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Concentration Range (concentration + range)
Kinds of Concentration Range Selected AbstractsQuantitative determination of the major saponin mixture bacoside A in Bacopa monnieri by HPLCPHYTOCHEMICAL ANALYSIS, Issue 1 2005M. Deepak Abstract Bacoside A, the putative bioactive component of the Indian medicinal plant Bacopa monnieri, was found to be a mixture of saponins with bacoside A3 (1), bacopaside II (2), jujubogenin isomer of bacopasaponin C (3) and bacopasaponin C (4) as major constituents. An HPLC method together with an optimised extraction procedure was developed for the estimation of 1,4 in B. monnieri to enable standardisation of the latter. Concentration ranges of the analytes in samples of B. monnieri collected from different regions of India were 0.14,0.85% (w/w) (1), 0.12,0.69% (2), 0.05,0.72% (3) and 0.05,0.44% (4). The importance of using bacoside A, with known concentrations of 1,4, as a reference standard for the routine analysis of B. monnieri is highlighted. Two common ,avonoids, luteolin and apigenin, were present in all samples of B. monnieri. Copyright © 2005 John Wiley & Sons, Ltd. [source] Manganese cell labeling of murine hepatocytes using manganese(III)-transferrin,CONTRAST MEDIA & MOLECULAR IMAGING, Issue 3 2008Christopher H. Sotak Abstract Manganese(III)-transferrin [Mn(III),Tf] was investigated as a way to accomplish manganese-labeling of murine hepatocytes for MRI contrast. It is postulated that Mn(III),Tf can exploit the same transferrin-receptor-dependent and -independent metabolic pathways used by hepatocytes to transport the iron analog Fe(III),Tf. More specifically, it was investigated whether manganese delivered by transferrin could give MRI contrast in hepatocytes. Comparison of the T1 and T2 relaxation times of Mn(III),Tf and Fe(III),Tf over the same concentration range showed that the r1 relaxivities of the two metalloproteins are the same in vitro, with little contribution from paramagnetic enhancement. The degree of manganese cell labeling following incubation for 2,7,h in 31.5,µm Mn(III),Tf was comparable to that of hepatocytes incubated in 500,µm Mn2+ for 1,h. The intrinsic manganese tissue relaxivity between Mn(III),Tf-labeled and Mn2+ -labeled cells was found to be the same, consistent with Mn(III) being released from transferrin and reduced to Mn2+. For both treatment regimens, manganese uptake by hepatocytes appeared to saturate in the first 1,2,h of the incubation period and may explain why the efficiency of hepatocyte cell labeling by the two methods appeared to be comparable in spite of the ,16-fold difference in effective manganese concentration. Hepatocytes continuously released manganese, as detected by MRI, and this was the same for both Mn2+ - and Mn(III),Tf-labeled cells. Manganese release may be the result of normal hepatocyte function, much in the same way that hepatocytes excrete manganese into the bile in vivo. This approach exploits a biological process,namely receptor binding, endocytosis and endosomal acidification,to initiate the release of an MRI contrast agent, potentially conferring more specificity to the labeling process. The ubiquitous expression of transferrin receptors by eukaryotic cells should make Mn(III),Tf particularly useful for manganese labeling of a wide variety of cells both in culture and in vivo. Published in 2008 by John Wiley & Sons, Ltd. [source] Serum ,-glutamyltransferase within its normal concentration range is related to the presence of diabetes and cardiovascular risk factorsDIABETIC MEDICINE, Issue 9 2005D.-J. Kim Abstract Aims Although many studies have reported an association between serum ,-glutamyltransferase (GGT) and cardiovascular risk factors, the mechanism of this relationship has not been clarified. Methods The medical records of 29 959 subjects (age, median 48, range 14,90 years; 16 706 men, 13 253 women) who visited the Center for Health Promotion at Samsung Medical Center for a medical check-up between January 2001 and December 2003, were investigated. Subjects with hepatic enzyme/GGT concentrations higher than three times the upper limit of the reference range, a positive test for hepatitis C virus antibody, a positive test for hepatitis B virus surface antigen, currently taking anti-diabetic/anti-hypertensive/anti-lipid medication, or a white blood cell (WBC) count higher than 10 000 cells/ml, were excluded. The subjects of each gender were classified into five groups according to their serum GGT concentrations, into quartiles of the normal range of GGT (groups 1, 2, 3 and 4) and into a group with elevated GGT (group 5). Results As the group number increased (group 1 , 5), the frequencies of all of the following increased: (i) diabetes and impaired fasting glucose (IFG); (ii) hypertension, obesity (body mass index , 27 kg/m2), dyslipidaemia (LDL-cholesterol , 4.1 mmol/l and/or triglyceride , 2.46 mmol/l, or HDL-cholesterol < 1.16 mmol/l); (iii) metabolic syndrome. Moreover, these significant relationships between