Search

ABSTRACT Aim Methods Results Conclusions This nationwide population‐based cohort study aimed to assess the incidence of implant complication treatments, including implant removal procedures and peri‐implantitis treatments, in relation to implant surfaces and abutment types.Data from the National Health Insurance Service, covering approximately 50 million individuals, were used. Implants and abutments were categorized by codes, including surfaces such as resorbable blasting media, sandblasted large grit and acid‐etched (SA) and hydroxyapatite coating, along with abutment structures (one‐piece straight, two‐piece straight, angled). The incidence of implant complication treatments was analysed using Kaplan–Meier curves and Cox proportional hazards regression (α = 0.05).The study included 2,354,706 implants. The SA group had the lowest hazard ratio for implant removal procedures (p < 0.0001). No significant differences were found in the risk of peri‐implantitis treatments between implant surfaces (p = 0.0587). The risk of implant complication treatments did not differ significantly by the abutment type (p = 0.9542). The incidence rate of implant complication treatments was < 3.9 per 1000 implant‐years across all groups.The SA group showed a slightly lower risk of late implant loss, whereas no significant association was found for the abutment type groups. All implant and abutment type groups showed an incidence rate of < 3.9 per 1000 implant‐years for complication treatments. [ABSTRACT FROM AUTHOR]

The suboptimal ionic conductivity of commercial polyolefin separators exacerbates uncontrolled lithium dendrite formation, deteriorating lithium metal battery performance and posing safety hazards. To address this challenge, a novel organic‐inorganic composite separator designed is prepared to enhance ion transport and effectively suppress dendrite growth. This separator features a thermally stable, highly porous poly(m‐phenylene isophthalamide) (PMIA) electrospun membrane, coated with ultralong hydroxyapatite (HAP) nanowires that promote “ion flow redistribution.” The synergistic effects of the nitrogen atoms in PMIA and the hydroxyl groups in HAP hinder anion transport while facilitating efficient Li+ conduction. Meanwhile, the optimized unilateral pore structure ensures uniform ion transport. These results show that the 19 µm‐thick HAP/PMIA composite separator achieves remarkable ionic conductivity (0.68 mS cm−1) and a high lithium‐ion transference number (0.51). Lithium symmetric cells using HAP/PMIA separators exhibit a lifespan exceeding 1000 h with low polarization, significantly outperforming commercial polypropylene separators. Furthermore, this separator enables LiFePO4||Li cells to achieve an enhanced retention of 97.3% after 200 cycles at 1 C and demonstrates impressive rate capability with a discharge capacity of 72.7 mAh g−1 at 15 C. [ABSTRACT FROM AUTHOR]

The fabrication of hydroxyapatite (HAP)/MgO composite coatings on Mg alloy is crucial for enhancing the corrosion resistance and biocompatibility of biomedical implants. In this study, we aimed to investigate the effects of two different surface modification methods, i.e., electrochemical (electrodeposition, ED) and chemical (solution treatment, ST), on the phase structure, degradation properties, and biocompatibility of the composite coatings in comparison to the anodized coating. The surface morphologies and crystalline structures of the coatings were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). Subsequently, the degradation rate of the coatings in simulated body fluid were comprehensively evaluated by using electrochemical impedance spectroscopy (EIS), potentiodynamic polarization and scanning electrochemical microscopy (SECM) tests. Additionally, in-vitro cell proliferation assays were employed to quantitatively assess the biocompatibilities of the coatings. The results showed that both ED and ST methods were effective in depositing HAP on anodized Mg alloy, resulting in different surface morphologies with hydroxyapatite layer thicknesses of 2.71 μm and 3.56 μm, respectively. In this way, the HAP-deposited coatings exhibited improved corrosion resistances and biocompatibilities compared with those of the anodized coating. Specifically, the ST-deposited composite film displayed superior degradability and biocompatibility which was attributed to its filiform surface morphology and thicker HAP layer. Overall, the present study demonstrates the potential of HAP/MgO composite coatings for biomedical applications, with implications for the development of advanced implant materials with improved performance and biocompatibility. [ABSTRACT FROM AUTHOR]

This study aimed to retrospectively analyze the follow-up results of cases in which the adjacent joint was preserved using a custom-made uncemented short-stem design (hollow stem) with optional external flanches in tumor endoprosthetic replacement due to bone sarcomas in 13 patients (with an average age of 9.6 years) between 2017 and 2023. Reconstructions were proximal femur (n = 6), intercalary femur (n = 4), intercalary tibia (n = 2), and proximal humerus (n = 1) tumor prostheses. The hollow body was used distally in 10 of the megaprotheses, proximally in 1, and both proximally and distally in 2 of them. The average distance from the joints was 6 cm in stems with flanches and 11.8 cm in stems without flanches. No aseptic loosening or deep infection was observed during an average follow-up of 34 months. Except for one case with a tibial intercalary prosthesis that needed a revision, all cases were well osteointegrated and all lower extremity cases could bear full weight without pain. In cases where the remaining bone stock after bone resection is insufficient for a standard stem implantation, reconstruction with a patient-specific short hollow-stem design appears to be a good alternative to protect healthy joints with high prosthesis survival and low revision rates in the short-term follow-up. [ABSTRACT FROM AUTHOR]

The increasing need for advanced orthopaedic implants necessitates improved materials that offer better biocompatibility and mechanical properties, addressing issues such as implant failure due to poor integration and corrosion. A 3″ diameter, 5-mm-thick pellet of hydroxyapatite (HAP) was prepared and was used as the cathode for the radio frequency (RF) magnetron sputtering system. One hundred nm nanocoating on alumina substrates (HAP/Al2O3) was done using RF magnetron sputtering. The hexagonal (HCP) HAP structure was chosen to deposit on hexagonal α-alumina for better growth and adhesion of the HAP film. The microstructure was analysed using field emission scanning electron microscopy, atomic force microscopy, and glancing angle X-ray diffraction. Elemental analysis was carried out using energy-dispersive X-ray spectroscopy. Mechanical and film adhesion properties were studied using Vicker's hardness and scratch test, respectively. The hardness of the coated sample increases 2.5 times. The optical contact angle increased from 82.88° for pure alumina to 113.53° for HAP/Al2O3 due to the decreased roughness, indicating enhanced hydrophobicity. Pore size, area, and volume were studied using the Brunauer–Emmett–Teller technique. Corrosion resistance in Ringer's solution and dielectric properties were investigated. The antimicrobial investigation was carried out against two different bacteria, namely gram-negative Escherichia coli (E. coli) and gram-positive Staphylococcus aureus (S. aureus). Improved adhesion, hardness, corrosion resistance, and biocompatibility properties are correlated with the surface and structural properties. [ABSTRACT FROM AUTHOR]

AbstractIn this manuscript, the application of hydroxyapatite coatings to total ossicular reconstruction prostheses (TORPs) using finite element modeling simulations was investigated to enhance the biocompatibility and mechanical performance of these prosthetic devices for middle ear implants. We focused on evaluating biocompatible materials, particularly polyetheretherketone (PEEK) and titanium, by analyzing their mechanical behavior under simulated conditions. The results revealed that PEEK demonstrates mechanical performance almost on par with titanium, exhibiting excellent stability and resilience within the middle ear environment. PEEK offers several key advantages over titanium, including easier fabrication, greater availability, and a simplified application process for hydroxyapatite coatings. These benefits suggest that PEEK could be a highly effective alternative to titanium for use in middle ear prostheses. The findings of this study highlight the potential of PEEK to improve the design and functionality of middle ear implants, providing a promising direction for future research and development in this field. By leveraging the advantages of PEEK, we can advance the effectiveness and accessibility of middle ear prosthetic devices, ultimately benefiting patients requiring such interventions. [ABSTRACT FROM AUTHOR]

