The increase in osteoporotic fracture worldwide is urging bone tissue engineering research to find new, improved solutions both for the biomaterials used in designing bone scaffolds and the anti-osteoporotic agents capable of promoting bone regeneration. This review aims to report on the latest advances in biomaterials by discussing the types of biomaterials and their properties, with a special emphasis on polymer-ceramic composites. The use of hydroxyapatite in combination with natural/synthetic polymers can take advantage of each of their components properties and has a great potential in bone tissue engineering, in general. A comparison between the benefits and potential limitations of different scaffold fabrication methods lead to a raised awareness of the challenges research face in dealing with osteoporotic fracture. Advances in 3D printing techniques are providing the ways to manufacture improved, complex, and specialized 3D scaffolds, capable of delivering therapeutic factors directly at the osteoporotic skeletal defect site with predefined rate which is essential in order to optimize the osteointegration/healing rate. Among these factors, strontium has the potential to increase osseointegration, osteogenesis, and healing rate. Strontium ranelate as well as other biological active agents are known to be effective in treating osteoporosis due to both anti-resorptive and anabolic properties but has adverse effects that can be reduced/avoided by local release from biomaterials. In this manner, incorporation of these agents in polymer-ceramic composites bone scaffolds can have significant clinical applications for the recovery of fractured osteoporotic bones limiting or removing the risks associated with systemic administration.

In this study, composite hydrogels with interpenetrated polymer networks (IPNs), based on bacterial cellulose (BC) and poly(acrylic acid-co-N,N′-methylene-bis-acrylamide) (PAA), were synthesized by radical polymerization and characterized herein for the first time. Liquid fertilizer (LF) formulations, containing potassium, phosphorus, ammonium oxides and micronutrients, were encapsulated directly into the IPNs of the composite hydrogels during synthesis. Thermal analyses and scanning electron microscopy of control and composite xerogels highlighted the formation of IPNs between BC and PAA. Swelling determinations confirmed the influence of the crosslinker and of the liquid fertilizer concentration upon the density of the IPNs. Further rheology studies and release profiles indicated how the presence of BC and the increase of the crosslinking density of IPNs improved the mechanical strength and the release profile of LF for the innovative composite BC-PAA hydrogels. Results regarding the fertilizer release indicated that the presence of the BC led to a more controlled liberation of the fertilizer proving that this new formulation is potentially viable for application in agricultural practices.

Multifunctional composite coatings composed of metal oxide nanoparticles dispersed in polymer matrices are an advanced solution to solve the problem of stone heritage deterioration. Their innovative design is meant to be stable, durable, transparent, easy to apply and remove, non-toxic, hydrophobic, and permeable. Coating formulations for the protection of buildings and monuments have been intensively researched lately. Such formulations are based on multifunctional composite coatings incorporating metal oxides. The present work aims to combine the hydrophobic properties of sodium polyacrylate (NaPAC₁₆) with the antimicrobial effectiveness, with promising antimicrobial results even in the absence of light, and good compatibility of MgO (a safe to use, low cost and environmentally friendly material) and TiO₂ (with antibacterial and antifungal properties), in order to develop coatings for stone materials protection. MgO (pure phase periclase) and TiO₂ (pure phase anatase) nanopowders were prepared through sol–gel method, specifically routes. Aqueous dispersions of hydrophobically modified polymer (NaPAC₁₆, polyacrylic acid sodium salt) and MgO/TiO₂ nanopowders were deposited through layer-by-layer dip coating technique on glass slides and through immersion on stone fragments closely resembling the mosaic stone from the fourth century AD Roman Mosaic Edifice, from Constanta, Romania. The oxide nanopowders were characterized by: Thermal analysis (TG/DTA), scanning electron microscopy (SEM), X-ray diffraction (XRD), BET specific surface area and porosity, and UV–Vis spectroscopy for band gap determination. An aqueous dispersion of modified polyacrylate polymer and oxide nanopowders was deposited on different substrates (glass slides, red bricks, gypsum mortars). Film hydrophobicity was verified by contact angle measurements. The colour parameters were evaluated. Photocatalytic and antimicrobial activity of the powders and composite coatings were tested.

The formation of separate phases in crystalline materials is promoted by doping with elements with different valences and ionic radii. Control of the formation of separate phases in multiferroics is extremely important for their magnetic, ferroelectric and elastic properties, which are relevant for multifunctional applications. The ordering of dopants and incipient phase separation were studied in lead titanate-based multiferroics with the formula (Pb_0.88Nd_0.08)(Ti_0.98−xFe_xMn_0.02)O₃ (x = 0.00, 0.03, 0.04, 0.05) by means of a combination of Mössbauer spectroscopy, XPS, HRTEM, dielectric and anelastic spectroscopy. We found that Fe ions are substituted as Fe³⁺ at Ti sites and preferentially exhibit pentahedral coordination, whereas Ti ions have coexisting valences of Ti⁴⁺/Ti³⁺. Fe³⁺ ions are preferentially ordered in clusters, and there exists a transition temperature T_C1, below which phase separation occurs between a tetragonal phase T1 free of magnetic clusters and a cubic phase, and a lower transition temperature T_C2, below which the cubic phase rich in magnetic clusters is transformed into a tetragonal phase T2. The phase separation persists at the nanoscale level down to room temperature and is visible in HRTEM images as a mixing of nanodomains with different tetragonality ratios. This phase separation was observed over the whole studied concentration range of x_Fe values. It occurs progressively with the value of x_Fe, and the transition temperature T_C2 decreases with the concentration from about 620 K (x_Fe = 0.03) to about 600 K (x_Fe = 0.05), while T_C1 remains nearly constant.