Polydopamine Research Articles

Zirconium(IV) coordination-mediated rapid and versatile post-modification of polydopamine coating as stationary phase for open-tubular capillary electrochromatography

In recent years, mussel-inspired polydopamine (PDA)-based materials have attracted significant attention in the field of open-tubular capillary electrochromatography (OT-CEC) owing to their diverse and appealing properties. However, previously established functionalized PDA coating-based CEC stationary phases predominantly relied on the latent reactivity of PDA with amine/thiol-containing molecules, limiting the types of applicable modifiers and requiring time-consuming reaction processes. Herein, we presented a versatile and efficient method for the facile and rapid fabrication of diverse functionalized PDA coatings as OT-CEC stationary phases through a Zr(IV) coordination-mediated post-modification strategy. Different kinds of modifiers, including octadecylamine (ODA), lauric acid (LA), and perfluorooctanoic acid (PFOA), were rapidly and robustly grafted onto the PDA coating, verified through multiple characterization techniques. The influences of preparation parameters on the grafting efficiency of the functionalized PDA coating were systematically investigated. Utilizing the Zr(IV)-mediated ODA-, LA- and PFOA-functionalized PDA-based OT-CEC columns, we achieved high-efficiency baseline separation of a series of neutral analytes with excellent repeatability, good stability, and long lifetime. Given the strong universality of the Zr(IV) coordination-mediated post-modification approach, our study provides an effective pathway for advancing the development of a wider range of functional PDA-based chromatographic stationary phases.

Sustained BMP-2 delivery via alginate microbeads and polydopamine-coated 3D-Printed PCL/β-TCP scaffold enhances bone regeneration in long bone segmental defects

Background/ObjectiveRepair of long bone defects remains a major challenge in clinical practice, necessitating the use of bone grafts, growth factors, and mechanical stability. Hence, a combination therapy involving a 3D-printed polycaprolactone (PCL)/β-tricalcium phosphate (β-TCP) scaffold coated with polydopamine (PDA) and alginate microbeads (AM) for sustained delivery of bone morphogenetic protein-2 (BMP-2) was investigated to treat long bone segmental defects. MethodsSeveral in vitro analyses were performed to evaluate the scaffold osteogenic effects in vitro such as PDA surface modification, namely, hydrophilicity and cell adhesion; cytotoxicity and BMP-2 release kinetics using CCK-8 assay and ELISA, respectively; osteogenic differentiation in canine adipose-derived mesenchymal stem cells (Ad-MSCs); formation of mineralized nodules using ALP staining and ARS staining; and mRNA expression of osteogenic differentiation markers using RT-qPCR. Bone regeneration in femoral bone defects was evaluated in vivo using a rabbit femoral segmental bone defect model by performing radiography, micro-computed tomography, and histological observation (hematoxylin and eosin and Masson's trichrome staining). ResultsThe PDA-coated 3D-printed scaffold demonstrated increased hydrophilicity, cell adhesion, and cell proliferation compared with that of the control. BMP-2 release kinetics assessment showed that BMP-2 AM showed a reduced initial burst and continuous release for 28 days. In vitro co-culture with canine Ad-MSCs showed an increase in mineralization and mRNA expression of osteogenic markers in the BMP-2 AM group compared with that of the BMP-2-adsorbed scaffold group. In vivo bone regeneration evaluation 12 weeks after surgery showed that the BMP-2 AM/PDA group exhibited the highest bone volume in the scaffold, followed by the BMP-2/PDA group. High cortical bone connectivity was observed in the PDA-coated scaffold groups. ConclusionThese findings suggest that the combined use of PDA-coated 3D-printed bone scaffolds and BMP-2 AM can successfully induce bone regeneration even in load-bearing bone segmental defects. The translational potential of this articleA 3D-printed PCL/β-TCP scaffold was fabricated to mimic the cortical bone of the femur. Along with the application of PDA surface modification and sustained BMP-2 release via AM, the developed scaffold could provide suitable osteoconduction, osteoinduction, and osteogenesis in both in vitro settings and in vivo rabbit femoral segmental bone defect models. Therefore, our findings suggest a promising therapeutic option for treating challenging long bone segmental defects, with potential for future clinical application.

