Surface Modification Research Articles

Modulating CO hydrogenation activity through silane functionalization of cobalt catalysts

Cobalt oxide (CoO) nanoparticles (NPs) were modified with different silanes (tetraethoxysilane – TEOS, triphenyl ethoxysilane – TPES, or trimethyl chlorosilane - TMCS) by dispersing the as-synthesized CoO NPs in n-hexane solutions containing the silanes. Fourier-transform infrared spectroscopy (FTIR) confirmed the presence of these silanes on the cobalt surfaces even after reduction in hydrogen (H2) at 573 K. Modifying CoO-NPs with TEOS resulted in face-centred cubic (fcc)-cobalt phase upon reduction whereas TPES or TMCS modification induced a mixture of hexagonal close-packed (hcp)- and fcc-cobalt phases. The modification of cobalt surfaces with the silanes alters the adsorption properties of carbon monoxide (CO) on the catalytically active sites. Furthermore, temperature programmed desorption of CO (CO-TPD) showed that the amount of dissociatively adsorbed CO relative to amount of associatively adsorbed CO increases on silane-modified cobalt surfaces, which correlates with an improved rate of CO conversion in the Fischer-Tropsch CO hydrogenation.

Surface modification of carbon dots with cyclodextrins as potential biocompatible photoluminescent delivery/bioimaging nanoplatform

BackgroundCyclodextrins are a well-established system which form inclusion complexes with many guest molecules. This property can be easily exploited to develop drug delivery systems. Additionally, carbon dots (CD) are a low-toxic photoluminescent product which have been used as luminescent tags. The combination of cyclodextrins and carbon dots allows obtaining a new nanoplatform, a biocompatible material, with both capabilities, increasing as well the internalization by the cells of the CD, induced by the cyclodextrins. ResultsIn the present work, we have modified the surface of carbon dots obtained from citric acid and glutathione with β and γ cyclodextrins. After a morphological and spectroscopic characterization, we concluded that the luminescence quantum yield and absorption molar coefficient of the derivatized and unmodified carbon dots was the same. These findings, together with the spectroscopic detection of active cyclodextrins, those bond to the CD able to interact with a guest molecule, allowed determination of the ratios: cyclodextrins/CD, active cyclodextrins/CD and an estimation of the CD molecular mass. Furthermore, the biocompatibility of the new materials was evaluated through cytotoxicity and cell-penetrance assays revealing that the materials were non cytotoxic up to 0.1 mg/mL. Moreover, the biocompatible developed nanoplatform penetrates in the cells maintaining the material's intrinsic fluorescence, thus constituting an adequate photoluminescent-tag with high-contrast for in vitro cell imaging. SignificanceThis work provides a new and easy method to combine cyclodextrins and carbon dots into a biocompatible material which can be used as nanoplatform both as drug delivery system and as photoluminescent tag in cell imaging. Likewise, this paper shows how to characterize the number of cyclodextrins and active cyclodextrins per CD, having an average stoichiometric relation of 1:1 for guest molecule – CD. Additionally, the minimum molecular mass of the unmodified CD was indirectly obtained, yielding about 1.6–1.9 kDa.

1D p-type molecular-based coordination polymer semiconductor with ultrahigh mobility

One-dimensional (1D) semiconductor nanostructures exhibit exceptional performance in mitigating short-channel effects and ensuring low power consumption. However, the scarcity of high-mobility p-type 1D materials impedes further advancement. Molecular-based materials offer high designability in structure and properties, making them a promising candidate for 1D p-type semiconductor materials. A molecular-based 1D p-type material was developed under the guidance of coordination chemistry. Cu–HT (HT is the abbreviation of p-hydroxy thiophenol) combines the merits of highly orbital overlap between Cu and S, fully covered surface modification with phenol functional groups, and unique cuprophilic (Cu–Cu) interactions. As such, Cu–HT has a remarkable hole mobility of 27.2 cm2 V−1 s−1, which is one of the highest reported values for 1D molecular-based materials to date and even surpass those of commonly used amorphous silicon as well as the majority of 1D inorganic materials. This achievement underscores the significant potential of coordination polymers in optimizing carrier transport and represents a major advancement in the synthesis of high-performance, 1D p-type semiconductor materials.

