Interfacial Adhesion Research Articles

Investigating Interface Adhesion of PLA-Coated Cellulose Paper Straws: Degradation, Plant Growth Effects, and Life Cycle Assessment

Although bioplastics and paper straws have been introduced as alternatives to single-use plastic straws, their potential environmental, economic, and social impacts have not been analyzed. This study addresses this gap by designing a polylactic acid layer interface adhesion on cellulose paper-based (PLA-P) composite straws by a dip molding process. This process is simple, efficient, and scalable for massive production. Optimizing key manufacturing parameters, including ice bath ultrasonic, overlapping paper strips (2 strips), winding angle (60°), soaking time (5min), and drying temperature (50°C), were systematically evaluated to improve straw quality and manufacturing efficiency. PLA chains were found to deposit onto the cellulose network through intermolecular interactions to form a consistent "sandwich" structure, which can improve adhesion, water resistance, and mechanical properties. Interestingly, PLA-P straws effectively decomposed in soil and compost environments, with a 35-40% degradation rate within 4 months. Besides, PLA-P straw residues affected seed germination and plant growth, but no significant toxic effects were detected. Further, microplastics were observed in soil and plant tissues (roots, stems, and leaves), and their possible diffusion mechanisms were explored. The results of a comprehensive life cycle assessment (LCA) and cost analysis showed that the process improvements reduced the ecological footprint of PLA-P straws and showed good prospects for commercial application. The study's findings contribute to the understanding of bioplastics and paper straws in effectively reducing environmental impact and fostering sustainable development.

Monomer in situ polymerization as topological sutures to achieve strong interfacial adhesion and long-term anti-mold of renewable adhesive

Integrated long-term anti-mold and high bonding capacity properties into renewable biomass adhesives hold significant importance for promoting the green and sustainable development of the wood industry, yet it remains an immense challenge. Drawing inspiration from the design of molecular suture materials, we successfully developed a series of innovative quaternary ammonium salt monomers (APM12) that polymerize in situ with glycidyl methacrylate (GMA) at the interface of bonded adherents. This process constructed molecular sutures on the molecular scale, forming a robust topological entanglement network between the adhesive and the wood substrate. Such a rational structure design allowed the modified soybean meal (SM) adhesive to present a boosted bonding strength and water resistance (2.08 and 1.05MPa). The stably riveting high-effect anti-germ platform imparted the protein adhesive with ultra-long mildew resistance of 150 days for liquid SM@GMA-APM12 adhesives, outperforming all the previously reported protein-based bio-adhesives. The implementation of the suture strategy through an in situ sutural interspersed crosslinking network provided a straightforward approach and offered a novel solution for creating renewable adhesives with multiple desirable properties. Moreover, this suture strategy can be applied to other interface strong adhesion and anti-bacterial materials comprised of polymer structure, such as hydrogel, organic coatings, and membrane, broadening its scope of applications.

Hyperbranched bio-based waterborne sizing coating for enhancing the wettability of carbon fibre and interfacial adhesion of fibre/epoxy composites

Hyperbranched bio-based waterborne sizing coating for enhancing the wettability of carbon fibre and interfacial adhesion of fibre/epoxy composites

Tough and biodegradable poly(lactic acid)/polybutylene adipate-co-terephthalate blends for screw-based 3D printing: Interfacial compatibilizing via reactive carbon nanotubes

Reactive nanoparticles were recently reported as novel and highly effective compatibilizers for biodegradable polymer blends. In this work, three kinds of reactive carbon nanotubes with low, medium, and high vinylsilane grafting ratios (VCNT-L, VCNT-M, and VCNT-H) were synthesized, and their compatibilizing efficiencies were studied. Poly(lactic acid)/polybutylene adipate-co-terephthalate (PLA/PBAT) blends for 3D printing were prepared by reactive blending PLA and PBAT with either of VCNT-L, VCNT-M, and VCNT-H in the presence of organic peroxide. Tough and biodegradable 3D printed samples were achieved by using PLA/PBAT blends reactively compatibilized by VCNT-M and VCNT-H. The impact strength of 3D printed blend samples containing VCNT-M and VCNT-H is 4.1 and 6.2 folds to that of 3D printed PLA samples, respectively. The high interfacial compatibilizing efficiency of both VCNT-M and VCNT-H for PLA/PBAT blend was evidenced by SEM and linear rheological examining results. However, the VCNT-L tended to induce large size PBAT phase domains, hence the poor interfacial adhesion. As a result, 3D printed PLA/PBAT blend samples containing VCNT-L exhibited low impact strength, closing to that of PLA samples. Apart from the remarkable compatibilizing effects, the VCNT-H was observed to significantly improve the interlayer adhesion of the 3D printed samples.

