PubMed Health⌕ Search

Biomedical subjects

Afsaneh Safavi

Publications and source records attributed to Afsaneh Safavi.

9 recordsLinked to original sources
PubMed2006

Highly stable electrochemical oxidation of phenolic compounds at carbon ionic liquid electrode.

A carbon ionic liquid electrode (CILE) was used for the investigation of the electrochemical oxidation of phenolic compounds in acidic media using cyclic voltammetry, chronoamperometry and square wave voltammetry techniques. The results indicate that, contrary to many other electrodes, the oxidation of phenolic compounds on CILE is highly stable and does not result in electrode fouling. Cyclic voltammetry showed that phenolic compounds such as phenol, 2,4-dichlorophenol and catechol were oxidized at CILE and remained electroactive after multiple cycles and at high concentrations of phenol. The cyclic voltammetric response of the CILE is very stable with more than 99% of the initial activity remaining after 20 s of stirring of a 0.5 mM solution of phenol.

Carbon↗
PubMed2006

Simultaneous determination of dopamine, ascorbic acid, and uric acid using carbon ionic liquid electrode.

A recently constructed carbon composite electrode using room temperature ionic liquid as pasting binder was employed as a novel electrode for sensitive, simultaneous determination of dopamine (DA), ascorbic acid (AA), and uric acid (UA). The apparent reversibility and kinetics of the electrochemical reaction for DA, AA, and UA found were improved significantly compared to those obtained using a conventional carbon paste electrode. The results show that carbon ionic liquid electrode (CILE) reduces the overpotential of DA, AA, and UA oxidation, without showing any fouling effect due to the deposition of their oxidized products. In the case of DA, the oxidation and reduction peak potentials appear at 210 and 135mV (vs Ag/AgCl, KCl, 3.0M), respectively, and the CILE shows a significantly better reversibility for dopamine. The oxidation peak due to the oxidation of AA occurs at about 60mV. For UA, a sharp oxidation peak at 340mV and a small reduction peak at 250mV are obtained at CILE. Differential pulse voltammetry was used for the simultaneous determination of ternary mixtures of DA, AA, and UA. Relative standard deviation for DA, AA, and UA determinations were less than 3.0% and DA, AA, and UA can be determined in the ranges of 2.0x10(-6)-1.5x10(-3), 5.0x10(-5)-7.4x10(-3), and 2.0x10(-6)-2.2x10(-4)M, respectively. The method was applied to the determination of DA, AA, and UA in human blood serum and urine samples.

Ascorbic Acid↗
PubMed2006

High-performance carbon composite electrode based on an ionic liquid as a binder.

Ionic liquid, n-octylpyridinum hexafluorophosphate (OPFP) has been used to fabricate a new carbon composite electrode with very attractive electrochemical behavior. This type of carbon electrode has been constructed using graphite mixed with OPFP as the binder. The electrode has combined advantages of edge plane characteristics of carbon nanotubes and edge plane pyrolytic graphite electrodes together with the low cost of carbon paste electrodes and robustness of metallic electrodes. It provides a remarkable increase in the rate of electron transfer of different organic and inorganic electroactive compounds and offers a marked decrease in the overvoltage for biomolecules such as NADH, dopamine, and ascorbic acid. It also circumvents NADH surface fouling effects as well as furnishing higher current density for a wide range of compounds tested. Depending on the choice of the electrolyte, the electrode can have the ion-exchange property and adsorptive characteristics of clay-modified electrodes. The proposed electrode thus allows sensitive, low-potential, simple, low-cost, and stable electrochemical sensing of biomolecules and other electroactive compounds. Scanning electron microscopy images indicate significant improvement in the microstructure of the proposed electrode compared to carbon paste electrodes. Such abilities promote new opportunities for a wide range of electrochemical and biosensing applications.

Journal Article↗
PubMed2006

Development of an optode membrane for high pH values.

