Polymeric hydrogels are used as wound dressing material since these materials show advantages such as pain relief, exudates absorption, barrier to microorganisms, permeability, and others. This article shows the results obtained in a study aiming to know the biological performance of different polymeric materials to be used in contact with skin: PVP hydrogels and acrylate adhesive. The biocompatibility was determined by in vitro assay of cytotoxicity and in vivo assay by using the contact test of irritability in rabbits. All the tested samples presented no toxicity and no dermal irritation.

The current challenge in treating periodontitis is regenerating the periodontium. This motivates tissue-engineering researchers to develop scaffolds as artificial matrices that give mechanical support for osteoblasts, cementoblasts, gingival and periodontal ligament fibroblast cells. In this study, modified hyaluronic acid (HA) and chitosan (CS) were employed to create a hybrid CS-HA hydrogel scaffold for periodontal regeneration. CS, HA, and CS-HA scaffolds were obtained by freeze-drying technique, resulting in porous structures suitable for use in tissue engineering. Scaffolds were submitted to gamma and UV-sterilization without significant morphology changes. The ATR-FTIR spectra of CS-HA hydrogels showed peaks at 377 cm , 1566 cm , and 1614 cm , representing secondary amide, primary amine, and carboxyl acid respectively, and it was also observed the emergence of peaks at 886 cm , which probably represents the Schiff base formed in the case of hybrid CS-HA hydrogels. The scaffolds presented a high rate of PBS uptake, reaching values higher than 95%. Thermal degradation of HA scaffolds was around 225°C and CS was around 285°C. The ATR-FTIR spectra and swelling degree were slightly disturbed mainly after gamma sterilization, but degradation temperature did not change after sterilization. The performance of the CS-HA hydrogel scaffolds for in vitro cell culture was tested using NIH3T3 and MG63 cell lines. The Alamar Blue test showed a significant increase in cellular viability and high CD44 expression, suggesting that the cells migrated more when seeded onto the scaffolds. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 104B: 1691-1702, 2016.

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Este trabalho apresenta os resultados do comportamento de blendas do polímero biodegradável PHB poli(hidroxibutirato) com os copoliésteres também biodegradáveis EastarBio® e Ecoflex®, na composição de 75% de PHB e 25% dos copoliésteres, em contato com solo composto simulado. Foi também avaliada a influência da adição de pó de serra ou farinha de madeira, na proporção de 70% da blenda e 30% de pó de serra (p.d.s.). A biodegradação foi avaliada para amostras após 30, 60 e 90 dias em contato com solo, através de análises gravimétricas, morfológicas e mecânicas. A preparação inicial dos grânulos dos compostos poliméricos foi feita por extrusão, utilizando uma extrusora dupla-rosca e a moldagem dos corpos de prova foi realizada através da moldagem por injeção. Os materiais estudados biodegradam nas condições testadas. A blenda PHB/EastarBio® (75/25) + 30% p.d.s. apresentou maior redução de massa, 29% após 90 dias. Notou-se que a biodegradação se inicia pela superfície do material e que 90 dias são insuficientes para observar alterações internas.

Dense and porous polyHEMA hydrogels were synthesized by bulk and solution radical-initiated polymerization techniques. The morphologic analysis (SEM) of obtained hydrogels showed an amorphous dense structure for the samples obtained by bulk polymerization and a porous structure with non connected porous as a result of bulk polymerization in the presence of water soluble crystals (sucrose/NaCl). The use of solution polymerization technique using different amounts of water as diluent resulted in the formation of a sponge-like structure with connected microporous in case of using water amount equal or higher than 57.5%. The saline solution uptake and dynamic mechanical behavior of dense hydrogels were influenced by the amount of crosslinking between the polymer chains

The increasing use of bioabsorbable polymeric materials in medicine has stimulated researchers in the materials field to search for solutions for the replacement of metallic artifacts by bioabsorbable polymers. Therefore, this study describes the in vitro degradation of PHBV, PCL and the blends of these polymers, both of which are bioabsorbable polymers. The samples were prepared by extrusion followed by injection, and subjected submitted to in vitro degradation in phosphate buffered saline solution with pH 7.3 and kept at 37° C. Through the characterization of the variation of mass, molar mass, mechanical properties and morphology, the results indicated that the samples analyzed are more stable to hydrolytic degradation when compared to other bioabsorbable polymers. The materials indicate signs of degradation after 30 days, with a small reduction in the molar mass. After 180 days, the materials indicated a significant reduction of molar mass and reduction in the mechanical properties

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The aim of this work was to perform a systematic study about the effects induced by chitosan solution concentration and by chitin or glycerol incorporation on dense chitosan membranes with potential use as burn dressings. The membrane properties analyzed were total raw material cost, thickness, morphology, swelling ratio, tensile strength, percentage of strain at break, crystallinity, in vitro enzymatic degradation with lysozyme, and in vitro Vero cells adhesion. While the use of the most concentrated chitosan solution (2.5% w/w) increased membrane cost, it also improved the biomaterial mechanical resistance and ductility, as well as reduced membrane degradation when exposed for 2 months to lysozyme. The remaining evaluated properties were not affected by initial chitosan solution concentration. Chitin incorporation, on the other hand, reduced the membranes cost, swelling ratio, mechanical properties, and crystallinity, resulting in thicker biomaterials with irregular surface more easily degradable when exposed to lysozyme. Glycerol incorporation also reduced the membranes cost and crystallinity and increased membranes degradability after exposure to lysozyme. Strong Vero cells adhesion was not observed in any of the tested membrane formulations. The overall results indicate that the majority of the prepared membranes meet the performance requirements of temporary nonbiodegradable burn dressings (e.g. adequate values of mechanical resistance and ductility, low values of in vitro cellular adhesion on their surfaces, low extent of degradation when exposed to lysozyme solution, and high stability in aqueous solutions).