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Treatment of injuries to bone structure represents a significant economic burden for health care institutions and systems worldwide. The development of tissue engineering scaffolds has expanded to include the incorporation of nanotechnology platforms such as liposomes for the efficient delivery of chemotherapeutic agents. Pyrroloquinoline quinone (PQQ) is a naturally occurring quinone with antioxidant and tissue regenerative properties. In this study, the liposome-based encapsulation of PQQ was achieved by studying the effect of different downsizing methods and lipid compositions. Liposomal sonication produced stable vesicles of sizes

In 10% to 40% of the cases of coronary stent implantation, patients face in-stent restenosis due to an inflammatory response, which induces artery thickening. Everolimus, a drug that inhibits growth factor-stimulated cell proliferation of endothelial cells, represents a promising alternative to prevent in-stent restenosis. In this study, everolimus was encapsulated by a film hydration technique in liposomes by using phosphatidylcholine and cholesterol at different ratios. As the ratio of cholesterol increases, it modulates the rigidity of the structure which can affect the encapsulation efficiency of the drug due to steric hindrance. Moreover, various lipid : drug ratios were tested, and it was found that as the lipid : drug ratio increases, the encapsulation efficiency also increases. This behavior is observed because everolimus is a hydrophobic drug; therefore, if the lipidic region increases, more drug can be entrapped into the liposomes. In addition, stability of the encapsulated drug was tested for 4 weeks at 4°C. Our results demonstrate that it is possible to prepare liposomal everolimus by film hydration technique followed by extrusion with high entrapment efficiency as a viable drug delivery system.

Glass ionomer cements and resin-based composites are promising materials in restorative dentistry. However, their limited mechanical properties and the risk of bulk/marginal fracture compromise their lifespan. Intensive research has been conducted to understand and develop new materials that can mimic the functional behavior of the oral cavity. Nanotechnological approaches have emerged to treat oral infections and become a part of scaffolds for tissue regeneration. Carbon nanotubes are promising materials to create multifunctional platforms for dental applications. This review provides a comprehensive survey of and information on the status of this state-of-the-art technology and describes the development of glass ionomers reinforced with carbon nanotubes possessing improved mechanical properties. The applications of carbon nanotubes in drug delivery and tissue engineering for healing infections and lesions of the oral cavity are also described. The review concludes with a summary of the current status and presents a vision of future applications of carbon nanotubes in the practice of dentistry.

This research was based on the synthesis of new materials with capacitive properties and low cost, seeking efficient energy storage, through the manufacture and characterization of composite materials of polyvinyl alcohol (PVA)/multiwalled carbon nanotubes with carboxyl group (MWCNTs-COOH) (1 %) for electrodes. Forcespinning and electrospinning techniques were used to develop composite fiber films and compare the physical structure of the fibers and its influence on their capacitive properties. These samples were characterized by SEM, FESEM, FT-IR, XRD, TGA, Raman spectroscopy and electrochemical techniques. The characterization of the composites makes evident the structural modification that the material underwent after the treatments. The electrochemical parameters were measured by electrochemical impedance spectroscopy (EIS), with the samples immersed in H2SO4 1 M as electrolyte. The PVA/MWCNTs-COOH composites with thermal treatment (340 °C) showed a considerable decrease in total impedance of up to 6 orders of magnitude (124 Ω) with respect to the blank sample (2.3 × 108 Ω), as a function of the immersion time in the acid solution. As well as, an increase in the specific capacitance of up to 8 orders of magnitude (1.01×10−2 F cm−2) with respect to the blank sample (5.07 × 10−10 F cm−2) for the composite manufactured by the electrospinning technique. The obtaining of fibers with directionality as a result of the forcespinning technique, the highly crossed network observed by electrospinning and the electrochemical properties shown by the structural modification of PVA/MWCNTs-COOH composite, make it, a material with potential technological applications such as electrode in electrochemical capacitors.

In this work, we present the results of two synthesis approaches for mesoporous magnesium carbonates, that result in mineralization of carbon dioxide, producing carbonate materials without the use of cosolvents, which makes them more environmentally friendly. In one of our synthesis methods, we found that we could obtain nonequilibrium crystal structures, with acicular crystals branching bidirectionally from a denser core. Both Raman spectroscopy and X-ray diffraction showed these crystals to be a mixture of sulfate and hydrated carbonates. We attribute the nonequilibrium morphology to coprecipitation of two salts and short synthesis time (25 min). Other aqueous synthesis conditions produced mixtures of carbonates with different morphologies, which changed depending on drying temperature (40 or 100 °C). In addition to aqueous solution, we used supercritical carbon dioxide for synthesis, producing a hydrated magnesium carbonate, with a nesquehonite structure, according to X-ray diffraction. This second material has smaller pores (1.01 nm) and high surface area. Due to their high surface area, these materials could be used for adsorbents and capillary transport, in addition to their potential use for carbon capture and sequestration.