In recent years, many different biomedical implants have been created for prolonged usage within the human body. The number of these implants has been steadily expanding. It is a common practice to use metallic bioimplants as substitutes when attempting to replace human body components in an anatomically acceptable manner. But the metallic bioimplant was mostly made biocompatible by putting a biocompatible coating on its surface and then using the right surface modification techniques. This was the primary method by which the biocompatibility of the bioimplant was achieved. Thermal spraying is a method that is frequently employed in surface modification treatments to modify metallic bioimplants. These methods can be found in the medical field. This is due to the adaptability of the thermal spraying method. Because of their capacity to respond and adapt to physiochemical circumstances, coatings that are based on hydroxyapatite (HAp) are the most popular type to be used in thermal spraying. This is due to the fact that HAp is a naturally occurring mineral. On the other hand, the majority of the HAp coatings are unsuccessful as a result of the coating’s weak mechanical qualities and insufficient adhesive strength. Supplying the coating in question with reinforcement in the form of hard particles and doing so in the appropriate proportions makes it feasible to alter the qualities of HAp-based coatings to fulfill a variety of requirements. This can be accomplished by providing the coating with reinforcement. The purpose of this inquiry was to deconstruct and analyze a variety of thermally sprayed (TS) coatings. These coatings were used to adhere HAp-based coatings on bioimplants. In addition, a detailed discussion is offered on how the reinforcements have an effect on the mechanical and biocompatible qualities of the coatings. In addition, we have discussed the difficulties associated with TS HAp coatings and their potential uses in the manufacturing of 3D biomedical implants through the utilization of cold spray (CS). [ABSTRACT FROM AUTHOR]

In this research, Sr-doped hydroxyapatite, HAp and NiO nanoparticles were used to produce a novel nanocomposite, Sr-doped HAp/NiO. Various analytical and instrumentation techniques such as FTIR, PXRD, UV-DRS, SEM, TEM, and XPS were used to characterize the as synthesized composite material. The nanocomposite acts as an efficient photocatalyst and is able to degrade Congo red (CR) dye up to 95.6% within 40 min under solar light irradiation without any kind of external additive. The HR LC–MS spectrum was recorded to determine the degradation products of the chosen organic dye. Furthermore, the as prepared nanocatalyst also effectively reduced 98.7% of carcinogenic Cr(VI) to Cr(III) within just 10 min. In order to propose the photocatalytic mechanism and to detect the active radicals present, a radical trapping experiment was conducted. As an appealing photocatalyst for wastewater treatment and reduction of toxic chemicals, the research concluded with a methodical and cost-effective process for producing the Sr-doped HAp/NiO nanocomposite. [ABSTRACT FROM AUTHOR]

The hydroxyapatite and copper-doped hydroxyapatite coatings (Ca10−xCux(PO4)6(OH)2; xCu = 0, 0.03; HAp and 3CuHAp) were obtained by the vacuum deposition technique. Then, both coatings were analyzed by the X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR) and water contact angle techniques. Information regarding the in vitro antibacterial activity and biological evaluation were obtained. The XRD studies confirmed that the obtained thin films consist of a single phase associated with hydroxyapatite (HAp). The obtained 2D and 3D SEM images did not show cracks or other types of surface defects. The FTIR studies' results proved the presence of vibrational bands characteristic of the hydroxyapatite structure in the studied coating. Moreover, information regarding the HAp and 3CuHAp surface wettability was obtained by water contact angle measurements. The biocompatibility of the HAp and 3CuHAp coatings was evaluated using the HeLa and MG63 cell lines. The cytotoxicity evaluation of the coatings was performed by assessing the cell viability through the MTT assay after incubation with the HAp and 3CuHAp coatings for 24, 48, and 72 h. The results proved that the 3CuHAp coatings exhibited good biocompatible activity for all the tested intervals. The ability of Pseudomonas aeruginosa 27853 ATCC (P. aeruginosa) cells to adhere to and develop on the surface of the HAp and 3CuHAp coatings was investigated using AFM studies. The AFM studies revealed that the 3CuHAp coatings inhibited the formation of P. aeruginosa biofilms. The AFM data indicated that P. aeruginosa's attachment and development on the 3CuHAp coatings were significantly inhibited within the first 24 h. Both the 2D and 3D topographies showed a rapid decrease in attached bacterial cells over time, with a significant reduction observed after 72 h of exposure. Our studies suggest that 3CuHAp coatings could be suitable candidates for biomedical uses such as the development of new antimicrobial agents. [ABSTRACT FROM AUTHOR]

Background: Periosteal expansion (PEO) results in the formation of new bone in the space created between existing bone by expanding the periosteum. PEO has already been performed on rabbit parietal bone and effective new bone formation has been demonstrated. In this study, the utility of a polyethylene terephthalate (PET) membrane as an activator was evaluated in the more complex morphology of the mandible. Methods: A PET membrane coated with hydroxyapatite (HA)/gelatine was placed in the rabbit mandibular bone at lower margin of mandibular molar region underneath periosteum, and screw‐fixed. In the experimental group, the membrane was bent and screw‐fixed along the lateral surface of the bone, with removal of the outer screw after 7 days followed by activation of the membrane. The experimental group was divided into two subgroups: with and without a waiting period for activation. Three animals were euthanized at 3 weeks and another three at 5 weeks postoperatively. Bone formation was assessed using micro‐CT as well as histomorphometric and histological methods. Results: No PET membrane‐related complications were observed. The area of newly formed bone and the percentage of new bone in the space created by the stretched periosteum did not significantly differ between the control and experimental groups. However, in the experimental group a greater volume was present after 5 weeks than after 3 weeks. Histologically, bone formation occurred close to the site of cortical bone perforation, with many sinusoidal vessels extending through the perforations in the new bone into the overlying fibrous tissue. Inflammatory cells were not seen in the bone. [ABSTRACT FROM AUTHOR]

The present work aimed to produce HAp nanoparticles doped with Zn and Ni in order to analyze the incorporation of these elements in the catalytic and antimicrobial properties of HAp. The samples were obtained by the microwave-assisted hydrothermal method in 30 min at 150 °C. XRD and FTIR results showed that HAp was formed without the presence of secondary phases, and Rietveld refinement indicated a reduction in crystallite size after doping. Nanorod-like morphologies were observed by SEM-FEG with reduction in particle size and increase in specific surface area. Furthermore, the hidden gap at 3.26 eV, photoluminescence indicated that there was a predominance of deep defects and XPS showed the presence of dopants on the HAp surface. The catalytic results in the degradation of methylene blue dye indicated that the zinc-doped sample removed 97.85 % under sunlight, 66.81 % under UV light and 70.64 % under ultrasound. After four cycles of reuse under sunlight, good photocatalytic performance was maintained, and inhibition tests indicated that holes and hydroxyls are the active radicals. Antimicrobial activity tests showed that zinc-doped and co-doped samples were efficient in inhibiting Gram-negative bacteria (Escherichia coli). This work brings a promising alternative application for hydroxyapatite in environmental and microbial remediation. [ABSTRACT FROM AUTHOR]

NiTi alloys are actively used in medicine as implants because of their mechanical properties. At the same time, however, the NiTi surface is not biologically active, which has a negative effect on osteogenesis. In addition, Ni is capable of causing various toxic reactions in the human body. It is therefore necessary to create a composite coating that is both bioactive and prevents the release of Ni ions. It has been shown that by changing the modes of plasma assisted RF sputtering of a calcium phosphate target, it is possible to obtain coatings with different contents of the amorphous phase. The coatings formed consist of hydroxyapatite and amorphous calcium phosphate. On the surface of a sample not treated with argon plasma, there are no phases containing calcium or phosphorus, although these elements are present on the surface. The different ways in which the CaP coatings were applied also affected their structure. It was found that the CaP coatings of samples M2 and M3 have mediocre corrosion resistance, dissolving quickly. This has a positive effect on the ability to osteogenesis, which was discovered as a result of in vitro tests. These tests have shown that the sample obtained at I discharge = 30 A and U bias = 30 V has the highest bioactivity and produces the lowest percentage of dead cells. [ABSTRACT FROM AUTHOR]

