalt-poly(methionine)(Co-poly(Met)) on a glassy carbon electrode (GCE) was developed and applied for the determination of estriol by differential pulse vol...A voltammetric sensor based on the electropolymerization of cobalt-poly(methionine)(Co-poly(Met)) on a glassy carbon electrode (GCE) was developed and applied for the determination of estriol by differential pulse voltammetry (DPV) for the first time. The electrochemical properties of the Co-poly(Met)/GCE were analysed by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) were used to characterize the polymers on the GCE surface. The deposition of the Co-poly(Met) film on the GCE surface enhanced the sensor electronic transfer. CV studies revealed that estriol exhibits an irreversible oxidation peak at t0.58 V for the Co-poly(Met)/GCE (vs. Ag/AgCl reference electrode) in 0.10 mol/L Britton-Robinson buffer solution (pH=7.0). Different voltammetric scan rates (10-200 mV/s) suggested that the estriol oxidation on the Co-poly(Met)/GCE surface is controlled by adsorption and diffusion processes. Based on the optimized DPV conditions, the linear responses for estriol quantification were from 0.596 μmol/L to 4.76 μmol/L (R2 =0.996) and from 5.66 μmol/L to 9.90 μmol/L (R2 =0.994) with a limit of detection (LOD) of 0.0340 μmol/L and a limit of quantification (LOQ) of 0.113 μmol/L. The DPV-Co-poly(Met)/GCE method provided good intra-day and inter-day repeatability with RSD values lower than 5%. Also, no interference of real sample matrices was observed on the estriol voltammetric response, making the DPV-Copoly( Met)/GCE highly selective for estriol. The accuracy test showed that the estriol recovery was in the ranges 96.7%-103% and 98.7%-102% for pharmaceutical tablets and human urine, respectively. The estriol quantification in pharmaceutical tablets performed by the Co-poly(Met)/GCE-assisted DPV method was comparable to the official analytical protocols.展开更多
The immobilization of SiW_(12)O_(40)^(4-)in poly(4-aminoazobenzene)film was done by electrochemical method.According to the continuous cyclic voltammograms of the modified electrode,it can be determined that SiW_(12)O...The immobilization of SiW_(12)O_(40)^(4-)in poly(4-aminoazobenzene)film was done by electrochemical method.According to the continuous cyclic voltammograms of the modified electrode,it can be determined that SiW_(12)O_(40)^(4-) in the polymer is very stable.The paper reports the elecctrochemical pro- perties of the modified electrode,Moreover,it was found that the modified electrode exhibits electrocatalysis for the reaction of oxygen.展开更多
A nanostructured polymer film incorporated gold nanoparticles modified electrode was fabricated. The fabrication process involved a previous electropolymerization of aspartic acid and followed by the eletrodeposition ...A nanostructured polymer film incorporated gold nanoparticles modified electrode was fabricated. The fabrication process involved a previous electropolymerization of aspartic acid and followed by the eletrodeposition of gold nano-particles on the glassy carbon electrode. The resulting poly (aspartic acid)-nanogold modified electrode (PAA- nano-Au/GCE) was characterized by scanning electron microscopy (SEM) and electrochemical impedance spectros-copy (EIS). A higher catalytic activity was obtained to electrocatalytic oxidation of dopamine (DA), ascorbic acid (AA) and uric acid (UA) due to the enhanced peak current and well-defined peak separations compared with three, bare GCE, PAA/GCE and nano-Au/GCE. Simultaneous determination of DA, AA, and UA were studied by voltammetry. The linear range of 5.0 × 10-7 - 1.0 × 10-4 M for DA, 5.0 × 10-6 - 2.0 × 10-3 M for AA and 5.0 × 10-6 - 1.0 × 10-3 M for UA was obtained. The detection limit was calculated for DA, AA and UA as being 6.5 × 10-8 M, 5.6 × 10-7 M and 3.0 × 10-7 M, respectively (S/N = 3). The practical application of the present modified electrode was demonstrated by the determination of DA, AA and UA in calf serum and fetal calf serum samples.展开更多