A small-period long-period fiber grating biosensor based on immobilization of concanavalin A on polydopamine nanospheres for simultaneous detection of D-glucose and temperature

The accurate and sensitive monitoring of glucose levels plays a crucial role in diagnosing diabetes in clinical settings. In this work, a novel small-period long-period fiber grating (SP-LPG) biosensor was first developed for D-glucose detection based on the immobilization of concanavalin A (Con A) on polydopamine (PDA) nanospheres. SP-LPG was fabricated by using femtosecond laser direct writing technology and the obtained grating region was only 2.4 mm. The recognition element of D-glucose, Con A, was attached to the surface of PDA nanospheres. Due to the high specific surface area of PDA nanospheres, a large number of binding sites were available for Con A. The as-prepared sensor showed selective and sensitive to D-glucose measurement in the range of 10 nM to 10 mM and a low detection limit of 1.95 nM (S/N = 3) was achieved. Moreover, the small grating period of SP-LPG allows for the observation of Bragg reflection, which can be utilized for temperature sensing. This property eliminates the issue of temperature cross-sensitivity present in refractive index sensing. And the sensor exhibited a thermal sensitivity of 10 pm/°C within the range of 30 ∼ 100 °C. The developed sensor offers a convenient and efficient platform of simultaneously measuring multiple parameters, including target molecules and temperature, for real-time medical monitoring applications.

Enhancing separation performance of thin film nanocomposite membranes by self-etching of polydopamine-modified calcium carbonate during interfacial polymerization process

The acid-accepting and gas-generating properties, along with the formation of extensive nanovoids, make CaCO3 nanoparticles attractive as sacrificial nanofillers for fabricating thin-film composite (TFN) nanofiltration membranes. However, challenges such as severe agglomeration and limited acid etching efficiency of the nanoparticles hinder the pursuit of superior membrane performance. In this study, the dispersion and compatibility of CaCO3 nanoparticles within the membrane matrix were improved by modifying them with a polydopamine (PDA) coating. The abundant phenolic hydroxyl groups of PDA enhanced the hydrophilicity and negative charges of membrane surface. Additionally, the PDA capsule increased the etching extent of the CaCO3 nanoparticles by improving the nanoparticle dispersion and generating additional acid, which created sufficient water channels within the polyamide layer. It was demonstrated that incorporating 45 μg/cm2 of PDA-modified CaCO3 nanoparticles doubled the water permeance to 16.7 LMH/bar, while maintaining a low molecular weight cut-off of 249 Da and achieving rejections over 90% for five types of per- and polyfluorinated substances. The PDA modification also overcame the membrane stability issue caused by the agglomerated CaCO3 nanoparticles. This study provides a novel strategy for applying properly modified self-etching nanofillers in TFN membrane development, showing great potential for water treatment applications.

Preparation of spherical HMX@PDA-based PBX by co-axial droplet microfluidic technology: Enhancing the interfacial effect and safety performance of composite microspheres

Surface engineering plays a crucial role in improving the performance of high energy materials, and polydopamine (PDA) is widely used in the field of energetic materials for surface modification and functionalization. In order to obtain high-quality HMX@PDA-based PBX explosives with high sphericity and a narrow particle size distribution, composite microspheres were prepared using co-axial droplet microfluidic technology. The formation mechanism, thermal behavior, mechanical sensitivity, electrostatic spark sensitivity, compressive strength, and combustion performance of the microspheres were investigated. The results show that PDA can effectively enhance the interfacial interaction between the explosive particles and the binder under the synergistic effect of chemical bonds and the physical "mechanical interlocking" structure. Interface reinforcement causes the thermal decomposition temperature of the sample microspheres to move to a higher temperature, with the sensitivity to impact, friction, and electrostatic sparks (for S-1) increasing by 12.5%, 31.3%, and 81.5% respectively, and the compressive strength also increased by 30.7%, effectively enhancing the safety performance of the microspheres. Therefore, this study provides an effective and universal strategy for preparing high-quality functional explosives, and also provides some reference for the safe use of energetic materials in practical applications.