Biomedical coatings were elaborated by pulsed electrodeposition with hydrogen peroxide (H 2 O 2) into electrolytes on Ti 6 Al 4 V substrates, and the effect of H 2 O 2 concentration on the electrolyte and the heat treatment was studied. The experimental procedures employed in this study produce a consistent hydroxyapatite coating. This coating is well-suited for use in bio-implants, as it enhances the integration of the implant with surrounding bone tissue and improves the mechanical performance. The coatings' surface morphology and chemical composition were assessed using scanning electron microscopy (SEM) in conjunction with energy-dispersive X-ray spectroscopy (EDXS) for x-ray microanalysis. X-ray diffraction (XRD) was also utilized to identify the phases and composition of the coatings. Nanoindentation and scratch tests were conducted to analyze the nanomechanical properties and adhesion behavior. Potentiodynamic polarization was employed in the Ringer solution to evaluate the corrosion resistance and replicate the conditions of the human body environment. The results of our thorough investigation revealed that employing pulsed electrodeposition with 9 % H 2 O 2 in the electrolyte, combined with subsequent heat treatment, facilitated the creation of coatings comprising two distinct phases: stoichiometric hydroxyapatite (HAP) and β-tricalcium phosphate (β-TCP). Our meticulous research underscores the significance of this process in achieving these specific coating compositions. Under these tests listed above, this composite demonstrated favorable mechanical properties (E = 30.45 GPa and H = 72.2 MPa). It also exhibited superior scratch adhesion and a critical load of 23 MPa and 12 N, respectively. Additionally, an improvement in tribological comportment was observed, and the wear volume decreased from 4.15 106 μm3 to 2.44 106 μm3. The HAP coating heat treated with 9 % H 2 O 2 exhibited the highest corrosion resistance, with E corr at −0.189 V/SCE and i corr at −1.11 μA cm−2 [ABSTRACT FROM AUTHOR]

[Display omitted] Stone-built cultural heritage faces threats from natural forces and anthropogenic pollutants, including local climate, acid rain, and outdoor conditions like temperature fluctuations and wind exposure, all of which impact their structural integrity and lead to their degradation. The development of a water-based, environmentally-friendly protective coatings that meet a combination of requirements posed by the diversity of the substrates, different environmental conditions, and structures with complex geometries remains a formidable challenge, given the numerous obstacles faced by current conservation strategies. Here we report the structural, electrical, and mechanical characterization, along with performance testing, of a nanostructured hydrophilic and self-healing hybrid coating based on hydroxyapatite (HAp) nanocrystals and polyelectrolyte multilayers (PEM), formed in-situ on Greek marble through a simple spray layer-by-layer surface functionalization technique. The polyelectrolyte-hydroxyapatite multilayer (PHM) structure resembled the design of naturally forming trabecular bone, attained at a short procedural time. It exhibited chemical affinity, aesthetical compatibility and resistance to weathering while offering reversibility. The proposed method is able to generate micron-sized coatings with controlled properties, such as adhesion and self-healing, leading to less weathered surfaces. Our results show that the PHM is a highly effective protective material that can be applied for stone protection and other similar applications. [ABSTRACT FROM AUTHOR]

Carbon fiber (CF) is one of ideal reinforcements to hydroxyapatite (HA) owing to its unique structure, excellent biocompatibility and high mechanical properties. However, the mechanical property of CF reinforced HA (CF/HA) composites cannot be effectively improved due to the mismatch in surface properties and thermal expansion coefficients between CF and HA. In order to solve the problems, nano-hydroxyapatite (nHA) coating with different thickness was fabricated on the CF surface. The effect of the coating thickness on mechanical property of nHA-coated CF/HA composites was studied by finite element analysis. The CF with proper nHA coating thickness was subsequently used to reinforce HA. The compressive strength of nHA-coated CF/HA composites was approximately 97.3 % and 164.6 % higher than those of the uncoated CF/HA composites and pure HA ceramics, respectively. The interface properties and crack propagation were analyzed by cohesive element in the finite element analysis. The toughening mechanism of the composites included interfacial debonding, crack deflection, crack branching, and crack bridging. The mechanical properties of nHA-coated CF/HA composites were enhanced due to the strong interfacial bonding strength and reducing cracking in HA matrix. The prepared nHA-coated CF/HA composites satisfy the requirement of the mechanical properties of human load-bearing bone. It can be used to prepare cages, plates, screws, pins and other compact bone substitute parts in bone grafting. The study provided a method for construction of nHA-coated CF/HA composites with the designed properties by adjusting the nHA coating on the fiber and can be used to design other fibers reinforced ceramic matrix composites. [Display omitted] [ABSTRACT FROM AUTHOR]

Controlling blood loss is crucial for saving lives during trauma. Based on the current application of solid waste in hemostatic materials, this study reports the synthesis of a hydroxyapatite/tourmaline composite material (referred to as ST) and a hemostatic sponge (referred to as STS). These materials were synthesized through hydrothermal processes and lyophilization techniques using seashells, tourmaline, and chitosan as precursors. The phase analysis and microstructure characterization were performed using XRD, SEM, TEM, and HRTEM. Owing to the spontaneous polarization of tourmaline attracting free ions in the system, the shells were deposited on the surface of tourmaline particles in the form of hydroxyapatite (HA) through dissolution and recrystallization during the hydrothermal process. HA can release free Ca2+, an important component in the coagulation system, while tourmaline can enhance cell metabolism by reducing water molecular clusters, thereby altering the permeability of cell membranes. ST particles were incorporated into the chitosan sponge matrix to prevent particle shedding. Through orthogonal design experiments on the preparation process of ST, the optimal preparation conditions were determined as follows: a hydrothermal temperature of 180 °C, a hydrothermal time of 12 h, a pH value of 8, and a shell-to-tourmaline ratio of 8 : 1. The composite materials were evaluated for their adsorption capacity, clotting time, hemolysis rate, antibacterial rate, and cytotoxicity. The results demonstrated a higher liquid adsorption rate, significantly reduced clotting time, a hemolysis rate of <5.0%, an antibacterial capacity of 88.5%, and lower cytotoxicity. These findings suggest that STS has the potential to be a safe, effective, and cost-efficient hemostatic agent. [ABSTRACT FROM AUTHOR]

In this study, hydroxyl apatite (HA) as a bio-ceramic is coated on the TiNi shape memory. In this approach, Tri-ethanolamine and butanol were used as suspensions. To set up Electrophoretic Deposition (EPD) process, voltages of 20, 30 and 40 volts were applied on the cathode for 1-5 minutes. The sintering process was done in the Ar atmosphere for two hours at 800°C. SEM and XRD were used to investigate surface morphologies and phases. Obtained results showed that higher electrical currents led to generation of thicker coatings registering 105% and 12.3% improvement for weight and thickness after 6 minutes, respectively. Moreover, Transformation of HA to other calcium phosphate phases doesn’t happen at a sintering temperature of 800°C. Moreover, a uniform, homogeneous and crackles coating can be reached in the voltage of 30 volts at low sintering temperatures. This process can be utilized an alternative technique for bioactive coatings. [ABSTRACT FROM AUTHOR]

Simple Summary: This research investigated the impact of different surface modifications on the osseointegration of dental implants. The study conducted experiments on rabbit tibiae comparing conventional machined surfaces (MSs) with those modified using a laser beam (LSs) or a laser beam incorporating hydroxyapatite (HA) by means of biomimetic methods without thermic treatment (LHSs). Utilizing scanning electron microscopy coupled with energy-dispersive X-ray spectrometry (SEM/EDX) and fluorochrome labeling techniques, the study evaluated bone formation over a four-week period. The results demonstrated significantly improved bone contact and newly formed bone area with LSs and LHSs compared to MSs. These findings suggest that surface modifications, particularly LS modifications and LHS modifications, enhance osseointegration, potentially leading to an enhanced longevity and performance of dental implants in clinical settings. (1) Objective: The aim of this study was to assess the biological behavior of bone tissue on a machined surface (MS) and modifications made by a laser beam (LS) and by a laser beam incorporated with hydroxyapatite (HA) using a biomimetic method without thermic treatment (LHS). (2) Methods: Scanning electron microscopy coupled with energy-dispersive X-ray spectrometry (SEM/EDX) was performed before and after installation in the rabbit tibiae. A total of 20 Albinus rabbits randomly received 30 implants of 3.75 × 10 mm in the right and left tibias, with two implants on each surface in each tibia. In the animals belonging to the 4-week euthanasia period group, intramuscular application of the fluorochromes calcein and alizarin was performed. In implants placed mesially in the tibiofemoral joint, biomechanical analysis was performed by means of a removal torque (N/cm). The tibias with the implants located distally to the joint were submitted for analysis by confocal laser microscopy (mineral apposition rate) and for histometric analysis by bone contact implant (%BIC) and newly formed bone area (%NBA). (3) Results: The SEM showed differences between the surfaces. The biomechanical analysis revealed significant differences in removal torque values between the MSs and LHSs over a 2-week period. Over a 4-week period, both the LSs and LHSs demonstrated removal torque values statistically higher than the MSs. BIC of the LHS implants were statistically superior to MS at the 2-week period and LHS and LS surfaces were statistically superior to MS at the 4-week period. Statistical analysis of the NBA of the implants showed difference between the LHS and MS in the period of 2 weeks. (4) Conclusions: The modifications of the LSs and LHSs provided important physicochemical modifications that favored the deposition of bone tissue on the surface of the implants. [ABSTRACT FROM AUTHOR]

