Antibacterial Performance Research Articles

Tailoring of magnetite nanocomposite of carboxymethyl chitosan (CMCs) impregnated with iron (III) oxide for enhanced degradation of reactive blue 19 dye and inactivation of harmful microbes in wastewater

The study investigates the fabrication of an innovative nanocomposite composed of carboxymethyl chitosan (CMC) combined with different amounts of iron (III) oxide (Fe₂O₃) to boost dye degradation and antibacterial effectiveness. A top-down ball milling technique formed the nanocomposites and was extensively investigated for their structural, morphological, and functional features. The mean particle size of the 0.3Fe₂O₃/CMC and 0.6Fe₂O₃/CMC nanocomposites was measured at 83.74 nm and 124.5 nm, respectively, with polydispersity index (PdI) values suggesting satisfactory homogeneity. The adsorption effectiveness of Reactive Blue 19 (RB 19) dye was evaluated under different circumstances, with the 0.6Fe₂O₃/CMC nanocomposite exhibiting the maximum adsorption capacity of 140 mg/g at an ideal pH of 5. Kinetic analyses indicated that the adsorption process adhered to a pseudo-second-order kinetic model. The nanocomposites had significant bactericidal performance, with the 0.6Fe₂O₃/CMC nanocomposite exhibiting the most extensive inhibition zones, particularly against E. coli (28.4 mm) and Pseudomonas aeruginosa (23.2 mm). Furthermore, the reusability of the 0.6Fe₂O₃/CMC nanocomposite was validated by five adsorption-desorption cycles, retaining over 90 % efficiency. The results underscore the efficacy of Fe₂O₃/CMC nanocomposites as viable materials for wastewater treatment and antibacterial purposes, offering a promising approach for environmental remediation.

Cellulose Acetate-Based Wound Dressings Loaded with Bioactive Agents: Potential Scaffolds for Wound Dressing and Skin Regeneration.

Wound healing and skin regeneration are major challenges in chronic wounds. Among the types of wound dressing products currently available in the market, each wound dressing material is designed for a specific wound type. Some of these products suffer from various shortcomings, such as poor antibacterial efficacy and mechanical performance, inability to provide a moist environment, poor permeability to oxygen and capability to induce cell migration and proliferation during the wound healing process. Hydrogels and nanofibers are widely reported wound dressings that have demonstrated promising capability to overcome these shortcomings. Cellulose acetate is a semisynthetic polymer that has attracted great attention in the fabrication of hydrogels and nanofibers. Loading bioactive agents such as antibiotics, essential oils, metallic nanoparticles, plant extracts, and honey into cellulose acetate-based nanofibers and hydrogels enhanced their biological effects, including antibacterial, antioxidant, and wound healing. This review reports cellulose acetate-based hydrogels and nanofibers loaded with bioactive agents for wound dressing and skin regeneration.

Poly(vinyl alcohol)/Chitosan Hydrogel Containing Gallic Acid-Modified Fe, Cu, and Zn Metal-Organic Frameworks (MOFs): Preparation, Characterization, and Biological Applications.

Hydrogel composites are water-swollen and three-dimensional materials that have been investigated for various biological applications, including controlled drug delivery and tissue engineering, owing to the similarity between their mechanical, electrical, and chemical properties with biological tissues. The hydrogel composites can provide a superior replication of living tissue compared to their single components. In this regard, Fe-BTC, Cu-BTC, and Zn-BTC MOFs were synthesized and modified with gallic acid (GA). The MOFs-based hydrogel composites (M-BTC-GA@PVA-CS) were finally fabricated by freezing-thawing the as-synthesized MOFs, gallic acid, chitosan, and poly(vinyl alcohol) mixture. The obtained hydrogels were characterized using techniques such as FTIR, XRD, UV-vis, SEM, EDS, and TEM. Additionally, their antibacterial activity against E. coli and S. aureus and biocompatibility were investigated. The results showed that the surface modification of M-BTC MOFs with GA improves the antibacterial performance of hydrogels and increases their biocompatibility and cell viability. Among the as-prepared M-BTC MOF-based composites, the Cu-BTC MOF-loaded hydrogels showed the highest antibacterial activity. In contrast, the lowest antibacterial effect was observed for the hydrogels with Fe-BTC MOFs. Furthermore, the H&E staining exhibited improved vascularization in Zn-BTC-GA@PVA-CS and Cu-BTC-GA@PVA-CS scaffolds compared to the Fe-BTC-GA@PVA-CS hydrogel. These MOFs-loaded hydrogels may be suitable for utilization in biological applications such as skin treatment, drug delivery, and cosmetics owing to their excellent antibacterial activity and low cytotoxicity.

