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1.
Carbohydr Polym ; 222: 114987, 2019 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-31320046

RESUMO

A study of the structural changes at micro- and nano-scale in a chitosan matrix after the adsorption of different metal ions is presented. Toward this aim, samples of chitosan films soaked in different concentrations of copper(II) and chromium(VI) aqueous solutions were prepared. Cu and Cr ions were selected as sorbates since they have different ionic properties. The effect of the adsorbed metal ions on the microstructure of the chitosan matrices were studied using Fourier transformed infrared spectroscopy, UV-vis spectroscopy, differential scanning calorimetry and thermogravimetric analysis. To go further into the study of the samples at the molecular level, the nuclear technique positron annihilation lifetime spectroscopy was used. Results are discussed in terms of the interaction between the metal ions and the chitosan functional groups.

2.
Carbohydr Polym ; 145: 86-94, 2016 07 10.
Artigo em Inglês | MEDLINE | ID: mdl-27106155

RESUMO

Two chitosan polymers with different deacetylation degree and molecular weight were subjected to grafting reactions with the aim to enhance the properties of these bio-based materials. Specifically, n-butyl acrylate in different proportions was grafted onto two different deacetylation degree (DD%) chitosan using radical initiation in a surfactant free emulsion system. Infrared spectroscopy was used to confirm grafting and products grafting percentage and efficiency were evaluated against acrylate/chitosan ratio and DD%. Thermal and structural properties and the behavior against water of the raw and grafted biopolymers were studied using several experimental techniques: differential scanning calorimetry, transmission electron microscopy, dynamic light scattering, water swelling, contact angle and positron annihilation lifetime spectroscopy. The influence of the grafting process on the morphological and physicochemical properties of the prepared natural/synthetic hybrid materials is discussed.


Assuntos
Acrilatos/química , Quitosana/química , Polímeros/química , Microscopia Eletrônica de Transmissão , Peso Molecular , Tamanho da Partícula , Espectroscopia de Infravermelho com Transformada de Fourier , Água/química , Difração de Raios X
3.
Acta Histochem ; 115(7): 649-57, 2013 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-23465485

RESUMO

Advanced glycation endproducts (AGEs) accumulate with age in various tissues, and are further increased in patients with Diabetes mellitus, in which they are believed to contribute to the development and progression of chronic complications that include a decrease in bone quality. Bisphosphonates are anti-osteoporotic drugs that have been used for the treatment of patients with diabetic bone alterations, although with contradictory results. In the present study, we have evaluated the in vitro alterations on osteoblastic morphology by environmental scanning electron microscopy, in actin cytoskeleton and apoptosis induced by AGEs, as well as the modulation of these effects by alendronate (an N-containing bisphosphonate). Our present results provide evidence for disruption induced by AGEs of the osteoblastic actin cytoskeleton (geodesic domes) and significant alterations in cell morphology with a decrease in cell-substratum interactions leading to an increase in apoptosis of osteoblasts and a decrease in osteoblastic proliferation. High concentrations of alendronate (10(-5)M, such as could be expected in an osteoclastic lacuna) further increase osteoblastic morphological and cytoskeletal alterations. However, low doses of alendronate (10(-8)M, compatible with extracellular fluid levels to which an osteoblast could be exposed for most of its life cycle) do not affect cell morphology, and in addition are able to prevent AGEs-induced alterations and consequently apoptosis of osteoblasts.


Assuntos
Alendronato/farmacologia , Conservadores da Densidade Óssea/farmacologia , Citoesqueleto/efeitos dos fármacos , Produtos Finais de Glicação Avançada/farmacologia , Osteoblastos/efeitos dos fármacos , Animais , Apoptose/efeitos dos fármacos , Diferenciação Celular/efeitos dos fármacos , Linhagem Celular Tumoral , Citoesqueleto/ultraestrutura , Relação Dose-Resposta a Droga , Interações Medicamentosas , Microscopia Eletrônica de Varredura , Osteoblastos/ultraestrutura , Ratos
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