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排序方式: 共有1019条查询结果,搜索用时 140 毫秒
1.
Keerakit Kaewket Pattanaphong Janphuang Peerawat Laohana Nantawat Tanapongpisit Wittawat Saenrang Kamonwad Ngamchuea 《Electroanalysis》2023,35(2):e202200200
Silver microelectrode arrays are fabricated by photolithography for a one-step analysis of H2O2 in low ionic strength samples. The effects of electrode length, width, band-to-band separation, connection height, and adhesion layer are evaluated. The developed sensor shows excellent repeatability (RSD=1.20 % (n=5)) and reproducibility (RSD=1.12 % (n=5)) with the linear range of 0.0–10.0 mM, the sensitivity of 9.84±0.34 μA mM−1, and the detection limit of 22.69 μM. The sensor has been successfully applied to detect H2O2 directly without the addition of supporting electrolyte in synthetic urine, tap water, drinking water, and milk samples. 相似文献
2.
Antônio Gomes dos Santos Neto Franciele de Matos Morawski Ana Caroline Ferreira Santos Cláudia Quintino da Rocha Roberto Batista de Lima Marília Oliveira Fonseca Goulart Clenilton Costa dos Santos Flávio Colmati Antônio Euzébio Goulart Santana Marco Aurélio Suller Garcia Auro Atsushi Tanaka 《Electroanalysis》2023,35(5):e202200390
Here, we report multiwalled carbon nanotubes (MWCNTs) functionalized with γ-cyclodextrins (γCD) as a novel electrochemical strategy for Rutin determination, showing superior performance than β-cyclodextrins (βCD) modified MWCNTs, suggesting an adequate environment for host-guest interactions. Under optimized conditions, the sensor showed a linear range of 39–975 nmol L−1 and a limit of detection of 7 nmol L−1. When tested with quercetin, catechin, and caffeine, the platform presented high selectivity with an interference response <10 %. The method was employed to quantify Rutin in spiked pharmaceutical and herbal extracts, providing recovery of 93–98.4 %. Also, HPLC-PDA confirmed the method‘s accuracy. 相似文献
3.
Teslime Erşan Didem Giray Dilgin Elif Kumrulu Umur Kumrulu Yusuf Dilgin 《Electroanalysis》2023,35(4):e202200295
This work describes the sensitive voltammetric determination of favipiravir (FAV) based on its reduction for the first time with a low-cost and disposable pencil graphite electrode (PGE). In addition, the determination of FAV was also performed based on its oxidation. Differential pulse (DP) voltammograms recorded in 0.5 M H2SO4 for the reduction of FAV show that peak currents increase linearly in the range of 1.0 to 600.0 μM with a limit of detection of 0.35 μM. The acceptable recovery values (98.9–106.0 %) obtained from a pharmaceutical tablet, real human urine, and artificial blood serum samples spiked with FAV confirm the high accuracy of the proposed method. 相似文献
4.
Electrochemical Behaviour and Rapid Determination of L‐Dopa at Electrochemically Pretreated Screen Printed Carbon Electrode 下载免费PDF全文
Andreea Alexandra Rabinca Mihaela Buleandra Adriana Balan Ioan Stamatin Anton Alexandru Ciucu 《Electroanalysis》2015,27(10):2275-2279
A simple and rapid voltammetric method based on a disposable electrochemically pretreated screen‐printed carbon electrode is proposed for the determination of L ‐dopa. Under optimum differential pulse voltammetry conditions a limit of detection of 3.6×10?7 M for L ‐dopa was obtained. The method was successfully applied to the determination of L ‐dopa in a commercial pharmaceutical formulation. 相似文献
5.
Microwire Chronoamperometric Determination of Concentration,Diffusivity, and Salinity for Simultaneous Oxygen and Proton Reduction 下载免费PDF全文
A microwire chronoamperometric method is reported employing a 25 µm diameter platinum microwire for multi‐parameter electroanalysis with digital simulation‐based evaluation (employing DigiElch 4.F). Concentration and diffusion coefficient data are obtained for the reduction of oxygen and for the reduction of protons individually and simultaneously in saline (0.1 M to 4.0 M NaCl) electrolyte media. The diffusion coefficient and concentration data for oxygen allows salinity levels to be estimated. The microwire chronoamperometry method offers versatility and precision due to (i) a slow approach to steady state (when compared to microdisc methods) and (ii) insignificant viscosity effects (when compared to hydrodynamic methods). 相似文献
6.
Nanomolar Determination of Methyldopa in the Presence of Large Amounts of Hydrochlorothiazide Using a Carbon Paste Electrode Modified with Graphene Oxide Nanosheets and 3‐(4′‐Amino‐3′‐hydroxy‐biphenyl‐4‐yl)‐acrylic Acid 下载免费PDF全文
A novel electrochemical sensor for sensitive detection of methyldopa at physiological pH was developed by the bulk modification of carbon paste electrode (CPE) with graphene oxide nanosheets and 3‐(4′‐amino‐3′‐hydroxy‐biphenyl‐4‐yl)‐acrylic acid (3,′AA). Applying square wave voltammetry (SWV), in phosphate buffer solution (PBS) of pH 7.0, the oxidation current increased linearly with two concentration intervals of methyldopa, one is 1.0×10?8–1.0×10?6 M and the other is 1.0×10?6–4.5×10?5 M. The detection limit (3σ) obtained by SWV was 9.0 nM. The modified electrode was successfully applied for simultaneous determination of methyldopa and hydrochlorothiazide. Finally, the proposed method was applied to the determination of methyldopa and hydrochlorothiazide in some real samples. 相似文献
7.
8.
Determination of Allura Red and Tartrazine in Food Samples by Sequential Injection Analysis Combined with Voltammetric Detection at Antimony Film Electrode 下载免费PDF全文
J. A. Rodríguez M. G. Juárez C. A. Galán‐Vidal J. M. Miranda E. Barrado 《Electroanalysis》2015,27(10):2329-2334
An antimony film electrode prepared on‐line and installed as part of a sequential injection system, was used as an electrochemical detector to determine azo dyes in food samples. The influence of several flow variables were evaluated using a central composite design. In optimal conditions, the linear range of the calibration curve varied from 1–5 µM, with a limit of detection limit of 0.3 µM. The relative standard deviation of analytical repeatability was <5.0 %.The method was validated by comparing the results obtained with those provided by HPLC; no significant difference were seen. 相似文献
9.
Tau protein undergoes complex biochemical processes involved in normal and diseased cellular functions; specifically, tau pathology has been linked to neurodegeneration. At the heart of tau biochemistry are three pillars: microtubules, phosphorylation, and aggregation. However, these three processes are also regulated through other biomolecules in the biological setting, such as metal ions and small and larger ligands, including proteins and nucleic acids. This review describes the latest electrochemical approaches toward greater understanding of tau biochemistry, early disease diagnosis, and drug inhibitor screening. 相似文献
10.
In this article, we introduced a novel electrochemical biosensor for the detection of microRNA-126. The biosensor utilizes a hybridization assay combined with multi-walled carbon nanotubes and gold nanorod-decorated screen-printed carbon electrodes. For electrode preparation, gold nanorods were first immobilized onto the surface of bare and multi-walled carbon nanotube-modified screen-printed carbon electrodes, and the thiol tagged-capture probe was immobilized on the electrode surface through gold and thiol group interaction. After the immobilization, thiol tagged-capture probe hybridized with the target sequence. Under optimum conditions, we determined limit of detection (LOD) and limit of quantification (LOQ) as high as 11 nM and 36 nM, respectively. 相似文献