Engineered Mesoporous Silica-Based Nanoparticles: Characterization of Surface Properties.

Mesoporous silica-based nanomaterials have emerged as multifunctional platforms with applications spanning catalysis, medicine, and nanotechnology. Since their synthesis in the early 1990s, these materials have attracted considerable interest due to their unique properties, including high surface area, tunable pore size, and customizable surface chemistry. This article explores the surface properties of a series of MSU-type mesoporous silica nanoparticles, elucidating the impact of different functionalization strategies on surface characteristics. Through an extensive characterization utilizing various techniques, such as FTIR, Z-potential, and nitrogen adsorption porosimetry, insights into the surface modifications of mesoporous silica nanoparticles are provided, contributing to a deeper understanding of their nanostructure and related interactions, and paving the way to possible unexpected actionability and potential applications.

Carbon nanotubes as efficient anode current collectors for stationary aqueous Zn–Br2 batteries

Static Zn–Br2 batteries are considered an attractive option for cost-effective and high-capacity systems for large energy storage. Yet, the corrosive nature of the Zn–Br2 electrolytes entails a careful selection of all cells' ingredients to avoid rapid degradation of the batteries upon cycling. Thanks to their high chemical resistance and excellent conductivity, carbonaceous electrodes are typically utilized as current collectors for the cathode side, while thin Zn or Ti foils are most widely used as the anodes' current collectors. However, these metals tend to corrode fast, thus undermining the desirable performance of the cells as durable and stable rechargeable batteries. We demonstrate the effective utilization of carbon nanotubes (CNT) films as highly stable anode current collector for Zn–Br2 batteries. Dispersion of the CNT beforehand in slurries containing anionic, cationic, or neutral surfactants yielded distinct chemical and physical characteristics of these carbonaceous electrodes. This, in turn, led to significant differences in the morphology of the deposited Zn, consequently affecting the electrochemical performance of the Zn anodes. These findings provide insight into the interactions between Zn cations and the surface of CNTs, offering opportunities for further surface modifications of CNTs as effective anodes’ substrates for Zn–Br2 batteries.

Computational design of an Au nanohexapod shape for internalization into an idealized plasma membrane, investigating sizes, shapes, and modified surfaces

Computational microscopy is a crucial tool for studying internalization of Au nanohexapods (AuNHs) and can be applied in designing nanostructures for biomedical applications. To further explore the molecular insights into interactions between AuNHs and a plasma membrane (PM), we conducted a coarse-grained molecular dynamic (CGMD) simulation. This simulation aimed to investigate the cellular internalization pathways of AuNHs, considering factors such as sizes (6, 8, 10, and 12 nm diameters) varying rod lengths (LR_S0.6) and spheres at end edges (LR_S0.9), shapes (varying sphere diameters (DS) end edges, and varying pyramid cores (DC) for fixed size at 8 nm AuNH), and surface-charge modifications (neutral and negatively charged). The simulation results indicated that size, shape, and surface modification significantly affect cellular uptake. Each AuNH size facilitated interaction and translocation through the PM by direct permeation and an endocytosis process, utilizing sharp ends or edges to disrupt/penetrate the PM and subsequently enter the inner cell. Direct translocations of shapes (DS and DC AuNHs) were not observed. The surface-charged modification (8 nm sized AuNHs) showed the direct translocation process. When comparing the cellular uptake of shaped AuNHs, the DC AuNH exhibited a higher free-energy barrier. Notably, anionic AuNHs demonstrated the lowest free-energy barrier among the various surface-charged AuNHs compared with neutrally charged AuNHs and bare AuNHs, resulting in anionic charges that were more easily translocated into the inner cell than other shapes and charges. Additionally, the permeability of the surface covering was lower than the unmodified surface due to charges and hydrocarbons facilitating translocation. These findings offer a comprehensive understanding of interactions between AuNHs with various characteristics and a realistic PM, thereby providing insights for the design of nanostructures with biological applications.

