Electrochemical sensing of methotrexate in the presence of folic acid using PAMAM dendrimer-functionalized multiwalled carbon nanotube-modified electrode.

This works presents a novel electrochemical sensor based on the third-generation poly(amidoamine) dendrimer (G3 PAMAM)-functionalized multiwalled carbon nanotube (MWCNT)-modified screen-printed graphite electrode (SPGE) for the simple and sensitive detection of methotrexate (MTX). The carboxylated MWCNTs were covalently functionalized with amino groups of G3 PAMAM and characterized using different techniques. The sensing ability of the designed nanosensor (MWCNTs-PAMAM/SPGE) was tested using differential pulse voltammetry (DPV), chronoamperometry (CHA), linear sweep voltammetry (LSV), and cyclic voltammetry (CV).

Molybdenum Disulfide/Nickel-Metal Organic Framework Hybrid Nanosheets Based Disposable Electrochemical Sensor for Determination of 4-Aminophenol in Presence of Acetaminophen.

The toxicity of commonly used drugs, such as acetaminophen (ACAP) and its degradation-derived metabolite of 4-aminophenol (4-AP), underscores the need to achieve an effective approach in their simultaneous electrochemical determination. Hence, the present study attempts to introduce an ultra-sensitive disposable electrochemical 4-AP and ACAP sensor based on surface modification of a screen-printed graphite electrode (SPGE) with a combination of MoS nanosheets and a nickel-based metal organic framework (MoS/Ni-MOF/SPGE sensor). A simple hydrothermal protocol was implemented to fabricate MoS/Ni-MOF hybrid nanosheets, which was subsequently tested for properties using valid techniques including X-ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy (EDX), Fourier transformed infrared spectroscopy (FTIR), and N adsorption-desorption isotherm.

A UiO-66-NH MOF/PAMAM Dendrimer Nanocomposite for Electrochemical Detection of Tramadol in the Presence of Acetaminophen in Pharmaceutical Formulations.

In this work, we prepared a novel electrochemical sensor for the detection of tramadol based on a UiO-66-NH metal-organic framework (UiO-66-NH MOF)/third-generation poly(amidoamine) dendrimer (G3-PAMAM dendrimer) nanocomposite drop-cast onto a glassy carbon electrode (GCE) surface. After the synthesis of the nanocomposite, the functionalization of the UiO-66-NH MOF by G3-PAMAM was confirmed by various techniques including X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), field emission-scanning electron microscopy (FE-SEM), and Fourier transform infrared (FT-IR) spectroscopy. The UiO-66-NH MOF/PAMAM-modified GCE exhibited commendable electrocatalytic performance toward the tramadol oxidation owing to the integration of the UiO-66-NH MOF with the PAMAM dendrimer.

Simultaneous Voltammetric Determination of Epinine and Venlafaxine Using Disposable Screen-Printed Graphite Electrode Modified by Bimetallic Ni-Co-Metal-Organic-Framework Nanosheets.

We constructed two-dimensional NiCo-metal-organic-framework (NiCo-MOF) nanosheets based on a facile protocol and then characterized them using multiple approaches (X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), field emission-scanning electron microscopy (FE-SEM), and N adsorption/desorption isotherms techniques). As a sensitive electroactive material, the as-fabricated bimetallic NiCo-MOF nanosheets were employed to modify a screen-printed graphite electrode surface (NiCo-MOF/SPGE) for epinine electro-oxidation. According to the findings, there was a great improvement in the current responses of the epinine because of the appreciable electron transfer reaction and catalytic performance of the as-produced NiCo-MOF nanosheets.

Graphene Oxide-PAMAM Nanocomposite and Ionic Liquid Modified Carbon Paste Electrode: An Efficient Electrochemical Sensor for Simultaneous Determination of Catechol and Resorcinol.

In this paper, a simple strategy was proposed for the analysis of catechol by a carbon paste electrode (CPE) modified with graphene oxide-third generation of poly(amidoamine) dendrimer (GO/G3-PAMAM) nanocomposite and ionic liquid (IL). The synthesis of GO-PAMAM nanocomposite was confirmed using X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), field emission scanning electron microscopy (FE-SEM), and Fourier transform infrared spectroscopy (FT-IR) techniques. The prepared modified electrode (GO-PAMAM/ILCPE) exhibited good performance to detect catechol with a notable decrease in overpotential and increase in current compared with an unmodified CPE.

Simultaneous Determination of Dopamine and Uric Acid in Real Samples Using a Voltammetric Nanosensor Based on Co-MOF, Graphene Oxide, and 1-Methyl-3-butylimidazolium Bromide.