A multifunctional electronic dressing with textile-like structure for wound pressure monitoring and treatment

In the treatment of infected wounds in bedridden or lying chair patients with mobility problems, improper wound care can lead to wound deterioration, prolong disease pain, increase treatment and care costs, and bring heavier psychological, physical, and economic burdens to patients. In the process of wound recovery, patients with mobility problems mainly face the comprehensive problems of poor air permeability, wound pressure could not be monitored, wound infection and slow healing. Therefore, in the process of wound care for such patients, it is imperative to develop a gas permeable dressing that can monitor the patient’s wound compression status in real time and promote wound healing. Here, we developed a textile-shaped gel dressing with pressure-responsive properties. Polydopamine (PDA)-silver coated calcium phosphate nanoparticles (CPNPs）and vascular endothelial growth factor (VEGF) were introduced into the gel to give the gel good antibacterial and therapeutic effects, while enhancing the pressure resistance of the gel to meet the needs of wound pressure monitoring. The textured gel morphology greatly improves the gas permeability of the gel and further improves the pressure sensitivity of the gel. This multifunctional textile-like gel dressing provides a new strategy for the development of treatment monitoring integrated dressing and has broad application prospects.

Highly stable scalable production of porous graphene-polydopamine nanocomposites for drug molecule sensing

As atenolol overdosing can lead to severe health complications, the rapid detection of atenolol intake in point-of-care settings is highly desirable. The recent advancement of redox analytical methodologies has facilitated the efficacious quantification of these compounds for drug analysis, but their performance still presents challenges in practical applications. This study addresses these challenges by controlling the electropolymerization of polydopamine (PDA) on highly porous laser-induced graphene (LIG) electrodes with enhanced electrochemical redox activity for the detection of drug molecules such as atenolol, with minimized interference with the other active substances to induce variation of electrochemical behavior. The enhanced sensitivity of atenolol is attributed to the superhydrophilicity and increased number of active surface sites and -NH2 groups in the PDA polymer through a controlled polymerization process. Moreover, the simulation results further reveal that highly sensitive sensing of atenolol molecules relies on optimal adsorption of the atenolol molecule on dopamine or dopaminequinone structural units. The resulting sensors with high repeatability and reproducibility can achieve a low detection limit of 80 μM and a sensitivity of 0.020 ± 0.04 μA/μM within a linear range from 100 to 800 μM. The materials and surface chemistry in the electrode design based on highly porous LIG provide insights into the integration and application of future scalable and cost-effective electrochemical sensors for use in point-of-care or in-field applications.

Tribological properties of oil impregnated carbon nanocapsules modified with polydopamine-polyethyleneimine

Self-lubricating microcapsules can reduce the coefficient of friction/wear and improve the tribological properties of polymer composites. Impregnation of prefabricated shell with core substances is a versatile and applicable route to obtain the microcapsules. In this work, double shell nanocapsules (PA@C HSM) with particle size of 448nm, shell thickness of 65nm are obtained by incorporating paraffin wax (PA) into the pre-synthesized hollow carbon nanospheres (PHCs)and then packaged by co-depositing with polydopamine (PDA) and polyethylenimine (PEI). The PDA/PEI transition shell increase the surface roughness of the nanocapsule and enhance the compatibility with the polymer matrix which will contribute to the improved oil storage ability and thermal stability of the nanocapsules as well. The distinguished mechanical interlocking and chemical interface bonding between PDA/PEI layer and EP matrix effectively facilitates mitigating the unfavorable impact of PA@C HSM on the mechanical properties of the composite with the modulus of the 7.5wt.% PA@C HSM/EP composites increased by 17.44%. As for the tribological performance of PA@C HSM/EP composite, the tribological properties are boosted remarkably and the friction coefficient and wear rate of 7.5%PA@C HSM/EP composite are reduced by 77.69% and 98.79% compared with pure EP material.

