Voltammetric sensing of tryptophan in dark chocolate bars,skimmed milk and urine samples in the presence of dopamine and caffeine

Journal of Applied Electrochemistry - The present work reports the development of screen-printed electrode (SPE) using flexible polyester sheets modified with nanodiamond (ND), Au nanoparticles...     

Water flux,DSC, and cytotoxicity characterization of membranes of cellulose acetate produced from sugar cane bagasse,using PEG 600

Summary In this article, cellulose acetate produced through the homogeneous acetylation of sugar cane bagasse cellulose was used to produce membranes, using poly(ethyleneglycol) 600 (PEG 600) as an admixture. The membranes were characterized using water flux measurements (Payne’s cup), differential scanning calorimetry (DSC) and neutral red uptake (cytotoxicity). The results showed that PEG 600 acts as a crystallinity inductor and/or pore former in the cellulose acetate matrix. The induction of crystallinity is important for this system since it had not been reported on the literature yet. The results also demonstrated that the studied membranes present a nontoxic behavior.     

Study of polypropylene/polybutene blends modified by gamma irradiation and (high melt strength polypropylene)/polybutene blends

It is well-known that polypropylene (PP) is difficult to process as a consequence of its linear structure. It is also known that grafting of long-chain branches on PP backbone using ionizing radiation is an effective approach to achieve high melt strength polypropylene (HMS PP). Chain-scission and, in minor extend, crosslinking and grafting are the predominant reaction in order to branch PP backbone. However, if multifunctional monomers are used to promote the grafting reaction, crosslinking can surpass chain scission and grafting, reducing drawability. Therefore, in an effort to enhance the processability and so the drawability, it has been found helpful to add a small amount of polybutene-1. Gamma irradiation technique was used to induce chemical changes in blends of PP and polybutene in acetylene atmosphere (crosslinker promoter) and in HMSPP/polybutene blends. The samples were irradiated with a ⁶⁰Co source with doses of 12.5 and 20 kGy in the presence of acetylene. In this work, two different methods of blends processing were compared regarding rheological and mechanical properties. Effects on the strength and elongation at the yield point and at rupture were observed by mechanical tests and showed decrease of tensile strength and increase of elongation at rupture for samples obtained by irradiation of blends. The results from rheology demonstrated an increase in melt strength and drawability of blends.     

EPDM recycling assisted by γ-processing

The integration of waste ethylene–propylene–diene terpolymer (EPDM), containing carbon black into pristine EPDM can be achieved by γ-irradiation as a versatile procedure to process ethylene–propylene elastomers. The presence of acrylic acid in the material formulation allows the formation of intermolecular bridges by threefold increase in gel content. The possibility of achieving greater stability by the addition of acrylic acid in EPDM systems was analyzed. The start materials were EPDM containing 30 and 50 phr of EPDM powder loaded with 40 phr of carbon black aged by pre-exposure to electron beam irradiation. The advanced γ-irradiation exceeding 100 kGy represented the optimal radiation processing condition. Two procedures of chemiluminescence under isothermal and non-isothermal regimes for the evaluation of radiation stability were applied on γ-irradiated samples. The thermal strength of irradiated samples was characterized based on the radiolysis mechanism of EPDM. The variation in the activation energy required for the thermal oxidation of these samples and the modification in gel contents due to the gelation action of acrylic acid were presented for the validation of proposed recycling radiochemical technique. Charlesby–Pinner representation provided different values for the ratios between radiochemical yields of cross-linking and scission, proving that the presence of acrylic acid promoted the conversion of EPDM wastes into valuable materials.     

CTHRSSVVC Peptide as a Possible Early Molecular Imaging Target for Atherosclerosis

The purpose of our work was to select phages displaying peptides capable of binding to vascular markers present in human atheroma, and validate their capacity to target the vascular markers in vitro and in low-density lipoprotein receptor knockout (LDLr^−/−) mouse model of atherosclerosis. By peptide fingerprinting on human atherosclerotic tissues, we selected and isolated four different peptides sequences, which bind to atherosclerotic lesions and share significant similarity to known human proteins with prominent roles in atherosclerosis. The CTHRSSVVC-phage peptide displayed the strongest reactivity with human carotid atherosclerotic lesions (p < 0.05), when compared to tissues from normal carotid arteries. This peptide sequence shares similarity to a sequence present in the fifth scavenger receptor cysteine-rich (SRCR) domain of CD163, which appeared to bind to CD163, and subsequently, was internalized by macrophages. Moreover, the CTHRSSVVC-phage targets atherosclerotic lesions of a low-density lipoprotein receptor knockout (LDLr^−/−) mouse model of atherosclerosis in vivo to High-Fat diet group versus Control group. Tetraazacyclododecane-1,4,7,10-tetraacetic acid-CTHRSSVVC peptide (DOTA-CTHRSSVVC) was synthesized and labeled with ¹¹¹InCl₃ in >95% yield as determined by high performance liquid chromatography (HPLC), to validate the binding of the peptide in atherosclerotic plaque specimens. The results supported our hypothesis that CTHRSSVVC peptide has a remarkable sequence for the development of theranostics approaches in the treatment of atherosclerosis and other diseases.     