Buttermilk differs from skim milk by the presence of milk fat globule membrane (MFGM) fragments that are released during cream churning. Milk fat globule membrane is rich in health-promoting components, such as phospholipids and membrane proteins, but these compounds have a negative impact on buttermilk techno-functional properties in dairy applications. The isolation of MFGM from buttermilk improved its functionality while also recovering the MFGM bioactive components. Hydroxyapatite (HA) can be used to extract MFGM by adsorption via charged site interactions. However, the affinity of HA to MFGM or the main buttermilk proteins (casein micelles [CM], β-LG, and α-LA) is not known. The influence of important physicochemical parameters such as pH and temperature on these interactions is also unclear. For each buttermilk component, a quartz crystal microbalance diffusion analysis was performed to determine the maximum adsorption time and the attached mass density on HA-coated gold sensors. The influence of pH, ionic strength (IS), and temperature (T) on the affinity of each buttermilk component for HA particles was assessed using a 3-levels and 3-factors Box-Behnken design. The absorption rate was highest for the CM, followed by β-LG and α-LA, and then by the MFGM. Nevertheless, the final maximal attached mass densities to the HA were similar for the MFGM and CM, and 2.5 times higher than for β-LG and α-LA. This difference can be explained by the higher number of binding sites found in CM and their heavier mass. The model obtained by the Box-Behnken design plan showed that the adsorption of the CM changed with T, pH, and IS. These results suggest that the techno-functional properties of buttermilk may be restored by specifically extracting MFGM with HA. Experiments are ongoing to determine conditions for fractionating MFGM directly from buttermilk. [Display omitted] [ABSTRACT FROM AUTHOR]

The high catalytic activity of arenediazonium, along with the ability of gold ions to form specific bonds with amikacin, has been used in the fabrication of an electrochemical sensor based on a glassy carbon electrode modified with a gold solution and arenediazonium tosylate (Ar/GGCE) for the detection and quantification of amikacin upon its release from implants. Atomic force microscopy, cyclic voltammetry, and square-wave voltammetry were used to demonstrate that the use of a gold solution and arenediazonium tosylate for the surface modification of a glassy carbon electrode significantly enhances the electrode characteristics. The determination of amikacin was achieved using square wave voltammetry, which enabled the detection of amikacin at the Ar/GGCE in the concentration range 0.2–60 μM and ensured a limit of detection of 0.058 μM for amikacin released from implants. [ABSTRACT FROM AUTHOR]

The aim of the present study is to create porous poly lactic acid (PLA)-based temporal cellular scaffolds with specifically designed topographical orientation by means of femtosecond laser (fs)-induced microstructuring, additionally functionalized by a nanometric layer of hydroxyapatite (HA) by the pulse laser deposition (PLD) method. For this purpose, surface micromodification of PLA samples by means of a CPA Ti:sapphire fs laser system (τ = 150 fs, λ = 800 nm, ѵ = 0.5 kHz), operating at fluence F = 0.8 J/cm2 and scanning velocity V = 3.8 mm/s, was combined with PLD of thin layer of HA on the patterned PLA matrices for cellular scaffold surface additional nanofunctionalization. Each laser structured PLA scaffold was analyzed with respect to its control and laser processed surface, covered with HA. The multilevel structured scaffolds were investigated by SEM, EDX, 3D profilometer, AFM, micro-Raman and WCA analyses. Cytocompatibility studies with MG63 osteoblastic cells were also performed. Moreover, the cellular behavior was compared with the one observed on HA spin-coated fs microstructured PLA temporary scaffolds, in order to compare the two methods of functionalization. A disordered spreading on smooth surfaces to a tendency of cell orientation and elongation along the laser created grooves was monitored, along with increased alkaline phosphatase activity, which could essentially improve their subsequent practical application in engineering of personalized bone tissue. [ABSTRACT FROM AUTHOR]

Keeping safety and sustainability in view with managing radioactive aqueous wastes and other wastewaters containing Sr(II) ions, the current work was designed and performed to immobilize this ion in ceramic matrices. The adsorption properties of Ti–Ca–Mg composite phosphates with different ratios of Ti/(Ca + Mg) towards Sr(II) ions have been studied. Chemical structures and phase transformations of phosphate adsorbents and Sr(II)-loaded products after heat treatment in the range of 20–1000 °C were scrutinized by XRD, DTA-DTG, FTIR and elemental analyses. Hardly soluble calcium, magnesium pyrophosphates, Ca–Mg and Ca–Ti phosphates with a NaZr 2 (PO 4) 3 or CaTi 4 (PO 4) 6 skeleton structure (abbreviated as NZP or CTP) were obtained through heat treatment of composite phosphates at 800–1000 °C. The effect of the Ti/(Ca + Mg) ratio existing in the initial adsorbents on the phase and chemical composition of heat-treated products was studied, and the mechanism of their formation was proposed. Heat treatment of Sr-saturated Ti–Ca–Mg phosphates at 1000 °C led to the formation of Sr-substituted hydroxyapatite and whitlockite, which caused a high immobilization strength for Sr(II) ions. The degree of desorption of Sr(II) ions after heat-treatment of Sr-saturated adsorbents decreased by 10–120 times, declining to the amounts of 0.31–0.54% in seawater and 0.03–0.12% in artesian. The obtained Ti–Ca–Mg composite phosphates are of interest for the adsorption and immobilization of Sr(II) ions from liquid radioactive wastes (LRW) into ceramic matrices and can be used in full-scale plants. [ABSTRACT FROM AUTHOR]

Although the hydroxyapatite (HA) coating implant prepared by laser cladding exhibits good biological activity due to its chemical composition similar to biological bone, the original surface roughness of the laser-clad coating is high, which is unfavorable for long-term cell adhesion and proliferation. In order to improve the biological activity of HA coating implants and increase the adhesion and proliferation rate of osteoblasts on their surface, microtextures with different length-diameter ratios and depth gradients were prepared on the HA coating surface by nanosecond laser with reference to the microscopic morphology characteristics of the biological bone surface. By investigating the effects of microtexture aspect ratio and depth gradient on osteoblast adhesion characteristics, it was found that bone-like microtextures better controlled and simulated cell-material surface interactions. The geometric morphology of microtextured bone with a wide front end and narrow rear end and a depth gradient from front to back was an important signal for osteoblast proliferation. When the aspect ratio of bone microtexture was 2.5:1 and the maximum depth gradient was 15.7 μm, osteoblasts within the microtexture showed optimal growth, proliferation, and adhesion. Additionally, due to induction by microtexture contour shape and depth gradient morphology, cell morphology showed varying adhesion morphology from the front to the back of the microtexture. The results demonstrated that HA coatings with bone-like microtextures had superior osteoblast proliferation and adhesion properties compared to the original cladded coating surface, beneficial for enhancing the application of HA-coated bone implants in large segment bone repair. [ABSTRACT FROM AUTHOR]

In this study, hydroxyapatite (HA) incorporated in mesoporous SiO 2 particles (SiO 2 /HA) was initially synthesized using a soft template method. The resulting structure owned a high surface area (796.62 m2 g-1) and a substantial pore volume (0.757 cm3 g-1). The TEM and FESEM images indicated that the synthesized mesoporous particles possessed a spherical morphology, with a diameter of approximately 200 nm, and pores of slit-shape. The mission was to improve the surface characteristics of NiTi implants by composite coatings. This investigation emphasized specifically the impact of different concentrations of mesoporous SiO 2 /HA particles within the electrolyte on the properties of HA/mesoporous composite coatings. The surface characteristics of the coatings were examined using ATR-FTIR, FESEM, EDS, AFM, and hydrophilicity measurements. Furthermore, the osteogenic activity of the coatings was evaluated by culturing the osteosarcoma cell line SAOS-2 on the coated samples. The introduction of mesoporous particles resulted in a decrease in the coatings' surface roughness along with an improvement in their wettability. Moreover, there was an enhancement in the cell viability (99% after 7 days), proliferation, adhesion, and growth of SAOS-2 cells at the optimized concentration of mesoporous SiO 2 /HA particles (1000 mg/L). DAPI images illustrated that the mesoporous particles did not cause any adverse impact on the cellular nuclei. Finally, in the apoptosis test, the composite coating displayed a reduced number of necrotic cells compared to the pure HA coating. [ABSTRACT FROM AUTHOR]

