Mesoporous bioactive glass as a multifunctional system for bone regeneration and controlled drug release

Purpose: Coupling the potential for bone regeneration and the ability for in situ controlled drug release in a single device is a challenging field of research in bone tissue engineering; in an attempt to pursue this aim, mesoporous bioactive glass (MBG) membranes belonging to the SiO2-P2O5-CaO ternary system were produced and characterized. Methods: The glass was synthesized via a sol-gel route coupled with an evaporation-induced self-assembly process by using a non-ionic block co-polymer as a mesostructure former. MBG structure and morphology, as well as mesopores size and shape, were investigated by x-ray diffraction, transmission electron microscopy, and N2 adsorption-desorption measurements. In vitro bioactivity was investigated by soaking MBG membranes in simulated body fluid (SBF) for different time frames. Ibuprofen was encapsulated into MBG pores and drug release kinetics in SBF were assessed. Biological tests by using SAOS-2 cells were performed to assess the material cytocompatibility. Results: The material revealed significant ability to induce hydroxyapatite formation on its surface (bioactivity). Drug release kinetics in SBF are very similar to those obtained for mesoporous silica having mesopore size comparable to that of the prepared MBG (∼5 nm). No evidence of cell viability depression was detected during in vitro culture, which demonstrates the good biological compatibility of the material. Conclusions: The easiness of tailoring and shaping, the highly bioactive and biocompatible behavior, and the drug uptake/release ability of the prepared materials may suggest their use as "smart" multifunctional grafts for bone reconstructive surgery

Phenolic resins emissions upon thermal degradation

Consumable materials pollution has been increasing during recent years. The optimization of vehicle engines lead to an important decrease of fine dust related to combustion. On the other hand fine dust, coming from brake pads, pneumatics and roads has been growing. Most of the fine dust produced by consumables is released in urban areas, making its analysis and monitoring an important issue. A significant part of this kind of pollution is generated by the braking system. In fact almost every terrestrial transport method (cars, bikes, trains or planes) has a braking system. The consumable part of the system is composed by a pad of friction material and a metallic rotor. These pads are composed by a series of ceramic and metallic materials joint together by a polymer matrix, generally a phenolic resin. The aim of this work is to determine the most significant gases that are released during the thermal degradation of phenolic resins. Thermo-gravimetric analysis (TGA) were carried out using an equipment coupled with mass spectrometer (MS). Two different samples of phenolic resin, commonly used in braking industry, named Phe_1 and Phe_2, have been investigated. Thermal degradation has been studied both in air and in inert atmosphere (Argon)

Silica–Cyclodextrin Hybrid Materials: Two Possible Synthesis Processes

: Both cyclodextrin (CD) and porous silica possess interesting properties of adsorption and release. A silica-CD hybrid, therefore, could synergically merge the properties of the two components, giving rise to a material with appealing properties for both environmental and pharmaceutical applications. With this aim, in the present study, a first hybrid is obtained through one-pot sol-gel synthesis starting from CD and tetramethyl orthosilicate (TMOS) as a silica precursor. In particular, methyl-β-cyclodextrin (bMCD) is selected for this purpose. The obtained bMCD-silica hybrid is a dense material containing a considerable amount of bMCD (45 wt.%) in amorphous form and therefore represents a promising support. However, since a high specific surface area is desirable to increase the release/adsorption properties, an attempt is made to produce the hybrid material in the form of an aerogel. Both the synthesis of the gel and its drying in supercritical CO2 are optimized in order to reach this goal. All the obtained samples are characterized in terms of their physico-chemical properties (infra-red spectroscopy, thermogravimetry) and structure (X-ray diffraction, electron microscopy) in order to investigate their composition and the interaction between the organic component (bMCD) and the inorganic one (silica)

Antimicrobial Nano-Zinc Oxide Biocomposites for Wound Healing Applications: A Review

Chronic wounds are a major concern for global health, affecting millions of individuals worldwide. As their occurrence is correlated with age and age-related comorbidities, their incidence in the population is set to increase in the forthcoming years. This burden is further worsened by the rise of antimicrobial resistance (AMR), which causes wound infections that are increasingly hard to treat with current antibiotics. Antimicrobial bionanocomposites are an emerging class of materials that combine the biocompatibility and tissue-mimicking properties of biomacromolecules with the antimicrobial activity of metal or metal oxide nanoparticles. Among these nanostructured agents, zinc oxide (ZnO) is one of the most promising for its microbicidal effects and its anti-inflammatory properties, and as a source of essential zinc ions. This review analyses the most recent developments in the field of nano-ZnO–bionanocomposite (nZnO-BNC) materials—mainly in the form of films, but also hydrogel or electrospun bandages—from the different preparation techniques to their properties and antibacterial and wound-healing performances. The effect of nanostructured ZnO on the mechanical, water and gas barrier, swelling, optical, thermal, water affinity, and drug-release properties are examined and linked to the preparation methods. Antimicrobial assays over a wide range of bacterial strains are extensively surveyed, and wound-healing studies are finally considered to provide a comprehensive assessment framework. While early results are promising, a systematic and standardised testing procedure for the comparison of antibacterial properties is still lacking, partly because of a not-yet fully understood antimicrobial mechanism. This work, therefore, allowed, on one hand, the determination of the best strategies for the design, engineering, and application of n-ZnO-BNC, and, on the other hand, the identification of the current challenges and opportunities for future research

The order affects the release of vitamin D from hybrid self-assembled silica systems