Structure and Properties of Bioactive Titanium Dioxide Surface Layers Produced on NiTi Shape Memory Alloy in Low-Temperature Plasma.

The NiTi alloy, known for its shape memory and superelasticity, is increasingly used in medicine. However, its high nickel content requires enhanced biocompatibility for long-term implants. Low-temperature plasma treatments under glow-discharge conditions can improve surface properties without compromising mechanical integrity. This study explores the surface modification of a NiTi alloy by oxidizing it in low-temperature plasma. We examine the impact of process temperatures and sample preparation (mechanical grinding and polishing) on the structure of the produced titanium oxide layers. Surface properties, including topography, morphology, chemical composition, and bioactivity, were analyzed using TEM, SEM, EDS, and an optical profilometer. Bioactivity was assessed through the deposition of calcium phosphate in simulated body fluid (SBF). The low-temperature plasma oxidization produced titanium dioxide layers (29-55 nm thick) with a predominantly nanocrystalline rutile structure. Layer thickness increased with extended processing time and higher temperatures (up to 390 °C), though the relationship was not linear. Higher temperatures led to thicker layers with more precipitates and inhomogeneities. The oxidized layers showed increased bioactivity after 14 and 30 days in SBF. Low-temperature plasma oxidation produces bioactive titanium oxide layers on NiTi alloys, with a structure and properties that can be tuned through process parameters. This method could enhance the biocompatibility of NiTi alloys for medical implants.

Optimisation of nitrogen plasma exposure time for surface modification of cotton fibre

Surface modification via plasma treatment is useful in improving textile-based wound dressing functionality. This study was conducted to optimise the nitrogen plasma exposure time and its effect on the cotton surface (CS) properties at a constant nitrogen flow rate of 20 sccm for 5 to 30 min. The optimisation was done by analysing the alteration in morphology, functional group composition, crystallinity phase, electrokinetic potential, and colour of CS as subjected to nitrogen plasma. CS experienced an etching effect due to the presence of microcracks on its surface, with its electrokinetic potential becoming less negative, ranging from -5.51 to –8.05 mV. Then, the nitrogen functional group was detected on CS ranging from 2.9% to 4.5%, with its whiteness index reduced to 8.67% compared to the pristine cotton. As a result, 20 min was selected as the optimum exposure time for surface treatment. An exposure time of 30 min showed an early sign of degradation, which reduced its crystallinity index by 11.1%. Apparently, the CS is activated as exposed to the nitrogen plasma and experiences slight changes in its molecular structure without affecting its bulk properties.

Investigation of the structural properties of Si4+-doped HAP coatings on Ti-6Al-4V substrate as a corrosion barrier in biomedical media