Based on the molecular recognition ability of conductive polymer and the peculiar properties of carbon nanotubes, a novel single wall nanotubes (SWNTs) compound poly(4- aminopyridine) modified electrode (SWNTs/POAPE) ...Based on the molecular recognition ability of conductive polymer and the peculiar properties of carbon nanotubes, a novel single wall nanotubes (SWNTs) compound poly(4- aminopyridine) modified electrode (SWNTs/POAPE) is prepared at glass carbon electrode (GCE). The electrochemistry response of nitrophenol isomers is studied at the SWNTs/POAPE. The re-sult indicates that o-, m- and p-nitrophenol are separated entirely at the SWNTs/POAPE interface. The electrode present here can be easily used to determine nitrophenol isomers simultaneously with higher sensitivity.展开更多
A composite film of DNA/poly(3-methylthiophene)(P3MT) modified glassy carbon electrode(GCE) has been fabricated by electro-deposition method.P3MT film was first electropolymerized at the GCE and the DNA layer was then...A composite film of DNA/poly(3-methylthiophene)(P3MT) modified glassy carbon electrode(GCE) has been fabricated by electro-deposition method.P3MT film was first electropolymerized at the GCE and the DNA layer was then immobilized on the P3MT layer by electrochemical method.The voltammetric behavior of 8-hydroxy-2'-deoxyguanosine(8-OH-dG) at the composite film modified electrode was studied.The effects of scan rates,pH and the interference of uric acid(UA) on the voltammetric behavior and detection of 8-OH-dG were also discussed.The experimental results suggest that the electrochemical behavior of 8-OH-dG at the composite film modified electrode was greatly improved due to the combination of the advantages of P3MT and DNA.In 0.1 M pH 7.0 phosphate buffer solution(PBS),the anodic peak currents of 8-OH-dG were linear with the 8-OH-dG concentration in two intervals,viz.0.28―4.2 μM and 4.2―19.6 μM.The detection limit of 56 nM 8-OH-dG could be estimated(S/N=3).This proposed composite film modified electrode shows excellent reproducibility and stability.It may have the potential application for the detection of 8-OH-dG in human urine.展开更多
The electrochemical behaviors of shikonin at a poly（diallyldimethylammonium chloride） functionalized graphene sheets modified glass carbon electrode（PDDA-GS/GCE） have been investigated. Shikonin could exhibit a pa...The electrochemical behaviors of shikonin at a poly（diallyldimethylammonium chloride） functionalized graphene sheets modified glass carbon electrode（PDDA-GS/GCE） have been investigated. Shikonin could exhibit a pair of well-defined redox peaks at the PDDA-GS/GCE located at 0.681 V（Epa） and 0.662 V（Epc）[vs. saturated calo- mel electrode（SCE）] in 0.1 mol/L phosphate buffer solution（pH=2.0） with a peak-to-peak separation of about 20 mV, revealing a fast electron-transfer process. Moreover, the current response was remarkably increased at PDDA- GS/GCE compared with that at the bare GCE. The electrochemical behaviors of shikonin at the modified electrode were investigated. And the results indicate that the reaction involves the transfer of two electrons, accompanied by two protons and the electrochemical process is a diffusional-controlled electrode process. The electrochemical para- meters of shikonin at the modified electrode, the electron-transfer coefficient（a）, the electron-transfer number（n） and the electrode reaction rate constant（ks） were calculated to be as 0.53, 2.18 and 3.6 s^-1, respectively. Under the optimal conditions, the peak current of differential pulse voltammetry（DPV） increased linearly with the shikonin concentra- tion in a range from 9A72×10^-8 mol/L to 3,789×10^-6 mol/L with a detection limit of 3,157× 10^-8 mol/L. The linear regression equation was Ip=O.7366c＋0.7855（R=0.9978; lp： 10-7 A, c： 10-8 mol/L）. In addition, the modified glass carbon electrode also exhibited good stability, selectivity and acceptable reproducibility that could be used for the sensitive, simple and rapid determination of shikonin in real samples. Therefore, the present work offers a new way to broaden the analytical application of graphene in pharmaceutical analysis.展开更多
基金supported by grant from National Natural Science Foundation of China(No.20775049).
