Metallic materials such as stainless steel (SS), titanium (Ti), magnesium (Mg) alloys, and cobalt-chromium (Co-Cr) alloys are widely used as biomaterials for implant applications. Metallic implants sometimes fail in surgeries due to inadequate biocompatibility, faster degradation rate (Mg-based alloys), inflammatory response, infections, inertness (SS, Ti, and Co-Cr alloys), lower corrosion resistance, elastic modulus mismatch, excessive wear, and shielding stress. Therefore, to address this problem, it is necessary to develop a method to improve the biofunctionalization of metallic implant surfaces by changing the materials’ surface and morphology without altering the mechanical properties of metallic implants. Among various methods, surface modification on metallic surfaces by applying coatings is an effective way to improve implant material performance. In this review, we discuss the recent developments in ceramics, polymers, and metallic materials used for implant applications. Their biocompatibility is also discussed. The recent trends in coatings for biomedical implants, applications, and their future directions were also discussed in detail.

The mechanical qualities of AZ31B magnesium alloys make them a promising material for biodegradable metallic implants. However, rapid degradation limits the application of these alloys. In the present study, 58S bioactive glasses were synthesized using the sol-gel method and several polyols such as glycerol, ethylene glycol, and polyethylene glycol, were used to improve the sol stability and to control the degradation of AZ31B. The synthesized bioactive sols were dip-coated onto AZ31B substrates and then, characterized by various techniques such as scanning electron microscopy (SEM), X-ray diffraction (XRD) and electrochemical techniques (potentiodynamic and electrochemical impedance spectroscopy), among them. FTIR analysis confirmed the formation of a silica, calcium, and phosphate system and the XRD the amorphous nature of the 58S bioactive coatings obtained by sol-gel. The contact angle measurements confirmed that all the coatings were hydrophilic. The biodegradability response under physiological conditions (Hank’s solution) was investigated for all the 58S bioactive glass coatings, observing a different behaviour depending on the polyols incorporated. Thus, for 58S PEG coating, an efficient control of the release of H2 gas was observed, and showing a pH control between 7.6 and 7.8 during all the tests. A marked apatite precipitation was also observed on the surface of the 58S PEG coating after the immersion test. Thus, the 58S PEG sol-gel coating is considered a promising alternative for biodegradable magnesium alloy-based medical implants.

This research study is primarily centred around calcination temperature and time influence on phase formation in bioactive glasses (BGs). In the present study, BG with a nominal composition of 45S5 was synthesized through the sol–gel process. The developed BGs then underwent heat treatment for various sintering durations and temperatures. X-ray diffraction (XRD) patterns of the BGs reveals that the sintering process led to the crystallization of both devitrite (Na₂Ca₃Si₆O₁₆) and combeite (Na₂Ca₂Si₃O₉) phases. The field emission scanning electron microscopy study divulges morphological alterations, from sheet-like to rod-like structures to eventually transforming into spherical and sheet-like structures. The surface area and Type-IV mesoporous porosity were validated through Brunauer Emmett Teller analysis, highlighting a notable increase in pore volume and mechanical strength at a lower sintering temperature. In vitro apatite formation was carried out in Hank’s balance salt in order to evaluate the bioactivity of the glass. After 7 d of immersion in simulated body fluid (SBF), XRD patterns and scanning electron microscopy micrographs results showed that formation of hydroxyapatite layer on the surface of the BGs. The BG compatibility with erythrocytes (red blood cells) was also studied, and the results revealed that there was only a low 2% lysis, showing good hemocompatibility. The drug loading and release behaviour of the BGs was studied in the in vitro analysis. The findings showed a high drug encapsulation effectiveness of up to 90% and continuous drug release from the BGs for 24 h. The materials biocompatibility was unambiguously confirmed by cytocompatibility and proliferation studies. This study provides compelling evidence for the exceptional efficacy and promise of the distinct 45S5 BGs in advancing the field of regenerative medicine.

Undoubtedly, biomaterials such as bioceramics, bioactive glasses, and gels have attracted a wide range of research interest in the field of tissue engineering (TE), as they facilitate the essential support and environment for cells to grow, differentiate, and, specifically, regenerate new tissues

One of the significant causes of failure in aerospace engine components is high-temperature oxidation. Therefore, it is necessary to investigate the high-temperature oxidation behavior of newly fabricated structural materials for aerospace components. From this perspective, the isothermal oxidation behavior and kinetics of newly developed stainless steel (SS) 08X14H were investigated at 750, 950 and 1050 °C for up to 100 h in an air environment. The weight results demonstrate that oxidation in 08X14H increases with time and temperature and follows a parabolic rate law. Major spallation was observed in samples oxidized for 100 and 24 h at 950 °C and 1050 °C, respectively. Structural and morphological analysis of oxidized samples through X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM) of the surface and cross section reveal the phases present and their distribution. The structural results confirm the formation of Fe₂O₃, Cr₂O₃, FeCr₂O₄ and intermediate (Cr, Fe)₂O₃ oxides in the oxidized samples. Surface morphologies reveal that the formation of a Cr₂O₃ layer effectively protects the material from further oxidation. At higher temperatures, the coarsening of Fe₂O₃ oxides takes place, which leads to the formation of loose and porous oxide scale with stress-induced cracks. The spallation of the outermost Fe₂O₃-rich oxide scale was observed, and the matrix is exposed during the extreme oxidation at 950 and 1050 °C for 100 and 50 h, respectively. The cross-sectional morphologies and elemental mapping results reveal a duplex oxide layer with an outermost Fe₂O₃ layer followed by an underlying layer of Cr₂O₃, (Cr, Fe)₂O₃ and FeCr₂O₄ spinel beneath the Fe₂O₃ layer.