A novel TFNi pervaporation membrane with g-C3N4 quantum dots for high-efficiency IPA dehydration

Pervaporation (PV) shows significant potential for the highly selective isopropanol (IPA). The pursuit of developing PV membranes with outstanding separation effect and enduring high purity permeation is an indispensable goal. Based on polyamide (PA) separation layers, a polydopamine (PDA) mixed g-C3N4 quantum dots (gCNQDs) coating as the interlayer was deposited onto a porous ceramic hollow fiber substrate to fabricate thin-film nanocomposite membranes with an interlayer (TFNi). The nanocomposite interlayer enabled the formation of a smoother and highly separated selective polyamide layer. The separation factor exhibited a 31-fold enhancement with the augmentation of the blending fraction of gCNQDs during the PDA coating process. The resulting TFNi membrane attained an exceedingly high separation factor of 10270 ± 90 with a permeate water concentration of 99.9% and demonstrated a satisfactory flux of 1.40 ± 0.08 kg⋅m-2⋅h-1 during the PV process of 90 wt% IPA dehydration at 60 °C. This study presents a fresh perspective on the implementation of nanocomposite interlayers, which is expected to expand the application of high-performance TFNi membranes in PV dehydration processes.

Persistent luminescent nanoparticles with enhanced afterglow through polydopamine modification for separation-free and visual detection of iron ions in water

Fluorescence analysis is one of the most popular methods in metal ions detection, but the background interference is an unavoidable obstacle in the fluorescence analysis of complex samples. In this work, a persistent luminescence nanoprobe was designed to detect iron ions in real samples by avoiding background interference. First, the Sr4Al14O25:Eu2+, Dy3+ persistent luminescent nanoparticles (PLNPs) were prepared by solid-state reaction protocols and polydopamine (PDA) encapsulation. After modification, these PLNPs@PDA showed better afterglow performance. More importantly, the PLNPs@PDA are highly selective toward iron ions, and could serve as an afterglow “turn off” nanoprobe for selective detection of iron ions through a dynamic quenching mechanism, with a detection limit of 2.86 μM. To further realize rapid and on-site detection, a test strip based on PLNPs@PDA was prepared and applied, which also showed good detection performance in real water samples. Compared with other detection methods, this afterglow imaging detection does not depend on expensive instruments, and can effectively shield the interference of background fluorescence from complex water samples, which has a good application prospects in the actual water sample. This work opens a new avenue for developing afterglow probe for the detection of metal ion in water samples without background interference.

Photothermally reinforced chemodynamic therapy in the treatment of osteosarcoma by polydopamine-modified, copper peroxide loaded ZIF8 nanoparticles

Chemodynamic therapy (CDT) has played an important role in osteosarcoma (OS) treatment. However, the insufficient content of endogenous H2O2 and high expression of glutathione (GSH) in tumor tissues limit the antitumor efficacy of CDT. In this work, we developed polydopamine (PDA) coated and CuO2 NPs loaded ZIF8 nanoparticles (CuO2@ZIF8@PDA NPs) for thermally reinforced CDT treatment of OS. The CuO2@ZIF8@PDA NPs exhibited excellent stability in neutral solutions while degraded in weakly acidic environments to generate hydrogen peroxide (H2O2) and Cu2+. Cu2+ consumes GSH in tumor tissues to generate Cu+. Both Cu2+ and Cu+ catalyzed the decomposition of H2O2, triggering a Fenton-like reaction to produce hydroxyl radicals (•OH). The PDA coating endowed the nanosystem with photothermal conversion capabilities under near-infrared laser irradiation, further promoting the generation of •OH, and inducing tumor cell death. In vitro experiments demonstrated that CuO2@ZIF8@PDA NPs exhibited significant toxicity towards K7M2 cells while remaining non-toxic to normal cells. In vivo studies revealed that under 808 nm laser irradiation, CuO2@ZIF8@PDA NPs exhibited stronger killing ability against K7M2 cells than CuO2@ZIF8@PDA NPs alone. This system, which combines GSH depletion, intratumoral H2O2 self-generation, and photothermally enhanced CDT, holds great promise for playing a pivotal role in the treatment of osteosarcoma.