文摘Poly-L-lysine(PLL) was first electrodeposited onto the surface of a glassy carbon(GC) electrode.The PLL modified electrode was used to immobilize chloroperoxidase(CPO) via 1-[(3-dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride(EDC).The electrochemical behaviors of immobilized CPO on PLL/GC electrode were investigated by cyclic voltammetry(CV).The CV results obtained showed that CPO was successfully immobilized on the PLL/GC electrode and a fast direct electron transfer between CPO and PLL-GC electrod...
基金CNPq (454438/2014-1)CAPES+1 种基金FINEPFAPEMIG for the financial support to this work
文摘A voltammetric sensor based on the electropolymerization of cobalt-poly(methionine)(Co-poly(Met)) on a glassy carbon electrode (GCE) was developed and applied for the determination of estriol by differential pulse voltammetry (DPV) for the first time. The electrochemical properties of the Co-poly(Met)/GCE were analysed by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) were used to characterize the polymers on the GCE surface. The deposition of the Co-poly(Met) film on the GCE surface enhanced the sensor electronic transfer. CV studies revealed that estriol exhibits an irreversible oxidation peak at t0.58 V for the Co-poly(Met)/GCE (vs. Ag/AgCl reference electrode) in 0.10 mol/L Britton-Robinson buffer solution (pH=7.0). Different voltammetric scan rates (10-200 mV/s) suggested that the estriol oxidation on the Co-poly(Met)/GCE surface is controlled by adsorption and diffusion processes. Based on the optimized DPV conditions, the linear responses for estriol quantification were from 0.596 μmol/L to 4.76 μmol/L (R2 =0.996) and from 5.66 μmol/L to 9.90 μmol/L (R2 =0.994) with a limit of detection (LOD) of 0.0340 μmol/L and a limit of quantification (LOQ) of 0.113 μmol/L. The DPV-Co-poly(Met)/GCE method provided good intra-day and inter-day repeatability with RSD values lower than 5%. Also, no interference of real sample matrices was observed on the estriol voltammetric response, making the DPV-Copoly( Met)/GCE highly selective for estriol. The accuracy test showed that the estriol recovery was in the ranges 96.7%-103% and 98.7%-102% for pharmaceutical tablets and human urine, respectively. The estriol quantification in pharmaceutical tablets performed by the Co-poly(Met)/GCE-assisted DPV method was comparable to the official analytical protocols.
文摘The immobilization of SiW_(12)O_(40)^(4-)in poly(4-aminoazobenzene)film was done by electrochemical method.According to the continuous cyclic voltammograms of the modified electrode,it can be determined that SiW_(12)O_(40)^(4-) in the polymer is very stable.The paper reports the elecctrochemical pro- perties of the modified electrode,Moreover,it was found that the modified electrode exhibits electrocatalysis for the reaction of oxygen.
文摘A nanostructured polymer film incorporated gold nanoparticles modified electrode was fabricated. The fabrication process involved a previous electropolymerization of aspartic acid and followed by the eletrodeposition of gold nano-particles on the glassy carbon electrode. The resulting poly (aspartic acid)-nanogold modified electrode (PAA- nano-Au/GCE) was characterized by scanning electron microscopy (SEM) and electrochemical impedance spectros-copy (EIS). A higher catalytic activity was obtained to electrocatalytic oxidation of dopamine (DA), ascorbic acid (AA) and uric acid (UA) due to the enhanced peak current and well-defined peak separations compared with three, bare GCE, PAA/GCE and nano-Au/GCE. Simultaneous determination of DA, AA, and UA were studied by voltammetry. The linear range of 5.0 × 10-7 - 1.0 × 10-4 M for DA, 5.0 × 10-6 - 2.0 × 10-3 M for AA and 5.0 × 10-6 - 1.0 × 10-3 M for UA was obtained. The detection limit was calculated for DA, AA and UA as being 6.5 × 10-8 M, 5.6 × 10-7 M and 3.0 × 10-7 M, respectively (S/N = 3). The practical application of the present modified electrode was demonstrated by the determination of DA, AA and UA in calf serum and fetal calf serum samples.
