Abstract In this paper, we report the synthesis and evaluation of a poly(vinyl alcohol)/poly(glycerol) dendrimer hydrogel incorporated with green synthesized silver nanoparticles (PVA/PGLD-AgNPs) using Cinnamomum verum extract as the reducting agent (Cz-extract). The Cz-extract was prepared using ultrasonic technique. UV-visible (UV-vis) spectra of Cz-extract confirmed the presence of cinnamaldehyde. PVA/PGLD-AgNPs films were prepared using 5, 10 and 20 mL of Cz-extract and characterized by UV-vis, Fourier transform infrared spectroscopy, Thermogravimetric analysis and X-ray diffraction (XRD). The surface plasmon resonance band in the UV-vis spectra confirmed the formation of AgNPs. XRD pattern confirmed the presence of silver, with average crystallite sizes calculated by Scherrer equal to 13.64 nm, 16.63nm and 20.27 nm for AgNPs prepared with 5 mL, 10 mL and 20 mL of Cz-extract, respectively. AgNPs release kinetic was studied by Korsmeyer- Peppas model. The antimicrobial results revealed that the PVA/PGLD-AgNPs hydrogels showed good antibacterial activity behavior against Escherichia coli.

Abstract Optical thermometry is a growing technological field which exploits the ability of certain materials to change their optical properties with temperature. In this work, poly(glycerol dendrimer) microspheres (PGLyD) encapsulating cobalt-doped hopeite (CoHo) was synthesized for its potential use as optical thermometer. The structure of the CoHo:PGLyD was studied using scanning electron microscopy (SEM), infrared spectroscopy (ATR-FTIR), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). On the basis of SEM images, the CoHo:PGLyD exhibited a spherical shape in which around 80% of the microspheres were within 0.82 µm. A multilayer feed-forward artificial neural network (MLP-ANN) was used to extract the chromaticity profile dependence of the CoHo:PGLyD with temperature. A color change was observed for the CoHo:PGLyD, going from dark blue (490-550 nm) to pale pink (650 nm) when the temperature changed from 20-200 °C, respectively. These results suggest that CoHo:PGLyD is a promising material for temperature sensing applications.

Abstract A platinum electrode (Pt) was coated with poly(2-hydroxyethyl methacrylate) (PHEMA) by electrochemical polymerization using chronopotentiometry. Electropolymerization of polyaniline nanowires doped with camphorsulfonic acid (PANI:CSA) was further performed on the surface of the Pt-PHEMA electrode by cyclic voltammetry. The coated Pt-PHEMA-PANI:CSA electrode was characterized by Fourier transform infrared spectroscopy (FTIR), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and scanning electron microscopy (SEM). According to EIS, the Pt-PHEMA electrode exhibits a charge transport resistance (Rct) of 169.19 kΩ. The EIS analysis of Pt-PHEMA-PANI:CSA electrode reveals a less resistive character (Rct=1.28 Ω) than the observed for the Pt electrode coated with PANI:CSA (Rct=0.47 kΩ). As demonstrated by SEM, the Pt-PHEMA-PANI:CSA electrode has a high surface area due to the PANI:CSA nanowires embedded in Pt-PHEMA. The biocompatibility of PHEMA, allied to the electrochemical characteristics of PANI:CSA, could be useful to the development of implantable electrodes for biomedical applications.

Este trabalho descreve as propriedades biológicas in vitro de três redes epoxídicas à base do éter diglicidílico do glicerol (DGEG) curadas com poli(oxipropileno) diamina (D230), isoforona diamina (IPD) e 4,4'-diamino-3,3'-dimetil-diciclohexilmetano (3DCM). As interações biológicas entre os polímeros e o sangue foram estudadas por ensaios biológicos in vitro. Estudos de adsorção de proteínas, adesão de plaquetas, atividade do lactato desidrogenase (LDH) e propriedades de tromboresistência estão apresentados. Os ensaios de adsorção de proteínas na superfície dos polímeros mostrou que as redes epoxídicas adsorvem mais albumina do que fibrinogênio. Os resultados relacionados à adesão de plaquetas, atividade do lactato hidrogenase e propriedades de tromboresistência indicaram que as redes DGEG/IPD e DGEG/3DCM exibem comportamento hemocompatível. Desta maneira, assumimos que estes polímeros epoxídicos são materiais compatíveis com o sangue.

