New series of metal complexes by amphiphilic biopolymeric Schiff bases from modified chitosans: Preparation, characterization and effect of molecular weight on its biological applications.

To improve biological activity of chitosans, new Zn(II), Pd(II) and Pt(II) complexes with biopolymeric amphiphilic Schiff bases anchored in different molecular weight chitosans matrices modified with salicylaldehyde and glycidol were prepared. Salicylaldehyde was introduced to generate complexing Schiff base sites in the chitosans matrix while glycidol is intended to increase the water solubility of the resulting biopolymeric complexes. These novel complexes were characterized using various techniques and assayed for antimicrobial and antitumor activity.

Simultaneous determination of environmental contaminants using a graphite oxide - Polyurethane composite electrode modified with cyclodextrin.

A composite electrode based on graphite oxide (GrO)-polyurethane (PU) modified with β-cyclodextrin (CD) was proposed for the simultaneous determination of three drugs: terbutaline (TER), nimesulide (NIM), and methocarbamol (MET), as possible contaminants in river water samples. To evaluate the performance of the proposed CD-GrOPUE, voltammetric techniques were used and two other electrodes were fabricated (GrOPUE and GrPUE) for comparison. The functionalization of the GrO was confirmed by scanning electron microscopy images, energy-dispersive X-ray spectroscopy analysis, and thermogravimetry.

The influence of reaction parameters on complexation of Zn(II) complexes with biopolymeric Schiff bases prepared from chitosan and salicylaldehyde.

Influence of some reactional parameters as mol ratio (Schiff base:metal), solvent, temperature and reaction time were evaluated in order to improve the extension of complexation during the preparation of zinc complexes of biopolymeric Schiff base from chitosan and salicylaldehyde. Zinc(II) complex was used as a model system in order to improve the degree of complexation for further synthesis of different Schiff bases complexes from other aldehydes and metallic centers. The complexation yields for each synthesis were estimated on the basis of the zinc oxide formed after thermal degradation.

Synthesis, Characterization and Biological Activities of Biopolymeric Schiff Bases Prepared with Chitosan and Salicylaldehydes and Their Pd(II) and Pt(II) Complexes.

In an attempt to enhance chitosan biological activities, biopolymeric Schiff bases of chitosan and different salicylaldehydes and their palladium(II) and platinum(II) complexes were synthesized and tested. The chemical structures of these derivatives were characterized using ¹H-NMR, FTIR spectroscopy and XPRD. Thermal analysis was done through TGA/DTG-DTA.

Comparative performances of a bare graphite-polyurethane composite electrode unmodified and modified with graphene and carbon nanotubes in the electrochemical determination of escitalopram.

A bare composite graphite-polyurethane electrode (EGPU) and two other modified with graphene (EGPU-GR) and functionalized multi-walled carbon nanotubes (EGPU-CNTs) were prepared and compared regarding their voltammetric response to escitalopran (EST). The modifiers were characterized by Raman spectroscopy and the resulting electrode materials by contact angle measurements with a hydrophilicity character in the ascending order for the composites: GPU > GPU-GR > GPU-CNTs and scanning electron microscopy (SEM). The electroactive areas of the EGPU, EGPU-GR, and EGPU-CNTs were 0.

Synthesis, characterization and biological activity of Cu(II), Ni(II) and Zn(II) complexes of biopolymeric Schiff bases of salicylaldehydes and chitosan.

Schiff bases have been prepared from biopolymer chitosan and salicylaldehyde, 5-methoxysalicylaldehyde, and 5-nitrosalicylaldehyde. Ligands were synthesized in a 1:1.5mol ratio, and their Cu(II), Ni(II) and Zn(II) complexes in a 1:1mol ratio (ligand:metal).

The use of a graphite-castor oil polyurethane composite electrode for the determination of hydroquinone in photographic developers.

The performance of a new graphite-castor oil polyurethane composite electrode in the determination of hydroquinone in photographic developers in a differential pulse voltammetric (DPV) procedure is described. The 60% (graphite, w/w) composite electrode presented good stability, repeatability and accurate response. Limit of detection of 934 nmol L(-1) was observed for hydroquinone within a linear dynamic range from 66 to 530 nmol L(-1).

Evaluation of a carbon paste electrode modified with organofunctionalised SBA-15 nanostructured silica in the simultaneous determination of divalent lead, copper and mercury ions.

The performance of a carbon paste electrode (CPE) modified with SBA-15 nanostructured silica organofunctionalised with 2-benzothiazolethiol in the simultaneous determination of Pb(II), Cu(II) and Hg(II) ions in natural water and sugar cane spirit (cachaça) is described. Pb(II), Cu(II) and Hg(II) were pre-concentrated on the surface of the modified electrode by complexing with 2-benzothiazolethiol and reduced at a negative potential (-0.80 V).

Graphite-silicone rubber composite electrode: Preparation and possibilities of analytical application.

Composite electrodes were prepared using graphite powder and silicone rubber in different compositions. The use of such hydrophopic materials interned to diminish the swallowing observed in other cases when the electrodes are used in aqueous solutions for a long time. The composite was characterized for the response reproducibility, ohmic resistance, thermal behavior and active area.

Determination of atenolol at a graphite-polyurethane composite electrode.

A bare graphite-polyurethane composite was evaluated as an alternative electrode in the determination of atenolol (ATN) in pharmaceutical formulations. Using a DPV procedure, a linear analytical curve was observed in the 4-100mumolL(-1) range with a LOD=3.16mumolL(-1), without need of surface renewing between successive runs, with recoveries between 95.

Evaluation of the electrochemical behavior and analytical potentialities of a carbon paste electrode modified with a ruthenium (III) piperidinedithiocarbamate complex.

The preparation and electrochemical characterization of a carbon paste electrode modified with bis(N,N-piperidinedithiocarbamate)-mu-tris(N,N-piperidinedithiocarbamate)diruthenium(III) complex, alpha-[Ru2(Pip)5]Cl are described. The best voltammetric response was obtained for a 10% (m/m) alpha-[Ru2(Pip)5]Cl content in the paste, potassium acid phthalate solution pH 4.0 as supporting electrolyte and scan rate of 100 mV s-1.

The use of carbon paste electrode in the direct voltammetric determination of tryptophan in pharmaceutical formulations.

A simple, fast and sensitive method is proposed for Tryptophan (Trp) determination in pharmaceutical formulations containing other non-electroative aminoacids, vitamins and hydroxycobalamines. Optimized conditions for differential pulse voltammetry allowed the determination of Trp with detection limit of 1.7 microM in 2-30 mM linear dynamic range (n=7; r=0.