A chemically modified carbon paste electrode, based on a CoMOF-graphene oxide (GO) and an ionic liquid of 1-methyl-3-butylimidazolium bromide (CoMOF-GO/1-M,3-BB/CPE), was fabricated for the simultaneous determination of dopamine (DA) and uric acid (UA). The prepared CoMOF/GO nanocomposite was characterized by field emission-scanning electron microscopy (FE-SEM), the X-ray diffraction (XRD) method, a N adsorption-desorption isotherm, and an energy dispersive spectrometer (EDS). The electrochemical sensor clearly illustrated catalytic activity towards the redox reaction of dopamine (DA), which can be authenticated by comparing the increased oxidation peak current with the bare carbon paste electrode.

Construction of modified screen-printed graphite electrode for the application in electrochemical detection of sunset yellow in food samples.

The current work introduced a novel electrochemical sensor (screen-printed graphite electrode (SPGE) modified with MnO nanorods anchored graphene oxide nanocomposite (MnO NRs/GO) for sensitive determination of sunset yellow. The characterization of MnO NRs/GO nanocomposite synthesized through a simple hydrothermal approach was determined employing varied analytical equipment like Field emission-scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FT-IR), and X-ray diffraction (XRD). Chronoamperometric measurements, differential pulse voltammetry (DPV), cyclic voltammetry (CV) and linear sweep voltammetry (LSV) were recruited to recognize the electrochemical oxidation of sunset yellow on the MnO NRs/GO/SPGE.

A Comprehensive Review of Metal-Organic Framework: Synthesis, Characterization, and Investigation of Their Application in Electrochemical Biosensors for Biomedical Analysis.

Many studies have addressed electrochemical biosensors because of their simple synthesis process, adjustability, simplification, manipulation of materials' compositions and features, and wide ranges of detection of different kinds of biomedical analytes. Performant electrochemical biosensors can be achieved by selecting materials that enable faster electron transfer, larger surface areas, very good electrocatalytic activities, and numerous sites for bioconjugation. Several studies have been conducted on the metal-organic frameworks (MOFs) as electrode modifiers for electrochemical biosensing applications because of their respective acceptable properties and effectiveness.

Simultaneous detection of carmoisine and tartrazine in food samples using GO-FeO-PAMAM and ionic liquid based electrochemical sensor.

This study was performed to investigate the simultaneous detection of carmoisine and tartrazine, two food azo dyes, with a new voltammetric sensor based on graphene oxide-FeO (GO-FeO) nanocomposite functionalized with fourth-generation poly(amidoamine) (G4 PAMAM) dendrimers (GO-FeO-G4 PAMAM) and ionic liquid (IL) modified carbon paste electrode (GO-FeO-G4 PAMAM/ILCPE). The GO-FeO-G4 PAMAM was synthesized and characterized by X-ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy (EDX), vibrating-sample magnetometer (VSM), and fourier transform infrared (FT-IR) techniques. Cyclic voltammetry (CV) was used to evaluate the electrochemical behavior of carmoisine, revealing the good electrocatalytic function of GO-FeO-G4 PAMAM/ILCPE.

Amplified electrochemical sensor employing screen-printed electrode modified with Ni-ZIF-67 nanocomposite for high sensitive analysis of Sudan I in present bisphenol A.

This study utilized a facile one-pot protocol to synthesize Ni-cobalt zeolitic imidazolate framework (Ni-ZIF-67) nanocomposite, which was then characterized by Fourier transform infrared spectroscopy, X-ray diffraction, energy dispersive X-ray spectroscopy and scanning electron microscopy. The Ni-ZIF-67 nanocomposite was subsequently applied to modify a screen-printed electrode (SPE) as a durable sensor for detection of Sudan I concomitantly with bisphenol A (BPA), with remarkably increased electrochemical response when comparing with a bare SPE. The results showed the calibration plot to be linear in the concentration range between 0.

Green Synthesis of Zeolitic Imidazolate Frameworks: A Review of Their Characterization and Industrial and Medical Applications.

Metal organic frameworks (MOF) are a class of hybrid networks of supramolecular solid materials comprising a large number of inorganic and organic linkers, all bound to metal ions in a well-organized fashion. Zeolitic imidazolate frameworks (ZIFs) are a sub-group of MOFs with imidazole as an organic linker to metals; it is rich in carbon, nitrogen, and transition metals. ZIFs combine the classical zeolite characteristics of thermal and chemical stability with pore-size tunability and the rich topological diversity of MOFs.

Synthesis and Characterization of GO/ZIF-67 Nanocomposite: Investigation of Catalytic Activity for the Determination of Epinine in the Presence of Dobutamine.