β-TiNb alloys have attracted much attention due to their excellent comprehensive mechanical properties and biocompatibility. However, its high cost and large difference between elastic modulus and human bone will limit its application. In this study, a porous Nb-32.5Ti-xTa alloy coating, approximately 1.3 mm thick, was prepared on the surface of Ti-6Al-4V using laser cladding technology. Subsequently, the properties of the composite coating were characterized. The results show that the addition of Ta and Nb elements contributes to the formation of β phase. The formation of Nb2O5 and Ta2O5 passivation films during electrochemical corrosion significantly enhanced the corrosion resistance of the coating, and the protection rate of Ti32.5Nb20Ta coating was 68.06 %. The cladding coating had better biocompatibility than the substrate. Furthermore, the sample deposited a large amount of hydroxyapatite (HA) in simulated body fluid (SBF), which proved that the coating had good bone formation ability. [ABSTRACT FROM AUTHOR]

Background/Objectives: A highly porous titanium cup with a three-dimensional metal interface was recently introduced to improve biological fixation and survival. However, radiography has revealed concerns regarding these cups, despite their excellent short- and mid-term clinical outcomes. This study compared the clinical and radiographic results of a highly porous titanium cup with those of a hydroxyapatite-coated porous titanium cup after primary total hip arthroplasty (THA). Methods: Fifty-one primary THAs were investigated. A highly porous titanium cup was used in 17 hips, and a hydroxyapatite-coated porous titanium cup was used in 34 hips. No significant differences in preoperative patient demographic characteristics were observed between the two groups. The 2-year postoperative clinical and radiographic results were compared. Results: Radiolucent lines were observed in 13 (76%) of 17 hips with highly porous titanium cups and in none (0%) of 34 hips with hydroxyapatite-coated porous titanium cups (p < 0.001). In the highly porous titanium cup group, radiolucent lines were observed in five hips (29%) in one zone, two hips (11%) in two zones, and six hips (35%) in three zones. No cup loosening was observed in either group. Conclusions: Radiolucent lines were significantly more frequent in highly porous titanium cups. This study suggests that, compared to the three-dimensional structure of porous titanium, the hydroxyapatite coating of porous titanium had a greater influence on bone ingrowth in the short term. The meaning of these findings in the long-term is unclear yet. [ABSTRACT FROM AUTHOR]

[3H]Hyaluronic acid with a molecular weight of 2.37 MDa and a specific radioactivity of 35 GBq/g was obtained using the tritium thermal activation method. Tritium labeled hyaluronic acid (HA) with a molecular weight of 2.37, 0.20, and 0.10 MDa were used to study their adsorption on hydroxyapatite (HAP) in two textural modifications: aqueous suspension and powder. Differences in adsorption kinetics and adsorption isotherms were observed due to variations in the interaction between polysaccharide molecules and the sorbent forms under consideration. The adsorption isotherms of HA on HAP were proven linear. It is shown that strong HA–HAP complexes are formed, and no desorption of HA into water and 0.9% NaCl solution were detected in 2 days. [ABSTRACT FROM AUTHOR]

Bone tissue engineering (BTE) is the most promising strategy to repair bones injuries and defects. It relies on the utilization of a temporary support to host the cells and promote nutrient exchange (i.e., the scaffold). Supercritical CO2 assisted drying can preserve scaffold nanostructure, crucial for cell attachment and proliferation. In this work, agarose aerogels, loaded with hydroxyapatite were produced in view of BTE applications. Different combinations of agarose concentration and hydroxyapatite loadings were tested. FESEM and EDX analyses showed that scaffold structure suffered from partial closure when increasing filler concentration; hydroxyapatite distribution was homogenous, and Young's modulus improved. Looking at BTE applications, the optimal combination of agarose and hydroxyapatite resulted to be 1% w/w and 10% w/v, respectively. Mechanical properties showed that the produced composites could be eligible as starting scaffold for BTE, with a Young's Modulus larger than 100 kPa for every blend. [ABSTRACT FROM AUTHOR]

In this study, to reactivate the oxide film and to secure biocompatibility, plasma electrolytic oxidation (PEO) treatment and hydroxyapatite (HA) deposition via mechanical coating (MC) processes were investigated. This experimental approach involved subjecting the Ti–6Al–4V alloy specimens to PEO treatment, followed by MC with HA powder for different hours as HA has the potential to increase bioactivity and surface characteristics due to its chemical composition and structural properties similar to natural bone. Therefore, the study aimed to examine the effects of MC with HA powder for 0, 1, 3, 5, 7, and 9 h on PEO-coated Ti–6Al–4V alloy discs for analyzing the surface characterization, phase analysis, surface roughness, wettability, adhesion strength, hardness, corrosion behavior, and cell proliferation properties for dental implant use. The findings demonstrate that prolonged HA milling enhances the substrate's mechanical strength, corrosion resistance, and adhesion properties. The presence of prominent anatase and HA peaks, particularly in the 5 MC-PEO, 7MC-PEO, and 9 MC-PEO samples, validates the synergistic impact of the PEO oxide layer and HA milling, resulting in outstanding corrosion resistance and biocompatibility. Cell culture analysis reveals a positive correlation between increased milling time and enhanced cell proliferation, particularly towards small-sized HA particles. [Display omitted] [ABSTRACT FROM AUTHOR]

Zinc (Zn) distinguishes itself as an excellent candidate for temporary orthopaedic implants due to its advantageous corrosion rate compared to other biodegradable metallic materials like Mg and Fe. The present research involved the fabrication of a porous, corrosion-resistant, and biocompatible plasma electrolytic oxidation (PEO) coating on a Zn–1Mg alloy. Bioactivity was imparted to the PEO coating by incorporating hydroxyapatite (HA) and silver-incorporated hydroxyapatite (SHA) nanoparticles into it by synergising the PEO process with electrophoretic deposition (EPD) in a single step. FESEM and EDS are utilised to confirm the porous PEO oxide layer formation and its sealing by HA and SHA particles in PEO-EPD coating. The coatings' phase composition, surface roughness, scratch resistance, and wettability were evaluated to assess their suitability for temporary implant applications. The coatings' wettability and roughness significantly improved compared to the untreated substrate, rendering it suitable for orthopaedic implant applications. The scratch resistance of the PEO coating was satisfactory and showed additional improvement in the thicker film with lower porosity, achieved through the combined PEO-EPD process. The electrochemical corrosion test in biological media revealed that the PEO coating enhanced the degradation resistance of Zn–1Mg, which was further enhanced by incorporating HA and SHA particles into the PEO coating. The in-vitro bioactivity test in simulated body fluid (SBF) and cytotoxicity test using L929 (Mouse fibroblast) cells proved that adding HA made the fabricated PEO coating biologically more favourable. Furthermore, the SHA-incorporated PEO coating is antibacterial against E. coli bacterial strains, enabling protection against post-implantation infections. • ZnO-HA ceramic composite coating developed on Zn–1Mg by PEO. • ZnO-HA coating showed 3 orders lower i corr compared to bare alloy. • Ceramic-composite coating proved to be bioactive and biocompatible. • Silver-incorporated coating exhibited the bactericidal property. [ABSTRACT FROM AUTHOR]

