Surface Modification Research Articles

An experimental approach on dynamic occlusal fingerprint analysis to simulate use-wear localisation and development on stone tools

Information about the use of stone tools in the past is encoded in the wear patterns left on their surface; however, post-depositional processes can modify and obstruct these traces. One aim in the field of lithic functional analysis is to develop methods to detect and quantify these traces on stone tools. The occlusal fingerprint analysis (OFA) is a well-established method in dental wear studies to virtually simulate dental occlusal (contact between teeth) stroke movements and thus locate and quantify the sequential contact between opposing tooth crowns. Reaching across disciplines, we conducted controlled experiments to test the applicability of the OFA method on stone tools to address the challenge of use-wear quantification and localisation, and therefore the identification of post-depositional wear. Our findings reveal a clear overlap between zones of experimentally produced use-wear and OFA-calculated contact areas. We demonstrate OFA as a potential method to generate models of multiscale use-wear that can be used as references on experimental tools to identify post-depositional surface modifications on stone tool artefacts.

A multifunctional aspect of surface modification of cotton fabric with green synthesized titanium dioxide/iron nanocomposite using Psidium guajava leave extract

This study explores the use of green TiO2/Fe nanocomposite for surface modification of cotton fabric, aiming to minimize its limitations such as wrinkle, shrinkage, lower photocatalytic activity, microbial degradation, and poor durability. To prepare the nanocomposite, the iron (Fe) and titanium dioxide (TiO2) nanoparticles were first green synthesized using an extract of guava leaf (Psidium guajava) and mixed by using citric acid as a cross-linking agent. The modified cotton fabric was characterized by FTIR, TGA, DTG, SEM, and EDS. The FTIR spectra of the modified fabrics showed additional peaks at 483 cm−1 for Ti-O- and 1059 cm−1 for Fe-O-, indicating the incorporation of TiO2/Fe- nanoparticles which was also confirmed by SEM images. Fe nanoparticles enhanced TiO2 NPs’ photocatalytic activity, enhancing self-cleaning, UV resistance, stain resistance, anti-water absorption, and antibacterial activity in modified cotton fabric. Additionally, the wettability, thermal stability, mechanical and chemical stability of modified cotton fabric were also improved. As a result, the method of surface modification has great potential to improve the sustainability and usability of cotton fabric, supporting its wide range of uses in clothing, medical, and personal hygiene goods.

Antioxidative implant coating with anti-infection and osteogenesis time-dependent bifunction for synergistic promotion of osteointegration

Infection and poor osteogenesis are two major causes of implant failure. Surface modification strategy provides solutions to the above problems. However, the functional requirements at different biological stages during infectious bone repair and the oxidative stimulation caused by reactive oxygen species (ROS) in an inflammatory environment pose challenges to the existing approaches. Layer-by-layer (LbL) self-assembly realizes layer by layer superposition and time-dependent acting of different bioactive components, but is demanding to functional groups. Tannic acid (TA) owns abundant phenolic hydroxyl groups, endowing various firm chemical bindings and excellent antioxidant property. To this end, we developed a time-dependent and antioxidant multifunctional coating via TA mediated LbL self-assembly. This layer exhibited higher ROS removal capacity and stronger binding ability. Furthermore, it showed rapid and excellent antibacterial ability of over 85 % against Staphylococcus aureus and Escherichia coli at 24 h, which additionally promoted osteogenic differentiation in vitro in long term. Moreover, the coating exhibited outstanding antibacterial and bone regeneration performance in vivo as well. Thus, this study is expected to provide an antioxidant and time-dependent multifunctional platform for surface modification engineering of dental and orthopedic implantation, as well as other potential biological material designs.

