Dopamine Modification Research Articles

Rapid Hemostasis Tumor In Situ Hydrogel Vaccines for Colorectal Cancer Chemo-Immunotherapy.

Due to the high heterogeneity and the immunosuppressive microenvironment of tumors, most single antigen tumor vaccines often fail to elicit potent antitumor immune responses in clinical trials, resulting in unsatisfactory therapy effects. Hence, personalized tumor vaccines have become a promising modality for cancer immunotherapy. Here, we have developed a tumor in situ hydrogel vaccine (AH/DA-OR) capable of rapid hemostasis for personalized tumor immunotherapy, composed of dopamine-grafted hyaluronic acid (HA/DA) combined with sodium alginate (ALG), with coloaded oxaliplatin (OXA) and resiquimod (R848). The ALG and HA framework imparts excellent biocompatibility to the hydrogel, and dopamine (DA) modification endows it with rapid hemostatic functionality. Following local peritumor injection of AH/DA-OR into the tumor, the in situ hydrogel vaccine achieved the sustained release of the chemotherapeutic agent, OXA, inducing immunogenic cell death in tumor cells and effectively releasing personalized tumor-associated antigens to activate immune responses. Simultaneously, local R848 adjuvant sustained release at the tumor site enhanced immune responses, minimized drug side effects, and amplified immunotherapy effects. Finally, the hydrogel vaccine effectively activated host immune responses to suppress CT26 colorectal cancer growth in vivo, also exhibiting superior inhibition of untreated tumor growth at distant sites. This strategy of rapid hemostasis of tumor in situ hydrogel vaccine holds significant clinical potential and provides a paradigm for achieving secure and robust immunotherapy.

Recycled PET Fibers with Dopamine Surface Modification for Enhanced Interlayer Adhesion in 3D Printed Concrete.

Three-dimensional printed concrete (3DPC) is increasingly recognized in the construction industry for its high design flexibility and the elimination of conventional formwork. However, weak interlayer adhesion remains a significant challenge. The potential of recycled polyethylene terephthalate (PET) fibers for reinforcing 3DPC is being explored, driven by their environmental sustainability and economic advantages. However, there is an inadequate interfacial adhesion between these recycled fibers and the 3DPC matrix. This study investigated the use of dopamine modification to address this issue and enhance the interlayer adhesion of fiber-reinforced 3DPC. Recycled PET fibers were surface-modified using dopamine treatment, forming a polydopamine (PDA) film that improved surface roughness and hydrophilicity. Both unmodified and modified fibers were incorporated into 3DPC at various volume fractions (0.1%, 0.3%, 0.5%). The effects on interlayer adhesion strength, compressive strength, and flexural strength were systematically evaluated and compared. The results showed that the inclusion of 0.3 vol% dopamine-modified fibers resulted in a 22.5% increase in interlayer adhesion strength compared to the control group, and a 14.8% improvement over unmodified fibers at the same content. Additionally, the compressive strength and flexural strength of 3DPC with 0.3 vol% MPET fibers increased by 22.5% and 27.6%, respectively, compared to the control group. Microstructural analysis using SEM and XRD revealed that the dopamine modification significantly improved the interfacial adhesion between fibers and the concrete matrix, explaining the superior performance of modified fibers. This study demonstrates that recycled PET fibers modified with dopamine can effectively enhance the interlayer adhesion of 3DPC. The findings affirm that surface modification techniques can significantly elevate the utility of recycled PET fibers in 3DPC, contributing to the sustainable advancement of construction materials.