The coatings of co-substituted bioactives play an important role in stimulating biological and physical properties for biomedical applications. Hydroxyapatite (HAP), a mineral compound possessing a hexagonal structure, exhibits high thermodynamic stability under typical physiological conditions. In this experimental study, Si4+-doped HAP coatings with varying concentrations (2.5 %, 5 %, and 10 % wt) were prepared on a Ti-6Al-4V substrate using the spin-coating technique and extreme centrifugal force (2500 rpm). The coated samples were characterized by XRD, FTIR, AFM, FESEM, and EDS techniques. The presence of cracks and voids in the HAP coatings detrimentally affected the performance of the implants. Tetraethyl orthosilicate (TEOS) was used in the coatings to mitigate the cracks and voids. Polarization and EIS studies in the simulated body fluid (SBF) were used to assess the corrosion resistance of the coatings. The decrease in current density and the improved resistance to corrosion observed in the coated samples, as compared to the uncoated Ti-6Al-4V, demonstrate the corrosion-inhibiting effects of anodizing. The integration of Si4+ ions in the structure of HAP caused the size of nanoparticles to decrease from 16.23 nm to 11.67 nm, and the surface roughness of the produced coatings exhibited a decrease from 29.18 to 5.65 nm. In the Nyquist plots, the 5 % Si4+-doped HAP coating displayed the highest Rct value of 17.99 MΩ.cm2 compared to the bare Ti-6Al-4V with a resistance of 0.13 MΩ.cm2. The 5 % Si4+-doped HAP coating was chosen as the optimal sample based on the study results. The results of this work show that surface modification with Si4+-doped HAP coatings is a promising approach for improving the functionality of the Ti-6Al-4 V alloy for biomedical applications.

Comment on Ma et al.’s “The Preventive Effect of Gentamicin in the Irrigating Solution on Endophthalmitis Caused by Methicillin-Resistant Staphylococcus epidermidis After Phacoemulsification with Intraocular Lens Implantation in Rabbits”

ABSTRACT In their recent publication, the authors explored the preventive effect of gentamicin in the irrigating solution on endophthalmitis caused by methicillin-resistant Staphylococcus epidermidis (MRSE) after phacoemulsification with intraocular lens (IOL) implantation in rabbits. This letter commends the authors for their innovative approach and discusses the potential of chitosan-based intraocular lenses as a future solution for reducing the incidence of endophthalmitis. Chitosan’s natural antibacterial properties, coupled with its capacity for sustained drug release and surface modification, make it a promising material for IOLs. This letter highlights recent advancements and suggests areas for further research to fully realize the potential of chitosan-based IOLs in ocular surgery.

Challenges and Prospects of Applying Nanocellulose for the Conservation of Wooden Cultural Heritage—A Review

Nanocellulose is a nanostructured form of cellulose, which retains valuable properties of cellulose such as renewability, biodegradability, biocompatibility, nontoxicity, and sustainability and, due to its nano-sizes, acquires several useful features, such as low density, high aspect ratio and stiffness, a high specific surface area, easy processing and functionalisation, and good thermal stability. All these make it a highly versatile green nanomaterial for multiple applications, including the conservation of cultural heritage. This review provides the basic characteristics of all nanocellulose forms and their properties and presents the results of recent research on nanocellulose formulations applied for conserving historical artefacts made of wood and paper, discussing their effectiveness, advantages, and disadvantages. Pure nanocellulose proves particularly useful for conserving historical paper since it can form a durable, stable coating that consolidates the surface of a degraded object. However, it is not as effective for wood consolidation treatment due to its poor penetration into the wood structure. The research shows that this disadvantage can be overcome by various chemical modifications of the nanocellulose surface; owing to its specific chemistry, nanocellulose can be easily functionalised and, thus, enriched with the properties required for an effective wood consolidant. Moreover, combining nanocellulose with other agents can also improve its properties, adding new functionalities to the developed supramolecular systems that would address multiple needs of degraded artefacts. Since the broad use of nanocellulose in conservation practice depends on its properties, price, and availability, the development of new, effective, green, and industrial-scale production methods ensuring the manufacture of nanocellulose particles with standardised properties is necessary. Nanocellulose is an interesting and very promising solution for the conservation of cultural heritage artefacts made of paper and wood; however, further thorough interdisciplinary research is still necessary to device new green methods of its production as well as develop new effective and sustainable nanocellulose-based conservation agents, which would replace synthetic, non-sustainable consolidants and enable proper conservation of historical objects of our cultural heritage.