Construction and biocompatibility evaluation of CS-FA/VA composite coating on the surface of ZE21B vascular stent

Magnesium alloys have become the focus of attention as a new generation of vascular stent materials due to their excellent mechanical properties and degradability. However, their rapid degradation rate and poor surface endothelialization performance have become key factors limiting their clinical application. In this study, the Mg-Zn-Y-Nd (ZE21B) surface was modified with the magnesium fluoride (MgF2) corrosion-resistant layer, and the polydopamine (PDA) layer was used to immobilize the chitosan (CS)-ferulic acid (FA)/vanillic acid (VA) bioactive composite coating. The results of the electrochemical and hydrogen evolution experiments showed that the corrosion current density and hydrogen release of the modified ZE21B alloy significantly decreased, and its corrosion resistance was enhanced; the results of the hemolysis rate and whole blood experiments showed that the adhesion of blood components such as white blood cells and platelets on the surface of the modified ZE21B alloy significantly decreased, improving the blood compatibility of the magnesium alloy; the results of in vitro cell experiments showed that the modified ZE21B alloy effectively promoted endothelial cell (ECs) adhesion and proliferation, and inhibited smooth muscle cell (SMCs) pathological proliferation. These enhancements suggest that the CS-FA/VA coating significantly improves both the corrosion resistance and biological compatibility of the ZE21B alloy.

Synchronized long-term delivery of growth hormone and insulin-like growth factor 1 through poly (lactic-co-glycolic acid) nanoparticles on polycaprolactone scaffolds for enhanced osteochondral regeneration

The regeneration of osteochondral defects is challenging due to the complex structure of the osteochondral unit. This study aimed to develop a biomimetic scaffold by loading growth hormone (GH) and insulin-like growth factor-1 (IGF-1) into poly (lactic-co-glycolic acid) (PLGA) nanoparticles and incorporating them into polycaprolactone (PCL) scaffolds to promote synchronized osteochondral regeneration. The nanoparticles were successfully immobilized onto PCL scaffolds pre-modified with polydopamine (PDA) to enhance cell adhesion and proliferation. The scaffolds exhibited a sustained release of GH and IGF-1 over 30 days. In vitro studies using rabbit adipose-derived stem cells (ADSCs) showed that the GH/IGF-1 nanoparticle-loaded scaffolds (PCL/PDA/M-PLGA) significantly promoted cell proliferation, chondrogenic differentiation, and osteogenic differentiation compared to control PCL/PDA scaffolds. In vivo experiments using a rabbit osteochondral defect model revealed that the PCL/PDA/M-PLGA scaffolds facilitated superior osteochondral regeneration, evidenced by increased subchondral bone formation and cartilage matrix deposition. Overall, this study demonstrates the potential of GH/IGF-1 nanoparticle-loaded PCL scaffolds for synchronized osteochondral regeneration and provides a promising strategy for treating osteochondral defects.