GGT concentrations within its normal range and the presence of diabetes/IFG, hypertension, obesity, dyslipidaemia, and metabolic syndrome persisted after adjusting for several clinical and biochemical variables and for the presence of fatty liver based on ultrasonographic findings. Odds ratios (95% CI) for group 4 (highest quartile of normal range of GGT) vs. group 1 (lowest quartile of normal range of GGT); the referent group, were 3.16 (2.15,4.65) for diabetes, 2.24 (1.73,2.90) for IFG, 1.93 (1.59,2.33) for obesity, 1.38 (1.23,1.55) for dyslipidaemia and 2.88 (2.28,3.65) for metabolic syndrome in men. In women, the odds ratios were 2.72 (1.34,5.52), 3.67 (2.26,5.97), 2.10 (1.61,2.74), 1.80 (1.58,2.04) and 3.57 (2.52,5.07), respectively. Conclusions Our data show that, even within its normal range, serum GGT concentrations are closely associated with the presence of diabetes and cardiovascular risk factors, and that these associations are independent of a fatty liver by ultrasonography. [source] Development and validation of fixed-time method for the determination of isoxsuprine hydrochloride in commercial dosages formsDRUG TESTING AND ANALYSIS, Issue 9 2010Dr Nafisur Rahman Abstract The main aim of this work was to develop a kinetic spectrophotometric method for the quantitative analysis of isoxsuprine hydrochloride in commercial tablets. The method is based on the reaction of isoxsuprine hydrochloride (ISx) with hydroxylamine hydrochloride and ammonium cerium (IV) nitrate in sulphuric acid medium at room temperature which resulted in the formation of yellow-coloured product peaking at 380 nm. The reaction is followed spectrophotometrically by measuring the absorbance as a function of time. Fixed time method (,A = A4,A2, where A2 and A4 refer to absorbance measurements taken at 2 and 4 min, respectively) was adopted for constructing the calibration curve which was found to be linear over the concentration range of 30,80 µgmL,1 with molar absorptivity of 5.95 × 103 L mol,1 cm,1. The method has been applied successfully to the determination of isoxsuprine hydrochloride in tablets. Statistical comparison (point and interval hypothesis tests) of the results showed that there is no significant difference between the proposed method and reference method. Copyright © 2010 John Wiley & Sons, Ltd. [source] Simultaneous determination of metronidazole and spiramycin in bulk powder and in tablets using different spectrophotometric techniquesDRUG TESTING AND ANALYSIS, Issue 1 2010Fatma I. Khattab Abstract Metronidazole (MZ) is an anti-infective drug used in the treatment of anaerobic bacterial and protozoa infections in humans. It is also used as a vetinary antiparasitic drug. Spiramycin (SP) is a medium-spectrum antibiotic with high effectiveness against Gram-positive bacteria. Three simple, sensitive, selective and precise spectrophotometric methods were developed and validated for the simultaneous determination of MZ and SP in their pure form and in pharmaceutical formulations. In methods A and B, MZ was determined by the application of direct spectrophotometry and by measuring its zero-order (D0) absorption spectra at its ,max = 311 nm. In method A, SP was determined by the application of first derivative spectrophotometry (D1) and by measuring the amplitude at 218.3 nm. In method B, the first derivative of the ratio spectra (DD1) was applied, and SP was determined by measuring the peak amplitude at 245.6 nm. Method C entailed mean centring of the ratio spectra (MCR), which allows the determination of both MZ and SP. The methods developed were used for the determination of MZ and SP over a concentration range of 5,25 µg ml,1. The proposed methods were used to determine both drugs in their pure, powdered forms with mean percentage recoveries of 100.16 ± 0.73 for MZ in methods A and B, 101.10 ± 0.90 in method C, 100.09 ± 0.70, 100.02 ± 0.88 and 100.49 ± 1.26 for SP in methods A, B and C, respectively. The proposed methods were proved using laboratory-prepared mixtures of the two drugs and were successfully applied to the analysis of MZ and SP in tablet formulation without any interference from each other or from the excipients. The results obtained by applying the proposed methods were compared statistically with a reported HPLC method and no significant difference was observed between these methods regarding both accuracy and precision. Copyright © 2010 John Wiley & Sons, Ltd. [source] Prussian Blue-Modified Titanate Nanotubes: A Novel Nanostructured Catalyst for Electrochemical Reduction of Hydrogen PeroxideELECTROANALYSIS, Issue 19 2010Damir Ivekovi Abstract Prussian blue (PB) modified titanate nanotubes (PB-TiNT) have been synthesized by the reaction of Fe2+ -modified TiNT with hexacyanoferrate(III) ions. The rate constant for heterogeneous catalytic reaction between PB-TiNT and H2O2 was found to be k=2×104,dm3,mol,1,s,1, which is an order of magnitude higher than the values of k reported for conventionally prepared, electrochemically deposited PB films. On the PB-TiNT modified