基金the Natural Science Foundation of Henan Province,China(Grant No.0311021000)the Key Laboratory of Environmental Science and Engineering,Education Commission of Henan Province.
文摘Based on the molecular recognition ability of conductive polymer and the peculiar properties of carbon nanotubes, a novel single wall nanotubes (SWNTs) compound poly(4- aminopyridine) modified electrode (SWNTs/POAPE) is prepared at glass carbon electrode (GCE). The electrochemistry response of nitrophenol isomers is studied at the SWNTs/POAPE. The re-sult indicates that o-, m- and p-nitrophenol are separated entirely at the SWNTs/POAPE interface. The electrode present here can be easily used to determine nitrophenol isomers simultaneously with higher sensitivity.
基金Supported by the National Natural Science Foundation of China (Grant Nos. 20475024 & 20775031)the Shandong Tai-Shan Scholar Research Fund
文摘A composite film of DNA/poly(3-methylthiophene)(P3MT) modified glassy carbon electrode(GCE) has been fabricated by electro-deposition method.P3MT film was first electropolymerized at the GCE and the DNA layer was then immobilized on the P3MT layer by electrochemical method.The voltammetric behavior of 8-hydroxy-2'-deoxyguanosine(8-OH-dG) at the composite film modified electrode was studied.The effects of scan rates,pH and the interference of uric acid(UA) on the voltammetric behavior and detection of 8-OH-dG were also discussed.The experimental results suggest that the electrochemical behavior of 8-OH-dG at the composite film modified electrode was greatly improved due to the combination of the advantages of P3MT and DNA.In 0.1 M pH 7.0 phosphate buffer solution(PBS),the anodic peak currents of 8-OH-dG were linear with the 8-OH-dG concentration in two intervals,viz.0.28―4.2 μM and 4.2―19.6 μM.The detection limit of 56 nM 8-OH-dG could be estimated(S/N=3).This proposed composite film modified electrode shows excellent reproducibility and stability.It may have the potential application for the detection of 8-OH-dG in human urine.
文摘The electrochemical behaviors of shikonin at a poly（diallyldimethylammonium chloride） functionalized graphene sheets modified glass carbon electrode（PDDA-GS/GCE） have been investigated. Shikonin could exhibit a pair of well-defined redox peaks at the PDDA-GS/GCE located at 0.681 V（Epa） and 0.662 V（Epc）[vs. saturated calo- mel electrode（SCE）] in 0.1 mol/L phosphate buffer solution（pH=2.0） with a peak-to-peak separation of about 20 mV, revealing a fast electron-transfer process. Moreover, the current response was remarkably increased at PDDA- GS/GCE compared with that at the bare GCE. The electrochemical behaviors of shikonin at the modified electrode were investigated. And the results indicate that the reaction involves the transfer of two electrons, accompanied by two protons and the electrochemical process is a diffusional-controlled electrode process. The electrochemical para- meters of shikonin at the modified electrode, the electron-transfer coefficient（a）, the electron-transfer number（n） and the electrode reaction rate constant（ks） were calculated to be as 0.53, 2.18 and 3.6 s^-1, respectively. Under the optimal conditions, the peak current of differential pulse voltammetry（DPV） increased linearly with the shikonin concentra- tion in a range from 9A72×10^-8 mol/L to 3,789×10^-6 mol/L with a detection limit of 3,157× 10^-8 mol/L. The linear regression equation was Ip=O.7366c＋0.7855（R=0.9978; lp： 10-7 A, c： 10-8 mol/L）. In addition, the modified glass carbon electrode also exhibited good stability, selectivity and acceptable reproducibility that could be used for the sensitive, simple and rapid determination of shikonin in real samples. Therefore, the present work offers a new way to broaden the analytical application of graphene in pharmaceutical analysis.