This work describes the in vitro biological properties of three epoxy networks based on diglycidyl ether of glycerol (DGEG) cured with poly(oxypropylene) diamine (D230), isophorone diamine (IPD) and 4,4'-diamino-3,3'-dimethyl-dicyclohexylmethano (3DCM). The biological interactions between epoxy polymers and blood were studied by in vitro assays. Studies of the protein adsorption, platelet adhesion, lactate dehydrogenase (LDH) activity and thromboresistance properties are presented. The protein adsorption assays onto polymeric surfaces showed that the epoxy networks adsorbed more albumin than fibrinogen. The results about platelet adhesion, lactate dehydrogenase (LDH) activity and thromboresistance properties indicated that the DGEG/IPD and DGEG/3DCM networks show hemocompatible behavior. In this way, we can assume that these epoxy polymers are blood compatible materials.

Polycrystalline ITO films with good optoelectronics characteristics and homogeneous surface has been obtained upon annealing at 550 °C in N² atmosphere using a low-cost chemical vapor deposition (CVD) system. The films were evaluated as pH sensors in separative extended gate field-effect transistor (SEGFET) apparatus, exhibiting a sensitivity of 53 mV/pH, close to the expected Nernstian theoretical value for ion sensitive materials. The use of CVD process to synthesize ITO, as described here, may represent an alternative for fabrication of SEGFET pH sensors at low cost to be used in disposable biosensors since H+ ions are the product of several oxireductase enzymes.

Nitric oxide (NO) is a diffusible messenger that has been involved in numerous physiological processes ranging from vasodilatation and antimicrobial properties to wound healing. The beneficial effects can be attributed to the role NO plays in angiogenesis, inflammation and tissue remodeling. In the present work, a polymeric device for the sustained site specific delivery of nitric oxide using a latex rubber matrix from Hevea brasiliensis which encapsulates the spin trap iron(II)- diethyldithiocarbamate complex (FeDETC) was developed. The release profiles of NO from latex rubber matrix were studied and stability studies were carried out. Electron Paramagnetic Resonance (EPR) signal of NO was detected in the membrane exposed to ambient atmosphere at room temperature (25 °C) even after 350 hours. FTIR spectroscopy data indicated that NO-FeDETC retained its structural and spectroscopic properties upon encapsulation in the latex matrix. The NO delivery system developed in this work as a membrane, presented high stability.

The utilization of nanostructured materials for development of biosensors is a growing field in medical diagnostics. In this work a glucose biosensor based on bioactive polyglycerol (PGLD) and chitosan dendrimers (CHD) was developed. PGLD and CHD were bioconjugated with the enzyme glucose oxidase (GOx) to obtain dendrimers with glucose sensing properties. Polyaniline nanotubes (PANINT´s) were used as electron mediator due to their high ability to promote electron-transfer reactions involving GOx. The PGLD-GOx and CHD-GOx were entrapped in PANINT´s during template electrochemical polymerization of aniline. The prepared PGLD-GOx/PANINT´s and CHD-GOx/PANINT´s biosensors exhibit a strong and stable amperometric response to glucose even at a low potential of +100 mV. The based PGLD-GOx/PANINT´s and CHD-GOx/PANINT´s biosensors showed a good performance in glucose concentrations range in human blood. A comparison of the sensitivities to glucose showed that both biosensors have a linearity range between 0.02 and 10 mM, though PGLD-GOx/PANINT´s is more sensitive (10.41 vs. 7.04 nA.mM-1). The difference in the biosensor behavior and the high sensitivity of the PGLD-GOx/PANINT´s may be due to the specific organization of GOx layer at surface of the modifier macromolecule PGLD and their distribution in PANINT´s. The enzyme affinity for the substrate, K Mapp remains quite good after GOx immobilization on PGLD and CHD dendrimers and entrapment of the bioconjugates in PANINT´s.