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2.
Mater Sci Eng C Mater Biol Appl ; 112: 110869, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32409038

ABSTRACT

The combination of chitosan (C) with alginate (A) has been explored for the production of dressings due to the positive results on wound healing. CA films can show a dense or porous flexible structure, with characteristics tunable for different applications. Porosity and flexibility can be achieved, respectively, by the addition of surfactants such as Kolliphor® P188 (P) and silicone-based compounds as Silpuran® 2130 A/B (S). Furthermore, composite matrices of these polysaccharides have potential applications as devices for releasing bioactive compounds to skin lesions. The purpose of this study was to evaluate the physicochemical and biological characteristics of flexible dense and porous CA membranes incorporating the standardized extract of Arrabidaea chica Verlot (A. chica), and also to analyze the release mechanism of the extract from different membrane formulations. The results show that the inclusion of P in the formulation allows obtaining porous matrices, promotes greater homogeneity of the mixture of the silicone gel with the suspension of polysaccharides, and increases the swelling of the polymer matrix. All formulations presented high stability, reaching a maximum mass loss of 18% after seven days. The formulations with S showed the best performance in terms of flexibility and strain at break. The presence of A. chica standardized extract did not affect negatively the characteristics of the membranes. Incorporation efficiencies of the bioactive compound above 87% were achieved, and the addition of P and S to the membrane formulation changed the release of the A. chica extract kinetics. In addition, the developed formulations did not significantly affect Vero cells proliferation.


Subject(s)
Alginates/chemistry , Bignoniaceae/chemistry , Chitosan/chemistry , Membranes, Artificial , Plant Extracts/chemistry , Animals , Bignoniaceae/metabolism , Cell Survival/drug effects , Chlorocebus aethiops , Drug Carriers/chemistry , Drug Carriers/toxicity , Methylene Blue/chemistry , Methylene Blue/metabolism , Plant Extracts/metabolism , Porosity , Surface-Active Agents/chemistry , Tensile Strength , Vero Cells
3.
Braz. j. med. biol. res ; 53(1): e8621, Jan. 2020. tab, graf
Article in English | LILACS | ID: biblio-1055482

ABSTRACT

The use of specially designed wound dressings could be an important alternative to facilitate the healing process of wounds in the hyperglycemic state. Biocompatible dressings combining chitosan and alginate can speed up wound healing by modulating the inflammatory phase, stimulating fibroblast proliferation, and aiding in remodeling phases. However, this biomaterial has not yet been explored in chronic and acute lesions of diabetic patients. The aim of this study was to evaluate the effect of topical treatment with a chitosan-alginate membrane on acute skin wounds of hyperglycemic mice. Diabetes mellitus was induced by streptozotocin (60 mg · kg-1 · day-1 for 5 days, intraperitoneally) and the cutaneous wound was performed by removing the epidermis using a surgical punch. The results showed that after 10 days of treatment the chitosan and alginate membrane (CAM) group exhibited better organization of collagen fibers. High concentrations of interleukin (IL)-1α, IL-1β, granulocyte colony-stimulating factor (G-CSF), and tumor necrosis factor-alpha (TNF-α) were detected in the first and second days of treatment. G-CSF and TNF-α level decreased after 5 days, as well as the concentrations of TNF-α and IL-10 compared with the control group (CG). In this study, the inflammatory phase of cutaneous lesions of hyperglycemic mice was modulated by the use of CAM, mostly regarding the cytokines IL-1α, IL-1β, TNF-α, G-CSF, and IL-10, resulting in better collagen III deposition. However, further studies are needed to better understand the healing stages associated with CAM use.


Subject(s)
Animals , Male , Rabbits , Bandages , Wound Healing/drug effects , Chitosan/administration & dosage , Cell Proliferation/drug effects , Diabetes Mellitus, Experimental/physiopathology , Alginates/administration & dosage , Time Factors , Biocompatible Materials/administration & dosage , Biomarkers/blood , Collagen/drug effects , Inflammation/prevention & control , Mice, Inbred C57BL
4.
Braz J Med Biol Res ; 53(1): e8621, 2020.
Article in English | MEDLINE | ID: mdl-31859909

ABSTRACT

The use of specially designed wound dressings could be an important alternative to facilitate the healing process of wounds in the hyperglycemic state. Biocompatible dressings combining chitosan and alginate can speed up wound healing by modulating the inflammatory phase, stimulating fibroblast proliferation, and aiding in remodeling phases. However, this biomaterial has not yet been explored in chronic and acute lesions of diabetic patients. The aim of this study was to evaluate the effect of topical treatment with a chitosan-alginate membrane on acute skin wounds of hyperglycemic mice. Diabetes mellitus was induced by streptozotocin (60 mg · kg-1 · day-1 for 5 days, intraperitoneally) and the cutaneous wound was performed by removing the epidermis using a surgical punch. The results showed that after 10 days of treatment the chitosan and alginate membrane (CAM) group exhibited better organization of collagen fibers. High concentrations of interleukin (IL)-1α, IL-1ß, granulocyte colony-stimulating factor (G-CSF), and tumor necrosis factor-alpha (TNF-α) were detected in the first and second days of treatment. G-CSF and TNF-α level decreased after 5 days, as well as the concentrations of TNF-α and IL-10 compared with the control group (CG). In this study, the inflammatory phase of cutaneous lesions of hyperglycemic mice was modulated by the use of CAM, mostly regarding the cytokines IL-1α, IL-1ß, TNF-α, G-CSF, and IL-10, resulting in better collagen III deposition. However, further studies are needed to better understand the healing stages associated with CAM use.


Subject(s)
Alginates/administration & dosage , Bandages , Cell Proliferation/drug effects , Chitosan/administration & dosage , Diabetes Mellitus, Experimental/physiopathology , Wound Healing/drug effects , Animals , Biocompatible Materials/administration & dosage , Biomarkers/blood , Collagen/drug effects , Inflammation/prevention & control , Male , Mice , Mice, Inbred C57BL , Time Factors
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