Modified nanoporous zeolites on a biodegradable polymer film with excellent hydrophobicity, ethylene gas adsorption, and antibacterial activity through surface charge accumulation

The high specific surface area and large pore volume of nanoporous zeolites (NZs) were utilized to impart a biodegradable polymer film with superhydrophobicity, ethylene gas adsorption capability, and active antibacterial activity. NZs were synthesized by using organic silanes via a sol–gel method. They were then dispersed on a biodegradable blended PPP [poly(lactic acid) (PLA)/poly butylene succinate (PBS)/poly butylene adipate terephthalate (PBAT)] film to enhance its mechanical properties and control water repellent. The hydrophobicity of the organic silanes on the zeolite surface gradually increased according to their length. The film prepared by utilizing octadecyltriethoxysilane (ODTES) was superhydrophobic with a contact angle 142.6°. The porous structure of the PPP with attached ODTES-NZs impeded the release of accumulated charges generated through friction, thereby yielding excellent output voltage when applying friction periodically. The output performance of the PPP-ODTES-NZs film was measured to be 723 V when a positive charge was injected into the film, which was about 3.1 times higher than the output performance of the PPP film without surface modification. The accumulated positive charges provided excellent antibacterial efficacy against externally introduced bacteria. Our approach of attaching ODTES-NZs to a blended polymer provides a multifunctional biodegradable film (ethylene gas adsorption, water repellent, and antibacterial activity via positive charge accumulation) with excellent food-storage capability.

Comprehensive study of plasma polymerization parameters on thiol-coated LDPE films for effective fibronectin adsorption targeting biomedical applications

In the realm of biomedical applications, biocompatible materials with optimized surface properties are crucial for facilitating cellular interactions. To attain the perfect balance of these properties, surface modification of non-toxic and stable bulk materials is often required. Within this context, this research aimed to improve the physiochemical and cell-responsive properties of a low-density polyethylene film. This was achieved by depositing thiol-rich coatings using a dielectric barrier discharge plasma reactor operating at medium pressures, with 1-propanethiol serving as polymerization precursor. The study systematically investigated the impact of key plasma polymerization parameters, including DBD chamber pressure, treatment time, and the combination of precursor flow rate and discharge power represented by the Yasuda parameter, to identify optimal plasma processing conditions for the formation of thiol-rich coatings. To characterize the coating thickness, hydrophilicity and surface chemical composition, atomic force microscopy, water contact angle measurements, and X-ray photoelectron spectroscopy were employed. The findings indicated that reducing the chamber pressure to 10 kPa led to more hydrophilic and thicker deposits possessing a higher sulphur content. Deposition time (5 to 15 min) also significantly impacted coating thickness and surface chemistry, where long times increased thickness, but also led to a reduced sulphur and increased oxygen content because of more pronounced etching. The optimal deposition time was therefore set at 10 min resulting in the deposition of dense coatings possessing a high number of sulphur-containing functionalities. The Yasuda parameter (W/FM) analysis demonstrated optimal thiol incorporation in combination with high coating stability at an intermediate W/FM value of 72 MJ/kg. Following the determination of the optimal plasma polymerization parameters, the effectiveness of thiol plasma polymerization and subsequent fibronectin immobilization for enhancing cell adhesion and proliferation was investigated. The thiol-coated substrates were found to exhibit superior protein immobilization, because of the high affinity for protein binding of the available thiol groups. To assess cellular responses, Schwann cells were cultured on uncoated and coated samples before and after fibronectin immobilization. The results revealed a superior cellular response of the thiol-coated samples after fibronectin immobilization, showing the highest cell viability and significantly enhanced cell adhesion and proliferation. Collectively, these results underscore the synergistic effect of thiol plasma polymerization and fibronectin immobilization in promoting the cellular response of LDPE substrates, thus highlighting their potential as a surface modification strategy of biomaterials.

The Effect of Gold Nanoparticles and Apricot Kernel Extract on the Osseointegration of Dental Implants - A Rabbit Model