Challenges and Prospects of Applying Nanocellulose for the Conservation of Wooden Cultural Heritage—A Review

Nanocellulose is a nanostructured form of cellulose, which retains valuable properties of cellulose such as renewability, biodegradability, biocompatibility, nontoxicity, and sustainability and, due to its nano-sizes, acquires several useful features, such as low density, high aspect ratio and stiffness, a high specific surface area, easy processing and functionalisation, and good thermal stability. All these make it a highly versatile green nanomaterial for multiple applications, including the conservation of cultural heritage. This review provides the basic characteristics of all nanocellulose forms and their properties and presents the results of recent research on nanocellulose formulations applied for conserving historical artefacts made of wood and paper, discussing their effectiveness, advantages, and disadvantages. Pure nanocellulose proves particularly useful for conserving historical paper since it can form a durable, stable coating that consolidates the surface of a degraded object. However, it is not as effective for wood consolidation treatment due to its poor penetration into the wood structure. The research shows that this disadvantage can be overcome by various chemical modifications of the nanocellulose surface; owing to its specific chemistry, nanocellulose can be easily functionalised and, thus, enriched with the properties required for an effective wood consolidant. Moreover, combining nanocellulose with other agents can also improve its properties, adding new functionalities to the developed supramolecular systems that would address multiple needs of degraded artefacts. Since the broad use of nanocellulose in conservation practice depends on its properties, price, and availability, the development of new, effective, green, and industrial-scale production methods ensuring the manufacture of nanocellulose particles with standardised properties is necessary. Nanocellulose is an interesting and very promising solution for the conservation of cultural heritage artefacts made of paper and wood; however, further thorough interdisciplinary research is still necessary to device new green methods of its production as well as develop new effective and sustainable nanocellulose-based conservation agents, which would replace synthetic, non-sustainable consolidants and enable proper conservation of historical objects of our cultural heritage.

Latest Delivery Advancements of Lipid Nanoparticles for Cancer Treatment.

As one of the primary causes of illness and death globally, cancer demands novel and potent treatment approaches, which is why lipid nanoparticles (LNPs) have gained attention as a promising delivery system for anticancer drugs with precision and efficacy. The article discusses the salient characteristics of LNPs, such as the lipid components, particle size, polydispersity index, and encapsulation efficiency, followed by strategies that enhance their remarkable drug delivery capabilities. The articles explore LNPs ability to improve the solubility, stability, and bioavailability of various chemotherapeutics, nucleic acids, and immunotherapeutic modalities. It also highlights the recent advancement in surface modification of LNPs, which is essential to improve their effectiveness. Tailored coatings of LNPs improve targeting precision, stability, and biocompatibility; enhancing their transport to boost therapeutic efficacy for cancer targeting. The review summarizes the recent advancements made in using LNPs to treat different forms of cancer and focuses on the most recent clinical studies. Overall, the review highlights that the LNPs can target and treat cancer in a tailored manner through gene therapy, RNA interference, and immunotherapy.

Formation of oxygen protective layer on monolayer MoS2 via low energy electron irradiation.

Monolayer molybdenum disulfide (MoS2) semiconductors are the new generation of two-dimensional materials that possess several advantages compared to graphene due to their tunable bandgap and high electron mobility. Several approaches have been used to modify their physical properties for optical device applications. Here, we report a facile and non-destructive surface modification method for monolayer MoS2 via electron irradiation at a low, 5 kV accelerating voltage. After electron irradiation, the results of Raman and photoluminescence spectroscopy confirmed that the structure remains unchanged. However, when the modified surface was illuminated with a 532 nm laser for a prolonged period, the PL intensity was quenched as a result of oxygen desorption. Interestingly, the PL intensity can be recovered when left in ambient conditions for 10 h. The analysis of the PL spectrum revealed a decrease of trion, which is consistent with the readsorbed O2 molecules on the surface that deplete electrons and lead to PL recovery. We attribute this effect to the enhancement of the n-type character of monolayer MoS2 after electron irradiation. The sensitive nature of the modified surface to oxygen suggests that this approach may be used as a tool for the fabrication of MoS2 oxygen sensors.