Self-driven photoelectrochemical sensor based on Z-type perovskite heterojunction for profenofos detection in milk and cabbage

With growing public concern about the accumulation of pesticide residues in food and their potential impacts on health and the environment, the demand for advanced detection technologies has become more critical. To address this need, we have developed an innovative self-driven photoelectrochemical (PEC) sensor, utilizing a Z-type heterojunction structure. This sensor exploited the synergistic interactions between the carbonyl groups in polyvinylpyrrolidone and the Pb2+ ions in the perovskite, and was further enhanced by the strong hydrogen bonds formed between polyethylene glycol and MA+. To optimize the sensor's performance, we incorporated perylene tetracarboxylic acid, which enhanced interface adhesion and promotes charge separation, elements crucial for the visible light-driven PEC process. This strategic design resulted in a sensor with high sensitivity and stability, which was capable of detecting profenofos residues in complex food matrices such as milk and cabbage. The sensor demonstrated a linear detection range from 0.1 to 107ngL-1 and an exceptional detection limit of 0.033ngL-1. When applied to real samples, the sensor achieved recovery rates ranging from 96.68% to 107.2%, with relative standard deviations between 1.08% and 4.54%. In light of these results, the sensor not only showed high efficiency in real-time monitoring of pesticide contamination, but also highlights its significant potential for broader application in the field of food safety.

Super‐adaptive electroactive programmable adhesive materials to challenging surfaces: From intelligent soft robotics to XR haptic interfaces

AbstractRecently, the intelligent strategies for adapting to multiple challengeable surfaces of electroactive programmable materials integrated with bio‐inspired architectures offer expanded directions beyond traditional limitations in soft grippers, medical mobile robots, and XR (Extended Reality) interfaces. These electroactive programmable adhesive materials are adaptively designed for a variety of complex surfaces, including soft, wet, non‐flat, or contamination‐susceptible feature such as bio‐surfaces and vulnerable objects. They can be produced via solution‐based methods of replica coating or 3/4‐dimensional printing. The integration of electroactive programmable materials and intelligent adhesive architecture enables super‐adaptive switchable adhesion to a variety of complex surfaces through control of physical deformation and mechanical properties at the adhesive interface, presenting a breakthrough in soft electro‐robotics and extended reality (XR) Haptic interfaces technology. These surface‐adaptive platform can provide multiple functionalities that can efficiently control physical deformations of soft bioinspired architectures or transfer physical energy (heat, vibration, pressure) into the engaged surfaces in a lightweight and human‐friendly form. This review focuses on intelligent strategies, principles, design, and fabrication methods of super‐adaptive electroactive programmable materials intelligently combined with bioinspired switchable adhesives for next‐generation human–robot interaction devices, along with current challenges and prospects.image

Environmentally friendly approaches for tailoring interfacial adhesion and mechanical performance of biocomposites based on poly(lactic acid)/rice straw.

In the present research, plant-based biocomposites containing poly(lactic acid) (PLA) and rice straw (RS) as an annually renewable agricultural waste were studied. To enhance the properties of these filled systems, two environmentally friendly pulping methods were applied to remove the non-cellulosic components of RS and fibrillate the fibers. In addition, two reactive compatibilizers based on functional epoxy and maleic anhydride groups were incorporated into the biocomposites, using a reactive extrusion process. By pulping the RS fibers and modifying the PLA/lignocellulosic filler interface, the plant-based biocomposites with enhanced performance were attained. Furthermore, the elastic modulus, tensile strength, tensile toughness, impact strength, hardness, density and Vicat softening point of PLA and filled PLA system with untreated RS were improved. The impact resistance, tensile strength and elastic modulus of neat PLA were enhanced by 40 %, 160 % and 100 % for the modified biocomposites containing the environmentally friendly RS pulps. The obtained results showed that, these biocomposites had even higher mechanical performance than the PLA biocomposites containing RS pulp obtained through common soda-pulping method. The reasons behind these improvements are the partial pulping of RS, as well as the chain extension of PLA macromolecules and PLA grafting onto the lignocellulosic fiber surfaces induced by the reactive compatibilizers.

Bacterial-host adhesion dominated by collagen subtypes remodelled by osmotic pressure.