electrode with subnanomolar surface concentration of PB (,(PB)=2.8×10,11,mol/cm2), a stable, reproducible and linear response towards H2O2 was obtained in the concentration range 0.02,4,mM, with the sensitivity of 0.10,AM,1,cm,2 at ,150,mV. [source] Electrocatalytic Reduction and Determination of Iodate and Periodate at Silicomolybdate-Incorporated-Glutaraldehyde- Cross-Linked Poly- L -lysine Film ElectrodesELECTROANALYSIS, Issue 10 2010Yu-Ching Pan Abstract The present work describes reduction of iodate (IO3,), and periodate (IO4,) at silicomolybdate-doped-glutaraldehyde-cross-linked poly- L -lysine (PLL-GA-SiMo) film coated glassy carbon electrode in 0.1,M H2SO4. In our previous study, we were able to prepare the PLL-GA-SiMo film modified electrode by means of electrostatically trapping SiMo12O404, mediator in the cationic film of PLL-GA, and the voltammetric investigation in pure supporting indicated that the charge transport through the film was fast. Here, the electrocatalytic activity of PLL-GA-SiMo film electrode towards iodate and periodate was tested and subsequently used for analytical determination of these analytes by amperometry. The two electron reduced species of SiMo12O404, anion was responsible for the electrocatalytic reduction of IO3, at PLL-GA-SiMo film electrode while two and six electron reduced species were showed electrocatalytic activity towards IO4, reduction. Under optimized experimental conditions of amperometry, the linear concentration range and sensitivity are 2.5×10,6 to 1.1×10,2,M and 18.47,,A mM,1 for iodate, and 5×10,6 to 1.43×10,4,M and 1014.7,,A mM,1 for periodate, respectively. [source] Voltammetric Determination of L -Dopa on Poly(3,4-ethylenedioxythiophene)-Single-Walled Carbon Nanotube Composite Modified MicroelectrodesELECTROANALYSIS, Issue 4 2010Jayaraman Mathiyarasu Abstract In the present communication, it is shown that platinum microelectrodes electrochemically coated with a composite of poly(3,4-)ethylenedioxythiophene and single-walled carbon nanotubes (PEDOT/SWNT) enable determinations of 3,4-dihydroxy- L -phenylalaines (L -dopa) in neutral phosphate buffer solutions containing an excess of ascorbic acid. The interpenetrated networked nanostructure of the composite was characterized by scanning electron microscope (SEM) and Raman spectroscopy. It is shown that the presence of the composite gives rise to an increase in the electroactive area of an order of magnitude in compared to the area for the bare microelectrodes. The composite film-coated microelectrode, which yielded reversible cyclic voltammograms for the ferro/ferricyanide redox couple for scan rates between 0.01 and 0.10,V s,1, also gave rise to two well-resolved oxidation peaks for L -dopa and ascorbic acid (AA). The latter effect, which was not seen in the absence of the composite, enabled differential pulse voltammetric determinations of L -dopa in the concentration range between 0.1 to 20,,M with a detection limit of 100,nM. [source] Highly Selective and Sensitive Tin(II) Membrane Electrode Based on a New Synthesized Schiff's BaseELECTROANALYSIS, Issue 7 2009Morteza Hosseini Abstract Studies on complex formation of tris(3-(2-hydroxybenzophenone)propyl)amine (THPA) with a number of metal ions in acetonitrile solution revealed the occurrence of a selective 1,:,1 complexation of the proposed ligand with Sn2+ ion. Consequently, THPA was used as a suitable neutral ionophore for the preparation of a polymeric membrane-selective electrode. The electrode exhibits a Nernstian behavior with a slope of 29.4±0.3,mV per decade and a detection limit of 2.0×10,7 M. It also showed a good selectivity for Sn2+ ions in comparison with some of group A and B metal ions over a wide concentration range of 5.0×10,7,1.0×10,1 M. Improved selectivity was achieved compared to the best selectivity recently reported by other authors for tin(II). The electrode was successfully applied to the determination of Sn2+ ion in waste water and various canned products. [source] Preparation and Characterization of a Tin Pentacyanonitrosylferrate-Modified Carbon Ceramic Electrode: Application to Electrocatalytic Oxidation and Amperometric Detection of L -CysteineELECTROANALYSIS, Issue 7 2009H. Razmi Abstract The sol-gel technique was used to construct tin pentacyanonitrosylferrate (SnPCNF) modified composite carbon ceramic electrode (CCE). This involves two steps: construction of CCE containing metallic Sn powder and then electrochemical creating of SnPCNF on the surface of CCE. The SnPCNF modified CCE (SnPCNFlCCE) was characterized by energy-dispersive X-ray (EDX), FTIR and cyclic voltammetry (CV) techniques. The SnPCNF film showed electrocatalytic activity toward the oxidation of L -cysteine. A linear calibration plot was obtained over the L -cysteine concentration range 1,51,,M using chronoamperometry. L -cysteine was determined amperometrically at the surface of this modified electrode. The detection limit (for a signal to noise of 3) and sensitivity were found to be 0.62,,M and 