The development of an optical pH sensor for high pH values is described based on the immobilization of Aniline Blue on an optically transparent triacetylcellulose membrane. The membrane is useful for repetitive and reversible pH measurements in the pH range of 8.8-13. The relative standard deviation is about 1.6% and 2% for seven measurements of the maximum change at 579 nm from pH 9 to 10.8 and from pH 11.1 to 12.8, respectively. Other advantages of the sensor include rapid equilibration time, long term stability, reversibility, high sensitivity, freedom from interference of other cations and ease of fabrication.

Aniline Compounds↗
PubMed2005

Flotation-separation and ICP-AES determination of ultra trace amounts of copper, cadmium, nickel and cobalt using 2-aminocyclopentene-1-dithiocarboxylic acid.

A rapid flotation method for separation and enrichment of ultra trace amounts of copper(II), cadmium(II), nickel(II) and cobalt(II) ions from water samples is established. At pH 6.5 and with sodium dodecylsulfate used as a foaming reagent, Cu2+, Cd2+, Ni2+ and Co2+ were separated simultaneously with 2-aminocyclopentene-1-dithiocarboxylic acid (ACDA) added to 1 l of aqueous solution. The proposed procedure of preconcentration is applied prior to the determination of these four analytes using inductivity coupled plasma-atomic emission spectrometry (ICP-AES). The effects of pH, concentration of ACDA, applicability of different surfactants and foreign ions on the separation efficiency were investigated. The preconcentration factor of the method is 1000 and the detection limits of copper(II), cadmium(II), nickel(II) and cobalt(II) ions are 0.078, 0.075, 0.072 and 0.080 ng ml(-1), respectively.

Cadmium↗
PubMed2003

Flow-injection chemiluminescence determination of chlorinated isocyanuric acids.

A rapid and sensitive flow-injection chemiluminescence method is described for the determination of dichloro- and trichloroisocyanuric acids based on the chemiluminescence produced during their reaction with luminol in alkaline medium. The effects of analytical and flow-injection variables on these chemiluminescence systems and determination of both oxidants are discussed. The optimized method yielded 3sigma detection limits of 8x10(-8) and 5x10(-8) mol L(-1) for the sodium dichloroisocyanurate and trichloroisocyanuric acid, respectively. The optimum conditions were found to be as follows: NaOH, 1x10(-1) mol L(-1); luminol, 5x10(-3) mol L(-1); KI, 2x10(-3) mol L(-1) and flow rate, 3.5 mL min(-1).

Detergents↗
PubMed2003

Flow injection determination of isoniazid using N-bromosuccinimide- and N-chlorosuccinimide-luminol chemiluminescence systems.

A chemiluminescent method for the determination of isoniazid is described. Method is based on the chemiluminescence (CL) generated during the oxidation of luminol by N-bromosuccinimide (NBS) and N-chlorosuccinimide (NCS) in alkaline medium. It was found that the isoniazid could greatly enhance this CL intensity when present in the luminol solution. Based on this observation, a new flow-injection CL method for the determination of isoniazid is proposed in this paper. The detection limits were 4 and 3 ng ml(-1) isoniazid for the NBS- and NCS-luminol CL systems, respectively. The relative CL intensity was linear with the isoniazid concentration in the range of 8-600 and 600-5000 ng ml(-1) for the NBS-luminol CL system, and 6-200 and 200-2000 ng ml(-1) for the NCS-luminol CL system. The results obtained for the assay of pharmaceutical preparations compared well with those obtained by the official method and demonstrated good accuracy and precision.

Bromosuccinimide↗
PubMed2002

Catalytic determination of traces of silver(I) using the oxidation of Janus Green with peroxodisulfate.

A method for sensitive and selective determination of silver based on the catalytic effect of silver(I) ion on the oxidation of Janus Green by peroxodisulfate is described. o-Phenanthroline is used as an activator. The rate of the decrease in absorbance of Janus Green (at 615 nm) is proportional to the concentration of silver in the range of 0.3-4.0 ng mL(-1) and 4.0-500.0 ng mL(-1). The theoretical limit of detection was 0.25 ng mL(-1). The method is free from most interferences. The method was applied to the determination of silver in plants (the uptake of silver by plants), in photographic solutions, lake water and several synthetic samples.

Journal Article↗