Introduction The osseointegration of dental implants is critical to their longevity and success. Various factors such as surface modifications, both additive and subtractive, systemic drug administration, growth factors, and plasma derivatives can influence osseointegration. Aims and Objectives This study aimed to study the effects of gold nanoparticles and aqueous extract of apricot kernels on the osseointegration of titanium implants in the tibia of rabbits. Materials and Methods Apricot kernels were dried, grounded, and dissolved in water to obtain an aqueous extract. It was filtered and stored in the refrigerator at 4oC. Gold nanoparticles (AuNPs) were prepared by mixing 3 ml of 0.02 mM hydrogen tetrachloroaurate with 1 ml of olive leaf extract. The mixture was stirred vigorously for 15 minutes on a heater stirrer at 50oC. Titanium screw implants were sterilized in an autoclave at 120oC with 15 pounds per square inch for 30 minutes. Sterilized implants were stored in sealed containers until use. The study was carried out at the College of Veterinary Medicine, University of Mosul, Iraq. The ethical approval for the study was obtained from the institutional animal care and use committee, College of Veterinary Medicine, University of Mosul, Mosul, Iraq, on 15/04/2023 on reference no UM.VET.2023.013. Nine healthy male adult white New Zealand rabbits aged between 10-12 months were utilized for the study. Three pure titanium implants, each of a type, were placed in each tibia. The implants were categorized as follows: control group (18 uncoated implants) and experimental group (36 coated implants). The implant placement was divided into three groups: controls with uncoated implants (n=18), AuNPs-coated implants (n=18), and apricot kernel extract-coated implants (n=18). General anesthesia was induced by intramuscular injection of ketamine hydrochloride 50mg (1ml /kg of body weight) plus xylazine 2% (0.2 ml /kg of body weight). The AuNPs-coated implants were implanted in the superior osteotomy site in the tibia. The apricot kernel extract-coated implants were implanted in the inferior osteotomy site and the uncoated implants were implanted in the middle osteotomy sites. Histological and histomorphometric tests were performed on all bone implant blocks at one-week, two-week, and three-week intervals after implant placement. The results were evaluated based on the amount of bone formation, cellular components, and inflammation. Tabulated data were statistically analyzed using SPSS v23.0 (IBM, Armonk, NY) using ANOVA with a statistical significance of p <0.05 Results We observed a significant amount of osteogenesis with reduced inflammation in AuNPs-coated implants and apricot kernel extract-coated implants compared to untreated implants. The osteoclastic activity was significantly higher in untreated implants than the treated implant sites. A statistically significant association was observed between coated implants and untreated implants. Conclusion The application of gold nanoparticles and aqueous extract of apricot kernels appears to be promising in reducing inflammation and improving bone apposition on the titanium implant surface. However, this preliminary investigation warrants further research.

Photothermal therapy and cell imaging tracking of porous silicon nanoparticle by magnesiothermic reduction and surface modification

The synthesis of silicon nanoparticles (PSi NPs) from silica nanoparticles (SiO₂) via magnesium (Mg) reduction is a promising technique due to its simplicity and cost-effectiveness. In this study, silica is utilized as the primary precursor and is subjected to a reduction process using magnesium powder as the reducing agent. By covalently attaching Fluorescein Isothiocyanate (FITC) to the surface of PSi NPs, we aim to enhance their fluorescence intensity and stability while also improving their surface reactivity and biocompatibility. The modified PSi NPs system was characterized using various microscopic techniques, Raman spectra, porosity and morphology analysis, Zeta potential, and analysis of organic functional groups to confirm successful conjugation and to evaluate changes in surface morphology, fluorescence properties, and colloidal stability. By leveraging the inherent photothermal conversion efficiency of PSi NPs, we explore their capacity to generate localized heat upon near-infrared (NIR) light irradiation, effectively inducing cancer cell apoptosis. Concurrently, the natural fluorescence of PSi NPs is harnessed to enable high-resolution imaging, facilitating real-time tracking and monitoring of therapeutic processes. The PSi NPs were subjected to a series of in vitro experiments to assess their photothermal efficiency, cytotoxicity, and imaging capabilities. Results demonstrate that PSi NPs exhibit excellent photothermal effects, leading to significant cell death in targeted cancer cells upon NIR exposure, while their fluorescence properties provide clear and detailed imaging. These findings highlight the potential of PSi NPs as multifunctional agents in cancer therapy, combining effective photothermal treatment with non-invasive imaging, thereby enhancing the precision and efficacy of therapeutic interventions.

Adhesion of retinal cells to gold surfaces by biomimetic molecules.