126,,A/mM, respectively. [source] Quantitative Analysis of Prometrine Herbicide by Liquid,Liquid Extraction Procedures Coupled to Electrochemical MeasurementsELECTROANALYSIS, Issue 6 2009V. Juarez Abstract A sensitive method is proposed for the preconcentration and quantification of the herbicide Prometrine (PROM) at a liquid-liquid interface employing square-wave voltammetry. The preconcentration stage was based on liquid-liquid extraction methodology and the PROM quantification was carried out from the peak current of square-wave voltammograms. Under the experimental conditions employed, linear calibration curves in the concentration range 1.0×10,6,M,5.0×10,5,M, with detection limit equal to 1.5×10,6,M were obtained without pretreatment of the samples. This linear range, as well as detection limit could be extended towards lower concentrations when a pretreatment procedure was employed. In this way, linearity of calibration curves between 8.0×10,8,M and 2.4×10,7,M and detection limit of 1.0×10,7,M, were observed. On the other hand, the standard addition method was also used as an alternative and an appropriated quantification technique for this system. A linear concentration range between 1.0×10,6,M and 2.7×10,5,M, with a correlation coefficient of 0.997, was obtained. This procedure has also a promising application in the separation of herbicides from other interferents, present in real samples, previous to their quantification. [source] Electrochemical Study of Anionic Ferrocene Derivatives Intercalated in Layered Double Hydroxides: Application to Glucose Amperometric BiosensorsELECTROANALYSIS, Issue 3-5 2009Christine Mousty Abstract Layered double hydroxides (Zn2Cr(OH)6X,nH2O LDH) containing (3-sulfopropyl)ferrocene-carboxylate (FcPSO3) and 1,1,-bis(3-sulfopropyl)ferrocene-carboxylate (Fc(PSO3)2) as interlayer anions (X) have been prepared by the co-precipitation method and characterized by PXRD, FTIR, SEM and XPS. The electrochemical behavior of these hybrid materials has been evaluated by cyclic voltammetry. A new amperometric biosensor based on the immobilization of glucose oxidase in ZnCr-FcPSO3 hybrid material was presented, the intercalated anions playing the role of mediators that shuttle electrons between the FAD centers in the enzyme and the electrode surface. The performance of the resulting biosensor for glucose determination under anaerobic conditions was evaluated by chronoamperometry at 0.5,V. The sensitivity (65,mA M,1 cm,2) determined in the concentration range 10,25,,M is higher than sensitivities reported for other glucose biosensors based on LDH host matrices. [source] Electrocatalytic and Analytical Response of Cobalt Phthalocyanine Modified Carbon Paste Electrodes Towards Antimalarial Endoperoxide ArtemisininELECTROANALYSIS, Issue 3-5 2009Chhanda Debnath Abstract A cobalt phthalocyanine modified carbon paste electrode was constructed for the analysis of artemisinin in Artemisia annua plant. Artemisinin, a sesquiterpene endoperoxide, is a novel, important antimalarial drug and is used in the therapy against Plasmodium falciparum. The developed cobalt phthalocyanine modified electrode exhibited a significant electrocatalytic activity in presence of artemisinin when using cyclic and differential pulse voltammetry. Under optimized conditions in phosphate buffer of pH,7 a well defined voltammetric peak appeared at about ,500,mV vs. Ag/AgCl. The differential pulse voltammetric peak current of artemisinin was increased linearly with the concentration range of 2.1×10,5 to 5.3×10,4 M (R=0.9997). The limit of detection (LOD) was found to be 6.5×10,6 M. The modified electrode was successfully tested for detecting artemisinin in complex plant materials. [source] Microflow Vessel Improving Reproducibility and Sensitivity of Electrochemical MeasurementsELECTROANALYSIS, Issue 23 2008Jan Krejci Abstract A new microflow system was designed and developed for electrochemical measurements. The electrochemical electrodes prepared using thick film technology were used in this arrangement. Results of various measurements such as simple amperometric measurement on the example of H2O2 detection, measurement with glucose oxidase (GOx) biosensor, soluble enzyme activity measurement etc. carried out using this system are reported. It was observed that the sensitivity and reproducibility of the electrochemical measurements is improved significantly. The new device performance was proved on H2O2 detection, activity of GOx measurement and heavy metals detection (measured concentration range: H2O2 10,9 to 10,1,M, glucose 10,6 to 10,2,M, activity of GOx 10,1 to 102,IU, heavy metals (Cu, Pb) 10,4 to 10,3,M). The microflow insert greatly reduces the overall size of the electrolyte vessel and measurements with sample quantity as low as 2,mL can be accomplished. [source] Amperometric Detection of 4-Chlorophenol on Two Types of Expanded Graphite Based Composite ElectrodesELECTROANALYSIS, Issue 22 2008Aniela Pop Abstract The assessment of an expanded graphite-Ag-zeolite-epoxy composite (EG-Z-Ag-Epoxy) electrode