Current advances concerning the most cited metal ions doped bioceramics and silicate-based bioactive glasses for bone tissue engineering

Studies related to biomaterials that stimulate the repair of living tissue have increased considerably, improving the quality of many people's lives that require surgery due to traumatic accidents, bone diseases, bone defects, and reconstructions. Among these biomaterials, bioceramics and bioactive glasses (BGs) have proved to be suitable for coating materials, cement, scaffolds, and nanoparticles, once they present good biocompatibility and degradability, able to generate osteoconduction on the surrounding tissue. However, the role of biomaterials in hard tissue engineering is not restricted to a structural replacement or for guiding tissue regeneration. Nowadays, it is expected that biomaterials develop a multifunctional role when implanted, orchestrating the process of tissue regeneration and providing to the body the capacity to heal itself. In this way, the incorporation of specific metal ions in bioceramics and BGs structure, including magnesium, silver, strontium, lithium, copper, iron, zinc, cobalt, and manganese are currently receiving enhanced interest as biomaterials for biomedical applications. When an ion is incorporated into the bioceramic structure, a new category of material is created, which has several unique properties that overcome the disadvantages of primitive material and favors its use in different biomedical applications. The doping can enhance handling properties, angiogenic and osteogenic performance, and antimicrobial activity. Therefore, this review aims to summarize the effect of selected metal ion dopants into bioceramics and silicate-based BGs in bone tissue engineering. Furthermore, new applications for doped bioceramics and BGs are highlighted, including cancer treatment and drug delivery.     

High Mechanical Strength Double‐Network Hydrogel with Bacterial Cellulose

Double‐network (DN) hydrogels with high mechanical strength have been synthesized using the natural polymers bacterial cellulose (BC) and gelatin. As‐prepared BC contains 90 % water that can easily be squeezed out, with no more recovery in its swelling property. Gelatin gel is brittle and is easily broken into fragments under a modest compression. In contrast, the fracture strength and elastic modulus of a BC–gelatin DN gel under compressive stress are on the order of megapascals, which are several orders of magnitude higher than those of gelatin gel, and almost equivalent to those of articular cartilage. A similar enhancement in the mechanical strength was also observed for the combination of BC with polysaccharides, such as sodium alginate, gellan gum, and ι‐carrageenan.     

Electrospinning of collagen-chitosan complex

The collagen-chitosan complex nanofibers have been prepared for the first time by electrospinning. The mixed HFP/TFA (the volume ratio of 90/10) was found to be the appropriate solvent for electrospinning. The concentration of the spinning solution and the ratio of chitosan/collagen were varied and adjusted to get smooth nanofibers. It was found that the diameter of the spun fibers became thick with the concentration of the solution increasing and became fine with the ratio of the chitosan/collagen increasing. We have characterised the molecular interactions in collagen-chitosan complex by Fourier transform infrared spectroscopy. The spun fibers are designed to mimic the native extracellular matrix for tissue engineering and to develop functional biomaterials.     

Multifunctional hydrogels that promote osteogenic hMSC differentiation through stimulation and sequestering of BMP2

The extracellular environment controls many cellular activities thereby linking external material cues to internal cell function. By better understanding these processes, synthetic extracellular material niches can be tailored to present cells with highly regulated physical and/or chemical cues that promote or suppress selected cell functions. Here, poly(ethylene glycol) (PEG) hydrogels were functionalized with fluvastatin-releasing grafts and growth factor binding heparin domains to enable the dynamic exchange of information between the material and cells from the outside-in and inside-out (i.e., bidirectional signaling). By incorporating a fluvastatin-releasing graft and carefully controlling the dose and temporal release, materials were designed to promote bone morphogenic protein (BMP2) and alkaline phosphatase (ALP) production by human mesenchymal stem cells (hMSCs). When the release of fluvastatin was controlled to occur over 2 weeks, BMP2 and ALP production was increased 2.2-fold and 1.7-fold, respectively, at day 28 compared to hMSCs cultured in the absence of fluvastatin. By introducing a heparin functionality into the gel to sequester and localize the hMSC-produced BMP2, the osteogenic differentiation of hMSCs was further augmented over fluvastatin delivery alone. Osteopontin and core binding factor α1 gene expression was 6-fold and 4-fold greater for hMSCs exposed to fluvastatin in the presence of the heparin functionalities, respectively. These results demonstrate how multifunctional gels that interact with cells in a bidirectional manner can efficiently promote selected cell functions, such as the osteogenic differentiation of hMSCs.     

