Publications by authors named "Kamal Alizadeh"

Two techniques, including chemical immobilization of a combination of two indicators of Alizarin and Orange dyes and the epoxy activation of the agarose membrane, were used for the preparation of a new optic pH sensor. For this purpose, the mentioned dyes were immobilized on agarose support activated by an epoxy, followed by optimizing the impacts of the coupling pH, as well as the ratio and concentration of the two dyes. The sensor was set up in a flow cell and effectively employed for online pH calculations.

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In this study, a novel method was developed to measure acidic and basic drugs in biological and wastewater samples. The method used magnetic nanoparticles based on Vortex-Assisted Dispersive Micro-Solid Phase Extraction (SPE) and then identifying with HPLC-UV. The magnetic nanoparticle (FeO@SiO@Kit-6@NH) has been used as an efficient adsorbent for the extraction of acidic and basic drugs ibuprofen (IFB), fenoprofen calcium (FPC), methocarbamol (MTC), and clonazepam (CZP).

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Drug delivery systems have been of interest to researchers. The effects of synthesized nano-polymers as silibinin and silymarin extract drug delivery systems on olfactory ensheathing cells under normal and high-glucose conditions were studied. The structure of the nanopolymer was characterized by IR, HNMR, GPC, DLS, and AFM.

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In the present study, UV-visible electronic spectra of three new 2,4-dinitrophenylhydrazone derivatives (C1, C2 and C3) have been studied. Different bands observed have been assigned to the proper electronic transitions. The solvatochromic behaviors of these compounds were investigated by studying their electronic spectra in several organic solvents with different polarities.

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A novel dispersive liquid-liquid microextraction method based on solidification of floating organic drop (DLLME-SFO) was developed for the preconcentration of ultratrace amounts of palladium (Pd)(II) before its determination by electrothermal atomic absorption spectrometry. Diphenyl ether (m.p.

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A simple, rapid and sensitive method was developed for the selective separation and preconcentration of Ni(II) using dispersive liquid-liquid microextraction, by a yellow Schiff's base bisazanyl derivative, as a selective complexing agent. In this method, a mixture of 45 μL chloroform (extraction solvent) and 450 μL tetrahydrofuran (dispersive solvent) is rapidly injected by syringe into a 5 mL aqueous sample containing 3% (w/v) sodium chloride and an appropriate amount of the Schiff's base. As a result, a cloudy solution is formed by entire dispersion of the extraction solvent into the aqueous phase.

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Complexation of a fluoroquinolone derivative (ciprofloxacin), L, and some amino acids has been studied using spectrofluorimetric method. Results indicated that ciprofloxacin have a greater tendency to form a 1:1 complex with aspartic acid and arginine than the other tested molecules. The fluorescence of ciprofloxacin exhibits quenching process while it has been titrated with these amino acids.

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1, 3-Bis(2-cyanobenzene)triazene, L, was used as a suitable ionophore for the fabrication of a new PVC-based polymeric membrane coated graphite electrode for selective sensing of Cd2+ ion. The electrode exhibited a selective linear Nernstian response to Cd2+ ion at an optimal pH range of 6-9 with a limit of detection of 8.0 × 10-6 M and a fast response time of about 2 s.

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In this work, UV-Vis. electronic spectra of 1-pyridinyl-2-methylene-benzene carbohydrazonic acid (L) have been studied. The different bands observed have been assigned to the proper electronic transitions.

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A highly selective optical sensor was developed for the Hg(2+) determination by chemical immobilization of 2-[(2-sulfanylphenyl)ethanimidoyl]phenol (L), on an agarose membrane. Spectrophotometric studies of complex formation between the Schiff's base ligand L and Hg(2+), Sr(2+), Mn(2+), Cu(2+), Al(3+), Cd(2+), Zn(2+), Co(2+) and Ag(+) metal ions in methanol solution indicated a substantially larger stability constant for the mercury ion complex. Consequently, the Schiff's base L was used as an appropriate ionophore for the preparation of a selective Hg(2+) optical sensor, by its immobilization on a transparent agarose film.

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A novel fluorescence chemical sensor for the highly sensitive and selective determination of Pb(2+) ions in aqueous solutions is described. The preliminary potentiometric and spectrofluorimetric complexation studies in solution revealed that the lipophilic ligand 5,8-bis((5'-chloro-8'-hydroxy-7'-quinolinyl)methyl)-2,11-dithia-5,8-diaza-2,6-pyridinophane (L2) forms a highly stable and selective [PbL2](2+) and [Pb(L2)(2)](2+) complexes which results in a strong fluorescence quenching of the ligand. Thus, a novel fluorescence Pb(2+) sensing system was prepared by incorporating L2 as a neutral lead-selective fluoroionophore in the plasticized PVC membrane containing tetrakis(p-chlorophenyl) borate as a liphophilic anionic additive.