Biochar with abundant functional groups, porous structure, and high specific surface area has been widely used as an adsorbent for the removal of metal ions, and its low production costs make it economically suitable for large-scale application in various industries. Hydroxyapatite nanoparticles were used to functionalize magnetic rice husk biochar (MBC) to produce hydroxyapatite functionalized magnetic rice husk biochar (HAP@MBC) in this study. The functional groups, magnetism performance, surface morphology, and aperture structure of HAP@MBC were characterized to explore the feasibility of its application in the treatment of wastewater containing Cu(II) ions. It is found that the maximum adsorption removal rate reaches 96.02% at 35°C, pH=5.0 , with an adsorbent dosage of 0.65 g/L and an initial Cu(II) ion concentration of 50 mg/L. Additionally, adsorption kinetics, isotherms, and thermodynamics were analyzed to probe into the adsorption mechanism of Cu(II) ions by HAP@MBC. The results show that the adsorption process is very close to the pseudo-second-order model, indicating that the adsorption process is mainly controlled by chemisorption. The adsorption of Cu(II) ions can also be fitted by the intraparticle diffusion model, revealing that the adsorption rate is limited by intraparticle diffusion as well as other factors. Moreover, the adsorption process is consistent with the Langmuir isotherm, and the saturated adsorption capacity is calculated to be 81.59 mg/g. Thermodynamic analysis shows that the value of adsorption enthalpy change is 48.35 kJ/mol , suggesting the adsorption process is chemisorption. More precisely, it is a spontaneous entropy-increasing reaction, and an increase in the temperature is conducive to the adsorption. To sum up, HAP@MBC exhibits perfect adsorption properties and has the potential to be a novel and promising adsorbent for the removal of Cu(II) ions. [ABSTRACT FROM AUTHOR]

Low P-containing wastewaters (LPWs) exhibit huge P recovery potential, considering their larger volume. P recovery via CaP crystallization using apatite as seed is documented as being potentially well suited for LPWs. However, its responsible mechanisms remain a subject for debate. Taking hydroxyapatite (HAP) as the seed of LPWs, this paper conducted HAP adsorption/dissolution experiments, titration experiments, and P recovery experiments to distinguish the primary responsible mechanism. Results showed that it was HAP dissolution, not P adsorption, that occurred when the initial P concentration was no higher than 5 mg/L, ruling out adsorption mechanism of P recovery from LPWs using HAP as the seed. Significant OH− consumption and rapid P recovery occurred simultaneously within the first 60 s in titration experiments, suggesting CaP crystallization should be responsible for P recovery. Moreover, the continuous increase in P recovery efficiency with seed dosages observed in P recovery experiments seemed to follow well the mechanism of pre-nucleation ion clusters (PNCs) aggregation. During PNCs aggregation, P aggregates with Ca2+ quickly, generating CaP PNCs; then, CaP PNCs aggregate with seed particles, followed by CaP PNCs fusion, and ultimately transform into fines attached to the seed surface. PNCs' aggregation mechanism was further supported by a comparison of seed SEM images before and after P recovery, since denser and smaller rod-shaped fines were observed on the seed surface after P recovery. This study suggests that PNCs' aggregation is the dominant mechanism responsible for the recovery of P from LPWs via CaP crystallization using HAP as the seed. [ABSTRACT FROM AUTHOR]

• Nano AlPO 4 can be obtained by sol–gel method. • Introduced nano AlPO 4 improves the integrity of the hydroxyapatite coating. • Nano AlPO 4 enhances the protective effect of the hydroxyapatite for stone relics. Open-air marble relics in Beijing are experiencing degradation due to sugaring, dissolution and other illnesses. Therefore, it is necessary to apply a protective and reinforcing coating to the weathered surface. Hydroxyapatite (HAP) has significantly lower solubility and dissolution rate compared to calcite. Additionally, HAP has similar lattice parameters with calcite, suggesting that a cohesive layer of HAP can be formed over calcite. In fact, HAP exhibits a lattice mismatch of 5 % with calcite, which might potentially lead to stress if the layer exceeds a few nanometre in thickness. On the other hand, aluminum phosphates (ideally, B-AlPO 4) only exhibit a 1 % mismatch with calcite and have a solubility lower than that of calcite. In this study, in order to improve the property of HAP in marble conservation, sol–gel method was employed to synthesize nano AlPO 4 , which were then incorporated into the phosphate solution to produce protective coating on the stone surface. The coatingʼs morphology and the structure were characterized by Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), high capacity 3D X-ray microscopy (XRM), optical microscope, and scanning electron microscopy coupled with energy dispersive spectroscopy (SEM-EDS). Moreover, the color, the contact angle, the three-point bending strength measurements, as well as the simulated acid rain test and freeze–thaw treatment were performed to assess the chromatic aberration, hydrophilicity, reliability, and durability of the coating. Results indicated that the nano AlPO 4 , with its matched lattice parameters and nucleation site provision, facilitated the formation a coherent HAP layer of crystal flakes. Subsequently, the anti‑corrosion property, freeze-thaw resistance and consolidation property of the coating were improved, demonstrating the potential application the hybrid of HAP with nano AlPO 4 in the preservation of marble. [ABSTRACT FROM AUTHOR]

This study explores the electrochemical deposition (ECD) of hydroxyapatite (HA) coatings onto commercially pure titanium (CP–Ti) substrates, with a focus on biomedical implant applications. The ECD process serves as a useful approach for controlling the growth and characteristics of these HA coatings. Additionally, to refine the crystalline structure and bolster biocompatibility, annealing techniques were employed. The results unveiled distinctive morphologies for HA coatings under varying pH levels of the electrolyte: granular at pH 4, flake-like at pH 6, and needle-like at pH 9, emphasizing the significant impact of electrolyte pH on coating structure. Surface roughness exhibited its peak at pH 4, indicative of the most uneven HA layer formation. In particular, all HA-coated samples displayed heightened hydrophilicity compared to their uncoated CP-Ti counterparts, with pH 6 showing the most substantial decrease in contact angle, suggesting pronounced biocompatibility enhancements. X-ray Diffraction affirmed HA as the predominant phase in the annealed coatings. Electrochemical assessments were conducted to gauge the electrochemical behavior of HA-coated samples. The findings revealed that pH 6 offered the most robust electrochemical behavior, rendering it a promising electrolyte pH condition for HA-coated CP-Ti biomedical implants. This comprehensive investigation highlights the profound influence of the pH of the electrolyte on HA morphology and surface properties, which in turn impact electrochemical behavior in HA-coated CP-Ti for biomedical implant applications. As such, the application of ECD techniques across varying pH levels of the electrolyte emerges as an effective strategy for tailoring HA coatings, thus enhancing their suitability for biomedical implants. [ABSTRACT FROM AUTHOR]

Effective prevention of recurrent kidney stone disease requires the understanding of the mechanisms of its formation. Numerous in vivo observations have demonstrated that a large number of pathological calcium oxalate kidney stones develop on an apatitic calcium phosphate deposit, known as Randall's plaque. In an attempt to understand the role of the inorganic hydroxyapatite phase in the formation and habits of calcium oxalates, we confined their growth under dynamic physicochemical and flow conditions in a reversible microfluidic channel coated with hydroxyapatite. Using multi-scale characterization techniques including scanning electron and Raman microscopy, we showed the successful formation of carbonated hydroxyapatite as found in Randall's plaque. This was possible due to a new two-step flow seed-mediated growth strategy which allowed us to coat the channel with carbonated hydroxyapatite. Precipitation of calcium oxalates under laminar flow from supersaturated solutions of oxalate and calcium ions showed that the formation of crystals is a substrate and time dependent complex process where diffusion of oxalate ions to the surface of carbonated hydroxyapatite and the solubility of the latter are among the most important steps for the formation of calcium oxalate crystals. Indeed when an oxalate solution was flushed for 24 h, dissolution of the apatite layer and formation of calcium carbonate calcite crystals occurred which seems to promote calcium oxalate crystal formation. Such a growth route has never been observed in vivo in the context of kidney stones. Under our experimental conditions, our results do not show any direct promoting role of carbonated hydroxyapatite in the formation of calcium oxalate crystals, consolidating therefore the important role that macromolecules can play in the process of nucleation and growth of calcium oxalate crystals on Randall's plaque. [ABSTRACT FROM AUTHOR]