Neural cell-electrode coupling is crucial for effective neural and retinal prostheses. Enhancing this coupling can be achieved through surface modification and geometrical design to increase neuron-electrode proximity. In the current research, we focused on designing and studying various biomolecules as a method to elicit neural cell-electrode adhesion via cell-specific integrin mechanisms. We designed extracellular matrix biomimetic molecules with different head sequences (RGD or YIGSR), structures (linear or cyclic), and spacer lengths (short or long). These molecules, anchored by a thiol (SH) group, were deposited onto gold surfaces at various concentrations. We assessed the modifications using contact angle measurements, fluorescence imaging, and X-ray Photoelectron Spectroscopy (XPS). We then analyzed the adhesion of retinal cells and HEK293 cells to the modified surfaces by measuring cell density, surface area, and focal adhesion spots, and examined changes in adhesion-related gene and integrin expression. Results showed that YIGSR biomolecules significantly enhanced retinal cell adhesion, regardless of spacer length. For HEK293 cells, RGD biomolecules were more effective, especially with cyclic RGD and long spacers. Both cell types showed increased expression of specific adhesion integrins and proteins like vinculin and PTK2; these results were in agreement with the adhesion studies, confirming the cell-specific interactions with modified surfaces. This study highlights the importance of tailored biomolecules for improving neural cell adhesion to electrodes. By customizing biomolecules to foster specific and effective interactions with adhesion integrins, our study provides valuable insights for enhancing the integration and functionality of retinal prostheses and other neural implants.

Thermal Performance Improvement of Composite Phase-Change Storage Material of Octanoic Acid–Tetradecanol by Modified Expanded Graphite

Phase-change cold storage technology is recommended as a solution for energy conservation and carbon neutrality in air conditioning systems of buildings. This study focuses on the development of binary composite phase-change materials comprising octanoic acid–tetradecanol (OA-TD). To enhance its thermal conductivity, expanded graphite (EG) was employed as an additive carrier, and the surface modification of EG particles using hexadecyltrimethoxysilane (HDTMOS) was attempted to make up for the instability and further to improve the performance of OA-TD/EG CPCMs. The OA-TD/EG-HDTMOS CPCMs were synthesized by EG mixed with EG-HDTMOS at a 1:1 mass ratio. The thermal performance and stability of the OA-TD/EG-HDTMOS CPCMs were thoroughly evaluated by multi-cycle melting–solidification and thermal conductivity measurements. The results revealed that the OA-TD mixture, when at a mass ratio of 77:23, exhibited a phase-transition temperature of 11.4 °C and a latent heat ranging from 150 to 155 J/g. Then, the OA-TD/EG-HDTMOS composite material, at a 12:1 mass ratio of OA-TD to EG-HDTMOS, solidified and melted at temperatures of 9.2 °C and 11.2 °C, with a latent heat ranging from 138 to 143 J/g, and significantly improved the thermal conductivity to 0.7 W/(m·K), representing a remarkable 133% increase compared to that of OA-TD alone. Even after undergoing 100 melting–solidification cycles, the OA-TD/EG-HDTMOS maintained superior phase-change thermal performance and stability, making it suitable for cold storage and energy conservation in air conditioning.

Inhibition of JAK/STAT3 Expression by Acute Myeloid Leukemia-Targeted Nanoliposome for Chemotherapy Enhancement.

Acute myeloid leukemia (AML) is a relatively common malignant hematological disease whose development is mostly associated with abnormal activation of the JAK/STAT3 signaling pathway. Our previous study revealed that SAR317461, a novel JAK2/STAT3 inhibitor, can effectively inhibit the activation of the JAK2/STAT3 signaling pathway and has significant damaging and pro-apoptotic effects on AML cell lines. This project aims to build upon our prior research to enhance the application of SAR317461 in AML. The surface modification of liposomes with the CD34 antibody, along with the inclusion of the SAR317461 and cytarabine (a common AML chemotherapeutic agent), is observed. Due to the high expression of CD34 on the surface of AML cells, the nanoliposome could target AML cells specifically, further achieving an effective treatment for AML through the synergistic effect of JAK2/STAT3 inhibitors and chemotherapeutic agents. The implementation of this project will provide more theoretical support and ideas for the clinical application of JAK/STAT3 inhibitors in malignant tumors and for overcoming chemotherapy resistance.