Vitamin D (VD) suffers from low water solubility and strong degradation, which both decrease its bioavailability. This work aims at obtaining a silica-surfactant-VD hybrid material and verifying if this system can protect VD from degradation and enhance its solubility. This preliminary study aspires at tuning the mesostructure order of the hybrid system (by modifying the surfactant amount) with the scope of controlling, somewhat, its drug release capability. To this purpose, two silica-surfactant-VD systems with different long-range order were synthesized and characterized in terms of physico-chemical properties and release behavior in a model solution mimicking the topical environment. Results show that the hybrid materials are able to incorporate VD, protect it from degradation up to 17 months and release it in aqueous media. The mesostructure order and the interaction between VD, surfactant and silica seem to play a key role in tuning kinetics and the amount of released drug. While the less ordered structure incorporates less VD with faster and higher release percentage, the more ordered one incorporates more VD but, due to the stronger interactions with the carrier, requires a partial dissolution of the matrix to occur before releasing the drug, so inducing a lag-time and a smaller released quantity

Zirconia-containing radiopaque mesoporous bioactive glasses

cited By 13International audienceA radiopaque mesoporous bioactive glass (named MBGZ-7) was obtained through a combined sol-gel and evaporation induced self-assembling (EISA) route, adding zirconium propoxide to the synthesis batch as the zirconia precursor. The nitrogen sorption analysis confirmed the mesoporous nature of the glass. The assessment of in vitro bioactivity by soaking in acellular simulated body fluid (SBF) and SEM observation showed the deposition of hydroxyapatite crystals on its surface after one week. The good radiopacity level was demonstrated by comparing X-ray images of MBGZ-7 and a blank sample that did not contain radiopaque additives. It is envisaged the use of MBGZ-7 as a promising dispersed phase in composite materials for minimally invasive surgery procedures, such as injectable bone cements, in order to allow the visualization of the implant under fluoroscopic control, during both injection and follow-up. © 2014 Elsevier B.V

Whey Proteins–Zinc Oxide Bionanocomposite as Antibacterial Films

The use of toxic crosslinking agents and reagents in the fabrication of hydrogels is a frequent issue which is particularly concerning for biomedical or food packaging applications. In this study, novel antibacterial bionanocomposite films were obtained through a simple solvent casting technique without using any crosslinking substance. Films were made from a flexible and transparent whey protein matrix containing zinc oxide nanoparticles synthesised via a wet chemical precipitation route. The physicochemical and functional properties of the ZnO nanoparticles and of the composite films were characterised, and their antibacterial activity was tested against S. epidermidis and E. coli. The synthesised ZnO nanoparticles had an average size of about 30 nm and a specific surface area of 49.5 m(2)/g. The swelling ratio of the bionanocomposite films increased at basic pH, which is an appealing feature in relation to the absorption of chronic wound exudate. A n-ZnO concentration-dependent antibacterial effect was observed for composite films. In particular, marked antibacterial activity was observed against S. epidermidis. Overall, these findings suggest that this novel material can be a promising and sustainable alternative in the design of advanced solutions for wound dressing or food packaging

A mesostructured hybrid CTA–silica carrier for curcumin delivery

Curcumin is a natural active principle with antioxidant, antibacterial and anti-inflammatory properties. Its use is limited by a low water solubility and fast degradation rate, which hinder its bioavailability. To overcome this problem, curcumin can be delivered through a carrier, which protects the drug molecule and enhances its pharmacological effects. The present work proposes a simple one-pot sol–gel synthesis to obtain a hybrid carrier for curcumin delivery. The hybrid consists of a mesostructured matrix of amorphous silica, which stabilizes the carrier, and hexadecyltrimethylammonium (CTA), a surfactant where curcumin is dissolved to increase its water solubility. The carrier was characterized in terms of morphology (FESEM), physicochemical properties (XRD, FTIR, UV spectroscopy) and release capability in pseudo-physiological solutions. Results show that curcumin molecules were entrapped, for the first time, in a silica-surfactant mesostructured hybrid carrier. The hybrid carrier successfully released curcumin in artificial sweat and in a phosphate buffer saline solution, so confirming its efficacy in increasing curcumin water solubility. The proposed drug release mechanism relies on the degradation of the carrier, which involves the concurrent release of silicon. This suggests strong potentialities for topical administration applications, since curcumin is effective against many dermal diseases while silicon is beneficial to the skin

New insights in large-pores mesoporous silica microspheres for hemostatic application

Hemorrhages are still considered a common cause of death and despite the availability of different hemostatic agents it is still necessary to develop more effective hemostats for bleeding managements in emergency situations. Herein, large-pores mesoporous silica microspheres (MSM) were synthesized, and their surface was modified to enrich the hydroxyls population with the aim of achieving a material with enhanced water adsorption capacity and high hemostatic ability. The success of surface modification was investigated by Fourier Transform Infrared spectroscopy (FT-IR) and thermogravimetric analysis (TGA), which confirmed the increase in the amount of surface hydroxyl groups. A hemolysis assay as well as a clotting test were carried out to evaluate the hemocompatibility and hemostatic ability, respectively. It was found that the modified material presented the lowest hemolytic ratio and the lowest clotting time. The novelty of the paper is mainly due to the coupling of the hemostatic ability test with the adsorption microcalorimetry of water. In fact, being the water adsorption on the material surface a crucial factor in the hemostatic activity, microcalorimetry was used for the first time to study the adsorption of water and estimate its heat of adsorption. The data obtained showed that the modified MSM presents a surface able to adsorb a higher amount of water, compared to the pristine MSM, with a low molar heat of adsorption (about 35 kJ/mol), which renders the modified MSM presented in the present study an excellent candidate for producing novel hemostats