Natural and unnatural silks

Natural silk is an important biopolymer with huge potential as it combines superb mechanical properties with environmentally sensitive production methods. Native silk dope taken straight from the gland can easily and without chemical assistance be drawn into strong fibres. Artificial silk fibres, on the other hand, rely on spinning dopes typically ‘reconstituted’ from natural silk fibres by strong chaotropic agents. Such fibres do not form readily, and often require chemical post-spin treatment for stabilisation. In addition these fibres tend to be brittle, and so far have been unable to match native fibres. Here we present novel rheometric data to argue that native and reconstituted silkworm silk dope differ in kind, not just in degree. While native silks behave like typical molten polymers, reconstituted silks do not. We conclude that rheology provides a powerful tool in the quest to learn from the Nature's polymer fibre technology.     

Alternative technique for hydroxyapatite coatings

Flame Assisted Chemical Vapor Deposition (FACVD), a novel technique that shows an enormous potential in porous oxides deposition, was employed for the first time aiming to obtain hydroxyapatite (HA) coatings on 316 L stainless steel metallic substrates. Calcium acetate and ammonium phosphate diluted in ethanol were employed as precursor salts. A Ca/P molar ratio of 1.66 was employed in precursor solution, which is equivalent to stoichiometric hydroxyapatite. A porous coating, formed by an open and interconnected network, was observed by scanning electronic microscopy (SEM) and associated with homogenous reactions. Thickness of hydroxyapatite coating was 412 ± 3 μm. X-ray diffraction (XRD) analysis indicated the presence of crystalline coatings, mainly constituted by hydroxyapatite phase and traces of tricalcium phosphate (β-TCP). Carbonate in the hydroxyapatite coatings was identified by Fourier transform-infrared (FTIR) spectroscopy.     

Experimental investigation and thermodynamic assessment of the Zn–Cu–Sr ternary system

Zn–Cu–Sr alloys play a crucial role in the development of biodegradable implant materials based on zinc. The current study aimed to investigate the phase equilibria of the Zn–Cu–Sr ternary system in the Cu–Zn-rich region, through experimental analysis. For this purpose, fifteen and fourteen samples were respectively prepared and equilibrated at 350 and 400 °C, to determine the isothermal sections. The equilibrated alloys were then subjected to various analytical techniques such as scanning electron microscopy (SEM) equipped with energy dispersive spectrometry analysis (EDS), electron probe microanalysis (EPMA), and powder X-ray diffraction analysis (XRD). The analysis revealed the presence of five three-phase equilibria and ten two-phase equilibria in the two isothermal sections. Differential scanning calorimetry (DSC) was used to investigate the phase transformation temperature with constant values of 8 at. % Sr and 30 at. % Cu. The obtained experimental results were used to perform a thermodynamic assessment of the Zn–Cu–Sr system especial in Zn-rich region using the calculation of phase diagrams (CALPHAD) method. The modified quasi-chemical model (MQM) was used to model the liquid solution, while the compound energy formalism (CEF) was used to represent Gibbs free energies of the solid phases. The present obtained thermodynamic parameters were found to accurately reproduce the experimentally measured phase relationships in the Zn–Cu–Sr ternary system.     

Integrated plasma-aided nanofabrication facility: Operation, parameters, and assembly of quantum structures and functional nanomaterials

The development, operation, and applications of two configurations of an integrated plasma-aided nanofabrication facility (IPANF) comprising low-frequency inductively coupled plasma-assisted, low-pressure, multiple-target RF magnetron sputtering plasma source, are reported. The two configurations of the plasma source have different arrangements of the RF inductive coil: a conventional external flat spiral “pancake” coil and an in-house developed internal antenna comprising two orthogonal RF current sheets. The internal antenna configuration generates a “unidirectional” RF current that deeply penetrates into the plasma bulk and results in an excellent uniformity of the plasma over large areas and volumes. The IPANF has been employed for various applications, including low-temperature plasma-enhanced chemical vapor deposition of vertically aligned single-crystalline carbon nanotips, growth of ultra-high aspect ratio semiconductor nanowires, assembly of optoelectronically important Si, SiC, and Al_1-xIn_xN quantum dots, and plasma-based synthesis of bioactive hydroxyapatite for orthopedic implants.