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111.
In this paper we report the desgin and synthesis of dihydroxyindoles oligomers based reversible fluorescence sensor.We find dihydroxyindoles-2-carboxylic acid derived oligmer(P-DHICA)has the highest selectivity and sensitivity for Cu^2+detection.This work provide a highly efficient,environmentally friendly biosensor for potential use in medical testing. 相似文献
112.
In this study, we fabricated an effective and sensitive DNA biosensor based on flower-like Pt/NiCo2O4 modified carbon paste electrode (FL-Pt/NiCo2O4/CPE) for detection of pramipexole (PPX). Spectrophotometry, differential pulse voltammetry (DPV) and docking methods were employed to evaluate the interaction of DNA-PPX. Moreover, the DPV technique was chosen to monitor the electrochemical response of guanine on the DNA biosensor. The relationship between the concentration of PPX and the oxidation signal of guanine was linear in the range of 0.4 to 310.0 μM and a limit of detection (LOD) of 0.09 μM was calculated. 相似文献
113.
In this study, an ITO (indium tin oxide) based biosensor was constructed to detect SOX2. SOX2 helps the regulation of cell pluripotency and is closely related to early embryonic development, neural and sexual differentiation. SOX2 is amplified and overexpressed in some malignant tumors such as squamous cell, lung, prostate, breast, esophageal cell, colon, ovarian, glioblastoma, pancreatic cancer, gastric cancer, head and neck squamous cell carcinoma. To generate a hydroxylated clean electrode surface, ITO electrodes were treated with NH4OH/H2O2/H2O. Later, ITO‐PET electrode surfaces were modified with 3‐glycidoxypropyl trimethoxysilane (3‐GOPS). Then, Anti‐SOX2 was covalently immobilized onto the electrode surfaces. 3‐GOPS concentration, Anti‐SOX2 concentration and incubation time, SOX2 incubation time were optimized. Electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) were utilized in order to follow up the immobilization processes and the optimization steps of the biosensor. To characterize the analytical properties of constructed immunosensor; linear range, repeatability, reproducibility and regeneration studies were investigated. The linear range of the immunosensor was detected as 0.625 pg/mL–62.5 pg/mL. Square wave voltammetry technique was also applied to the biosensor. Storage life of the biosensor was determined for identifying the possible usability of the biosensor in clinical field. Finally, the designed biosensor was applied to the real human serum samples. The results obtained with the presented biosensor were also compared with ELISA results. 相似文献
114.
115.
AbstractThe presented method of surface modification of single-crystal silicon by chemical etching makes it possible to obtain homogeneous nanostructured silicon layers with a thickness from 3 to 60?nm for application in micro- and nano-electronics as new multifunctional material. These results could be applied to the creation of sensitive photodetectors for visible and ultraviolet ranges. The method of scanning tunneling spectroscopy shows, that the changes in the thickness of nanostructured silicon layers affect the type of conductivity, and it opens new prospective for a practical application of nanostructured silicon in nano-electronics. The obtained current-voltage characteristics of nanostructured silicon layers showed different degrees of filling of the valence band, the conduction band and the appearance on the curve of the tunneling conductance of new peaks in the gas environment. The latter gives the possibility to use the method of scanning tunneling spectroscopy for a generation of gas and biosensors. The immune biosensor is proposed in the lab on a chip form based on the nanostructured silicon for the simultaneous analysis of numerous samples. The developed biosensor based on nanostructured silicon is very promising for use in so-called systems of lab-on-chip because it can be used for rapid analysis of various immune responses and is fully compatible with silicon planar technology used in the manufacturing of the semiconductor devices. 相似文献
116.
Rūta Araminaitė Rasa Garjonytė Albertas Malinauskas 《Central European Journal of Chemistry》2008,6(2):175-179
Kinetic study on the decomposition of Prussian Blue electrocatalytic layer during electrochemical reduction of hydrogen peroxide
has been studied in relation to biosensor application of this electrocatalyst. The decomposition has been shown to proceed
as a nearly exponential decay process and the corresponding first-order rate coefficients were determined. It has been shown
that the decomposition proceeds about 10 times faster in pH 7.3 buffer solution as compared to pH 5.5 buffer. A linear dependence
of the decomposition rate on the concentration of hydrogen peroxide has been found.