for the determination of 4-chlorophenol (4-CP) is described and compared to the corresponding expanded graphite-epoxy composite (EG-Epoxy) electrode. Cyclic voltammetry was used to characterize the electrochemical behavior and determination of 4-CP at both electrodes in 0.1,M Na2SO4 and 0.1,M NaOH supporting electrolytes. A substantial enhancement of sensitivity for the determination of 4-CP at the EG-Z-Ag-Epoxy electrode was reached by applying a chemical preconcentration step prior to voltammetric quantification. Also, under these last conditions the lowest limit of detection of 1,,M illustrates the analytical versatility of this electrode in a concentration range where aquatic 4-chlorophenol pollution is known to occur. [source] A Biomimetic Potentiometric Sensor Using Molecularly Imprinted Polymer for the Cetirizine Assay in Tablets and Biological FluidsELECTROANALYSIS, Issue 18 2008Mehran Javanbakht Abstract Despite the increasing number of applications of molecularly imprinted polymers (MIPs) in analytical chemistry, the construction of a biomimetic potentiometric sensor remains still challenging. In this work, a biomimetic potentiometric sensor, based on a non-covalent imprinted polymer was fabricated for the recognition and determination of cetirizine. The MIP was synthesized by precipitation polymerization, using cetirizine dihydrochloride as a template molecule, methacrylic acid (MAA) as a functional monomer and ethylene glycol dimethacrylate (EGDMA) as a cross linking agent. The sensor showed high selectivity and a sensitive response to the template in aqueous system. The MIP-modified electrode exhibited Nernstian response (28.0±0.9 mV/decade) in a wide concentration range of 1.0×10,6 to 1.0×10,2 M with a lower detection limit of 7.0×10,7 M. The electrode has response time of ca. 20,s, high performance, high sensitivity, and good long term stability (more than 5,months). The method was satisfactory and used to the cetirizine assay in tablets and biological fluids. [source] Lead(II) Potentiometric Sensor Based on 1,4,8,11-Tetrathiacyclotetradecane Neutral Carrier and Lipophilic AdditivesELECTROANALYSIS, Issue 11 2008Mohamed Abstract A potentiometric sensor for lead(II) ions based on the use of 1,4,8,11-tetrathiacyclotetradecane (TTCTD) as a neutral ionophore and potassium tetrakis-(p -chlorophenyl)borate as a lipophilic additive in plasticized PVC membranes is developed. The sensor exhibits linear potentiometric response towards lead(II) ions over the concentration range of 1.0×10,5,1.0×10,2,mol L,1 with a Nernstian slope of 29.9,mV decade,1 and a lower limit of detection of 2.2×10,6,mol L,1 Pb(II) ions over the pH range of 3,6.5. Sensor membrane without a lipophilic additive displays poor response. The sensor shows high selectivity for Pb(II) over a wide variety of alkali, alkaline earth and transition metal ions. The sensor shows long life span, high reproducibility, fast response and long term stability. Validation of the method by measuring the lower limit of detection, lower limit of linear range, accuracy, precision and sensitivity reveals good performance characteristics of the proposed sensor. The developed sensor is successfully applied to direct determination of lead(II) in real samples. The sensor is also used as an indicator electrode for the potentiometric titration of Pb(II) with EDTA and potassium chromate. The results obtained agree fairly well with data obtained by AAS. [source] Properties of Poly(sodium 4-styrenesulfonate)-Ionic Liquid Composite Film and Its Application in the Determination of Trace Metals Combined with Bismuth Film ElectrodeELECTROANALYSIS, Issue 5 2008Jianbo Jia Abstract A new kind of bismuth film modified electrode to sensitively detect trace metal ions based on incorporating highly conductive ionic liquids 1-butyl-3-methyl-imidazolium hexafluorophosphate (BMIMPF6) in solid matrices at glassy carbon (GC) was investigated. Poly(sodium 4-styrenesulfonate) (PSS), silica, and Nafion were selected as the solid matrices. The electrochemical properties of the mixed films modified GC were evaluated. The electron transfer rate of Fe(CN)64,/Fe(CN)63, can be effectively improved at the PSS-BMIMPF6 modified GC. The bismuth modified PSS-BMIMPF6 composite film electrodes (GC/PSS-BMIMPF6/BiFEs) displayed high mechanical stability and sensitive stripping voltammetric performances for the determination of trace metal cations. The GC/PSS-BMIMPF6/BiFE exhibited well linear response to both Cd(II) and Pb(II) over a concentration range from 1.0 to 50,,g L,1. And the detection limits were 0.07,,g L,1 for Cd(II) and 0.09,,g L,1 for Pb(II) based on three times the standard deviation of the baseline with a preconcentration time of 120,s, respectively. Finally, the GC/PSS-BMIMPF6/BiFEs were successfully applied to the determination of Cd(II) and Pb(II) in real sample, and the results of present method agreed well with those of atomic absorption spectroscopy. [source] Novel Potentiometric Sensors of Molecular Imprinted Polymers for Specific