Biocompatible chitin-based Janus hydrogel membranes for periodontal repair

Periodontal defects caused by severe periodontitis are a widespread issue globally. Guided tissue regeneration (GTR) using barrier membranes for alveolar bone repair is a common clinical treatment. However, most commercially available collagen barrier membranes are expensive and lack the antibacterial properties essential for effective bone regeneration. Herein, we report a natural polysaccharide chitin hydrogel barrier membrane with a Janus structure (ChT-PDA-p-HAP), featuring high antibacterial and protein-repelling activity on the outer side and good osteogenesis ability on the inner side. This multifunctional membrane is fabricated though a three-step process: (i) dissolution and regeneration of chitin, (ii) co-deposition with polydopamine (PDA) and poly(sulfobetaine methacrylate) (pSBMA), and (iii) coating with gelatin-hydroxyapatite (gelatin-HAP). In vitro cell experiments demonstrated the membrane's high biocompatibility and significant osteogenic activity. In vivo implantation in rats with periodontal defects revealed that the cemento-enamel junction index of the ChT-PDA-p-HAP membrane (1.165 mm) was superior to that of the commercial Bio-Gide® membrane (1.350 mm). This work presents a method for fabricating a chitin-based Janus barrier membrane, potentially expanding the use of chitin in tissue engineering. Statement of significanceThis study introduces a Janus hydrogel membrane based on chitin, tailored for guided tissue regeneration in periodontal defects. By combining antibacterial properties and osteogenic capabilities in a single membrane, the ChT-PDA-p-HAP membrane represents a significant advancement over traditional collagen barriers. Its outer surface, enhanced by Cu2+ and PDA-pSBMA coatings, resists bacterial colonization and protein adhesion effectively, while the inner side, coated with gelatin-HAP, promotes robust bone formation. In vitro experiments demonstrate high biocompatibility and substantial osteogenic differentiation, while in vivo testing in rat models confirms good therapeutic efficacy compared to commercial membranes. This multifunctional approach not only utilizes chitin's abundant natural resource but also integrates simple coating techniques to enhance therapeutic outcomes in periodontal tissue engineering, offering promising avenues for broader biomedical applications.

Bio-inspired fabrication of Ag-ZnO nanoparticle decorated Nylon 11 nanofibers: Multifunctional membrane for environmental remediation

Traditional wastewater treatment methods using nanoparticles encounter challenges with catalyst recovery. In this study, we fabricated a Nylon 11 nanofibrous membrane (NFM) via electrospinning and functionalized it with polydopamine to immobilize Ag-ZnO nanoparticles for photocatalytic degradation of organic pollutants. The Nylon 11 NFM was treated with a dopamine tris buffer solution for polydopamine (PDA) coating, which facilitated mussel-inspired attachment of the ZnO nanoparticles. These nanoparticles served as a nucleation site for the biomimetic nucleation of Ag-ZnONPs during the hydrothermal process. The synthesized composite membrane was characterized by various microscopic and spectroscopic techniques. The water contact angle decreased from 135° (Nylon 11 NFM) to 41° (PDA/Nylon 11 NFM) and the filtration efficiency improved 10 folds (from 15.92 Lm-2 hr-1 to 170.60 Lm-2hr-1) at ambient conditions. The Ag-ZnO/PDA/Nylon 11 NFM showed strong antimicrobial activity against different bacterial strains and excellent photocatalytic degradation for methyl orange with a rate constant of 0.0431 min-1, significantly surpassing other configurations. The membrane exhibited excellent stability, reusability and consistent photocatalytic efficiency over multiple cycles. It is easily recoverable from the reaction mixture, and suitable for repeated use, making it a promising candidate for environmental remediation due to its antibacterial properties, photocatalytic activity, enhanced filtration efficiency, and reusability.

