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Electrochemical determination of pharmaceuticals in spiked water samples

May 3, 2010 by · Leave a Comment 

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This digital document is a journal article from Journal of Hazardous Materials, published by Elsevier in . The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

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The electrochemical behaviour of acidic and neutral pharmaceutical active compounds (PhACs) was studied by cyclic voltammetry and pulse voltammetric techniques on mercury, carbon nanotube paste, carbon paste and gold electrodes. The best results, in terms of sensitivity, linearity range and detection limits, were obtained by differential pulse voltammetry (DPV) for ofloxacin (LOD 5.2@mM), differential pulse polarography (DPP) for clofibric acid (LOD 4.7@mM) and normal pulse voltammetry (NPV) for diclofenac (LOD 0.8@mM) and propranolol (LOD 0.5@mM). An enrichment step of approximately two orders of magnitude was performed by a solid-phase extraction procedure (SPE) in order to concentrate the samples. The developed method was optimized and tested on spiked river water samples.

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Amperometric determination of -N-methylsalsolinol and monoamine neurotransmitters with liquid chromatography using functionalized multi-wall …

May 3, 2010 by · Leave a Comment 

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This digital document is a journal article from Analytica Chimica Acta, published by Elsevier in 2004. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

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The fabrication and application of a novel electrochemical detection (ED) system with the functionalized multi-wall carbon nanotubes (MWNTs) chemically modified electrode (CME) for liquid chromatography (LC) were described. The electrochemical behaviors of dopamine (DA) at the CME were investigated by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). It was found that the CME exhibited efficiently electrocatalytic effect on the current responses of (R)-salsolinol ((R)-Sal), (R)-N-methylsalsolinol ((R)-NMSal), and monoamine neurotransmitters with high sensitivity, stability, and long-life of activity. In LC-ED, all (R)-Sal, (R)-NMSal, DA, norepinephrine (NE), 3-methoxy-4-hydroxyphenylglycol (MHPG), 3,4-dihydroxyphenylacetic acid (DOPAC), 5-hydroxytryptamine (5-HT), 5-hydroxyindoleacetic acid (5-HIAA), and homovanillic acid (HVA) had good and stable current responses at the CME. The linear ranges of the nine analytes were over three orders of magnitude (R^2>0.995). The application of this method coupled with microdialysis sampling for the determination of (R)-Sal, (R)-NMSal, and monoamine neurotransmitters in Parkinson’s patients’ cerebrospinal fluid was satisfactory.

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Electrical detection of deoxyribonucleic acid hybridization based on carbon-nanotubes/nano zirconium dioxide/chitosan-modified electrodes

May 1, 2010 by · Leave a Comment 

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This digital document is a journal article from Analytica Chimica Acta, published by Elsevier in 2007. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

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A novel and sensitive electrochemical DNA biosensor based on nanoparticles ZrO”2 and multi-walled carbon nanotubes (MWNTs) for DNA immobilization and enhanced hybridization detection is described. The MWNTs/nano ZrO”2/chitosan-modified glassy carbon electrode (GCE) was fabricated and oligonucleotides were immobilized to the GCE. The hybridization reaction on the electrode was monitored by differential pulse voltammetry (DPV) analysis using electroactive daunomycin as an indicator. Compared with previous DNA sensors with oligonucleotides directly incorporated on carbon electrodes, this carbon nanotube-based assay with its large surface area and good charge-transport characteristics increased DNA attachment quantity and complementary DNA detection sensitivity. The response signal increases linearly with the increase of the logarithm of the target DNA concentration in the range of 1.49×10^-^1^0 to 9.32×10^-^8molL^-^1 with the detection limit of 7.5×10^-^1^1molL^-^1 (S/N=3). The linear regression equation is I=32.62+3.037logC”D”N”A (molL^-^1) with a correlation coefficient value of 0.9842. This is the first application of carbon nanotubes combined with nano ZrO”2 to the fabrication of an electrochemical DNA biosensor with a favorable performance for the rapid detection of specific hybridization.

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Electrochemical DNA biosensors based on platinum nanoparticles combined carbon nanotubes

May 1, 2010 by · Leave a Comment 

Product Description
This digital document is a journal article from Analytica Chimica Acta, published by Elsevier in . The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
Platinum nanoparticles were used in combination with multi-walled carbon nanotubes (MWCNTs) for fabricating sensitivity-enhanced electrochemical DNA biosensor. Multi-walled carbon nanotubes and platinum nanoparticles were dispersed in Nafion, which were used to fabricate the modification of the glassy carbon electrode (GCE) surface. Oligonucleotides with amino groups at the 5′ end were covalently linked onto carboxylic groups of MWCNTs on the electrode. The hybridization events were monitored by differential pulse voltammetry (DPV) measurement of the intercalated daunomycin. Due to the ability of carbon nanotubes to promote electron-transfer reactions, the high catalytic activities of platinum nanoparticles for chemical reactions, the sensitivity of presented electrochemical DNA biosensors was remarkably improved. The detection limit of the method for target DNA was 1.0×10^-^1^1moll^-^1.

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