Bimetallic metal organic framework/Ni doped ZnO nanomaterials modified carbon paste electrode for selective electrochemical determination of ciprofloxacin.

In this work, an efficient and sensitive electrochemical sensor for the determination of ciprofloxacin (CIP) is reported. The sensor was prepared by using a carbon paste electrode (CPE) modified with a combination of bimetallic copper/cerium-based metal organic framework (Cu/Ce-MOF) and nickel doped zinc oxide nanoparticles (NZP). The modifiers were characterized by Brunauer-Emmett-Teller (BET) analysis, Fourier-transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), and elemental mapping analysis (EDS).

Investigating the effect of magnesium supplement in patients with major depressive disorder under selective serotonin reuptake inhibitor treatment.

Background: Major depression disorder (MDD) is a mental disorder that affects millions of people worldwide. This disease has negative impacts on quality of life and psychological-related functions. This is a multifactorial disorder; both genetic background and environmental factors have their role.

A sensitive fluorescent probe based on dithizone-capped ZnS quantum dots for quercetin determination in biological samples.

A simple turn on/off fluorescence approach based on dithizone-capped ZnS quantum dots (ZnS@DZ QDs) with the help of lead ions as a fluorescent probe for the quantitative determination of quercetin is reported. The interaction of lead ions with dithizone led to the formation of a rigid structure on the surface of ZnS@DZ QDs and turned on the fluorescence intensity of the QDs. After addition of quercetin to this probe and interaction with lead ions, the fluorescence emission turned off.

CdSe quantum dots capped with a deep eutectic solvent as a fluorescent probe for copper(II) determination in various drinks.

The present study shows that copper(II) ions can be determined with a new fluorescent probe that is based on the use of CdSe quantum dots capped with deep eutectic solvent (DES-CdSe QDs). The capped QDs were prepared in aqueous phase by a one-step procedure under ambient atmosphere using selenium dioxide as a stable precursor for selenium, and ascorbic acid as non-toxic reducing agent. The deep eutectic solvent is composed of choline chloride and thioglycolic acid and acts as stabilizing and functionalizing agent.

Capped cadmium sulfide quantum dots with a new ionic liquid as a fluorescent probe for sensitive detection of florfenicol in meat samples.

The new ionic liquid capped CdS quantum dots (IL-CdS QDs) as a fluorescent probe was successfully synthesized by a hydrothermal method in a one step process and used for the facile and sensitive determination of florfenicol (FLF) in aqueous media. The new ionic liquid 3-(2-[(5-amino-1,3,4-thiadiazol-2-yl)thio]ethyl)-1-methyl-1H-imidazol-3-ium chloride (IL) was synthesized by introducing 5-amino-1,3,4-thiadiazole-2-thiol as a ligand onto the alkyl chain of the 1-chloroethyl-3-methylimidazolium chloride ILs. This task specific ionic liquid reagent was used for the capping of CdS QDs which played the role of recognition element of FLF.

Simultaneous determination of Brilliant Green and Crystal Violet dyes in fish and water samples with dispersive liquid-liquid micro-extraction using ionic liquid followed by zero crossing first derivative spectrophotometric analysis method.

In this study, dispersive liquid-liquid micro-extraction using ionic liquid (IL-DLLME) combined with zero crossing first derivative spectrophotometric method was applied to quantitative determination of triphenylmethane dyes in binary mixtures. The 1-methyl-3-octylimidazolium hexafluorophosphate [OMIM][PF] ionic liquid was used to extract Brilliant Green (BG) and Crystal Violet(CV) dyes from aqueous solutions. The amplitude of the zero crossing first derivative spectra at 670 nm and 532 nm were selected for the determination of BG and CV, respectively.

Iron species determination by task-specific ionic liquid-based in situ solvent formation dispersive liquid-liquid microextraction combined with flame atomic absorption spectrometry.

Background: The task-specific ionic liquid (TSIL) of 1-ethyl-3-methylimidazolium bromide functionalized with 8-hydroxyquinoline was used as a chelating agent and extracting solvent for dispersive liquid-liquid microextraction and subsequent determination of Fe(III) by flame atomic absorption spectrometry. The in situ solvent formation of TSIL using KPF provided the desired water-immiscible ionic liquid. The total Fe concentration could be determined after pre-oxidation of Fe(II) to Fe(III).