A Hollow Hemispherical Mixed Matrix Lithium Adsorbent with High Interfacial Interaction for Lithium Recovery from Brine

Mixed matrix lithium adsorbents have attracted much interest for lithium recovery from brine. However, the absence of an interfacial interaction between the inorganic lithium-ion sieves (LISs) and the organic polymer matrix resulted in the poor structural stability and attenuated lithium adsorption efficiency. Here, a novel hollow hemispherical mixed matrix lithium adsorbent (H-LIS) with high interfacial compatibility was constructed based on mussel-bioinspired surface chemistry using a solvent evaporation induced phase transition method. The effects of types of functional modifiers, LIS loading amount, adsorption temperature and pH on their structural stability and lithium adsorption performance were systematically investigated. The optimized H-LIS adsorbent with the LIS loading amount of 50 wt.% possessed the structural merit that the LIS functionally modified by dopamine exposed on both the inner and outer surfaces of the hollow hemispheres. At the best adsorption pH of 12.0, it showed a comparable lithium adsorption capacity of 25.68 mg·g−1 to the powdery LIS within 4 h, favorable adsorption selectivity of Mg/Li and good reusability that could maintain over 90% of lithium adsorption capacity after the LiCl adsorption—0.25 M HCl pickling-DI water cleaning cycling processes for three times. The interfacial interaction mechanism of H-LIS for lithium adsorption was innovatively explored via advanced microcalorimetry technology. It suggested the nature of the Li+ adsorption process was exothermic and dopamine modification could reduce the activation energy for lithium adsorption from 15.68 kJ·mol−1 to 13.83 kJ·mol−1 and trigger a faster response to Li+ by strengthening the Li+-H+ exchange rate, which established the thermodynamic relationship between the structure and Li+ adsorption performance of H-LIS. This work will provide a technical support for the structural regulation of functional materials for lithium extraction from brine.

Effects of collagen modification on the osteogenic performance of different surface-modified titanium samples in vitro.

The aim of this study was to evaluate the effects of collagen modification on the osteogenic performance of different surface-modified titanium, including alkaline etching, alkaline etching followed by silanization, and alkaline etching followed by dopamine modification. The proliferation, adhesion, and osteogenic differentiation abilities of MC3T3-E1 cells on the surfaces with collagen modification were analyzed and compared. Collagen was immobilized on the surfaces of pure titanium (Ti-C), alkaline-etched titanium (Ti-Na-C), alkaline-etched and silanized titanium (Ti-A-C), and alkaline-etched and dopamine-modified titanium (Ti-D-C), with pure titanium (Ti) as the control group. The surface morphology was observed by scanning electron microscopy (SEM), and the surface elemental composition was analyzed by X-ray photoelectron spectroscopy (XPS). Contact angle measurements were conducted to evaluate the hydrophilicity of the surfaces. MC3T3-E1 cells were cultured on the surfaces, and their proliferation, adhesion, and osteogenic differentiation abilities were assessed using CCK-8 assay, laser scanning confocal microscope, alkaline phosphatase (ALP) staining, Alizarin red staining and quantitative analysis, as well as real-time quantitative polymerase chain reaction (RT-qPCR) to evaluate the mRNA expression levels of osteogenic-related genes, including ALP, typeⅠcollagen (COL-1), osteocalcin (OCN), osteopontin (OPN). SEM and XPS results confirmed the successful immobilization of collagen on the titanium surfaces, with the Ti-Na-C group exhibiting a higher amount of collagen modification. Contact angle measurements showed improved hydrophilicity of the surfaces after collagen modification. CCK-8 results indicated good compatibility of the materials with MC3T3-E1, with enhanced cell proliferation on the collagen-modified surfaces. Cell fluorescence staining revealed better cell spreading on the collagen-modified surfaces, and ALP and Alizarin red staining results suggested that the Ti-Na-C group exhibited the best osteogenic performance, with significantly higher absorbance values in the Alizarin red quantification analysis. RT-qPCR analysis showed that the Ti-Na-C group had the highest expression of the osteogenic-related gene OPN. Among the different collagen modification approaches employed in this study, collagen modification on alkaline-etched titanium surfaces showed the most conducive effects on MC3T3-E1 cell adhesion, spreading, proliferation, and osteogenic differentiation. This approach can be considered as the optimal collagen modification strategy for enhancing osteogenesis on titanium surfaces.