The non-negligible non-specific adsorption of oligonucleotides in target-immobilized Mag-SELEX

Target-immobilized magnetic beads-based Systematic Evolution of Ligands by Exponential Enrichment (target-immobilized Mag-SELEX) has emerged as a powerful tool for aptamer selection owing to its convenience, efficiency, and versatility. However, in this study we systematically investigated non-specific adsorption in target-immobilized Mag-SELEX and found that the non-specific adsorption of the oligonucleotides to target-labeled magnetic beads was comparable to that of the screening libraries, indicating a substantial portion of captured sequences likely stem from non-specific adsorption. Longer nucleic acid sequences (80 nt and above, such as polyA80 and yeast tRNA) were found to attenuate this non-specific adsorption, with more complex higher-order structures demonstrating greater efficacy, while dNTP and short sequences such as primer sequences (20 nt), polyT(59), or polyA(59), did not possess this capability. Various evidence suggested that hydrophobic interactions and other weak interactions may be the primary underlying cause of non-specific adsorption. Additionally, surface modification of magnetic beads with polar molecule polyethylene glycol (PEG) also yielded a significant reduction in non-specific adsorption. In conclusion, our research underscores the critical importance of closely monitoring non-specific adsorption in target-immobilized Mag-SELEX.

The non-negligible non-specific adsorption of oligonucleotides in target-immobilized Mag-SELEX

Target-immobilized magnetic beads-based Systematic Evolution of Ligands by Exponential Enrichment (target-immobilized Mag-SELEX) has emerged as a powerful tool for aptamer selection owing to its convenience, efficiency, and versatility. However, in this study we systematically investigated non-specific adsorption in target-immobilized Mag-SELEX and found that the non-specific adsorption of the oligonucleotides to target-labeled magnetic beads was comparable to that of the screening libraries, indicating a substantial portion of captured sequences likely stem from non-specific adsorption. Longer nucleic acid sequences (80 nt and above, such as polyA80 and yeast tRNA) were found to attenuate this non-specific adsorption, with more complex higher-order structures demonstrating greater efficacy, while dNTP and short sequences such as primer sequences (20 nt), polyT(59), or polyA(59), did not possess this capability. Various evidence suggested that hydrophobic interactions and other weak interactions may be the primary underlying cause of non-specific adsorption. Additionally, surface modification of magnetic beads with polar molecule polyethylene glycol (PEG) also yielded a significant reduction in non-specific adsorption. In conclusion, our research underscores the critical importance of closely monitoring non-specific adsorption in target-immobilized Mag-SELEX.

Surface Engineering Enhances Vanadium Carbide MXene-Based Nanoplatform Triggered by NIR-II for Cancer Theranostics.

Despite the advantages of high tissue penetration depth, selectivity, and non-invasiveness of photothermal therapy for cancer treatment, developing NIR-II photothermal agents with desirable photothermal performance and advanced theranostics ability remains a key challenge. Herein, a universal surface modification strategy is proposed to effectively improve the photothermal performance of vanadium carbide MXene nanosheets (L-V2C) with the removal of surface impurity ions and generation of mesopores. Subsequently, MnOx coating capable of T1-weighted magnetic resonance imaging can be in situ formed through surface redox reaction on L-V2C, and then, stable nanoplatforms (LVM-PEG) under physiological conditions can be obtained after further PEGylation. In the tumor microenvironment irradiated by NIR-II laser, multivalent Mn ions released from LVM-PEG, as a reversible electronic station, can consume the overexpression of glutathione and catalyze a Fenton-like reaction to produce ·OH, resulting in synchronous cellular oxidative damage. Efficient synergistic therapy promotes immunogenic cell death, improving tumor-related immune microenvironment and immunomodulation, and thus, LVM-PEG can demonstrate high accuracy and excellent anticancer efficiency guided by multimodal imaging. As a result, this study provides a new approach for the customization of 2D surface strategies and the study of synergistic therapy mechanisms, highlighting the application of MXene-based materials in the biomedical field.