The development of a new optical sensor based on the Mn doped ZnS quantum dots modified with the molecularly imprinted polymers for sensitive recognition of florfenicol.

The Mn doped ZnS quantum dots (Mn:ZnS QDs) capped with the florfenicol molecularly imprinted polymer (Mn:ZnS QDs@MIP) were prepared via the sol-gel surface imprinting approach using 3-aminopropyltriethoxysilane (APTES) as the functional monomer and tetraethoxysilane (TEOS) as the cross-linker for the optosensing of the florfenicol. Transmission electron microscopy (TEM), X-ray diffractometer, IR spectroscopy, UV-Vis absorption spectrophotometry, and spectrofluorometry were used to elucidate the formation, morphology, and identification of the products. To illustrate the usefulness of the new imprinted material, the non-imprinted coated Mn:ZnS QDs (Mn:ZnS QDs@NIP) were synthesized without the presence of the florfenicol.

A new method for separation and determination of Cr(III) and Cr(VI) in water samples by high-performance liquid chromatography based on anion exchange stationary phase of ionic liquid modified silica.

In this work, N-methylimidazolium-chloride ionic liquid functionalized silica was prepared and used as an anion-exchange stationary phase for separation of chromium species by high-performance liquid chromatography (HPLC) with UV detection at 200 nm. The Cr(VI) as HCr2O7(-) and chelated Cr(III) with potassium hydrogen phthalate (PHP) as Cr(PHP)2 (-) was retained on the prepared column and separated using a mobile phase composed of 5% methanol in 25 mM phosphate buffer at pH 6.5.

A highly selective sorbent for removal of Cr(VI) from aqueous solutions based on Fe₃O₄/poly(methyl methacrylate) grafted Tragacanth gum nanocomposite: optimization by experimental design.

In this work, poly(methyl methacrylate) grafted Tragacanth gum modified Fe3O4 magnetic nanoparticles (P(MMA)-g-TG-MNs) were developed for the selective removal of Cr(VI) species from aqueous solutions in the presence of Cr(III). The sorbent was characterized by Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), a vibrating sample magnetometer (VSM), and thermo-gravimetric analysis (TGA). A screening study on operational variables was performed using a two-level full factorial design.

A new amperometric biosensor based on Fe3O4/polyaniline/laccase/chitosan biocomposite-modified carbon paste electrode for determination of catechol in tea leaves.

In the present study, a new biosensor based on laccase from Paraconiothyrium variabile was developed for catechol. The purified enzyme entrapped into the Fe3O4/polyaniline/chitosan (Fe3O4/polyaniline (PANI)/chitosan (CS)) biocomposite matrix film without the aid of other cross-linking reagents by a one-step electrodeposition on the surface of carbon paste electrode (CPE). The formed layer of biocomposite was characterized with scanning electron microscopy (SEM), electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV).

A nanocomposite/crude extract enzyme-based xanthine biosensor.

A novel amperometric biosensor for xanthine was developed based on covalent immobilization of crude xanthine oxidase (XOD) extracted from bovine milk onto a hybrid nanocomposite film via glutaraldehyde. Toward the preparation of the film, a stable colloids solution of core-shell Fe3O4/polyaniline nanoparticles (PANI/Fe3O4 NPs) was dispersed in solution containing chitosan (CHT) and H2PtCl6 and electrodeposited over the surface of a carbon paste electrode (CPE) in one step. Scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectrophotometry, cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS) were used for characterization of the electrode surface.

A highly sensitive and selective electrochemical sensor for determination of Cr(VI) in the presence of Cr(III) using modified multi-walled carbon nanotubes/quercetin screen-printed electrode.

A novel screen-printed carbon electrode modified with quercetin/multi-walled carbon nanotubes was fabricated for determination of Cr(VI) in the presence of excess of Cr(III) without any pretreatment. The method is based on accumulation of the quercetin-Cr(III) complex generated in situ from Cr(VI) at the modified electrode surface in an open circuit followed by differential pulse voltammetry detection. The new method allowed selective determination of Cr(VI) in the presence of Cr(III).

Voltammetric sensor based on carbon paste electrode modified with molecular imprinted polymer for determination of sulfadiazine in milk and human serum.

A new sensitive voltammetric sensor for determination of sulfadiazine is described. The developed sensor is based on carbon paste electrode modified with sulfadiazine imprinted polymer (MIP) as a recognition element. For comparison, a non-imprinted polymer (NIP) modified carbon paste electrode was prepared.