Improved performance of epoxy resin coating with the modification of dopamine doped Ti4O7

AbstractIn this paper, a dense and well‐adherent polydopamine‐Ti4O7/epoxy resin (PDA‐Ti4O7/EP) composite coating is successfully prepared. The modified grafting of Ti4O7 by polydopamine (PDA) is achieved through the coordination complexation of unstable catechol groups in PDA with coordination unsaturated Ti atoms in Ti4O7. The potentiodynamic polarization curve and electrochemical impedance spectroscopy test results show that the performance of the composite coating is improved compared with that of the pure epoxy coating, and the composite coating slows down the penetration of electrolytes and aggressive ions and improves the corrosion resistance. The composite coating with 2 wt.% PDA‐Ti4O7 filler shows the best corrosion resistance, and its |Z|0.01 Hz remains above 1011 Ω cm2 after 30 days of immersion in 3.5 wt% NaCl solution. This can be attributed to the good barrier property of PDA‐Ti4O7 filler, which carries NH2 and OH reactive groups, interacting with the resin and matrix to improve the dispersion of the filler and the adhesion of the composite coating. The NH2 group reacts with the epoxy group in the epoxy resin in a ring‐opening reaction, which avoids the agglomeration of the filler and the uniformly dispersed filler fills the pores in the coating due to curing to improve the denseness of the coating and give full play to the barrier property of the filler. At the same time, the hydrogen bonding between the filler and the OH group in the resin and the substrate increases the adhesion of the coating. In addition, the unstable catechol group in PDA chelates with iron ions to further improve the overall corrosion resistance of the coating.Highlights A dense and well‐adherent PDA‐Ti4O7/EP coating is successfully prepared. PDA connect with Ti4O7 through coordination of catechol groups and Ti atom. PDA‐Ti4O7 are chemically bonded to the EP through a ring‐opening reaction. PDA‐Ti4O7 improves the crosslinking density and barrier ability of the coating.

A stable and efficient hydrogel/sponge solar evaporator with splendid water supply

Solar-driven interfacial evaporation is an effective and realizable way of water purification. However, a short supply of water limits the evaporation performance of evaporator greatly. Here, an integrated photothermal evaporator owning double-layer structure of hydrogel and sponge with strong water transport ability is successfully prepared by cross-linking and dopamine modification. Abundant pores and hydrophilic functional groups in hydrogel and modified sponge benefit to enhance water transport of the whole evaporator and further relieve salt accumulation. Carbon black having the advantages of low cost and full spectrum absorption is dispersed into hydrogel networks to improve the capacity of photothermal conversion. Under the illumination of 1 kW m−2, the evaporator exhibits an excellent evaporation rate of 1.71 kg m-2h−1, corresponding to an evaporation efficiency of 93.8 %. Furthermore, the evaporator shows excellent stability during 8 cycles of solar evaporation. And the evaporator demonstrates superior salt tolerance in 3.5 wt% NaCl solution during the continuous evaporation of 8 h and has an outstanding efficiency of 99.8 % in 4-NP wastewater purification. The outdoor experiment proves that the evaporator of 1 m2 can produce 7.28 L of fresh water per day, which meet the drinking water demand of two adults. The hydrogel/sponge integrated photothermal evaporator has great application potential in seawater desalination and wastewater purification.

Lipid-Polymer Hybrid Nanoparticles with Both PD-L1 Knockdown and Mild Photothermal Effect for Tumor Photothermal Immunotherapy.