Environmental osmolarity plays a crucial role in regulating the functions and behaviors of both host cells and pathogens. However, it remains unclear whether and how environmental osmotic stimuli modulate bacterial‒host interfacial adhesion. Using single-cell force spectroscopy, we revealed that the interfacial adhesion force depended nonlinearly on the osmotic prestimulation of host cells but not bacteria. Quantitatively, the adhesion force increased dramatically from 25.98 nN under isotonic conditions to 112.45 or 93.10 nN after the host cells were treated with the hypotonic or hypertonic solution. There was a strong correlation between the adhesion force and the number of host cells harboring adherent/internalized bacteria. We further revealed that enhanced overexpression levels of collagen XV and II were responsible for the increases in interfacial adhesion under hypotonic and hypertonic conditions, respectively. This work provides new opportunities for developing host-directed antibacterial strategies related to interfacial adhesion from a mechanobiological perspective.

Extremely Ultrahigh Stretchable Starch‐Based Hydrogels with Continuous Hydrogen Bonding

AbstractNatural polysaccharides‐based hydrogels have drawn extensive attention yet have been plagued by less desirable stretchability due to their inherent nature. Here, ultra‐stretchable starch‐based hydrogels (amylopectin/polyacrylamide, AAM) are developed by constructing reversible intramolecular physical interactions. This strategy endows the hydrogel with exceedingly ultrahigh deformation due to a continuous hydrogen bonding network. It can be stretched from less than 0.5 to >300 cm without breakage that the elongation exceeds 600 times the original length. The elongation collected by the universal testing machine reaches up to 36 000% without breakage outperforming previous reports and demonstrating extraordinary stretchability. Furthermore, an interwoven structure of hydrogen bonding interaction and trace covalent bonds make the stress of hydrogel reach 0.28 MPa, accompanied by an ultra‐high strain of 22 500% and significant toughness (47 MJ·m−3). The hydrogel displays high transparency (≈93%), low‐temperature resistance, moisturizing property, and extraordinary interfacial adhesion property. Intriguingly, the aqueous precursor can act as inks to prepare various forms of hydrogel within minutes through the facile writing or drawing method. This hydrogel verifies strong potential in both fields of human motion sensor (After long‐term or low‐temperature conditions) and energy storage. This study will facilitate the progress of ultra‐stretchable or multifunctional hydrogels.

Comparative Analysis of Mechanical and Morphological Properties of Cordenka and Ramie Fiber-Reinforced Polypropylene Composites

The depletion of conventional materials and their adverse environmental impacts have prompted a shift toward sustainable alternatives in composite materials engineering. In pursuit of this objective, this study investigated the mechanical properties of polypropylene matrix composites reinforced with Cordenka, an artificial cellulose fiber, and compared them to those reinforced with ramie, a natural cellulose fiber. Continuous strand composites were developed using the Multi-Pin-assisted Resin Infiltration (M-PaRI) process. The strands were subsequently sectioned into 15 mm lengths and injection-molded into dumbbell and strip specimens for mechanical characterization. The results showed that 20 wt% Cordenka/PP composites exhibited a tensile strength of 68.7 MPa, 2.04 times higher than neat PP and 1.66 times greater than the 20 wt% ramie/PP composites. Impact testing further demonstrated that Cordenka/PP composites absorbed 2 to 2.5 times more impact energy than ramie/PP composites, regardless of the presence of notches. Fiber length analysis indicated that Cordenka fibers maintained their length beyond the critical fiber length, allowing for efficient stress transfer and acting as a more effective reinforcement compared to ramie fibers, which were below this threshold. Consequently, the Cordenka/PP composites exhibited significantly enhanced mechanical performance. Scanning electron microscopy (SEM) analysis revealed fewer fiber pullouts in ramie-reinforced composites, suggesting superior interfacial adhesion to the PP matrix, although it did not translate to higher mechanical properties. These findings underscore the potential of Cordenka as a sustainable alternative to synthetic, non-biodegradable fibers in PP composites, providing improved mechanical properties and promising prospects for advanced composite applications.