Enhancing OLED electroluminescence by surface modification and work function adjustment of anode through NiO:Co coating

This study presents an approach to improve the electroluminescence (EL) of organic light-emitting diodes (OLEDs) by coating an ultra-thin NiO:Co (NCO) layer on the anode. The NCO layer was pivotal in modifying anodic properties, including surface roughness, hydrophilicity, and work function, thereby promoting ohmic hole injection from the anode into the NPB layer and enhancing the current density and carrier recombination in OLEDs. Compared to OLEDs with a pristine ITO anode, the OLEDs with an NCO-coated ITO anode showed a significant enhancement in EL performance, including a 24.5 % increase in current density, an 84.9 % enhancement in brightness, and a 48.7 % boost in efficiency. Notably, coating NCO on the anode consistently enhanced hole injection regardless of whether ITO or PEDOT:PSS was used as the anode.

A solid state electrolyte based enzymatic acetone sensor

This paper introduces a novel solid-state electrolyte-based enzymatic sensor designed for the detection of acetone, along with an examination of its performance under various surface modifications aimed at optimizing its sensing capabilities. To measure acetone concentrations in both liquid and vapor states, cyclic voltammetry and amperometry techniques were employed, utilizing disposable screen-printed electrodes consisting of a platinum working electrode, a platinum counter electrode, and a silver reference electrode. Four different surface modifications, involving different combinations of Nafion (N) and enzyme (E) layers (N + E; N + E + N; N + N + E; N + N + E + N), were tested to identify the most effective configuration for a sensor that can be used for breath acetone detection. The sensor's essential characteristics, including linearity, sensitivity, reproducibility, and limit of detection, were thoroughly evaluated through a range of experiments spanning concentrations from 1 µM to 25 mM. Changes in acetone concentration were monitored by comparing currents readings at different acetone concentrations. The sensor exhibited high sensitivity, and a linear response to acetone concentration in both liquid and gas phases within the specified concentration range, with correlation coefficients ranging from 0.92 to 0.98. Furthermore, the sensor achieved a rapid response time of 30–50 s and an impressive detection limit as low as 0.03 µM. The results indicated that the sensor exhibited the best linearity, sensitivity, and limit of detection when four layers were employed (N + N + E + N).

Amorphous titanium oxide (aTiO2) thin films biofunctionalized with CAP-p15 induce mineralized-like differentiation of human oral mucosal stem cells (hOMSCs)

Insufficient osseointegration of titanium-based implants is a factor conditioning their long-term success. Therefore, different surface modifications, such as multifunctional oxide coatings, calcium phosphates, and the addition of molecules such as peptides, have been developed to improve the bioactivity of titanium-based biomaterials. In this work, we investigate the behavior of human oral mucosal stem cells (hOMSCs) cultured on amorphous titanium oxide (aTiO2), surfaces designed to simulate titanium (Ti) surfaces, biofunctionalized with a novel sequence derived from cementum attachment protein (CAP-p15), exploring its impact on guiding hOMSCs towards an osteogenic phenotype. We carried out cell attachment and viability assays. Next, hOMSCs differentiation was assessed by red alizarin stain, ALP activity, and western blot analysis by evaluating the expression of RUNX2, BSP, BMP2, and OCN at the protein level. Our results showed that functionalized surfaces with CAP-p15 (1 µg ml−1) displayed a synergistic effect increasing cell proliferation and cell attachment, ALP activity, and expression of osteogenic-related markers. These data demonstrate that CAP-p15 and its interaction with aTiO2 surfaces promote osteoblastic differentiation and enhanced mineralization of hOMSCs when compared to pristine samples. Therefore, CAP-p15 shows the potential to be used as a therapeutical molecule capable of inducing mineralized tissue regeneration onto titanium-based implants.