BACKGROUND: Medical titanium and titanium alloy have achieved good therapeutic effects in clinical applications, but there are still some phenomena such as peri-implant inflammation, loosening and shedding. OBJECTIVE: To explore the physicochemical properties of graphene oxide coating materials and their effects on bone marrow mesenchymal stem cells. METHODS: (1) Hydroxyapatite coating and graphene oxide/hydroxyapatite composite coating were prepared on a titanium surface by electrochemical deposition. The surface morphology, phase structure, functional groups, elemental composition and surface hydrophilicity of the coating were analyzed by scanning electron microscopy, X-ray energy dispersion spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, Raman spectroscopy, and contact angle measurement instrument. (2) Mouse bone marrow mesenchymal stem cells were isolated and cultured and inoculated on pure titanium, hydroxyapatite coating and graphene oxide/hydroxyapatite composite coating, respectively. CCK-8 assay and scanning electron microscopy were used to evaluate the proliferation, morphology and growth status of the coated cells. RESULTS AND CONCLUSION: (1) Scanning electron microscopy and X-ray energy dispersion spectra showed that the surface of graphene oxide/hydroxyapatite composite coating was more flat, compact and uniform than that of hydroxyapatite coating and pure titanium. X-ray photoelectron spectroscopy, X-ray diffraction and Raman spectroscopy showed that hydroxyapatite coating and graphene oxide/hydroxyapatite composite coating were successfully prepared on the surface of the titanium sheet. The hydrophilicity of graphene oxide/hydroxyapatite composite coating was better than that of hydroxyapatite coating and pure titanium. (2) CCK-8 assay showed that the number of bone marrow mesenchymal stem cells on the surface of the three groups increased with the extension of co-culture time. On days 1, 4, and 7, the proliferative absorbance of the cells on the graphene oxide/hydroxyapatite composite coating was higher than that on hydroxyapatite coating and pure titanium (P < 0.000 1). Scanning electron microscopy after 4 days of co-culture showed that bone marrow mesenchymal stem cells on the surface of the three groups of materials were fusiform. The cells on the surface of graphene oxide/hydroxyapatite composite coating showed good tensile properties and were polygonal. Multiple antennae could be seen attached to the coating surface at the edge of the cells, and the elongation of the filamentous foot on the surface was more than that on pure titanium and hydroxyapatite coatings. (3) The results show that graphene oxide/ hydroxyapatite composite coating material is a kind of coating material with excellent physicochemical and biological properties. [ABSTRACT FROM AUTHOR]

With the increasing incidences of orbital wall injuries, effective reconstruction materials and techniques are imperative for optimal clinical outcomes. In this literature review, we delve into the efficacy and potential advantages of using titanium implants coated with nanostructured hydroxyapatite for the reconstruction of the orbital wall. Titanium implants, recognized for their durability and mechanical strength, when combined with the osteoconductive properties of hydroxyapatite, present a potentially synergistic solution. The purpose of this review was to critically analyze the recent literature and present the state of the art in orbital wall reconstruction using titanium implants coated with nanostructured hydroxyapatite. This review offers clinicians detailed insight into the benefits and potential drawbacks of using titanium implants coated with nanostructured hydroxyapatite for orbital wall reconstruction. The highlighted results advocate for its benefits in terms of osseointegration and provide a novel strategy for orbital reconstruction, though further studies are essential to establish long-term efficacy and address concerns. [ABSTRACT FROM AUTHOR]

Titanium and its alloys are extensively applied in artificial tooth roots because of their excellent corrosion resistance, high specific strength, and low elastic modulus. However, because of their biological inertness, their surface needs to be modified to improve the osteointegration of titanium implants. The preparation of biologically active calcium–phosphorus coatings on the surface of an implant is one effective method for enhancing the likelihood of bone integration. In this study, osteoinductive peptides were extracted from oyster shells by using acetic acid. Two peptide-containing hydroxyapatite (HA) composite coatings were then prepared: one coating was prepared by hydrothermally synthesizing an HA coating in the presence of peptides (HA/P/M), and the other coating was prepared by hydrothermally synthesizing HA and then immersing the hydrothermally synthesized HA in a peptide solution (HA/P/S). Characterization results indicated that the composite HA coatings containing oyster shell-based peptides were successfully prepared on the alkali-treated pure titanium surfaces. The HA/P/M and HA/P/S composite coatings were found to exhibit excellent hydrophilicity. Protein adsorption tests confirmed that the HA/P/M and HA/P/S coatings had an approximately 2.3 times higher concentration of adsorbed proteins than the pure HA coating. [ABSTRACT FROM AUTHOR]

This study focuses on the usage of chitosan/hydroxyapatite composites for pertechnetate removal from aqueous solutions. Pertechnetate, a prominent radionuclide in nuclear waste, presents environmental hazards due to its long half-life and mobility. The composites, formed by intergrating hydroxyapatite into chitosan matrices, demonstrate in situ nanohydroxyapatite generation. Investigation of the adsorption process involves assessing parameters like pH, contact time, and the influence of competetive ions. This research provides valuable insights for using composites to mitigate pertechnetate contamination. [ABSTRACT FROM AUTHOR]

Electrophoretic deposition (EPD) is a versatile fabrication method allowing the deposition of coatings on substrates with complicated shapes. The main disadvantage of this method, especially in relation to bio applications, lies in hazardous stabilisers frequently used to optimise suspension parameters. This work deals with the plasma treatment of hydroxyapatite (HA) powder for stabilising the suspension without any additives. This approach was already successfully used for alumina powder. EPD of untreated and plasma treated HA powder is performed to compare the final deposits' microstructure. Besides this primary goal, the powder and suspension characteristics are monitored to clarify the effect of plasma treatment on processing and final properties. Moreover, the impact of the rapid sintering approach on deposits' densification is tested. Finally, the suitability of EPD of plasma treated powder for the preparation of homogeneous coating on the orthopaedic screw is manifested. • Electrophoretic deposition of ceramics usually requires physical, environmental, or health hazardous additives. • Atmospheric plasma treatment changes the powder's surface properties. • Homogeneous and uniform hydroxyapatite coatings are obtained without additives. • Rapid pressureless sintering leads to quick and sufficient densification in a fraction of the time. • Orthopaedic screws are uniformly coated. [ABSTRACT FROM AUTHOR]

This study discusses the contribution of Cu2+ and Mg2+, two biologically important ions substituted into the structure of fluorohydroxyapatite. FHA, a partial substitution of fluorine ion in HA has received a great attention because it improves the corrosion resistance of orthopedic implants. Copper, Magnesium and copper-Magnesium doped fluorohydroxyapatite (FHA) coatings were electrochemical deposited on titanium (Ti) using a cyclic voltammetry technique. The coatings properties were identified by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The corrosion behavior of coated and uncoated samples, immersed for 7 days in aerated simulated body fluid (SBF) in a presence of 0.2 g/l human serum albumin (HAS) was investigated by potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). The synergetic effect of albumin and doped elements on the degradation of Ti was studied. As a result of these investigations, it is revealed that: fluoride, copper and magnesium were successfully incorporated into apatite lattice structure. The additions of ions in FHA crystal matrix reduced the crystallite size, increased the crystallinity and changed the structure of F-hydroxyapatite. All the electrochemical techniques employed demonstrated that the coatings that were produced offered superior protection against corrosion for titanium when exposed to artificial body fluids. The nano-Mg-FHA coating improves effective protection to Ti and presents the highest corrosion resistance. The outcomes of this investigation were also compared with already published works to validate the research results. [ABSTRACT FROM AUTHOR]

To effectively combat infectious osteoporosis, Ti‐based implants with enhanced antibacterial and osseointegrative properties are urgently required. Herein, a one‐step method involving Mg thermal‐reduction is employed to modify a hydroxyapatite (HA) array on Ti, which comprises an inner TiO2 layer and an outer nanorod‐like HA layer. This process introduces oxygen vacancies (OVs) into the TiO2 layer and deposits a Mg─O‐contained amorphous nanolayer on each HA nanorod. The introduced OVs enhance reactive oxygen species (ROS) yield by the array during ultrasound treatment via narrowing TiO2 bandgap and improving H2O molecules absorption. The produced ROS, combined with a weak alkaline microenvironment created by the degraded Mg─O nanolayer, endows the array with potent bacterial‐killing and biofilm‐eradicating efficacies within a 5 min ultrasound treatment via the combination of proton‐consumption and cell envelop‐detriment effects. Moreover, due to the alkaline microenvironment and the released Mg2+, the array hinders osteoclastogenesis by activating the inflammation‐related FAK‐PI3K‐AKT signaling pathway in macrophages, as revealed by transcriptomic analysis, resulting in robust osseointegration in rat femoral shaft with concurrent bacterial‐infection and osteoporosis. This work paves a new way for simultaneously endowing a sonosensitive coating on Ti with sonodynamic treatment‐derived high antibacterial ability and alkaline microenvironment‐mediated strong osseointegration for infectious osteoporosis treatment. [ABSTRACT FROM AUTHOR]