Combined release of LL37 peptide and zinc ion from a mussel-inspired coating on porous titanium for infected bone defect repairing

Implant-associated infections impose great burden on patient health and public healthcare. Antimicrobial peptides and metal ions are generally incorporated onto implant surface to deter bacteria colonization. However, it is still challenging to efficiently prevent postoperative infections at non-cytotoxic dosages. Herein, a scaffold based on porous titanium coated with a mussel-inspired dual-diameter TiO2 nanotubes is developed for loading dual drugs of LL37 peptide and Zn2+ with different sizes and characteristics. Benefiting from in-situ formed polydopamine layer and dual-diameter nanotubular structure, the scaffold provides an efficient platform for controllable drugs elution: accelerated release under acidic condition and sustained release for up to 28 days under neutral/alkalescent circumstances. Such combination of dual drugs simultaneously enhanced antibacterial efficacy and osteogenesis. In antibacterial test, LL37 peptide serving as bacteria membrane puncture agent, and Zn2+ acting as ROS generator, cooperatively destroyed bacterial membrane integrity and subsequently damaged bacterial DNA, endowing dual-drug loaded scaffold with remarkable bactericidal efficiency of > 92 % in vitro and > 99 % in vivo. Noteworthily, dual-drug loaded scaffold promoted bone-implant osteointegration under infectious microenvironment, overmatching single-drug load ones. It provides a promising strategy on surface modification of implant for infected bone defect repairing.

The effect of nano-zinc oxide on the mechanical properties of the cured ethylene-propylene-diene monomer rubber with a semi-efficient vulcanisation system

The present investigation is dedicated to the impact of replacing conventional zinc oxide (ZnO) with nano-zinc oxide (nZnO) in ethylene-propylene-diene monomer (EPDM) rubber compounds. Multiple rubber compounds were prepared utilising conventional and nano-zinc oxides, followed by vulcanisation employing a semi-efficient vulcanisation system (SEV). Results indicate that nZnO promotes a more uniform dispersion within the rubber matrix compared to ZnO. Moreover, the incorporation of nZnO enhances the vulcanisation process, yielding a notable 27% increase in crosslink density. Nevertheless, the mechanical properties of the cured rubber, encompassing tear strength, hardness, tensile strength and elongation at break, remained either unaffected or exhibited slight deterioration. This observed discrepancy is ascribed to the inherent tendency of nZnO particles to self-aggregate, thereby disrupting the homogeneous distribution of the activator within the rubber matrix and fostering the formation of localised crosslink networks around the nano-particles. To overcome this challenge, the study proposes potential strategies, including nano-particle surface modification, optimisation of mixing parameters, and integration of compatibilisers, aiming to enhance the interaction between nZnO and rubber chains, mitigate agglomeration and facilitate a more even dispersion. The study suggests the potential of nZnO in augmenting the crosslinking efficiency of rubber compounds while emphasising the imperative need to address nano-particle agglomeration to optimise overall mechanical properties.

Synthesis, Characterization and Application of Advanced Antimicrobial Electrospun Polymers.

The aim of this work was to synthesize, characterize and apply advanced antimicrobial biocompatible electrospun polymers suitable for medical implants for surgical repairs. Injuries to the musculoskeletal system often necessitate surgical repair, but current treatments can still lead to high failure rates, such as 40% for the repair of rotator cuff tears. Therefore, there is an urgent need for the development of new biocompatible materials that can effectively support the repair of damaged tissues. Additionally, infections acquired during hospitalization, particularly those caused by antibiotic-resistant bacteria, result in more fatalities than AIDS, tuberculosis, and viral hepatitis combined. This underscores the critical necessity for the advancement of antimicrobial implants with specialized coatings capable of combating Methicillin-resistant Staphylococcus aureus (MRSA) and Methicillin-sensitive Staphylococcus aureus (MSSA), two strains notoriously known for their antibiotic resistance. Therefore, we developed an antimicrobial coating incorporating nanoparticle mixtures using the sol-gel process and applied it to electrospun polycaprolactone (PCL) filaments, followed by thorough characterization by using spectroscopic (FTIR, Raman, NMR) microscopic (SEM and SEM-EDX), and tensile test. The results have shown that the integration of electro-spinning technology for yarn production, coupled with surface modification techniques, holds significant potential for creating antimicrobial materials suitable for medical implants for surgical repairs.