Anti-corrosion Properties of Functionalized Organo-silane Coupling Agents for Galvanized Steel

Silane precursor selection is an important criterion for achieving great anticorrosive performance on steel substrates using sol-gel technology. A density functional theory (DFT) study was performed on functional and nonfunctional organosilane precursors. The global reactivity parameters, such as the global hardness (ƞ), dipole moment (μ), and number of electrons transferred (∆N) to the metal substrate, were calculated to identify suitable silane coupling agents. DFT studies revealed that precursors containing functional groups such as epoxy, amine, and mercapto offer better protection against corrosion to galvanized steel by providing stronger interfacial adhesion than precursors without functional moieties. The DFT-calculated adsorption energy (Eads) is more than 40.0kcal/mol for the adsorption of functional organosilanes onto the (ZnO)12 cluster. Evidence of chemical bond formation at the interface for functional organosilanes is found in the electron density overlap in the MOs. Natural charge analyses revealed clear charge transfer from the organosilane moiety to the (ZnO)12 cluster. The theoretical predictions were validated via experiments. Electrochemical studies demonstrated a protective efficiency of 92.5% for Ie with an impedance of 92.9kΩ·cm2. The presence of the respective functional groups and surface morphology were evaluated by FTIR and SEM. The order of corrosion inhibition of organosilanes was found to be MPTMS≈APTES>GPTMS>TEOS.

Layer interface characteristics and adhesion of 3D printed cement-based materials exposed to post-printing temperature disturbance

The layer interface, which is vital for the performance and longevity of 3D printed cement-based materials (3DPCM), is very sensitive to the environmental conditions because of the lack of formwork. Nevertheless, the current limited understanding of how temperature affects the layer interface has restricted the application of 3D printing in different construction scenarios. Here, we revealed the effects of temperature on the multi-scale phase distribution features of the layer interface through mercury intrusion porosimetry, X-ray computed tomography, nanoindentation and scanning electron microscopy with energy dispersive spectroscopy techniques. Additionally, the interlayer bond strength of 3DPCM was evaluated via the splitting tensile test. Small amplitude oscillation, surface roughness and isothermal calorimetry measurements were employed for an in-depth analysis of the mechanisms. Results indicate that an increase in temperature post-printing reduces the discrepancies in aggregate volume fraction between the layer interface and bulk matrix due to the increasing structuration rate and the amount of cement paste at the interface due to the reduced settlement of aggregates. The porosity difference between the layer interface and bulk matrix decreased with increasing temperature due to the pore size refinement by faster filling with hydrates. In addition, a more concentrated distribution of atomic ratios and elastic modulus of hydrates were observed at the layer interface of 3DPCM hardened at higher temperatures. Increased curing temperature improves the interlayer bond strength of 3DPCM owing to the enhanced aggregate interlocking, reduced porosity and improved high-density CSH content.

Effects of Mechanized Irrigation Protocols on Endodontic Obturation Using Calcium Silicate-Based Sealer

The aim of this study was to evaluate the effects of mechanized final irrigation protocols (XPE, XP-Endo Finisher; XPC, XP-Clean; and ECL, Easy Clean) compared to PUI (passive ultrasonic irrigation) on the debris incidence and open dentinal tubules, and their effects on the adhesion interface after 48 h and 6 months. One hundred twenty maxillary central incisors were submitted to chemical–mechanical preparation using a rotary instrument and 2.5% sodium hypochlorite. Specimens were distributed in 4 groups (n = 30) in accordance with the mechanized final irrigation protocol: XPE, XPC, ECL, or PUI. Forty specimens (n = 10/group) were submitted to SEM analysis to evaluate the residue incidence and dentin open tubules. The other specimens were obturated using Bio-C Sealer and submitted to push-out bond strength and adhesive failure mode evaluations in the cervical, middle, and apical thirds after 48 h or 6 months (n = 10/group). Only in the apical third, ECL presented the highest residue incidence and fewer open dentinal tubules when compared to the XPE, XPC, and PUI groups (p < 0.05). In the cervical and middle root thirds, no significant differences were observed regardless of the group evaluated (p > 0.05). After 48 h, ECL resulted in the lowest bond strength only in the apical third (p < 0.05), while the XPE, XPC, and PUI groups remained similar in the cervical and middle thirds (p > 0.05). At 6 months, all groups showed lower bond strength values regardless of the root third evaluated, but ECL showed the lowest bond strength in the apical and middle root thirds when compared to the other groups (p < 0.05). The ECL protocol did not provide adequate residue removal on the apical radicular third and negatively affected the longevity of endodontic obturation using a calcium silicate-based sealer.