Selective solid-phase extraction using molecular imprinted polymer sorbent for the analysis of florfenicol in food samples.

A molecularly imprinted polymer (MIP) for the selective solid phase extraction (SPE) of florfenicol (FF) was prepared using FF as template and 4-vinyl pyridine (4-VP) as functional monomer. For comparison, non-imprinted polymer (NIP) was synthesized in the absence of FF. The synthesized polymers were characterised by infrared spectroscopy (IR), scanning electron microscopy (SEM), thermogravimetry analysis (TGA) and differential thermal analysis (DTA).

Preconcentration and speciation of trace amounts of chromium in saline samples using temperature-controlled microextraction based on ionic liquid as extraction solvent and determination by electrothermal atomic absorption spectrometry.

A sensitive and selective method for the preconcentration and speciation of sub ng L(-1) levels of chromium species in aqueous solutions with high salt contents is described. The developed method is based on temperature-controlled microextraction of chromium species using the 1-hexyl-3-methylimidazolium hexafluorophosphate ([HMIM][PF(6)]) ionic liquid as an extractant followed by electrothermal atomic absorption spectrometry (ETAAS) determination. The extraction of chromium species from aqueous solution into the fine droplets of [HMIM][PF(6)] was performed with ammonium pyrrolidine dithiocarbamate (APDC) as the chelating agent.

Surface modified magnetic Fe3O4 nanoparticles as a selective sorbent for solid phase extraction of uranyl ions from water samples.

In this study, silica-coated magnetic nanoparticles modified with quercetin were synthesized by a sol-gel method. These magnetic nanoparticles were assessed as a new solid phase sorbent for extraction of uranyl ions from aqueous solutions. The crystal and chemical structures and magnetic property of the new sorbent were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectrophotometer (FT-IR), and vibration sample magnetometer (VSM).

Spectrophotometric determination of rifampicin through chelate formation and charge transfer complexation in pharmaceutical preparation and biological fluids.

Two simple and accurate spectrophotometric methods for determination of Rifampicin (RIF) are described. The first method is based on charge transfer (CT) complex formation of the drug with three pi-electron acceptors either 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ), 7,7,7,8-Tetracyanoquinodimethane (TCNQ) or 2,3,5,6-Tetrachloro-1,4-benzoquinone (p-chloranil) in acetonitrile. The method is followed spectrophotometrically by measuring the maximum absorbance at 584 nm, 761 nm (680 nm) or 560 nm for DDQ, TCNQ and p-chloranil, respectively.

Copper (II) ion selective liquid membrane electrode based on new Schiff base carrier.

Cu2+ selective PVC membrane electrode based on new Schiff base 2, 2'-[1,9 nonanediyl bis (nitriloethylidyne)]-bis-(1-naphthol) as a selective carrier was constructed. The electrode exhibited a linear potential response within the activity range of 1.0 x 10(-6) - 5.

Selective transport of copper(II) ions across a liquid membrane mediated by Piroxicam.

Piroxicam was found to be a highly selective carrier for uphill transport of Cu2+ ions through a chloroform liquid membrane. The transport occurs via a counterflow of protons from the receiving phase to the source phase. The effects of several parameters on the transport of Cu2+ ions, such as the carrier concentration, pH of the source phase, composition of the receiving phase, and duration are described.

Molecularly imprinted solid-phase extraction for the screening of antihyperglycemic biguanides.

A new molecularly imprinted polymer (MIP) was specifically synthesized as a smart material for the recognition of metformin hydrochloride in solid-phase extraction. Particles of this MIP were packed into a stainless-steel tubing (50 mm x 0.8 mm i.

Solid-phase extraction-spectrophotometric determination of uranium(VI) in natural waters.

A method for the extraction and determination of uranyl ion in natural waters using octadecyl bonded silica membrane disks modified with piroxicam and spectrophotometry with arsenazo(III) is proposed. The perconcentration step was studied with regard to experimental parameters such as amount of extractant, type and amount of eluent, pH, flow rates and tolerance limit of diverse ions on the recovery of uranyl ion. The limit of detection of the proposed method is 0.

Triiodide PVC membrane electrodes based on charge-transfer complexes.

Three new electrodes were prepared by incorporating two different charge-transfer complexes and amino crown ether into plasticized PVC membranes. The electrodes showed Nernstian response to triiodide ion over the activity range from 1.0 x 10(-5) to 1.