Coral-like AgNPs hybrided MOFs modulated with biopolymer polydopamine for synergistic antibacterial and biofilm eradication

Bacterial contamination is an intractable challenge in food safety, environments and biomedicine fields, and places a heavy burden on society. Polydopamine (PDA), a high molecular biopolymer, is considered as a promising candidate to participate in the design of novel antibacterial agents with unique contributions in biocompatibility, adherence, photothermal and metal coordination ability. In this study, coral-like ZIFL-PDA@AgNPs with excellent antibacterial properties and biocompatibility were prepared by embedding AgNPs into the biopolymer PDA-modulated ZIFL-PDA nanostructures by green reduction method to solve the problem with poor stability of AgNPs. Based on the plasma resonance effect of AgNPs, coral-like ZIFL-PDA@AgNPs had enhanced photothermal properties compared with ZIFL-PDA. Due to the synergistic effect between antibacterial metal ions mainly Ag+ and the photothermal effect, coral-like ZIFL-PDA@AgNPs showed enhanced anti-mature biofilm and antibacterial properties, which was dependent on its concentration and sterilization time. In addition, regulated by the ZIFL-PDA nanostructure, coral-like ZIFL-PDA@AgNPs demonstrated a unique Ag+ long-time sustained release behavior, giving it an extended antibacterial validity period and good biocompatibility. Antibacterial mechanism experiments indicated that coral-like ZIFL-PDA@AgNPs can significantly damage the integrity of bacterial cell membrane, reduce the content of ATP in bacterial by affecting the activity of succinate dehydrogenase, and induce the accumulation of reactive oxygen species, ultimately leading to bacterial death.

Anti-pyroptosis biomimetic nanoplatform loading puerarin for myocardial infarction repair: From drug discovery to drug delivery

Pyroptosis is a critical pathological mechanism implicated in myocardial damage following myocardial infarction (MI), and the crosstalk between macrophages and pyroptotic cardiomyocytes presents a formidable challenge for anti-pyroptosis therapies of MI. However, as single-target pyroptosis inhibitors frequently fail to address this crosstalk, the efficacy of anti-pyroptosis treatment post-MI remains inadequate. Therefore, the exploration of more potent anti-pyroptosis approaches is imperative for improving outcomes in MI treatment, particularly in addressing the crosstalk between macrophages and pyroptotic cardiomyocytes. Here, in response to this crosstalk, we engineered an anti-pyroptosis biomimetic nanoplatform (NM@PDA@PU), employing polydopamine (PDA) nanoparticles enveloped with neutrophil membrane (NM) for targeted delivery of puerarin (PU). Notably, network pharmacology is deployed to discern the most efficacious anti-pyroptosis drug (puerarin) among the 7 primary active monomers of TCM formulations widely applied in clinical practice and reveal the effect of puerarin on the crosstalk. Additionally, targeted delivery of puerarin could disrupt the malignant crosstalk between macrophages and pyroptotic cardiomyocytes, and enhance the effect of anti-pyroptosis by not only directly inhibiting cardiomyocytes pyroptosis through NLRP3-CASP1-IL-1β/IL-18 signal pathway, but reshaping the inflammatory microenvironment by reprogramming macrophages to anti-inflammatory M2 subtype. Overall, NM@PDA@PU could enhance anti-pyroptosis effect by disrupting the crosstalk between M1 macrophages and pyroptotic cardiomyocytes to protect cardiomyocytes, ameliorate cardiac function and improve ventricular remodeling, which providing new insights for the efficient treatment of MI.

Biomimetic Nanomodulators With Synergism of Photothermal Therapy and Vessel Normalization for Boosting Potent Anticancer Immunity.