Impact of Graphene Nano particles on static and dynamic mechanical properties of basalt-glass fibre reinforced epoxy polymer hybrid composites

ABSTRACT This paper investigates the structure-property relationships in basalt – glass fabric reinforced hybrid polymer composites doped with graphene nanoplatelets. Basalt Glass fabrics were reinforced with 0.2 wt.% − 0.8 wt.% graphene using hand layup and compression moulding to fabricate laminated plates. The mechanical, morphological, and thermomechanical properties were characterised using tensile, flexural, impact, SEM, FTIR, XRD, and DMA testing. Results showed that low graphene loadings of 0.2 wt.% − 0.4 wt.% led to small, isolated graphene platelets decorating the basalt fibres. At 0.8 wt.% loading, extensive wrinkling, folding, and stacking of graphene sheets on the basalt was observed. FTIR revealed increasing sp2 C=C vibrations and XRD showed rising graphene peak intensities with higher loadings. While tensile and flexural strengths improved up to 0.6 wt.% graphene due to efficient stress transfer, impact energy increased consistently until 0.8 wt.% graphene owing to reinforcement effects. DMA exhibited enhanced storage modulus and restricted mobility with more graphene. An optimum graphene loading of 0.6 wt.% was found to maximise the mechanical performance through uniform dispersion and strong interfacial adhesion. The results demonstrate that graphene incorporation can substantially augment the strength, toughness, and thermomechanical properties of the composites at appropriate compositions prior to aggregation.

Enhancing Interface Performance Through Self-Assembly Mechanisms of APTES on Surface-Modified Tuff Aggregates

To enhance the adhesion between tuff and asphalt, this study investigates the efficacy of alkalinization treatment technology using a molecular self-assembly layer derived from the silane-coupling agent γ-aminopropyltriethoxysilane (APTES). APTES hydrolysis solutions at varying concentrations were prepared to assess their impact on the adhesive strength of the aggregate–asphalt interface and water damage resistance. Using surface energy theory, the interface adhesion work of tuff was analyzed, while SEM and EDS were employed to examine changes in surface morphology and composition after treatment. The results demonstrate that an APTES:water:ethanol mass ratio of 5:45:50, along with a curing temperature of 200 °C, significantly improves the bonding strength between tuff and asphalt. The silanol groups on APTES react with hydroxyl groups on the tuff surface to form siloxane bonds (Si-O-Si), anchoring APTES to the tuff. This study elucidates the self-assembly mechanisms of APTES on tuff aggregates and demonstrates the consequent enhancement of interfacial adhesion, providing valuable insights for the application of tuff as tunnel spoil in road engineering.

Densifying Conduction Networks of Vertically Aligned Carbon Fiber Arrays with Secondary Graphene Networks for Highly Thermally Conductive Polymer Composites

AbstractThermally conductive polymer composites hold great potential for thermal management applications in the electronics industry, but achieving metal‐like thermal conductivity (>200 W m−1 K−1) remains challenging due to the inevitable phonon scattering and the thermal resistance at filler‐filler and filler‐matrix interfaces. Herein, an efficient approach is presented to overcome this long‐standing barrier by designing a densified interconnecting filler framework, featuring a macro‐level carbon fiber (CF) array welded with a high‐quality, self‐assembled graphene network. In this framework, vertically aligned continuous CFs function as primary through‐plane thermal conduction paths, minimizing phonon scattering and thermal resistance. Meanwhile, the secondary graphene network interconnects the CFs into a more integrated and densified framework while introducing supplementary thermal conduction paths. Following polymer backfilling, the resulting epoxy nanocomposite exhibits an unprecedented through‐plane thermal conductivity of 262 W m−1 K−1 at a filler loading of 23.3 vol%, establishing a new benchmark among the thermally conducting polymer composites. When employed as a thermal interface material, this composite offers a 68.2% enhancement in cooling efficiency compared to standard commercial counterparts. Furthermore, the functional composite presents excellent Joule heating and interfacial adhesion properties, making it promising for thermal interface healing and multifunctional thermal management applications in complex environments.

Dipodal silane‐treated ramie woven matt reinforced polylactic acid biocomposites for improved mechanical and thermal properties

AbstractHot compression molding was used to produce biocomposites from ramie plain‐woven fabric‐reinforced polylactic acid (PLA). Prior to composite fabrication, alkali and dipodal silane (bis(3‐trimethoxysilylpropyl) amine) (BAS) were applied to improve fiber‐matrix adhesion. Mechanical tests revealed improvements in tensile and flexural strength due to interfacial adhesion. The flexural strength of ramie PLA composite samples treated only with silane (SR‐PLA) was the highest, at 136.35 MPa. Young's modulus was 7.51 GPa. BAS treatment was crucial for ensuring strong adhesion between the fabric and the PLA matrix. In combined alkali‐BAS‐treated composites (ASR‐PLA), the glass transition and crystallization temperatures disappeared completely, affecting PLA morphology. The maximum heat of absorption (373°C) was found in SR‐PLA composites, suggesting electrostatic interactions created a three‐dimensional network. In conclusion, the initial incorporation of dipodal silane resulted in the formation of six silanol linkages with ramie fabric, leading to enhancements in the mechanical and thermal characteristics of ramie–PLA composites.Highlights Alkali and BAS treated Fabrics ironed to remove treatment‐induced wrinkles. Carded PLA fiber with consistent density and weighted in four equal portions. Fabric and PLA lay alternatively in warp direction before compression molding. SR‐PLA composites exhibited improved thermal and mechanical properties.

