A novel potentiometric naproxenate ion sensor immobilized in a graphite matrix for determination of naproxen in pharmaceuticals (original) (raw)
Related papers
Properties of naproxen ion-selective electrodes
Central European Journal of Chemistry, 2008
Naproxen membrane electrodes based on different plasticizers and the quaternary ammonium salts (QASs) dimethyldidecylammonium bromide, methyltrioctylammonium chloride, or tetraoctylammonium chloride, were prepared. The following basic parameters were investigated for the optimal electrode: measurement range (10−4 − 10−1 mol L−1), slope of the linear range of the calibration curve (−58.3 mV decade−1), limit of detection (6.0 × 10−5 mol L−1), lifetime (2.5 months), dependence of the electrode potential on pH (5.5 − 9.0), reproducibility of potential (1.2 mV) and selectivity coefficients in relation to selected organic and inorganic anions. The electrode was utilized for determination of naproxen in tablets by the calibration curve method and the standard addition method.
Voltammetric and Chromatographic Determination of Naproxen in Drug Formulation
Journal of Scientific Perspectives, 2019
In this work, the electrochemical oxidation of naproxen (NAP) was studied at an ultra-trace graphite electrode (UTGE). The cyclic voltammetry (CV) technique was used to determine the optimum conditions and the effect of pH on the electrochemical oxidation of NAP. Acetate buffer (pH 4.50) was selected as the support electrolyte due to obtaining the highest electronic signal increase during oxidation of NAP at UTGE. The differential pulse voltammetry (DPV) technique was performed for electrochemical determination of NAP. In the optimum conditions, the limits of detection (LOD) and quantification (LOQ) were determined to be 8.66 10-8 M and 2.88 10-7 M. In addition, the amount of NAP was determined in drug tablets. The recovery studies of NAP from the drug tablet were completed in order to check the accuracy and precision of the applied voltammetric method. Furthermore, the determination of NAP was performed with the high-performance liquid chromatography (HPLC) method. These two methods were compared in terms of accuracy, precision and recovery studies.
An effective, novel, and cheap carbon paste electrode for naproxen estimation
Reviews in Analytical Chemistry
Herein, a carbon paste electrode (CPE) modified with poly(reduced-o-nitrobenzoic acid [r-o-NBA]) supported in graphene quantum dots (GQDs) was fabricated for the first time. The fabricated electrode’s surface morphology and composition were characterised by scanning electron microscope and transmission electron microscope. The poly(r-o-NBA)/GQDs/CPE showed high electrocatalytic activity towards the oxidation of naproxen (NPX) using cyclic and differential pulse voltammetric methods. The effect of scan rate on the oxidation peak of NPX suggests that the electrode process was typically diffusion-controlled. In addition, the effect of pH reflects the participation of protons in the oxidation process of NPX. The peak current is linearly proportional to the concentration of NPX ranging from 1.0 to 100.0 µM, with the correlation coefficient (R 2), sensitivity, limit of detection (3σ), and limit of quantification (10σ) being 0.9995, 0.419 µA·µM−1·cm−2, 0.672, and 2.241 µM, respectively. Us...
A novel and fast electroanalytical method for naproxen determination in pharmaceutical formulations using batch injection analysis (BIA) with pulsed amperometric detection is described. Bare glassy carbon electrode was used as working electrode and 0.05 mol L-1 phosphate buffer solution as supporting electrolyte. The amperometric method involved the continuous application of two sequential potential pulses to the working electrode in order to detect naproxen by its electrochemical oxidation (+1.5 V for 200 ms) and to clean the electrode surface from adsorption products (+1.0 V for 100 ms), avoiding electrode contamination. The proposed method has several advantages for routine analysis, including: a low relative standard deviation between injections (3.0%, n = 10), high analytical frequency (90 h-1), satisfactory accuracy (based on comparative determinations by spectroflorimetry) and low limit of detection (0.3 µmol L-1).
Journal of Analytical Methods in Chemistry
The present work describes a novel, simple, and fast electroanalytical methodology for naproxen (NAP) determination in pharmaceutical formulations and biological fluids in the presence of its degradation products. Carbon paste electrodes (CPEs) modified with different carbon nanomaterials, namely, glassy carbon powder (GCE), multiwall carbon nanotubes (MWCNTs), single-walled carbon nanotubes (SWCNTs), graphene nanosheets (Gr), and graphene oxides (GO) were tested. Comprehensive studies were performed on the electrode matrix composition including the nature of the pasting liquids, pH, carbon nanomaterials, and mode of electrode modification. Two anodic oxidation peaks were recorded at 0.890 and 1.18 V in 1 × 10−1 mol·L−1 phosphate buffer solution at pH 6. Oxidation of naproxen (NAP) is an irreversible diffusion-controlled process. Calibration plots were rectilinear in the concentration ranging from 0.067 to 1.0 µg·mL−1 with correlation coefficient 0.9979. Photodegradation of NAP resu...
Analytica Chimica Acta, 2003
The anodic oxidation of naproxen has been carried out on a platinum electrode using cyclic, linear sweep and differential pulse voltammetry (DPV). Naproxen exhibited a single well-defined and irreversible peak in acetonitrile/0.1 M LiClO 4 with a peak potential at 1146 mV versus Ag/AgCl. This allowed the development of a simple, selective and sensitive differential pulse voltammetric method for the determination of naproxen in pharmaceuticals. The calibration plot was linear (R 2 = 0.998) over the range 1-25 g ml −1 . The limit of detection (3σ/m) was 0.24 g ml −1 and the relative standard deviation of the measurements was 1.2% (n = 6).