Binding of ChlormequatELECTROANALYSIS, Issue 2 2008Ayman Abstract Molecularly imprinted polymers (MIP) were used as potentiometric sensors for the selective recognition and determination of chlormequat (CMQ). They were produced after radical polymerization of 4-vinyl pyridine (4-VP) or methacrylic acid (MAA) monomers in the presence of a cross-linker. CMQ was used as template. Similar non-imprinted (NI) polymers (NIP) were produced by removing the template from reaction media. The effect of kind and amount of MIP or NIP sensors on the potentiometric behavior was investigated. Main analytical features were evaluated in steady and flow modes of operation. The sensor MIP/4-VP exhibited the best performance, presenting fast near-Nernstian response for CMQ over the concentration range 6.2×10,6,1.0×10,2,mol L,1 with detection limits of 4.1×10,6,mol L,1. The sensor was independent from the pH of test solutions in the range 5,10. Potentiometric selectivity coefficients of the proposed sensors were evaluated over several inorganic and organic cations. Results pointed out a good selectivity to CMQ. The sensor was applied to the potentiometric determination of CMQ in commercial phytopharmaceuticals and spiked water samples. Recoveries ranged 96 to 108.5%. [source] A Cobalt Film Electrode for Nitrite Determination in Natural WaterELECTROANALYSIS, Issue 24 2007Koïkoï Soropogui Abstract In this study a cobalt film electrodeposited on a copper disk (Ø=3.1,mm) was tested as electrode to measure nitrite ions in raw water. This electrode was able to determine the nitrite ions concentration in nondeaerated synthetic media and in natural water. The electrode reached a detection limit of 0.2,,mol L,1 and has a linear concentration range of 0.4 to 2,,mol L,1 NO2,. The influence of several ions such as NO3,, Cl,, SO42,, Mg2+, HCO3, and NH4+ was also tested. The electrode was used to determine the concentration of nitrite ions in a real sample. [source] Bismuth Film Electrode as an Alternative for Mercury Electrodes: Determination of Azo Dyes and Application for Detection in Food StuffsELECTROANALYSIS, Issue 21 2007Benoît Claux Abstract Bismuth electrodes were investigated and exhibit electrochemical properties similar to mercury electrodes but with much lower toxicity. An electrochemical application of bismuth film modified glassy carbon electrode for azo dyes determination was investigated. The plating step was optimized in order to achieve its analytical efficiency. A plating potential of ,0.9,V in a solution of 200,mg/L Bi(NO3)3, 0.5,M HNO3 for 100,s yields to a suitable electrode (in terms of stability and detection). Azo dyes such as azorubine (i.e., carmoisine, E122), amaranth (E123), ponceau 4R (i.e., new coccine, E124) and allura red (E129) were determined by differential pulse voltammetry in a NaCl solution in the concentration range of few ppm to 100 ppm. The reproducibility of the signal, characterized by the relative standard deviation, was found to be less than 5%, the detection and quantification limits were few mg/L. The influence of other food components on the signal was studied and the applicability was tested on real beverages samples. [source] Chitosan Incorporating Cetyltrimethylammonium Bromide Modified Glassy Carbon Electrode for Simultaneous Determination of Ascorbic Acid and DopamineELECTROANALYSIS, Issue 17 2007Xuelian Zou Abstract Simultaneous determination of a neurotransmitter, dopamine (DA), and ascorbic acid (AA) is achieved at neutral pH on a chitosan incorporating cetyltrimethylammonium bromide (CTAB) modified glassy carbon (GC) electrode. Differential pulse voltammetry (DPV) technique was used to investigate the electrochemical response of DA and AA at a glassy carbon electrode modified with chitosan incorporating CTAB. An optimum 6.0,mmol L,1 of CTAB together with 0.5 wt% of chitosan was used to improve the resolution and the determination sensitivity. In 0.1,mol L,1 aqueous phosphate buffer solution of pH,6.8, the chitosan-CTAB modified electrode showed a good electrocatalytic response towards DA and AA. The anodic peak potential of DA shifted positively, while that of AA shifted negatively. Thus, the difference of the anodic peaks of DA and AA reached 0.23,V, which was enough to separate the two anodic peaks very well. The presented method herein could be applied to the direct simultaneous determination of DA and AA without prior treatment. The anodic peak currents (Ipa) of DPV are proportional to DA in the concentration range of 8,,M to 1000,,M, to that of AA 10,,M to 2000,,M, with correlation coefficients of 0.9930 and 0.9945, respectively. The linear range is much wider than previously reported. [source] New Methylene Blue (NMB) Encapsulated in Mesoporous AlMCM-41 Material and Its Application for Amperometric Determination of Ascorbic Acid in Real SamplesELECTROANALYSIS, Issue 15 2007Shabnam Sohrabnezhad Abstract New methylene blue (NMB) dye incorporated into AlMCM-41 surfactant-free and hybrid surfactant-AlMCM-41 mesophase. UV-vis evidence shows that