Efficient extraction and HPLC determination of sulfonamide residues in milk samples using acylated graphene oxide-functionalized polyurethane sponges: A tailored approach for efficient analyte recovery

This study reports a novel surface modification of polyurethane sponge (PUS) with acylated graphene oxide (AGO), yielding a versatile sorbent material (AGO@PUS) for the efficient extraction of sulfonamide residues from milk samples. The AGO@PUS combines the extractive properties of AGO with the advantages of PUS, enabling easy, fast, cost-effective, and efficient sample preparation. The material was characterized using FTIR, SEM, XRD and the extraction protocol was optimized for the determination of three sulfonamides (SGD, SDS, and SDZ) by HPLC-UV. The proposed method exhibited excellent linearity (0.01–1000 µg mL−1), low limits of detection (0.04–0.06 µg mL−1) and quantification (0.13–0.21 µg mL−1), and high coefficients of determination (R2 = 0.993–0.997). The maximum recovery rate reached 99.63 %, demonstrating the exceptional sorption capacity of AGO@PUS. Notably, the clear extracts obtained with this material highlight its potential for efficient sample preparation and analysis.

Off-Stoichiometry Thiol-Ene (OSTE) Micro Mushroom Forest: A Superhydrophobic Substrate

Superhydrophobic surfaces have been used in various fields of engineering due to their resistance to corrosion and fouling and their ability to control fluid movement. Traditionally, superhydrophobic surfaces are fabricated via chemical methods of changing the surface energy or mechanical methods of controlling the surface topology. Many of the conventional mechanical methods use a top-to-bottom scheme to control the surface topolopy. Here, we develop a novel fabrication method of superhydrophobic substrates using a bottom-to-top scheme via polymer OSTE, which is a prototyping polymer material developed for the fabrication of microchips due to its superior photocuring ability, mechanical properties, and surface modification ability. We fabricate a superhydrophobic substrate by OSTE–OSTE micro mushroom forest via a two-step lithography process. At first, we fabricate an OSTE pillar forest as the mushroom stems; then, we fabricate the mushroom heads via backside lithography with diffused UV light. Such topology and surface properties of OSTE render these structures superhydrophobic, with water droplets reaching a contact angle of 152.9 ± 0.2°, a sliding angle of 4.1°, and a contact angle hysteresis of less than 0.5°. These characteristics indicate the promising potential of this substrate for superhydrophobic applications.

Study on the regulation of droplet motion behavior on superhydrophobic surfaces

Wettability properties of the surface is essential for controlling the dynamic sliding of droplets, thereby facilitating surface self-cleaning and drag reduction. This study makes use of chemical etching and surface modification techniques to prepare superhydrophobic surfaces with micro-nano pore structures on copper. This research examines and evaluates the chemical composition, surface morphology, and hydrophobic characteristics of superhydrophobic surfaces, also investigates the exhibited excellent superhydrophobic properties, a positive correlation observed between the concentration of the modifier solution and the surface’s hydrophobic strength. Droplets move in an accelerated fashion on superhydrophobic surfaces, and the total resistance to droplet sliding decreases as the surface hydrophobicity increases and the wall tilt angle decreases. During the motion of droplets, the fluctuation range of the receding angle is considerably greater than that of the advancing angle, thereby rendering the receding angle as the primary determinant factor for droplet movement, and as the hydrophobicity of the surface improves, the fluctuation extent of the droplet’s receding angle experiences a significant diminution. Droplet motion on superhydrophobic surfaces comprises both slipping and rolling behaviors, the increased hydrophobicity of the surface and the larger tilt angle facilitate droplet movement in a slipping mode on the surface, within the experimental parameters, the proportion of rolling distance to slipping distance varies from 35 % to 15 %. This study has revealed innovative regulatory approaches for modulating the moving behavior of liquids on microstructured surfaces, potentially enabling the development of superior functional surfaces for fluid drag reduction or droplet manipulation in the future.

Air-microwave simultaneously induced carbon fiber surface oxidation and magnetism adjustment by CoOx nanoparticles rapid assembly for interface enhancement and electromagnetic wave absorption of its composites

It is a significant challenge to develop a fast carbon fiber (CF) surface modification method, especially for the high strength electromagnetic wave (EMW) absorption materials. Herein, magnetic CoOx nanoparticles are successfully synthesized and uniformly assembled on CF surface with high oxygen-containing groups by rapid ambient microwave carbon thermal shock (MCTS). The presence of oxygen defect sites on CF surface promotes CoOx nanoparticles nucleation. The number of oxygen defects and the types of magnetic nanoparticles on the CF surface effectively adjust the surface chemical activity and the electromagnetic properties of CF, which is conducive to improving the EMW absorption performance and interface compatibility of the CoOx nanoparticles modified CF reinforced polyamide 6 (CO@CF/PA6) composites. Compared with CO@CF-0 s/PA6, the tensile strength and modulus of CO@CF-3.5 s/PA6 composite are increased by 18.1 % and 18.6 %, respectively. It also displays a minimum reflection loss value (−59.9 dB) at a thinner thickness of 1.9 mm while the maximum effective absorption bandwidth reaches 5.02 GHz with a thickness of 1.8 mm. Its radar cross-section values exhibit less than −10 dBm2 at all tested detection angles. This rapid MCTS shows great potential for large-scale production of CF modification with low-cost, efficient and environmentally friendly process.