In this study, we prepared graphene oxide (GO)/ZIF-67 nanocomposites. Therefore, GO/ZIF-67 nanocomposites were used as a modifier on a screen-printed electrode (GO/ZIF-67/SPE) for studying the electrochemical behavior of epinine in phosphate buffer saline (PBS) at pH 7.0 with voltammetry techniques.

Voltammetric detection of sumatriptan in the presence of naproxen using FeO@ZIF-8 nanoparticles modified screen printed graphite electrode.

A novel electrochemical sensing platform was designed and prepared for the simultaneous detection of sumatriptan and naproxen by exploiting the prowess of the FeO@ZIF-8 nanoparticles (NPs); as-synthesized FeO@ZIF-8 NPs were characterized by energy-dispersive X-ray spectroscopy, fourier transform infrared spectroscopy, X-ray diffraction, field emission scanning electron microscopy (FESEM), transmission electron microscopy and thermal gravimetric analysis. The immobilized FeO@ZIF-8 NPs on a screen printed graphite electrode (SPGE) was evaluated electrochemically via cyclic voltammetry, linear sweep voltammetry, and differential pulse voltammetry as well as chronoamprometery means; FeO@ZIF-8/SPGE exhibited good sensing performance for sumatriptan in a range of 0.035-475.

Low-temperature synthesis of hetero-structures of magnetically separable iron oxide@Au-rGO nanocomposite for efficient degradation of organic dye under visible light irradiation.

In the present study, FeO@Au core-shell nanoparticles decorated on reduce graphene oxide (FeO@Au/rGO) nanocomposite were synthesized using the reduction method by sodium citrate, Hummer's method, and hydrothermal method, respectively. The as-prepared nanostructures were characterized by X-ray diffraction (XRD), Energy Dispersive X-ray (EDX), transmission electron microscopy (TEM), scanning electron microscopy (SEM)to assess the surface features, crystallinity and morphological characteristics. These nanostructures were employed for photocatalytic degradation of crystal violet (CV), and amongst them, FeO@Au/rGO nanocomposite offered the best results under the visible light irradiation and optimal conditions.

Magnetic nanomaterials based electrochemical (bio)sensors for food analysis.

It is widely accepted that nanotechnology attracted more interest because of various values that nanomaterial applications offers in different fields. Recently, researchers have proposed nanomaterials based electrochemical sensors and biosensors as one of the potent alternatives or supplementary analytical tools to the conventional detection procedures that consumes a lot of time. Among different nanomaterials, researchers largely considered magnetic nanomaterials (MNMs) for developing and fabricating the electrochemical (bio)sensors for numerous utilizations.

Recent developments in voltammetric and amperometric sensors for cysteine detection.

This review article aims to provide an overview of the recent advances in the voltammetric and amperometric sensing of cysteine (Cys). The introduction summarizes the important role of Cys as an essential amino acid, techniques for its sensing, and the utilization of electrochemical methods and chemically modified electrodes for its determination. The main section covers voltammetric and amperometric sensing of Cys based on glassy carbon electrodes, screen printed electrodes, and carbon paste electrodes, modified with various electrocatalytic materials.

Fabrication of a new superparamagnetic metal-organic framework with core-shell nanocomposite structures: Characterization, biocompatibility, and drug release study.

The Superparamagnetic CoFeONPs@Mn-Organic Framework core-shell nanocomposites that had potential application in targeted drug-delivery were synthesized by layer to layer method. The structure and composition of the obtained microspheres were characterized by SEM, TEM, DLS, XRD, VSM, FTIR, and TG analysis. Results showed that the structures have a high degree crystalline, high temperature stability, magnetics and core-shell nanocomposites.

Simultaneous electrochemical determination of levodopa and piroxicam using a glassy carbon electrode modified with a ZnO-Pd/CNT nanocomposite.

A highly conductive electrochemical sensor was constructed for the simultaneous electrochemical determination of levodopa and piroxicam by modification of a glassy carbon electrode with a ZnO-Pd/CNT nanocomposite (GCE/ZnO-Pd/CNTs). The ZnO-Pd/CNT nanocomposite was synthesized by the sol-gel procedure and was characterized by EDAX, MAP and SEM. The sensor was shown to improve the oxidation signal of levodopa and piroxicam by ∼70.

Fabrication of novel TiO2 nanoparticles/Mn(III) salen doped carbon paste electrode: application as electrochemical sensor for the determination of hydrazine in the presence of phenol.