new methylene blue dye protonated in both cases of zeolites. New methylene blue is electroactive in zeolites and their electrochemical activity has been studied by cyclic voltammetry and compared to that of NMB in aqueous solutions. New methylene blue molecules are not released to the solution during CV measurements and are accessible to H3O+ ions. The presence of surfactant affects the kinetics of the redox process through proton ions diffusion. The midpoint potentials (Em) values show that new methylene blue dye incorporated into AlMCM-41 can be reduced easily with respect to solution new methylene blue. New methylene blue interacting with surfactant polar heads and residual Br, ions as a results, it shows a couple of peaks in high potential with respect to new methylene blue solution. The electrode made with methylene blue-AlMCM-41 without surfactant was used for the mediated oxidation of ascorbic acid. The anodic peak current observed in cyclic voltammetry was linearly dependent on the ascorbic acid concentration. The calibration plot was linear over the ascorbic acid concentration range 1.0×10,5 to 5.0×10,4 M. The detection limit of the method is 1.0×10,5 M, low enough for trace ascorbic acid determination in various real samples. [source] DNA Determination in the Presence of Copper in Diluted Alkaline Electrolyte by Adsorptive Stripping Voltammetry at the Mercury Film ElectrodeELECTROANALYSIS, Issue 11 2007Augusto, Mardini Farias, Percio Abstract A stripping method for the determination of single-stranded DNA in presence of copper at the submicromolar concentration levels is described. The method is based on controlled adsorptive accumulation of adenine (from acid-treated DNA) at thin-film mercury electrode followed by linear scan voltammetry measurement of the surface species. Optimum experimental conditions were found to be the use of a 5.0×10,3,M NaOH solution, an accumulation potential of ,0.40,V and a scan rate of 200,mV s,1. The response of adenine,copper is linear over the concentration range 50,250,ppb. For an accumulation time of 15,minutes, the detection limit was found to be 4,ppb. The more convenient relation to measuring the ssDNA in presence of metals and nitrogenated bases were also investigated. The utility of the method is demonstrated by the presence of adenosine-triphosphate (ATP) and amino acids. [source] Comparative Studies of Tridentate Sulfur and Nitrogen-Containing Ligands as Ionophores for Construction of Cadmium Ion-Selective Membrane SensorsELECTROANALYSIS, Issue 11 2007Ashok, Kumar Singh Abstract New polymeric membrane cadmium-ion selective sensors have been prepared by incorporating nitrogen and sulfur containing tridentate ligands as the ionophores into the plasticized PVC membranes. Poly(vinyl chloride) (PVC) based membranes of potassium hydrotris[N -(2,6-xylyl)thioimdazolyl) borate] (KTt2,6-xylyl) and potassium hydrotris(3-phenyl-5-methylpyrazolyl) borate (KTpPh,Me) with sodium tetraphenyl borate (NaTPB) as an anionic excluder and dibutylphthalate (DBP), tributylphthalate (TBP), dioctylsebacate (DOS), and o -nitrophenyloctyl ether (o -NPOE) as plasticizing solvent mediators were investigated in different compositions. KTt2,6-xylyl was found to be a selective and sensitive ion carrier for Cd(II) membrane sensor. A membrane composed of KTt2,6-xylyl:NaTPB:PVC:DBP with the % mole ratio 2.3,:,1.1,:,34.8,:,61.8 (w/w) works well over a very wide concentration range (7.8×10,8,1.0×10,2,M) with a Nernstian slope of 29.4±0.2,mV/decades of activity between pH values of 3.5 to 9.0 with a detection limit of 4.37×10,8,M. The sensor displays very good discrimination toward Cd(II) ions with regard to most common cations. The proposed sensor shows a short response time for whole concentration range (ca. 8,s). The effects of the cationic (tetrabutylammonium chloride, TBC), anionic (sodium dodecyl sulfate, SDS) and nonionic (Triton X-100) surfactants were investigated on the potentiometric properties of proposed cadmium-selective sensor. The proposed sensor based on KTt2,6-xylyl ionophore has also been used for the direct determination of cadmium ions in different water samples and human urine samples. [source] Electrocatalytic Oxidation of Sulfur Containing Amino Acids at Renewable Ni-Powder Doped Carbon Ceramic Electrode: Application to Amperometric Detection L -Cystine, L -Cysteine and L -MethionineELECTROANALYSIS, Issue 21 2006Abdollah Salimi Abstract A sol-gel technique was used here to prepare a renewable carbon ceramic electrode modified with nickel powder. Cyclic voltammograms of the resulting modified electrode show stable and a well defined redox couple due to Ni(II)/Ni(III) system with surface confined characteristics. The modified electrode shows excellent catalytic activity toward L -cystine, L -cysteine and L -methionine oxidation at reduced overpotential in alkaline solutions. In addition the antifouling properties at the modified electrode toward the above analytes and their oxidation products increases the reproducibility of results. L -cystine, L -cysteine and L -methionine were determined chronoamperometricaly at the surface of this modified electrode at pH range 9,13. Under the optimized conditions the calibration curves are linear in the concentration range 1,450,,M, 2,90,,M and 0.2,75,,M for L -cystine, L -methionine and L -cysteine determination, respectively. The detection limit and sensitivity were 0.64,,M, 3.8,nA/ ,M for L -cystine, 2,,M, 5.6,nA/ ,M for L -methionine and 0.2,,M and 8.1,nA/,M for L -cysteine. The advantageous of this modified electrode is high response, good stability and reproducibility, excellent catalytic activity for oxidation inert molecules at reduced overpotential and possibility of regeneration of the electrode surface by potential cycling for 5,minutes. Furthermore, the modified electrode has been prepared without using specific reagents. This sensor can be used as an amperometric detector for disulfides detection in chromatographic or flow systems. [source] A Peroxidase-Based Biosensor Supported by Nanoporous Magnetic Silica Microparticles for Acetaminophen Biotransformation and Inhibition StudiesELECTROANALYSIS, Issue 17 2006Donghui Yu Abstract Magnetized nanoporous silica based microparticles (MMPs) were used for horseradish peroxidase (HRP) immobilization and applied for amperometric peroxidase-based biosensor development. A magnetized carbon paste electrode permitted the MMPs attraction. The biosensor was applied to the investigation of the enzymatic oxidation of acetaminophen (paracetamol). The biosensor operated at low applied potential and the signal corresponded to the electroreduction of N -acetylbenzoquinoneimine (NAPQI) generated by the enzyme HRP in the presence of hydrogen peroxide. The biosensor allowed performing the quantitation of acetaminophen in the micromolar concentration range and the comparative study of thiols which inhibited the biosensor response. Distinct inhibition results were observed for HRP entrapped in the silica microparticles compared to the soluble HRP. [source] A Novel Al(III)-Selective Electrochemical Sensor Based on N,N,-Bis(salicylidene)-1,2-phenylenediamine ComplexesELECTROANALYSIS, Issue 16 2006B. Gholivand Abstract A polyvinylchloride membrane sensor based on N,N,-bis(salecylidene)-1,2-phenylenediamine (salophen) as membrane carrier was prepared and investigated as a Al3+ -selective electrode. The sensor exhibits a Nernstian response toward Al(III) over a wide concentration range (8.0×10,7,3.0×10,2,M), with a detection limit of 6.0×10,7,M. The potentiometric response of the sensor is independent of the pH of the test solution in the pH range 3.2,4.5. The electrode possesses advantages of very fast response and high selectivity for Al3+ in comparison with alkali, alkaline earth and some heavy metal ions. The sensor was used as an indicator electrode, in the potentiometric titration of aluminum ion and in determination of Al3+ contents in drug, water and waste water samples. [source] Preparation, Characterization and Analytical Applications of a New and Novel Electrically Conducting PolymerELECTROANALYSIS, Issue 15 2006F. D'Eramo Abstract In this study, a glassy carbon electrode (GC) was modified with an electropolymerized film of 1-naphthylamine (1-NAP) with a subsequent overoxidation treatment in 0.2,M sodium hydroxide solution. This polymer p-1-NAPox film coated GC electrode was used for the selective determination of dopamine (DA) in the presence of a triple concentration of ascorbic acid (AA). These studies were performed using cyclic voltammetry and square-wave voltammetry at physiological pH. p-1-NAPox shows an attractive permselectivity, a marked enhancement of the current response and antifouling properties when compared to a bare GC electrode activated in basic media. With a preconcentration time of 3,minutes at open circuit, linear calibration plots were obtained for DA in buffer solution (pH,7.4) over the concentration range from 1×10,6,1×10,4 M with a detection limit of 1.59×10,7 M. [source] Silver(I)-Selective PVC Membrane Potentiometric Sensor Based on a Recently Synthesized Calix[4]areneELECTROANALYSIS, Issue 10 2006Ayça Demirel Abstract A new PVC membrane potentiometric sensor for Ag(I) ion based on a recently synthesized calix[4]arene compound of 5,11,17,23-tetra- tert -butyl-25,27-dihydroxy-calix[4]arene-thiacrown-4 is developed. The electrode exhibits a Nernstian response for Ag(I) ions over a wide concentration range (1.0×10,2,1.0×10,6 M) with a slope of 53.8±1.6,mV per decade. It has a relatively fast response time (5,10,s) and can be used for at least 2 months without any considerable divergence in potentials. The proposed electrode shows high selectivity towards Ag+ ions over Pb2+, Cd2+, Co2+, Zn2+, Cu2+, Ni2+, Sr2+, Mg2+, Ca2+, Li+, K+, Na+, NH4+ ions and can be used in a pH range of 2,6. Only interference of Hg2+ is found. It is successfully used as an indicator electrode in potentiometric titration of a mixture of chloride, bromide and iodide ions. 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