In developing countries, the incidence of colorectal cancer (CRC) is on the rise. The combination of programmed cell death ligand-1 (PD-L1) siRNA (siPD-L1) and mild photothermal therapy (PTT) is a promising strategy for CRC treatment. In this study, dopamine-modified polyethylenimine (PEI) was prepared to fabricate an IR780 and siPD-L1 codelivery lipid-polymer hybrid nanoparticle (lip@PSD-siP) for the photothermal immunotherapy of CRC. The modification of dopamine can significantly reduce the cytotoxicity of PEI. lip@PSD-siP can be effectively taken up by CT26 cells and successfully escaped from lysosomes after entering the cells for 4 h. After CT26 cells were transfected with lip@PSD-siP, the PD-L1 positive cell rate decreased by 82.4%, and its PD-L1 knockdown effect was significantly stronger than the positive control Lipo3000-siP. In vivo studies showed that lip@PSD-siP-mediated mild PTT and efficient PD-L1 knockdown exhibited primary and distal tumor inhibition, metastasis delay, and rechallenged tumor inhibition. The treatment with lip@PSD-siP significantly promoted the maturation of dendritic cells in lymph nodes. The amount of T cell infiltration in the tumor tissues increased significantly, and the frequency of CD8+ T cells and CD4+ T cells was significantly higher than that of other groups. The percentage of immunosuppressive regulatory cells (Tregs) in the tumor tissue on the treatment side decreased by 88% compared to the PBS group, and the proportion of CD8+CD69+ T cells in the distal tumor tissue was 2.8 times that of the PBS group. The memory T cells of mice in the long-term antitumor model were analyzed. The results showed that after treatment with lip@PSD-siP, the frequency of effector memory T cells (Tem cells) significantly increased, suggesting the formation of immune memory.

Preparation and Characterization of Dopamine-Modified Carbon Fiber Paper Composites for Gas Diffusion Layers.

Carbon fibers (CFs) cannot be directly used for the preparation of CF paper because of their chemically inert nature. Herein, the surface of CFs was modified using the spontaneous oxidative self-polymerization of dopamine. By taking full advantage of the spontaneous oxidation and self-polymerization properties of PD to maintain the maximum strength of CFs, a polydopamine-modified CF paper (PDA-CFP) with excellent performance was prepared using PD-modified CFs (PDA-CFs). This increased the proportion of hydrophilic functional groups on the surface of carbon fibers, increased the O/C ratio on the CF surface by 6 times, and improved the bond strength between the modified CF and the adhesive by making full use of the interaction force between polydopamine and PVA fibers. In this way, the primary properties of the CF paper were improved. Overall, the results showed that the dispersion of CF was considerably improved with dopamine modification. In addition, the primary physical properties of PDA-CFP were better than those of virgin CF paper (CFP-0). PDA-CFP exhibited a maximum tensile strength of 2.04 kN·m-1, a minimum resistivity of 0.06055 Ω·cm-1, and a minimum porosity of 72.4%. The tightness was increased by up to 12.1%.

Fetal milieu-simulating hyaluronic acid-dopamine-chondroitin sulfate hydrogel promoting angiogenesis and hair regeneration for wound healing

Wound regeneration with complete functions and skin appendages is still challenging in wound dressing application. Inspired by the efficient wound healing in the fetal environment, we developed a fetal milieu-mimicking hydrogel for accelerating wound healing simultaneously with hair follicle regeneration. To mimic the fetal extracellular matrix (ECM), which contains high content of glycosaminoglycans, hyaluronic acid (HA) and chondroitin sulfate (CS) were selected to fabricate hydrogels. Meanwhile, dopamine (DA) modification endowed hydrogels with satisfactory mechanical properties and multi-functions. The hydrogel encapsulated atorvastatin (ATV) and zinc citrate (ZnCit), namely HA-DA-CS/Zn-ATV, exhibited tissue adhesion, self-healing capacity, good biocompatibility, excellent anti-oxidant ability, high exudate absorption, and hemostasis property. In vitro results revealed that hydrogels exerted significant angiogenesis and hair follicle regeneration efficacy. In vivo results confirmed that hydrogels significantly promoted wound healing, and the closure ratio reached over 94 % after 14 days of hydrogels-treatment. The regenerated skin exhibited a complete epidermis, dense and ordered collagen. Furthermore, the number of neovessels and hair follicles in the HA-DA-CS/Zn-ATV group were 1.57- and 3.05-fold higher than those of the HA-DA-CS group. Thus, HA-DA-CS/Zn-ATV serves as multifunctional hydrogels for simulating the fetal milieu and achieving efficient skin reconstruction with hair follicle regrowth, exhibiting potential in clinical wound healing.