相似文献
117.
Povilas Virbickas Gerda Ziziunaite Arunas Ramanavicius Aušra Valiūnienė 《Electroanalysis》2023,35(4):e202200230
In this research a Hg2+ ion biosensor was developed by combining Prussian blue (PB) with glucose oxidase (GOx) – an enzyme that can be inhibited by Hg2+ ions. An application of PB in the design of Hg2+ ion biosensor enabled detecting changes in hydrogen peroxide reduction current at low operational potential of 0.2 vs Ag|AgCl,KClsat. The described Hg2+ ion biosensor exhibited wide linear range from 27 μM to 247 μM of Hg2+ and higher maximal detectable concentration of Hg2+ than other GOx inhibition-based biosensors, making it convenient for the analysis of samples with high concentration of Hg2+ ions. 相似文献
118.
Hydrogen peroxide biosensor based on electrodeposition of zinc oxide nanoflowers onto carbon nanotubes film electrode 总被引:2,自引:0,他引:2
Hui Ping Bai Xu Xiao Lu Guang Ming Yang Yun Hui Yang~* Department of Chemistry Chemical Engineering Yunnan Normal University Kunming China 《中国化学快报》2008,19(3):314-318
A new amperometric biosensor for hydrogen peroxide was developed based on adsorption of horseradish peroxidase at the glassy carbon electrode modified with zinc oxide nanoflowers produced by electrodeposition onto multi-walled carbon nanotubes (MWNTs) film. The morphology of the MWNTs/nano-ZnO electrode has been investigated by scanning electron microscopy (SEM), and the electrochemical performance of the electrode has also been studied by amperometric method. The resulting electrode offered an excellent detection for hydrogen peroxide at -0.11 V with a linear response range of 9.9×10^-7 to 2.9×10^-3 mol/L with a correlation coefficient of 0.991, and response time 〈5 s. The biosensor displays rapid response and expanded linear response range, and excellent stability. 相似文献
119.
A paste electrode (SWNT&RTIL PE) has been prepared using carboxylic group‐functionalized short single‐walled carbon nanotubes (SWNTs) mixed with 1‐butyl‐3‐methylimidazolium hexafluorophosphate (BMIMPF6, one kind of room temperature ionic liquid, RTIL). Its electrochemical behavior was investigated by cyclic voltammetry and electrochemical impedance spectroscopy in comparison with the paste electrode using mineral oil as a binder. Results highlighted the advantages of the paste electrode: not only higher conductivity, but also lower potential separation (ΔEp), higher peak current (ip) and better reversibility towards dopamine (DA), methylene blue (MB) and K3[Fe(CN)6]. The SWNT&RTIL PE could be used to detect the number of guanine bases and adenine bases contents in per mol oligonucleotides according to the current response in the range of 0.05–2.0 nM. Based on the current response of guanine bases, oligonucleotides could be detected sensitively in the B–R buffer solution with a detection limit of 9.9 pM. The heterogeneous electron transfer rate constant (ks) of guanine bases contents in the oligonucleotides was investigated and its value was 0.90 s?1. In essence the SWNT&RTIL PE showed high sensitivity, reliability, stability and reproducibility for the detection of DNA. 相似文献
120.
Andrea Kagie Daniel K. Bishop Jared Burdick Jeffrey T. La Belle Robert Dymond Robin Felder Joseph Wang 《Electroanalysis》2008,20(14):1610-1614
We describe here a miniaturized flexible thick‐film electrochemical biosensor flow detector, suitable for insertion into the lacrimal canaliculus towards minimally invasive amperometric monitoring of biomarkers in the tear fluid. Our focus here is on the microfabrication and in‐vitro testing of the new laterally rolled screen‐printed sensor. The new device responds rapidly and sensitively to dynamic changes in the levels of norepinephrine and glucose (the later in connection to glucose‐oxidase containing ink). Coverage of the enzyme electrode with an electropolymerized polytyramine minimizes contributions from the common electroactive interferences ascorbic and uric acids. Such attractive performance indicates great promise for minimally invasive monitoring of health biomarkers in the tear fluid, or in alternative usage such as capillary microelectrophoresis, ultralow volume sampling, or in‐flow (tubular) systems for batch processing of blood or culture media. 相似文献