Baccharin Prevents Genotoxic Effects Induced by Methyl Methanesulfonate and Hydrogen Peroxide in V79 Cells

Baccharin is one of the major chemical compounds isolated from the aerial parts of Baccharis dracunculifolia DC (Asteraceae), a native plant of South America and the most important botanical source of the Brazilian green propolis that has been used in alternative medicine to treat inflammation, liver disorders, and stomach ulcers. The present study was carried out in V79 cells to determine the possible genotoxic and antigenotoxic activities of baccharin utilizing comet and micronucleus assays, where 2 known mutagenic agents with different mechanisms of DNA damage were used as positive controls. The V79 cells were treated with concentrations of baccharin (0.25, 0.5, 1.0, and 2.0 μg/mL) and for to investigate the antigenotoxicity these concentrations were associated with methyl methanesulfonate (MMS; 200 μM-comet assay and 400 μM-micronucleus assay) or hydrogen peroxide (H(2) O(2;) 50 μM-comet assay and 100 μM-micronucleus assay). Statistically significant differences in the rate of DNA damage were observed in cultures treated with the highest concentration of baccharin when compared to the control group, but this difference was not found in the micronucleus assay. The results also showed that the frequencies of DNA damage and micronuclei induced by MMS and H(2) O(2) were significantly reduced after treatment with baccharin. The baccharin showed a chemoprevention effect and can be the chemical compound responsible for the antigenotoxicity also demonstrated by the B. dracunculifolia. The antioxidant potential of baccharin may be related to its chemoprevention activity induced against both genomic and chromosomal damages.     

Polymerization shrinkage evaluation on nanoscale‐layered silicates: Bis‐GMA/TEGMA nanocomposites,in photo‐activated polymeric matrices

This study concerns to the investigation of the polymerization shrinkage in dental experimental composites filled with silanized silica Aerosil^® OX‐50 and clay nanoparticulated Montmorilonita (MMT) Cloisite^® 30B, in glycidyl methacrylate resin. The characterization of the experimental composites was established with the following analyses: Thermo‐Mechanical Analysis (TMA) at isotherm temperature, Differential Scanning Calorimetry Analysis (DSC) under nitrogen atmosphere, X‐Ray diffraction (DRX), and Micro Hardness analysis. Through the TMA analysis was observed that the polymerization shrinkage varies according to the filler type and concentration in the experimental composite. The polymerization shrinkage ranged from 0.98% to 0.22% in the experimental composites added with Cloisite^® 30B and ranged from 2.73% to 1.01% in the experimental composites containing silanized silica. Due to the intercalation of the clay nanoparticle in relation to the polymer matrix, the experimental nanocomposites with Cloisite^® 30B showed better performance compared to the composites with silanized silica. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2014 , 131, 40010.     

Controlled degradation and crosslinking of polypropylene induced by gamma radiation and acetylene

Isotactic polypropylene (iPP) undergoes crosslinking and extensive main chain scissions when submitted to irradiation. The simultaneous irradiation of PP and acetylene is able to control chain scission and produce grafting. The grafted PP further reacts with PP radicals resulting in branching and crosslinking. In this work, commercial polypropylenes (iPP) of different molecular weights were irradiated with a ⁶⁰Co source at dose of 12.5 kGy in the presence of acetylene in order to promote the crosslinking. The mechanical and rheological tests showed a significant increase in melt strength and drawability of the modified samples obtained from resins with high melt flow index. The characterization of the molecular modifications induced by gamma irradiation of isotactic polypropylenes under acetylene atmosphere proved the existence of branching, crosslinking and chain scission in a qualitative way. The G′ and G″ indicated the presence of LCB in all samples. Therefore, PP irradiation under acetylene was proved to be an effective approach to achieve high melt strength polypropylene (HMSPP).     

Direct UV photocrosslinking of poly(N-vinyl-2-pyrrolidone) (PVP) to produce hydrogels

Hydrogels for biomedical purposes, made from synthetic polymers as starting materials and free of co-adjuvant molecules, have been produced almost exclusively by high-energy radiative processes. On the other hand, UV photocrosslinking of such materials has been used in conjunction of monomers and/or photoinitiators. This work was addressed to the analysis of poly(N-vinyl-2-pyrrolidone) (PVP) submitted to direct photocrosslinking in aqueous solution, using low pressure Hg lamp (λ_em=254 nm). The process efficiency was evaluated, and the properties of the hydrogel formed were determined. The product thus formed has similar micro- and macroscopic properties, as compared to hydrogels produced by high-energy radiation and presents no cytotoxicity. These results demonstrated the viability of using this method as a versatile alternative to hydrogel production, broadening the possibility of its production where high-energy radiation facilities are not available.