Extrusion-Based 3D Bioprinting of Adhesive Tissue Engineering Scaffolds Using Hybrid Functionalized Hydrogel Bioinks.

Adhesive tissue engineering scaffolds (ATESs) have emerged as an innovative alternative means, replacing sutures and bioglues, to secure the implants onto target tissues. Relying on their intrinsic tissue adhesion characteristics, ATES systems enable minimally invasive delivery of various scaffolds. This study investigates development of the first class of 3D bioprinted ATES constructs using functionalized hydrogel bioinks. Two ATES delivery strategies, in situ printing onto the adherend versusprinting and then transferring to the target surface, aretested using two bioprinting methods, embedded versus air printing. Dopamine-modified methacrylated hyaluronic acid (HAMA-Dopa) and gelatin methacrylate (GelMA) are used as the main bioink components, enabling fabrication of scaffolds with enhanced adhesion and crosslinking properties. Results demonstrate that dopamine modification improved adhesive properties of the HAMA-Dopa/GelMA constructs under various loading conditions, while maintaining their structural fidelity, stability, mechanical properties, and biocompatibility. While directly printing onto the adherend yields superior adhesive strength, embedded printing followed by transfer to the target tissue demonstrates greater potential for translational applications. Together, these results demonstrate the potential of bioprinted ATESs as off-the-shelf medical devices for diverse biomedical applications.

Robust mechanical and water responsive mechanically adaptive property of physically cross-linked sustainable nanocellulose composites

The development of wood derived cellulose nanocrystal (CNCs) based sustainable composites is potential to address the plastic pollution issue. However, because of strong hydrogen bonding interactions inside the CNCs, it is still challenging to obtain composites with satisfied comprehensive performance via the incorporation of CNCs into poly (vinyl alcohol) (PVA) matrix directly, so two strategies combined with dopamine modification, base bath solution and ferric (III) ion treatment were reported to tailor the comprehensive performance of PVA/CNC composites. The comparative study indicated that both of physically cross-linked PDA@CNC/PVA and PVA/CNC composites have obvious improvement in term of mechanical and water resistance property owing to the multiple physical interactions, e.g., hydrogen bonding and ferric ion-carboxyl group coordination interactions as well as catechol group and ferric ion coordination interactions. In addition, the physical performance (water resistance and mechanical property) of cross-linked PVA/CNC composites is more better than that of cross-linked PDA@CNC/PVA composites. Besides, physically cross-linked PVA/CNC composites also showed the water responsive mechanically adaptive property. This work provides the foundation for the further development of direct ink writing four-dimensional printing of physically cross-linked PVA/CNC sustainable composites.

Improving Hydrophilicity and Adhesion of PDMS through Dopamine Modification Assisted by Carbon Dioxide Plasma

In this paper, the carbon dioxide (CO2) plasma-assisted method was firstly developed for the preparation of dopamine coating polydimethylsiloxane (PDMS). The PDMS films were pre-treated by CO2 plasma at the power of 30–60 W for 5–10 min and then modified by dopamine for 18 h. The results showed that many polar groups such as C-O bonds, C=O bonds, and O-C=O bonds were introduced into the surface of PDMS films, which successfully promoted the formation of poly(dopamine) coating. Finally, the results of contact angle measurements showed that the surface of the plasma-assisted dopamine grafted samples changed from 118° to 64°. The shearing adhesion strength increased from 2.22 N/cm2 to 6.02 N/cm2, almost three times that of the original sample. This method provides a successful strategy for obtaining good poly(dopamine) coating layers on PDMS with strong hydrophilicity and shearing adhesion, which can be widely applied in the fields of medical and adhesive materials.