Ozonation combined to BAC filtration for secondary effluent treatment containing moderate concentration of heavy metals

The treatment of industrial and urban effluents is a recognized strategy for environmental preservation, which brings benefits not only to fauna and flora but also to human health. In this paper, the combination effect of ozonation (O3) and biological activated carbon (BAC) filtration treatments on the inorganic contaminants removal, disinfection, and mitigation of toxicity in secondary effluent from wastewater treatment plants (WWTP) were evaluated. Disinfection efficiency was evaluated using total coliforms and Escherichia coli inactivation, and toxicity was investigated by Eruca sativa germination, Artemia salina larvae and Daphnia similis. The O3-BAC system was efficient to remove metals, disinfect the samples and reduce toxicity. The combined treatment reduced 99.9 % of the assessed metal concentration and ≥ 96 % on samples enriched with 2x the concentration allowed by Brazilian legislation. O3-BAC also demonstrated superior bactericidal performance compared to BAC and O3 alone, exhibiting a 5-log reduction within 24 h against total coliforms and 4-log reduction in E. coli, whereas BAC and O3 achieved ≤ 3-log inactivation. Regarding toxicity, the bioassays demonstrated that the combined treatment effect improved the relative germination of E. sativa (∼97 %), and the relative root elongation showed no differences compared to the control group (∼100 %). Similar behavior was also observed in the analysis with wheat and radish seeds, with no differences noted between the treated samples and the positive control. In relation to A. salina, no toxic results were observed even at high metals concentration. Additionally, BAC treatment reduced D. similis immobilization from 97 ± 6 % to a level with no observed effect. The observed synergy suggests that the O3-BAC combination may address a variety of pollutants and improve treatment efficacy.

Recent Advances in Antibacterial Strategies Based on TiO2 Biomimetic Micro/Nano-Structured Surfaces Fabricated Using the Hydrothermal Method

Ti and its alloys, widely utilized in orthopedic and dental implants, inherently lack antibacterial properties, posing significant infection risks, especially in the context of growing antibiotic resistance. This review critically evaluates non-antibiotic antibacterial strategies, with a particular focus on surface modifications and micro/nano-structured surfaces. Micro/nano-structured surfaces, inspired by natural topographies, utilize physical mechanisms to eradicate bacteria. Despite their potential, the antibacterial efficacy of these surfaces remains insufficient for clinical application. Titanium dioxide (TiO2), known for its excellent photocatalytic antibacterial activity and biocompatibility, is emerging as an ideal candidate for enhancing micro/nano-structured surfaces. By combining the photocatalytic antibacterial effects of TiO2 with the mechanical bactericidal properties of micro/nano-structured surfaces, superior antibacterial performance can be achieved. The hydrothermal method is frequently employed to fabricate TiO2 micro/nano-structured surfaces, and this area of research continues to thrive, particularly in the development of antibacterial strategies. With demonstrated efficacy, combined antibacterial strategies based on TiO2 micro/nano-structured surfaces have become a prominent focus in current research. Consequently, the integration of physical stimulation and chemical release mechanisms may represent the future direction for TiO2 micro/nano-structured surfaces. This review aims to advance the study of TiO2 micro/nano-structured surfaces in antibacterial applications and to inspire more effective non-antibiotic antibacterial solutions.

Synthesis, Characterizationand Antibacterial Activity Studyof Para-substituted Derivatives of N -benzyl-3-methylbuten-2-enamides.

In order to deeply explorethe effect of para-substituentson the antibacterial activity ofN-benzyl-3-methylbuten-2-enamidederivatives,we elaborately synthesizedthreesuchpara-substituted derivatives(compounda: N-(4-hydroxybenzyl)-3-methylbut 2-enamide;compoundb:N-(4-isobutoxybenzyl)-3-methylbut-2-enamide;compoundc:N-(4-isopropoxybenzyl)-3-methylbut-2-enamide),of which thestructures were determined by ways of single crystal X-ray diffraction data analysis mainly. The antibacterial performance experiments showed thatcompounds a, band cwere evaluated for their antibacterial (Escherichia coli, Staphylococcus aureus,andEnterobacter aerogenes)activities.Among them, compounds a, band chavean effective antibacterial reagents forE.coliexhibiting MIC values of 0.01,0.01 and0.01g/mL, respectively, but inactive for E. aerogenes.In addition, compounds band chave better activity than compounda against S. aureuswithMIC values of 0.01 and0.02g/mL.These results provide an important basis for further study of the antibacterial properties and structure-activity relationship of these compounds, and are expected to provide valuable reference for the development of new antibacterial drugs.