Hydrazine and phenol are two important environmental pollutants. In this work, an electrochemical sensor for the selective and sensitive detection of hydrazine in presence of phenol was developed by the bulk modification of carbon paste electrode (CPE) with TiO2 nanoparticles and Mn(III) salen. Large peak separation, good sensitivity, and stability allow this modified electrode to analyze hydrazine individually and simultaneously along with phenol.

Synthesis, characterization, X-ray crystal structure, DFT calculation, DNA binding, and antimicrobial assays of two new mixed-ligand copper(II) complexes.

Two new Cu(II) complexes, [Cu(L)(phen)] (1), [Cu(L)(bipy)] (2), where L(2-)=(3-methoxy-2oxidobenzylidene)benzohydrazidato, phen=1,10 phenanthroline, and bipy=2,2' bipyridine, were prepared and fully characterized using elemental analyses, FT-IR, molar conductivity, and electronic spectra. The structures of both complexes were also determined by X-ray diffraction. It was found that, both complexes possessed square pyramidal coordination environment in which, Cu(II) ions were coordinated by donor atoms of HL and two nitrogens of heterocyclic bases.

Combined experimental and theoretical studies on the X-ray crystal structure, FT-IR, 1H NMR, 13C NMR, UV-Vis spectra, NLO behavior and antimicrobial activity of 2-hydroxyacetophenone benzoylhydrazone.

A Schiff base ligand, 2-hydroxyacetophenone benzoylhydrazone (HL) was synthesized and fully characterized with FT-IR, elemental analyses, UV-Vis, (1)H NMR and (13)C NMR spectra. DFT calculations using B3LYP/6-31+G(d,p) and PW91/DZP are performed to optimize the molecular geometry. Optimized structures are used to calculate FT-IR, UV-Vis, (1)H NMR and (13)C NMR spectra of the compound.

A new tridentate Schiff base Cu(II) complex: synthesis, experimental and theoretical studies on its crystal structure, FT-IR and UV-Visible spectra.

A new Cu(II) complex [Cu(L)(NCS)] has been synthesized, using 1-(N-salicylideneimino)-2-(N,N-methyl)-aminoethane as tridentate ONN donor Schiff base ligand (HL). The dark green crystals of the compound are used for single-crystal X-ray analysis and measuring Fourier Transform Infrared (FT-IR) and UV-Visible spectra. Electronic structure calculations at the B3LYP and MP2 levels of theory are performed to optimize the molecular geometry and to calculate the UV-Visible and FT-IR spectra of the compound.

Potentiometric determination of trace amounts of aluminium utilizing polyvinyl chloride membrane and coated platinum sensors based on E-N'-(2-hydroxy-3-methoxybenzylidene) benzohydrazide.

This paper describes the construction and performance characteristics of novel polyvinyl chloride membrane (PME) and coated platinum (CPtE) aluminium (Al) ion selective electrodes based on E-N'-(2-hydroxy-3-methoxybenzylidene) benzohydrazide. The electrodes exhibited linear responses with near Nernstian slopes of 19.9 +/- 0.

A novel tridentate Schiff base dioxo-molybdenum(VI) complex: synthesis, experimental and theoretical studies on its crystal structure, FTIR, UV-visible, ¹H NMR and ¹³C NMR spectra.

A new dioxo-molybdenum(VI) complex [MoO(2)(L)(H(2)O)] has been synthesized, using 5-methoxy 2-[(2-hydroxypropylimino)methyl]phenol as tridentate ONO donor Schiff base ligand (H(2)L) and MoO(2)(acac)(2). The yellow crystals of the compound are used for single-crystal X-ray analysis and measuring Fourier Transform Infrared (FTIR), UV-visible, (1)H NMR and (13)C NMR spectra. Electronic structure calculations at the B3LYP and PW91PW91 levels of theory are performed to optimize the molecular geometry and to calculate the UV-visible, FTIR, (1)H NMR and (13)C NMR spectra of the compound.

A new Mo Schiff base complex: methanol[N'-(3-meth-oxy-2-oxidobenzyl-idene)benzohydrazidato]dioxido-molybdenum(VI).

In the title benzil-idene Schiff base molybdenum(VI) complex, [Mo(C(15)H(12)N(2)O(3))O(2)(CH(3)OH)], the Mo(VI) ion is coordinated by two oxide O atoms and by two O atoms and one N atom of the tridentate N'-(3-meth-oxy-2-oxidobenzyl-idene)benzo-hydrazidate (L) Schiff base ligand. The methanol O atom completes the distorted octa-hedral configuration of the Mo(VI) atom. Strong O-H⋯N hydrogen bonds form a C(5) chain around a 2(1) screw axis.