A Ce-MOF@polydopamine composite nanozyme as an efficient scavenger for reactive oxygen species and iron in thalassemia disease therapy.

Patients with β-thalassemia are prone to complications such as cardiovascular diseases and secretory gland injury due to iron overload (IO) and reactive oxygen species (ROS) production caused by blood transfusions. Simultaneously scavenging ROS and eliminating IO using nanomedicine remains challenging. Herein, we designed a dual-functional Ce-based metal-organic framework@polydopamine (Ce-MOF@PDA) composite that integrates oxidative stress reduction and IO elimination and evaluated its protective effect on IO injury in thalassemia. Using Ce-MOF with multiple active sites as the core, dopamine, which can coordinate iron ions, was modified on the surface of Ce-MOF and spontaneously polymerized to obtain PDA with iron elimination ability. Dopamine modification also adjusted the Ce3+/Ce4+ ratio to further enhance the catalytic activity for scavenging ROS. Ce-MOF@PDA exhibited multiple nanozyme activities, such as superoxide dismutase- and catalase-like activities, and decreased iron-mediated oxidative stress levels in vitro. Furthermore, the serum ferritin levels and iron concentrations in the liver of IO mice were reduced following treatment with Ce-MOF@PDA, and the fecal clearance ability was comparable to that of deferoxamine. These results indicate that Ce-MOF@PDA can eliminate IO while scavenging ROS and reduce tissue damage caused by oxidative stress. Therefore, the Ce-MOF@PDA nanozyme is a promising therapeutic nanomedicine for treating thalassemia IO.

A double crosslinking MXene/cellulose nanofiber layered film for improving mechanical properties and stable electromagnetic interference shielding performance

With the discovery of the two-dimensional (2D) MXene, it shows a great application potential in the field of electromagnetic interference (EMI) shielding, but the mechanical brittleness and easy oxidation of MXene limit its wide application. For this reason, a double crosslinking strategy is provided to solve the above problems in a nacre-like “brick-mortar” layered MXene/cellulose nanofiber (MXene/CNF) film. Typically, the film was firstly suffered by dopamine modification, then was further reinforced by secondary Ca2+ bridging, so as to obtain excellent mechanical properties and antioxidative EMI shielding performance. Comparing with the single crosslinking, the double crosslinking strategy reveals a higher efficiency in improving the mechanical property. The mechanical strength and toughness of the double crosslinking MXene/CNF film can increase to 142.2 MPa and 9.48 MJ/m3, respectively. More importantly, while achieving good mechanical properties, the MXene composite film still holds a very stable EMI shielding performance of more than 44.6 dB when suffering from the oxidation treatment of high-temperature annealing, showing excellent anti-oxidation ability and environment tolerance. Therefore, this work provides a universal but effective double crosslinking strategy to solve the mechanical brittleness and easy oxidation of MXene-based composites, thus showing a huge potential in flexible EMI shielding applications.

Boosting fire safety and mechanical performance of thermoplastic polyurethane by the face-to-face two-dimensional phosphorene/MXene architecture

