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Öğe Voltammetric behavior of testosterone on bismuth film electrode: Highly sensitive determination in pharmaceuticals and human urine by square‐wave adsorptive stripping voltammetry(Wiley Online Library, 2015-03-20) Levent, Abdulkadir; Altun, Ahmet; Taş, Süleyman; Yardım, Yavuz; Şentürk, ZühreIn this paper, an electrochemical application of bismuth‐film electrode (BiFE) fabricated via ex‐situ electrodeposition onto a glassy carbon electrode for testosterone determination was investigated in aqueous and aqueous/surfactant solutions. In cyclic voltammetry, the compound showed one irreversible and adsorption‐controlled reduction peak. The BiFE revealed good linear response in the examined concentration range of 1 to 45 nmol L−1 testosterone in BrittonRobinson buffer, pH 5.0 containing 3 mmol L−1 cetyltrimethylammonium bromide. The limit of detection was 0.3 nmol L−1 (0.09 ng mL−1). Finally, the BiFE was satisfactorily applied for quantitation of testosterone in both pharmaceutical (oil‐based ampoule) and biological (human urine) samples.Öğe Electrochemical performance of boron-doped diamond electrode in surfactant-containing media for ambroxol determination(Elsevier, 2014-07-17) Levent, Abdulkadir; Yardım, Yavuz; Şentürk, ZühreA novel application of boron-doped diamond electrode is introduced for the determination of ambroxol, a potential antioxidant drug belonging to the expectorant class. The electrochemical oxidation of ambroxol was first investigated by cyclic voltammetry using boron-doped diamond and glassy carbon electrodes in aqueous solutions both with and without the addition of surfactant. The compound was irreversibly oxidized in one/two steps at high positive potentials, resulting in the formation of a couple with a reduction and re-oxidation wave at less positive potentials. Special attention was given to the use of adsorptive stripping voltammetry at a surface of mildly oxidized boron-doped diamond electrode in aqueous solutions over the pH range of 1.0–10.0. Addition of anionic surfactant (sodium dodecylsulfate) to ambroxol-containing electrolyte enhanced the stripping current signal. Using square-wave stripping mode, the drug yielded a well-defined voltammetric response in phosphate buffer pH 2.5 containing 4 × 10−4 M sodium dodecylsulfate at +1.02 V (versus Ag/AgCl) (after 30 s accumulation at +0.50 V). The process could be used to determine ambroxol in the concentration range of 0.05–0.7 μM, with a detection limit of 0.010 μM (4.2 ng mL−1). The suggested method was successfully applied to pharmaceuticals and spiked human urine samples.Öğe Electrooxidation of thiourea and its square-wave voltammetric determination using pencil graphite electrode(Walter de Gruyter, 2011-04-01) Levent, Abdulkadir; Keskin, Ertuğrul; Yardım, Yavuz; Şentürk, ZühreThe electrochemical properties of thiourea (TU) were investigated in pH range 2.0-12.0 by cyclic and square-wave voltammetry. The compound was irreversibly oxidized at a pencil graphite electrode in one or two oxidation steps which are pH-dependent. Based on the voltammetric peak for the second oxidation process of TU in phosphate buffer at pH 12.0, a square-wave voltammetric method was proposed for the determination of the compound in the range 6.3-30μm, with a detection limit of 1.29μm. The applicability to direct assays of wastewaters was also tested.Öğe Sensitive voltammetric determination of testosterone in pharmaceuticals and human urine using a glassy carbon electrode in the presence of cationic surfactant(Elsevier, 2014-05-10) Levent, Abdulkadir; Altun, Ahmet; Yardım, Yavuz; Şentürk, ZühreIn this work, the electrochemical investigation of testosterone, a steroid hormone from the androgen group, was carried out in aqueous and aqueous/surfactant solutions using a glassy carbon (GC) electrode. In cyclic voltammetry, the compound showed one irreversible and adsorption-controlled reduction peak. Addition of cationic surfactant (cetyltrimethylammonium bromide, CTAB) was found to enhance the reduction current signal of testosterone, whereas, anionic (sodium dodecylsulfate, SDS) and non-ionic (Tween 80) surfactants exhibited opposite effect. Using square-wave adsorptive stripping voltammetry, the current showed a linear dependence with concentration in the range between 10 and 70 nM in Britton–Robinson buffer, pH 5.0 containing 3 mM CTAB. A detection limit of 1.18 nM (0.34 ng mL−1), and relative standard deviation of 4.12% for a concentration level of 35 nM (n = 11) were calculated. This method was successfully applied for the analysis of testosterone in oil-based pharmaceutical preparations and urine samples without any separation.