Edwardsholder0722

Subsequently, in vitro studies like cell adhesion, proliferation and osteogenic differentiation of MC3T3-E1 were evaluated. The incorporation of UHAPNWs improved mechanical properties and hydrophilicity with an enhancement in cell adhesion, proliferation, and osteogenic differentiation. More importantly, 10 wt% UHAPNWs/MXene exhibited the optimal mechanical properties while biological improvement was more pronounced along with the addition of UHAPNWs when the weight fraction of UHAPNWs was from 0 to 30 wt%. Furthermore, in vivo experiments the UHAPNWs/MXene nanocomposite membranes effectively enhanced bone tissue formation quantitatively and qualitatively in a rat calvarial bone defect. Therefore, an appropriate amount of UHAPNWs into MXene plays a positive and evident role in enhancing mechanical properties, biocompatibility and osteoinductivity, leading a novel inorganic composite material for regeneration of bone tissue.Multiple studies exist on the influence of TiO2 nanoparticle uptake on cell behavior. Yet little is known about the lingering influence of nanoparticles accumulation within the external environment which is particularly important to stem cell differentiation. Herein, dental pulp stem cells were cultured on hard and soft polybutadiene substrates, where 0.1 mg/mL rutile TiO2 nanoparticles were introduced once, 24 h after plating. In the absence of TiO2, the doubling time on soft substrate is significantly longer, while addition of TiO2 decreases it to the same level as on the hard substrate. FACS analysis indicates particle uptake initially at 25% is reduced to 2.5% after 14 days. In the absence of TiO2, no biomineralization on the soft and snowflake-like hydroxyapatite deposits on the hard substrate are shown at week 4. b-AP15 ic50 With the addition of TiO2, SEM/EDAX reveals copious mineral deposition templated on large banded collagen fibers on both substrates. The mineral-to-matrix ratios analyzed by Raman spectroscopy are unremarkable in the absence of TiO2. However, with addition of TiO2, the ratios are consistent with native bone on the hard and dentin on the soft substrates. This is further confirmed by RT-PCR, which showed upregulation of markers consistent with osteogenesis and odontogenesis, respectively.The adsorption of isoniazid in the Faujasite zeolite channels has been studied. For that, the influence of the pH from the solution media in the adsorption process was verified to enable higher amount of isoniazid retained. With the information of the best pH and the equilibrium time obtained with the kinetic study, an isotherm was constructed and the hybrid material obtained with the plateau concentration equilibrium was characterized with several techniques. Molecular modeling calculations were also performed for a better understanding of the adsorption process and how the interaction between zeolite and isoniazid occurs. The geometrical disposition of the drug molecules into the zeolite channels, the saturation levels, the different isoniazid protonation states with respect to the pH media and the interaction energy between the zeolite surface and the isoniazid molecule was studied. Finally, a drug release study was made to verify if the Faujasite-Y zeolite could change the isoniazid release in acid and phosphate buffer media. The results show that the Faujasite-Y has the possibility to work as carrier for isoniazid, where the adsorption process is more effective in media at pH 3, result confirmed by the molecular modeling. The isoniazid release essay showed that the hybrid material does not change the drug release profile, provides more stability in acid media, indicating that the zeolite can be used as carrier for isoniazid, and improve the medicine formulations on antituberculosis treatment.The biocompatibility, flexibility, and tissue-like mechanical properties of hydrogels suggest they are promising materials for wearable devices. However, the production of smart, self-healing hydrogels is limited by the unstable structure of load-bearing stressors and the need for long-term healing capacity. An important goal when developing such hydrogels is to improve their mechanical characteristics and rapid ability to self-repair in physiological environments. In this study, we aimed to create a thermo-responsive hydrogel that possessed thermal-healing and enhanced mechanical properties, without losing its self-healing capabilities, by employing two interpenetrating cross-linked networks of polyvinyl alcohol (PVA) and boron nitride nanosheets (BNNSs). We observed that addition of BNNSs significantly increased the glass transition temperature (Tg) and temperature-dependent swelling of PVA hydrogels, indicating a high compatibility between these two materials and a high thermal response to external stimuli. Our results suggest that PVA hydrogels combined with BNNSs outperform single-network PVA hydrogels in terms of thermal-healing capacity. As above Tg, the thermal energy gained during moisture loss leads to an increase in the thermal mobility of the polymer chains and in the free volume available for new hydrogen bonds at the fracture surface. This unique structure increases water content and confers better mechanical properties. Interestingly, this structure of the second network benefits the first PVA network during deformation by effectively dissipating energy and bearing force, and contrarily to single-network PVA hydrogels. Taken together, our results show that combining PVA and BNNSs to create a hybrid structure, exerts a synergistic effect and successfully improves the thermal-healing performance of wet hydrogels.Increasing evidences are demonstrating that structural and functional properties of non-neuronal brain cells, called astrocytes, such as those of cytoskeleton and of ion channels, are critical for brain physiology. Also, changes in astrocytes structure and function concur to and might determine the outcome of neuronal damage in acute neurological conditions or of chronic disease. Thus, the design and engineering of biomaterials that can drive the structural and functional properties of astrocytes is of growing interest for neuroregenerative medicine. Poly-ɛ-caprolactone (PCL), is FDA-approved polyester having excellent mechanical and chemical properties that can be tailored to obtain neural implants for regenerative purposes. However, the study on the use of PCL substrates for neuroregenerative purposes are mainly aimed at investigating the interaction of the material with neurons. Here, we report on the long-term viability, morphology, structural and functional properties of primary astrocytes grown on electrospun fibres of PCL (-GEL) and on blending of PCL and Gelatin protein (+GEL).