The Effectiveness of Curcumin Nanoparticle-Coated Titanium Surfaces in Osteogenesis: A Systematic Review

(1) Background: This systematic review critically appraises and synthesizes evidence from in vitro studies investigating the effects of curcumin nanoparticles on titanium surface modification, focusing on cell adhesion, proliferation, osteogenic differentiation, and mineralization. (2) Methods: A comprehensive electronic search was conducted in PubMed, Cochrane Central Register of Controlled Trials, and Google Scholar databases, yielding six in vitro studies that met the inclusion criteria. The search strategy and study selection process followed PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines. A qualitative methodological assessment was performed using the SciRAP (Science in Risk Assessment and Policy) method, which evaluated the reporting and methodological quality of the included studies. (3) Results: All six studies consistently demonstrated that curcumin-coated titanium surfaces inhibited osteoclastogenesis and promoted osteogenic activity, evidenced by enhanced cell adhesion, proliferation, osteogenic differentiation, and mineralization. The mean reporting quality score was 91.8 (SD = 5.7), and the mean methodological quality score was 85.8 (SD = 10.50), as assessed by the SciRAP method. Half of the studies used hydroxyapatite-coated titanium as a control, while the other half used uncoated titanium, introducing potential variability in baseline comparisons. (4) Conclusions: This systematic review provides compelling in vitro evidence supporting the osteogenic potential of curcumin nanoparticle-coated titanium surfaces. The findings suggest that this surface modification strategy may enhance titanium implants’ biocompatibility and osteogenic properties, potentially improving dental and orthopedic implant outcomes. However, the review highlights significant heterogeneity in experimental designs and a concentration of studies from a single research group. Further research, particularly in vivo studies and clinical trials from diverse research teams, is essential to validate these findings and comprehensively understand the translational potential of this promising surface modification approach.

A REVIEW ON THE MECHANICAL AND TRIBOLOGICAL PROPERTIES OF THERMALLY SPRAYED HYDROXYAPATITE COATINGS FOR BIOMEDICAL IMPLANT MATERIALS

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).

Enhanced Antifouling Capability of In Situ-Grown Hydrophilic-Hydrophobic Nanodomains on Membrane Surface in the Ultralow Pressurized Ultrafiltration Process.

Although hydrophilic modification of the membrane surface is widely adopted, polymeric membranes still suffer from irreversible fouling caused by hydrophilic components in surface water. Here, an ultrathin hydrogel layer (40 nm) with hydrophilic-hydrophobic textures was in situ grown onto the polysulfone ultrafiltration membrane surface using an organic-radical-initiated interfacial polymerization technique. The interfacial polymerization of hydrophilic and hydrophobic monomers ensured the molecular-scale distribution of hydrophilic and hydrophobic nanodomains on the membrane surface. These nanodomains, with their molecular lengths, facilitated dynamic repulsion interactions between the uniformly textured surface and foulant components with different degrees of hydrophilicity. Chemical force characterization confirmed that the adhesion force between the hydrophilic-hydrophobic textured membrane surface and foulants (dodecane, bovine serum albumin, and humic acid) was greatly reduced. Dynamic filtration experiments showed that a hydrophilic-hydrophobic textured membrane always possessed the largest water flux and the best antifouling performance. Furthermore, the foulant coverage ratio on the membrane surface was first evaluated by measuring changes in surface streaming potentials, which demonstrated a 69% reduction in the amount of foulant adhering to the hydrophilic-hydrophobic textured membrane surface. Therefore, the construction of hydrophilic-hydrophobic nanodomains on the membrane surface provides a promising strategy for alleviating membrane fouling caused by both hydrophobic and hydrophilic components during ultralow pressurized ultrafiltration processes.