Öğe Graphene/Nafion composite film modified glassy carbon electrode for simultaneous determination of paracetamol, aspirin and caffeine in pharmaceutical formulations(ScienceDirect, 2016-05-16) Yiğit, Aydın; Yardım, Yavuz; Çelebi, Metin; Levent, Abdulkadir; Şentürk, ZühreA graphene-Nafion compositefilm was fabricated on the glassy carbon electrode (GR-NF/GCE), and usedfor simultaneous determination of paracetamol (PAR), aspirin (ASA) and caffeine (CAF). The electro-chemical behaviors of PAR, ASA and CAF were investigated by cyclic voltammetry and square-waveadsorptive anodic stripping voltammetry. By using stripping one for simultaneous determination of PAR,ASA and CAF, their electrochemical oxidation peaks appeared atþ0.64, 1.04 and 1.44 V, and good linearcurrent responses were obtained with the detection limits of 18 ng mL 1(1.2 10 9M), 11.7 ng mL 1(6.5 10 8M) and 7.3 ng mL 1(3.8 10 8M), respectively. Finally, the proposed electrochemical sensorwas successfully applied for quantifying PAR, ASA and CAF in commercial tablet formulations.Öğe Voltammetric behavior of benzo[a]pyrene at boron-doped diamond electrode: A study of its determination by adsorptive transfer stripping voltammetry based on the enhancement effect of anionic surfactant, sodium dodecylsulfate(Elsevier, 2011-07-15) Yardım, Yavuz; Keskin, Ertuğrul; Levent, Abdulkadir; Şentürk, ZühreBenzo[a]pyrene (BaP), a member of the polycyclic aromatic hydrocarbon (PAH) class, is one of the most potent PAH carcinogens. The electrochemical oxidation of BaP was first studied by cyclic voltammetry at the boron-doped diamond electrode in non-aqueous solvent (dimethylsulphoxide with lithium perchlorate). The compound was irreversibly oxidized in a single step at high positive potential, resulting in the well-resolved formation of a couple with a reduction and re-oxidation wave at much lower potentials. Special attention was given to the use of adsorptive stripping voltammetry together with a medium exchange procedure in aqueous and aqueous/surfactant solutions over the pH range of 2.0–8.0. The technique in aqueous solutions had little value in practice because of too small oxidation peak current. This problem was solved when surfactants were added into the sample solution, by which the oxidation peak currents of BaP were found enhanced dramatically. The employed surfactants were sodium dodecylsulfate (anionic, SDS), cetyltrimethylammonium bromide (cationic, CTAB) and Tween 80 (non-ionic). Using square-wave stripping mode, the compound yielded a well-defined voltammetric response in Britton–Robinson buffer, pH 2.0 containing 2.5 × 10−4 M SDS at +1.07 V (vs. Ag/AgCl) (after 120 s accumulation at +0.10 V). The process could be used to determine BaP in the concentration range of 16–200 nM (4.04–50.46 ng mL−1), with a detection limit of 2.86 nM (0.72 ng mL−1). This method was also applied to determine BaP in model water sample prepared by adding its different concentrations into tap water.Öğe Determination of 7,12-dimethylbenz[a]anthracene in orally treated rats by high-performance liquid chromatography and transfer stripping voltammetry(Bentham, 2012-06) Yardım, Yavuz; Levent, Abdulkadir; Ekin, Suat; Keskin, Ertuğrul; Oto, Gökhan; Şentürk, ZühreA number of polycyclic aromatic hydrocarbons (PAHs) have been shown to be toxicants, and induce carcinogenic and immunotoxic effects. As a model PAH agent, 7,12-dimethylbenz[a]anthracene (DMBA) was the strongest one tested in terms of its biological activities and biotransformation. A new and simple high-performance liquid chromatographic (HPLC) method with diode-array detection at 290 nm was developed and validated for monitoring of DMBA in different matrices (serum, liver and kidney) of rats orally treated with DMBA. Furthermore, the applicability of adsorptive transfer stripping voltammetry (AdTSV) on the pencil-lead graphite electrode to these samples was illustrated using our previously reported data for bulk aqueous solutions of DMBA. HPLC and AdTSV methods, which were compatible with each other, allowed DMBA to be detected down to the levels of 3.82x10-9 M (0.98 ppb) and 6.73x10-9 M (1.73 ppb), respectively. Olive oil solutions of DMBA in dose 50 mg/kg were orally administered. 60 days after a single dose of DMBA, its concentrations in these biological samples from rats were measured by means of both methods. Because of rapid biotransformation, DMBA could not be detected in serum. Only low levels of the compounds were deposited unchanged in kidney whereas its levels were considerably higher in liver. These methods were also applied to the assay whether there is an influence of the intake of aqueous extracts of Hypericum Perforatum L. plant on the parent DMBA levels accumulated in rat tissues.