Synthesis of a gallic acid-based self-healing waterborne polyurethane with a thermo-responsive dynamic phenol-carbamate network for enhanced mechanical strength, antimicrobial activity, and shape memory properties

To expedite the advancement of multifunctional next-generation smart materials, it is imperative to create polymers derived from renewable, green bio-based resources. This paper presents a direct synthesis of thermo-responsive aqueous polyurethanes by combining gallic acid (GA) with isocyanate groups to form a dynamic phenol-carbamate crosslinked network and the incorporation of the metal-organic framework Cu-MOF-2 for synergistic effects. The resulting GA-based polyurethane (MOF-GWPU) exhibits excellent thermal stability and mechanical properties, achieving an ideal balance between mechanical strength and self-healing efficiency. The MOF-GWPU film demonstrates strong antimicrobial efficacy against Escherichia coli and Staphylococcus aureus, highlighting its exceptional antibacterial performance. The thermo-responsive dynamic covalent bonds enable the MOF-GWPU film to rapidly revert from a temporary shape back to its original form. Post-processing experiments further indicate that the crosslinked GA-PU polymer can be efficiently recycled through solution casting and hot-pressing techniques. This design offers a novel approach and valuable insights for advancing the development of multifunctional smart polymers derived from bio-based resources.

Surface immobilization and properties optimization of phage hydrolase against Gram-negative bacteria

Immobilized hydrolase not only reduces the production of antibiotic-resistant bacteria, but also effectively improves the stability of hydrolase in external use. In this study, phage hydrolase LysSSE1 against Gram-negative bacteria were surface immobilized and optimized for their bactericidal activity. Different anti-pathogen surface materials were prepared, where LysSSE1 was immobilized on the glass surface with a silica-affinity peptide and into which different peptide linkers were introduced. Immobilized enzymes inserted into the natural amino acid peptide linker exhibited higher bactericidal activity, greater stability, and more consistent bactericidal performance compared to those without the peptide linker. Among these immobilized enzymes, LysSSE1-NL-SiAP1 exhibited the strongest bactericidal activity and the best repeatable bactericidal performance, which only reduced the original performance by about 5% after three bactericidal cycles. Modeling analysis suggested that the presence of peptide linker might increase the molecular flexibility of the proximal hydrolase domain to better interact with the bacterial substrate. Our surface immobilization strategy could be extended to other lytic proteins, providing support for the development of surface sterilization methods and materials.

Bimetallic FeCo metal–organic framework based cascade reaction system: Enhanced peroxidase activity for antibacterial performance

Metal-organic frameworks (MOFs), as a peroxidase (POD), can catalyze the conversion of H2O2 to reactive oxygen species (ROS) for antibacterial application. To achieve strong antibacterial activity, it is necessary to improve the enzyme-like activity of MOFs. In this study, FexCoMOF was synthesized by incorporating Co(II) to improve the electron transfer of Fe(III)/Fe(II), which enhanced its redox capacity as a nanozyme and further promoted the generation of hydroxyl radical (⋅OH), exhibiting higher POD activity. Doping with different amounts of Co(II) altered the particle size, specific surface area, and surface defects of FexCoMOF, thus exhibiting differential enzyme-like activities. Additionally, a glucose-responsive enzyme cascade reaction system based on Fe4CoMOF/glucose oxidase (GOx) was established. In the presence of glucose, the in situ-generated substrate H2O2 was in contact with the catalytic site and the generated gluconic acid enabled Fe4CoMOF to maintain maximum enzyme activity under physiological pH conditions, avoiding damage caused by the use of exogenous high concentrations of H2O2. In the in vitro antibacterial experiment, the minimum inhibitory concentration (MIC) of Fe4CoMOF/GOx was 10 μg mL−1 for Escherichia coli (E. coli) and 5 μg mL−1 for Staphylococcus aureus (S. aureus) (∼108 CFU mL−1). The increase in enzyme activity resulted in a considerable reduction in the dose of the antibacterial agent, which was conducive to improving bio-safety. The in vivo experiment in mice demonstrated that the glucose-responsive Fe4CoMOF-based cascade reaction system had excellent antibacterial properties and remarkably promoted wound healing. The antibacterial agent based on bimetallic MOF developed in this work provides a new idea for cascade catalytic antibacterial therapy and will have remarkable application prospects in biomaterials and nanomedicine.