Sensors, 2020
Here we report on a selective and sensitive graphene-oxide-based electrochemical sensor for the detection of naproxen. The effects of doping and oxygen content of various graphene oxide (GO)-based nanomaterials on their respective electrochemical behaviors were investigated and rationalized. The synthesized GO and GO-based nanomaterials were characterized using a field-emission scanning electron microscope, while the associated amounts of the dopant heteroatoms and oxygen were quantified using x-ray photoelectron spectroscopy. The electrochemical behaviors of the GO, fluorine-doped graphene oxide (F-GO), boron-doped partially reduced graphene oxide (B-rGO), nitrogen-doped partially reduced graphene oxide (N-rGO), and thermally reduced graphene oxide (TrGO) were studied and compared via cyclic voltammetry (CV) and differential pulse voltammetry (DPV). It was found that GO exhibited the highest signal for the electrochemical detection of naproxen when compared with the other GO-based nanomaterials explored in the present study. This was primarily due to the presence of the additional oxygen content in the GO, which facilitated the catalytic oxidation of naproxen. The GO-based electrochemical sensor exhibited a wide linear range (10 µM–1 mM), a high sensitivity (0.60 µAµM−1cm−2), high selectivity and a strong anti-interference capacity over potential interfering species that may exist in a biological system for the detection of naproxen. In addition, the proposed GO-based electrochemical sensor was tested using actual pharmaceutical naproxen tablets without pretreatments, further demonstrating excellent sensitivity and selectivity. Moreover, this study provided insights into the participatory catalytic roles of the oxygen functional groups of the GO-based nanomaterials toward the electrochemical oxidation and sensing of naproxen.
Macedonian Journal of Chemistry and Chemical Engineering
In this study, an electrochemical sensor based on a boron doped diamond electrode (BDDE) was developed for the determination of naproxen (NAP) using a poly(aniline-2-sulfonic acid)/boron doped diamond electrode, p(A2SA/BDDE). Polymerization of A2SA was conducted in a water/acetonitrile (1:1) mixture containing 0.1 M sodium perchlorate (NaClO4) on bare BDDE and the electrochemical properties studied by cyclic voltammetry in ferricyanide/KNO3 solution. The prepared p(A2SA/BDDE) was used for detection of NAP. Effects of parameters such as monomer type and concentration, the number of cycles, and scan rate were investigated using differential pulse voltammetry (DPV) in phosphate buffer containing 0.75 mM NAP. The effect of electrolyte type and pH on DPV responses to NAP were also studied. The oxidative current peak stem from NAP concentration observed at 1.1 V potential. A linear calibration curve was obtained in the range of 0.05–1.00 mM NAP concentration. Correlation coefficient (R2),...
2019
The electrochemical response of Sand R-naproxen enantiomers were investigated on L-cysteine/reduced graphene oxide modified glassy carbon electrode (L-Cys/RGO/GCE). The production of the reduced graphene oxide and L-cysteine on the surface of the glassy carbon electrode was done by using electrochemical processes. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were used to study the enantioselective interaction between the chiral surface of the electrode and naproxen (NAP) enantiomers. The L-Cys/RGO/GCE was found to be successfully enantioselective toward sensing S-NAP in the presence of R-NAP. The linear dynamic range was found to be 5.0 × 106-1.3 × 104 M for both naproxen enantiomers with detection limits of 3.5 × 107 and 2.5 × 106 M for Sand R-NAP, respectively.
Stereoselective determination of S-naproxen in tablets by capillary electrophoresis
Journal of Pharmaceutical and Biomedical Analysis, 1998
A capillary electrophoresis (CE) method was developed for the stereoselective determination of the non-steroidal anti-inflammatory drug (NSAID), S-naproxen, in tablets. Several i-cyclodextrin derivatives (CDs) were tested as chiral selectors, including sulfobutyl-i-CD (SBCD), carboxymethyl-i-CD (CMCD), dimethyl-i-CD (DMCD) and trimethyl-i-CD (TMCD), in a phosphoric acid/triethanolamine pH 3 buffer. Under these conditions, the analyte was mainly present in an uncharged form and therefore, the use a neutral CD (DMCD or TMCD) alone could not lead to enantiomeric separation. On the contrary, by addition of a charged CD (SBCD or CMCD) to the running buffer, giving the analyte enantiomers an adequate mobility, chiral resolution could be achieved, although the resolution values obtained in this case were not quite satisfactory (RsB 1.5). Dual systems, based on the use of mixtures of charged and neutral CDs, were then investigated. The SBCD/TMCD system was found to be particularly well suited to the enantioseparation of naproxen and after optimisation of the concentrations of both CDs, a resolution value of 5.4 could be obtained. The method was validated for the determination of R-naproxen (enantiomeric impurity) in the 0.1-2% range, using the racemic mixture of the analyte. A second validation was performed in the 50 -150% range for the quantitation of S-naproxen. In both cases, good results with respect to linearity, precision and accuracy were obtained.