• A black phosphorus-MXene@polydopamine nanohybrid was synthesized. • The TPU/BP-MXene@PDA nanocomposite simultaneously showed reinforcing and toughening effects towards TPU. • The TPU/BP-MXene@PDA nanocomposite could be achieved excellent thermal stability, mechanical properties and flame retardancy. • A synergistic flame-retardant mechanism between black phosphorus and MXene in the TPU were discussed and clarified. Black phosphorus (BP), as one of the most promising fillers for flame retarding polymer, has been seriously limited in practical application, due to the agglomeration and poor structural stability challenges. Here, the BP was modified by MXene and polydopamine (PDA) via ultrasonication and dopamine modification strategy to improve the structural stability and dispersibility in the matrix. Then, the obtained (BP-MXene@PDA) nanohybrid was employed to promote the mechanical performance, thermal stability, and flame retardancy of thermoplastic polyurethane elastomer (TPU). The resultant TPU composite containing 2 wt.% of BP1-MXene2@PDA showed a 19.2% improvement in the tensile strength and a 13.8% increase in the elongation at break compared to those of the pure TPU. The thermogravimetric analysis suggested that BP-MXene@PDA clearly enhances the thermal stability of TPU composites. Furthermore, the introduction of the BP-MXene@PDA nanohybrids could considerably improve the flame retardancy of TPU composite, i.e., 64.2% and 27.3% decrease in peak heat release rate and total heat release, respectively. The flame-retardant mechanisms of TPU/BP-MXene@PDA in the gas phase and condensed phase were investigated systematically. This work provides a novel strategy to simultaneously enhance the fire safety and mechanical properties of TPU, thus expanding its industrial applications.

Enhanced Bioactive Properties of Halloysite Nanotubes via Polydopamine Coating.

Halloysite nanotubes (HNT) were coated five times with dopamine (DOPA) in a tris buffer medium at pH 8.5 to acquire polydopamine-coated HNTs (PDOPA@HNT), e.g., PDOPA1@HNT, PDOPA3@HNT, and PDOPA5@HNT. Upon coating HNT with PDOPA, the surface area, pore volume, and pore size were decreased depending on the number of coatings. While the surface area of HNT was 57.9 m2/g, by increasing the number of coatings from 1 to 5, it was measured as 55.9, 53.4, 53.3, 47.4, and 46.4 m2/g, respectively. The isoelectric point (IEP) for HNTs was determined as 4.68, whereas these values are estimated as 2.31 for PDOPA1@HNTs, 3.49 for PDOPA3@HNT, and 3.55 for PDOPA5@HNT. Three different antioxidant studies were conducted for HNT and PDOPA@HNT, and the total phenol (TPC) value of HNT was found to be 150.5 ± 45.9 µmol gallic acid (GA) equivalent. The TPC values for PDOPA1@HNT, PDOPA3@HNT and PDOPA5@HNT coatings were found to be 405.5 ± 25.0, 750.0 ± 69.9, and 1348.3 ± 371.7 µmol GA equivalents, respectively. The Fe(II) chelation capacity of HNT was found to be 20.5% ± 1.2%, while the PDOPA1@HNT, PDOPA3@HNT and PDOPA5@HNT values were found to be 49.9 ± 6.5, 36.6 ± 12.7 and 25.4 ± 1.2%, respectively. HNT and PDOPA@HNTs inhibited the α-glucosidase (AG) enzyme to greater extents than acetylcholinesterase (AChE). As a result, the DOPA modification of HNTs was rendered to provide additional characteristics, e.g., antioxidant properties and higher AChE and AG enzymes inhibition capabilities. Therefore, PDOPA@HNTs have great potential as biomaterials.

Preparation of silver nanoparticle functionalized aramid fiber by employing dopamine and silane coupling agent modification

AbstractSilver nanoparticles functionalized poly‐p‐phenylene terephthamide (PPTA) fiber was fabricated through the electroless plating method. To facilitate the efficient deposition of silver nanoparticles, the PPTA fiber surface was modified by using dopamine and γ‐methacryloxypropyl trimethoxy silane (MPTES). Various techniques including scanning electron microscope (SEM), X‐ray photoelectron spectroscopy (XPS) and X‐ray diffraction (XRD) were used to characterize the surface morphology and chemical composition of surface modified and silver‐plated PPTA fibers. The silver‐plated PPTA fiber showed a surface resistance of 0.53 Ω over a length of 1 cm with reliable coating fastness under ultrasonic washing and high temperature treatment. Furthermore, the silver‐plated PPTA fiber exhibited antibacterial resistance against Escherichia coli and Staphylococcus aureus, as well as good electrical heating performance with surface temperature of 100.4°C at a voltage of 4.5 V.