Combination therapy using photothermal therapy (PTT) and immunotherapy is one of the most promising approaches for eliciting host immune responses to ablate tumors. However, its therapeutic efficacy is limited due to inefficient immune cell infiltration and cellular immune responses. In this study, a biomimetic immunostimulatory nanomodulator, Tm@PDA-GA (4T1 membrane@polydopamine-gambogic acid), with homologous targeting is developed. The 4T1 membrane (Tm) coating reduced immunogenicity and facilitated uptake of Tm@PDA-GA by tumor cells. Polydopamine (PDA) as a drug carrier can induce PTT under near-infrared ray (NIR) irradiation and immunogenic cell death (ICD) to activate dendritic cells (DCs). Moreover, Tm@PDA-GA on-demand released gambogic acid (GA) in an acidic tumor microenvironment, inhibiting the expression of heat shock proteins (HSPs) for synergetic chemo-photothermal anti-tumor activity and increasing the ICD of 4T1 cells. More importantly, GA can normalize the vessels via HIF-1α and VEGF inhibition to enhance immune infiltration and alleviate hypoxia stress. Thus, Tm@PDA-GA induced ICD, activated DCs, stimulated cytotoxic T cells, and suppressed Tregs. Moreover, Tm@PDA-GA is combined with anti-PD-L1 to further augment the tumor immune response and effectively suppress tumor growth and lung metastasis. In conclusion, biomaterial-mediated PTT combined with vessel normalization is a promising strategy for effective immunotherapy of triple-negative breast cancer (TNBC).

Robust photothermal anti/de-icing hydrophobic coating based on polydopamine (PDA) composition

The hydrophobic soft coating has low ice adhesion strength and hydrophobic stability in low-temperature and high-humidity environments, which is crucial for preventing ice formation on infrastructure and transportation systems. However, creating mechanically durable hydrophobic soft coatings using simple methods remains challenging. In this study, a high-hardness particle-toughened, self-stratifying organic layer with high photothermal conversion rate was developed to enhance coating durability and ice-repellent performance. By optimizing the ratio of dopamine (DA) and sodium alginate (SA), a hydrophobic photothermal agent (DPSn) with high hardness and a significant light-heat effect was synthesized. A durable, hydrophobic photothermal anti-ice coating (AR/20 %PDMS/x%DPS1) with varying DPS1 amounts was successfully created using a straightforward one-step spray method, utilizing the self-stratification characteristics of acrylic resin (AR) and polydimethylsiloxane (PDMS), along with the toughening effect of DPSn. The fiber cross-linked structure of DPS1 achieved a photothermal conversion rate of 87.5 %. Adding 4 wt% DPS1 increased the surface temperature of the AR/20 %PDMS coating to 96.5 ± 2.4 °C and boosted the coating’s adhesion strength from 6.70 ± 0.3 MPa to 7.23 ± 0.7 MPa. The AR/20 %PDMS/4%DPS1 coating demonstrated excellent anti-/de-icing performance after 60 friction cycles, 60 icing/de-icing cycles, and 132 h of acid-base immersion. Its simple preparation process and durable ice-repellent properties make it highly suitable for practical applications in photothermal hydrophobic soft coatings.

Polydopamine modified carbon fiber to improve the comprehensive properties of carbon paper for proton exchange membrane fuel cell

In this study, polydopamine (PDA) was used to modify functional groups on the surface of carbon fiber (CF), and the effects of different dopamine hydrochloride (DPH) concentrations on the surface morphology, functional groups, contact angle and dispersion stability of CF were studied. Subsequently, the raw carbon paper (RCP), hot-pressed carbon paper (HPCP) and carbon paper (CP) were prepared successively using the modified CF through wet forming, impregnation/hot-pressing, and carbonization methods. The surface morphology, tensile strength, flexural strength, electrical resistivity, air permeability and pore size distribution were analyzed for these materials. It was observed that the introduction of −OH and − NH2 groups improved the hydrophilicity and dispersion of PDA modified CFs, resulting in an increase in formation index (FI) from 39.2 to 48.1 for RCP samples. With increasing DPH concentration, the tensile strength of CP initially increased but then decreased while its electrical resistivity showed an opposite trend. Finally, PDA modified CP was assembled into proton exchange membrane fuel cells (PEMFC). The PEMFC assembled from DPH-CP-2.5 achieved a maximum limiting current density of 1440.0 mA/cm2 and power density of 458.25 mW/cm2. Meanwhile, the lower material transmission impedance for DPH-CP-2.5 as well as excellent water management ability and gas transmission performance.