Porous structures can reduce the elastic modulus of implants, decrease stress shielding, and avoid bone loss in the alveolar bone and aseptic loosening of implants; however, there is a mismatch between yield strength and elastic modulus as well as biocompatibility problems. This study aimed to investigate the parametric design method of porous root-shaped implants to reduce the stress-shielding effect and improve the biocompatibility and long-term stability and effectiveness of the implants. Firstly, the porous structure part was parametrically designed, and the control of porosity gradient distribution was achieved by using the fitting relationship between porosity and bias and the position function of bias. In addition, the optimal distribution law of the porous structure was explored through mechanical and hydrodynamic analyses of the porous structure. Finally, the biomechanical properties were verified using simulated implant–bone tissue interface micromotion values. The results showed that the effects of marginal and central porosity on yield strength were linear, with the elastic modulus decreasing from 18.9 to 10.1 GPa in the range of 20–35% for marginal porosity, with a maximum decrease of 46.6%; the changes in the central porosity had a more consistent effect on the elastic modulus, ranging from 18.9 to 15.3 GPa in the range of 50–90%, with a maximum downward shift of 19%. The central porosity had a more significant effect on permeability, ranging from 1.9 × 10−7 m2 to 4.9 × 10−7 m2 with a maximum enhancement of 61.2%. The analysis showed that the edge structure had a more substantial impact on the mechanical properties. The central structure could increase the permeability more effectively. Hence, the porous structure with reasonable gradient distribution had a better match between mechanical properties and flow properties. The simulated implantation results showed that the porous implant with proper porosity gradient distribution had better biomechanical properties. [ABSTRACT FROM AUTHOR]

The bacterial enzyme chondroitinase ABCI (chABCI), which has been isolated from Proteus Vulgaris, is crucial in the treatment of spinal cord injuries. However, due to its short lifespan, the maintenance and clinical application of this enzyme are very constrained. In this study, the immobilization of this enzyme on hydroxyapatite has been carried out and assessed with the aim of enhancing the characteristics and efficiency of chABCI. Hydroxyapatite particles (HAPs) are a potential candidate for drug-delivery carriers because of their excellent biocompatibility, shape controllability, and high adsorption. The use of the nanometer scale allows efficient access to the enzyme's substrate. It demonstrates important biological application capabilities in this way. Field emission gun-scanning electron microscopy (FEG-SEM), X-ray diffraction (XRD), infrared spectroscopy (FT-IR), in vitro release study, and cytotoxicity test were used to characterize the drug nanosystem's properties. According to the findings, electrostatic bindings was formed between charged groups of the enzyme and hydroxyapatite nanoparticles. The results also demonstrated that immobilized chABCI on hydroxyapatite has beneficial properties, such as more manageable drug release, minimal toxicity and side effects, and a high potential to enhance the efficacy of drug delivery and decrease the need for repeated injections. Key points: It has been proven that hydroxyapatite increases the shelf life of chondroitinase when it is used as a carrier matrix. Stability of the enzyme loaded onto hydroxyapatite was enhanced significantly after immobilization. The proposed process can make the hydroxyapatite nanoparticles a useful stabilizer drug delivery vehicle. The release of the chondroitinase is more controllable than previous studies; therefore the stability of the nanosystem has been increased. [ABSTRACT FROM AUTHOR]

Titanium dental implants are one of the best replacements for the natural teeth. It can reduce early failures compared to other implant materials. During mastication, generally, implant loosening occurs between the bone and the implant surface. Therefore, to resolve this issue, surface modification of the implant surface was done which can provide better bonding between the implant and the bone. In this study, we designed five different types of surface texture on the implant and compared them with the solid non-textured implant. In addition to that, we used four different hybrid composite coating materials along with hydroxyapatite, for better osseointegration and bone formation. Thus, we modeled a bony structure like mandible using solid modeling technique. We considered average biting force of 250 N with different bone conditions. After the analysis, it has been observed that 'U' and 'V' shape textures exhibited the optimized textures for dental implant with coating combination of HA1.5TO1.5SR and HA3Sr for weak and very weak bone conditions. The coating for straight and dome shaped textures for strong and very strong bone conditions showed better results, whereas 'U' shaped and dome shaped textures showed better results for normal bone condition. [ABSTRACT FROM AUTHOR]

Electrospinning is a facile popular method for the creation of nano-micro fibers tissue engineering scaffolds. Here, polycaprolactone (PCL)/collagen (COL): polyvinyl pyrrolidone (PVP) scaffolds (PCL/COL: PVP) were fabricated for bone regeneration. Various concentrations of Cephalexin (CEF) (0.5, 1, 1.5 wt. %) were added to PCL/COL: PVP scaffold to provide an antibacterial scaffold, and different concentrations of hydroxyapatite (HA) (1, 2, 5 wt. %) was electrospray on the surface of the scaffolds. The PCL/COL: PVP scaffold contained 1.5% CEF and coated with 2% HA was introduced as the best sample and in-vitro tests were performed on this scaffold based on the antibacterial and MTT test results. Morphology observations demonstrated a bead-free uniform combined nano-micro fibrous structure. Fourier transform infrared spectroscopy and X-ray diffraction tests confirmed the successful formation of the scaffolds and the wettability, swelling, and biodegradability evaluations of the scaffolds confirmed the hydrophilicity nature of the scaffold with high swelling properties and suitable biodegradation ratio. The scaffolds supported cell adhesion and represented high alkaline phosphatase activity. CEF loading led to antibacterial properties of the designed scaffolds and showed a suitable sustained release rate within 48 h. It seems that the electrospun PCL/COL: PVP scaffold loaded with 1.5% CEF and coated with 2% HA can be useful for bone regeneration applications that need further evaluation in the near future. [ABSTRACT FROM AUTHOR]

In recent years, additive manufacturing of nickel-titanium (NiTi) alloys as medical implant materials have attracted a lot of interest due to their precise, rapid, and integrated molding. However, the NiTi alloy as a bioinert material exhibits poor osteogenic activity and biomineralization properties. In this work, a graphene oxide (GO) coating containing nano-hydroxyapatite (HA) is fabricated on the NiTi alloys by a one-step DC electrodeposition method. The effects of HA (0.1 g/L) on the corrosion resistance, biomineralization properties and long-term stability of GO composite coating were investigated by electrochemical tests and immersion experiments. The result shows that the corrosion current density of GO coating reduces by one order of magnitude due to the introduction of nano-HA (from 2.24 × 10−8 A/cm2 to 3.18 × 10−9 A/cm2), the surface remains dense after 15 days of immersion, and a dense apatite layer is mineralized on the surface. In addition, in vitro MC3T3-E1 cell viability and cell morphology results showed that the coating can effectively enhance the biocompatibility of additively manufactured NiTi alloy because it provides a better microenvironment and interface for cell growth and adhesion. Taken together, the additively manufactured NiTi alloys with GO/HA coating present great potential for biological application, especially as orthopedic implants. [ABSTRACT FROM AUTHOR]

Purpose: Titanium alloys are among the most widely used materials in medicine, especially in orthopedics. However, their use requires the application of an appropriate surface modification method to improve their properties. Such methods include anodic oxidation and the application of polymer coatings, which limit the release of alloying element ions. In addition, biodegradable polymer coatings can serve as a carrier for drugs and other substances. The paper presents the results of research on the physical properties of biodegradable polymer coatings containing na-noparticle hydroxyapatite on a titanium alloy substrate. Methods: A PLGA coating was used in the tests. The coatings on the substrate of the anodized Ti6Al7Nb alloy were applied by ultrasonic spray coating. The tests were carried out for coatings with various hydroxyapatite content (5, 10, 15, 20%) and thickness resulting from the number of layers applied (5, 10, 15 layers). The scope of the research included microscopic observations using scanning electron microscopy, topography tests with optical profilometry, structural studies using X-ray diffraction, as well as wettability and adhesion tests. Results: The results shows that with the use of ultrasonic spray coating system is possible to obtain the continuous coatings containing hydroxyapaptite. Conclusions: The properties of the coating can be controlled by changing the percentage of hydroxyapatite and the number of layers of which the coating is composed. [ABSTRACT FROM AUTHOR]