Dopamine facilitates Al2O3 film growth on polyethylene terephthalate by low-temperature plasma-enhanced atomic layer deposition

Polymeric materials, including polyethylene terephthalate (PET), are widely used in various fields because of their beneficial properties. Functional films are deposited on these materials through different approaches, such as plasma-enhanced atomic layer deposition (PEALD), to enhance their performance and prolong their life span. However, the inert and thermally fragile nature of most polymers hinders deposition. We developed a strategy for the PEALD of nanoscale Al2O3 films on PET substrates. First, a PET substrate is subjected to alkali treatment, which gives it basic hydrophilicity for the subsequent dopamine modification. After 24 h of dopamine deposition, the substrate shows adequate active sites (phenolic hydroxyl groups), which can chemisorb large amounts of precursor during the initial deposition. The island growth mode was observed during the PEALD processes. We analyzed the detailed chemical components of Al2O3 on alkali-treated PET and dopamine-modified PET. After 100 cycles of deposition, the Al2O3 films on both samples contained much hydrogen. Benefitting from the more active sites, we observed more continuous Al2O3 film on dopamine-modified PET, which exhibited excellent water vapor blocking performance. Our findings suggest that dopamine could act as a ‘bridge’ between polymers and PEALD functional films.

Dopamine-modified chitosan hydrogel for spinal cord injury

Spinal cord injury (SCI) decreases people's both physical and psychological levels. The rehabilitation of SCI is still a clinical challenging process owing to the inflammatory environment for cell survival. Herein, we designed a dopamine-modified chitosan hydrogel to improve poor microenvironment of spinal cord injury. Dopamine modified chitosan hydrogel was fabricated by crosslinking with citric acid (CS-CA-DA), which address the insufficient mechanical properties. In vitro analysis showed that dopamine modification improved the cell survival and cell adhesion. Moreover, implantation of CS-CA-DA hydrogel alone into rat injured spinal cord helped improving cell survivals, modulating immunity, promoting macrophage polarization to the M2 phenotype and promoting axonal regeneration in vivo in brutal areas of SCI. This strategy of modified chitosan with dopamine undergoing a high mechanical properties, excellent cell compatibility and antioxidant performance, providing a new insight into repairing spinal cord injury.

Micro mechanism of latent heat enhancement of polyethylene glycol/aminated modified palygorskite composite phase change materials

Surface functional modification of clay minerals showed a positive effect on promoting phase change behavior and improving heat storage characteristic of phase change material (PCM). Currently, there was a lack of quantitative evidence to explain the micro mechanism between surface functional modification and latent heat enhancement. In this work, the dopamine-modified palygorskite/polyethylene glycol (MPP) composite PCMs were prepared and their latent heat enhanced micro mechanism was studied in depth based on density functional theory (DFT) calculations. Due to the strong surface interaction, the phase change behavior of palygorskite/polyethylene glycol composite PCMs was strongly restricted so that no latent heat was released when the content of polyethylene glycol was <50 wt%. After dopamine modification, the latent heat (> 37.63 J/g) of MPP was released when the content of polyethylene glycol was higher than 30 wt%, indicating that the surface interaction was weakened. The DFT calculation results revealed that before and after dopamine modification, the surface interaction changed from weak SiO chemical bonds to no combination approaches and the interaction energy sharply dropped from 195.25 eV to 0.40 eV, demonstrating that the surface interaction between polyethylene glycol and palygorskite was greatly reduced, which was further confirmed by the crystallization and heat storage/release results, which was responsible for the promoted phase change behavior and enhanced latent heat. Furthermore, the MPP exhibited excellent chemical compatibility and acceptable thermal stability. This work was of great significance in revealing the inner relationship between the microstructure and property enhancement of clay minerals-based composite PCMs.