Covalently grafting silane coupling agents onto MXene‐reinforced carbon fibers for epoxy composites with improved mechanical properties

AbstractTwo‐dimensional (2D) MXene (MX) and silane coupling agents are increasingly used to modify carbon materials for the fabrication of composite functional materials, which exhibit enhanced electrical, optical, and mechanical properties due to the synergistic effects of both MX and silane. We demonstrate the modification of carbon fibers (CFs) with MX and three different kinds of silane coupling agents, including 3‐aminopropyltriethoxysilane, 3‐glycidyloxypropyldimethoxymethylsilane, and 3‐mercaptopropyltriethoxysilane, which are named as CF‐MX@N, CF‐MX@O, and CF‐MX@S, respectively, and further prepare the CF‐MX@silane/epoxy (EP) composites. The utilized silane coupling agents serve as bridges between MX and CFs, forming CF‐MX@silane composites. Through comparative analysis, it is found that the CF‐MX@S composites form a strong interface phase through covalent bonds, significantly enhancing the interface compatibility and revealing strong interface adhesion. The interfacial shear strength of the molded CF‐MX@S/EP composites increases to 119.7 MPa, with an 173.9% enhancement comparing to unmodified composites. This work can offer useful guidance and reference for selecting appropriate silane coupling agent to modify CFs with 2D materials to form high‐performance composite materials.Highlights Silane coupling agents are used as bridges to graft MXene‐modified CFs The surface modification of CFs is achieved by a simple one‐step approach Excellent interfacial phase is constructed through forming strong covalent bonds Microstructure and failure interface are responsible to interface strengthen.

Interphase mechanics vs chemical compatibility: Generating a deformable PA6-carbon fiber interphase

Good interfacial adhesion is typically correlated to obtaining the best tensile/flexural performance for carbon fibre-reinforced composites. The nature or even presence of the interphase, a localized region around the fibre-matrix junction, is often discussed but notoriously difficult to visualize and characterise. Here, a surface-initiated electro-polymerization approach to covalently graft either polyacrylamide or polygylcidyl methacrylate to the carbon fibres was used. This was followed by continuous melt compounding into the polyamide-6 matrix prior to injection moulding. Analysis via X-ray photoelectron spectroscopy (XPS) coupled with topological/visual study through scanning electron microscopy (SEM), showed distinct surface changes after modification and at the composite fracture surface. Additionally, mechanical (tensile, flexural, and tribological characteristics) and thermal (differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA)) investigations were performed. The results showed that the unmodified CF samples exhibit higher tensile and flexural modulus than the modified CF samples. However, the wear rate has been significantly decreased for modified CF samples. SEM of fractured composite surfaces showcased a clear interphase region surrounding the fibre, highlighting the importance of interphase/interphase mechanics in the design of optimal composite interfaces.

Metalloproteinase inhibitors in the adhesion process dental

Matrix metalloproteinases (MMPs) are enzymes involved in tooth physiological development, caries processes, and hybrid layer degradation, in addition to being associated with dentin collagen breakdown. The interplay of MMP activity, masticatory forces, and biofilm action may, over time, compromise composite resin restorations. To reduce hybrid layer degradation by endogenous proteases and extend the longevity of resin restorations, MMP inhibitors and collagen cross-linking agents have been extensively studied. This work aims to identify, through a literature review, agents capable of inactivating MMPs at the dentin adhesive interface. This integrative review, based on studies retrieved from PUBMED/MEDLINE, LILACS, BBO, and VHL databases, identified 19 agents able to inhibit MMP activity at the adhesive-dentin interface in studies published between January 2018 and June 2023. It can be concluded that several agents can partially or completely block MMP activity, thereby enhancing restoration longevity. However, further studies are required to facilitate the clinical use of these agents, beyond chlorhexidine, in dental practice, with the application techniques suited to dentists’ daily clinical routines.