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N,N'-phenylenebis(salicylideaminato) (L) has been used to detect trace amounts of zinc ion in acetonitrile-water solution by fluorescence spectroscopy. The fluorescent probe undergoes fluorescent emission intensity enhancement upon binding to zinc ions in MeCN/H(2)O (1:1, v/v) solution. The fluorescence enhancement of L is attributed to the 1:1 complex formation between L and Zn(II), which has been utilized as the basis for selective detection of Zn(II).

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The UV-visible electronic spectra of some azo dyes have been studied. The different bands observed in the electronic spectra of the compounds in various organic solvents have been assigned to the proper electronic transitions. The solvatochromic behaviour of these compounds was investigated by studying their visible spectra in several pure and mixed organic solvents.

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A new sulfur-containing macrocyclic diamide, 1,15-diaza-3,4,12,13-dibenzo-5,11-dithia-8-oxa-1,15-(2,6-pyrido)cyclooctadecan-2,14-dione, L, was synthesized, characterized and used as an active component for fabrication of PVC-based polymeric membrane (PME), coated graphite (CGE) and coated silver wire electrodes (CWE) for sensing Cd(2+) ion. The electrodes exhibited linear Nernstian responses to Cd(2+) ion in the concentration range of 3.3 x 10(-6) to 3.

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A novel fluorescence chemical sensor for the highly sensitive and selective determination of Co(2+) ions in aqueous solutions is prepared. The cobalt sensing system was prepared by incorporating 7-[(5-chloro-8-hydroxy-7-quinolinyl)methyl]-5,6,7,8,9,10-hexahydro-2H-1,13,4,7,10-benzodioxatriazacyclopentadecine-3,11(4H,12H)-dione (L) as a neutral cobalt-selective fluoroionophore in the plasticized PVC membrane containing sodium tetraphenylborate as a liphophilic anionic additive. The response of the sensor is based on the strong selective fluorescence quenching of L by Co(2+) ions.

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This work reports the preparation of a new copper(II) ion-imprinted polymer (IIP) material, using 5,6;14,15-dibenzo-1,4-dioxa-8,12-diazacyclopentadecane-5,14-diene (DBDA15C4) and 2-vinylpyridine (VP) as a non-vinylated chelating agent and a functional vinyl monomer, respectively. The Cu2+ ion can form stable complexes with DBDA15C4 and VP. The stoichiometries of Cu2+-DBDA15C4 and ternary Cu2+-DBDA15C4-VP complexes were elucidated using conductometric and spectrophotometric methods, and found to be Cu2+ (DBDA15C4), Cu2+ (DBDA15C4)2 and Cu2+ (DBDA15C4)(VP)2.

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A multiwavelength spectrophotometric titration method was applied to study the acidity constants of some azo dyes in water. The UV-vis absorption spectra of azo dye solutions were recorded in the course of their pH-metric titration with a standard base solution. The protolytic equilibrium constants, spectral profiles, concentration diagrams and also the number of components have been calculated.

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Solution studies on the binding properties of uranyl ion toward four different recently synthesized benzo-substituted macrocyclic diamides L1-L4 revealed the occurrence of a 1:1 complexation of the ligands with UO(2)(2+) ion, with a stability order of L2>L1>L4>L3. Consequently, L2 was used as a suitable neutral ionophore for the preparation of novel polymeric membrane (PME) and coated graphite (CGE) UO(2)(2+)-selective electrodes. The electrodes exhibit a Nernstian behavior for UO(2)(2+) ions over wide concentration ranges (1.

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Spectrofluorometric studies on the binding properties of 5-pyridino-2,8-dithia[9](2,9)-1,10-phenanthrolinephane (L) toward La3+, Sm3+, Gd3+, Yb3+, and Nd3+ in methanol solution revealed the occurrence of both 1:1 and 2:1 (ligand/metal) complexation with a stability order of Nd3+ > Yb3+ > Gd3+ > Sm3+ > La3+. Consequently, L was used as a suitable neutral ionophore for the preparation of a novel polymeric membrane-selective electrode for Nd3+ ion. The electrode exhibited a Nernstian response over a wide concentration range (1.

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Solution studies on the binding properties of 4,5,6,7-tetrathiocino[1,2-b:3,4-b']diimidazolyl-1,3,8,10-tetraethyl-2,9-dithione (Et(4)todit) toward a number of cationic species including some lanthanide ions revealed the occurrence of a selective 1:1 complexation of the ligand with Sm(3+) ion. Consequently, Et(4)todit was used as a suitable neutral ionophore for the preparation of novel polymeric membrane (PME) and coated graphite (CGE) Sm(3+)-selective electrodes. The electrodes exhibit a Nernstian behavior for Sm(3+) ions over wide concentration ranges (1.

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