Super protective effect, ultra-high juice absorption and long-term antibacterial of Ag-2MI@Chitosan biodegradable sponge for fruit preservation and transportation

Plastic foam packaging is often used for the transportation to avoid mechanical damage to the fruit, but it lacks antibacterial properties, water absorption and is non-degradable, leading to fruit decay and safety risks as well as serious environmental pollution. Herein, Ag-2-Methylimidazole@Chitosan (Ag-2MI@CS) was successfully synthesized by in situ synthesis at normal temperature and pressure, and improved the antibacterial performance of Ag-2MI@CS by using green solvent ethanol to adjust the solvent polarity. The results showed that the long-lasting inhibitory performance of Ag-2MI@CS was significantly improved, the long-lasting antibacterial time has been extended from 24 h to 96 h. Furthermore, Ag-2MI@CS can significantly protect fruits and reduce the damage of fruits, even when falling from a height of 60 cm or under extreme transportation conditions. Besides, Ag-2MI@CS had extremely high absorption rates of water and fruit juice, 1447.69 % and 1356.59 %, respectively, which was conducive to absorbing water generated by respiration and juice generated by damage during transportation, so as to avoid the growth of bacteria caused by water and fruit juice. Ag-2MI@CS can achieve fruit preservation in both indoor static and transportation dynamic conditions. This study offers novel insights into new biodegradable packaging material in fruit transportation.

Iron Single-Atom Nanozyme with Inflammation-Suppressing for Inhibiting Multidrug-Resistant Bacterial Infection and Facilitating Wound Healing.

Infection with drug-resistant bacteria and the formation of biofilms are the main factors contributing to wound healing insufficiency. Antibacterial agents with enzyme-like properties have exhibited considerable potential for efficient eradication of drug-resistant microorganisms due to their superior sensitivities and minimal side effects. In this work, we prepared a kind of Fe-centered single-atom nanozyme (Fe-SAzyme) with high biocompatibility and stability via a facile one-pot hydrothermal method, which was suitable for the treatment of wounds infected with drug-resistant bacteria. The Fe-SAzyme exhibited remarkable peroxidase-like catalytic activities, catalyzing the conversion of hydrogen peroxide (H2O2) to highly toxic hydroxyl radicals (•OH), which could not only damage bacterial cells but also inhibit, disrupt, and eradicate the formation of bacterial biofilms. Thus, Fe-SAzyme demonstrated a broad-spectrum antibacterial performance capable of effectively eliminating multidrug-resistant bacteria. The coexistence of ferrous (Fe2+) and ferric (Fe3+) ions in Fe-SAzyme conferred the nanozyme with anti-inflammatory activity, effectively suppressing excessive inflammation. Meanwhile, Fe-SAzyme could significantly downregulate inflammatory cytokines tumor necrosis factor-α and interleukin-1β and upregulate growth factors VEGF and epidermal growth factor, which can prevent bacterial infection, mitigate inflammation, promote fibroblast proliferation, and improve wound closure. Thus, Fe-SAzyme had shown favorable therapeutic efficiency in promoting bacteria-infected wound healing. This study provides Fe-SAzyme as a promising candidate for the development of new strategies to treat multidrug-resistant bacterial infections.

Aminosilane@mesoporoussilica/chitosan∗salicylaldehyde nanohybrid: synthesis, characterization and applications

“Hydrogen-borrowing” mechanism has enables the production of biologically active molecules with minimal waste, high efficiency and mild reaction conditions. However, majority of research on the above mechanism has been focused on small molecule transformations. Hence, using Fe-tetraphenylcyclopentadienone tricarbonyl complex as a catalyst for “hydrogen-borrowing” mechanism between amines and alcohols, a novel pH-responsive inorganic-organic hybrid nanocarrier based on mesoporous silica-chitosan (MSN@CONH2/CS∗SCA) was developed to overcome these limitations. The nanocarrier was fabricated through C-N bond formation between 1-[3-trimethoxysiliylpropyl] urea functionalized mesoporous silica and salicylaldehyde modified chitosan derivative for antibacterial, antioxidant and drug delivery application. The chemical composition of synthesized nanocarrier was characterized by FTIR, 1H NMR and XRD techniques while the thermal stability examined through TGA. The surface morphology and porosity were evaluated using BET, SEM, and TEM whereas elemental composition, particle size and surface charge were determined by EDX with mapping, PSA and Zeta-potential method respectively. The nanohybrid was loaded with quercetin and curcumin drug, with 82.68 % and 83.24 % encapsulation efficiency respectively. The controlled drug release for quercetin was observed with 76 % (pH-5.0) and 20 % (pH-7.4), while for curcumin it observed 70.36 % (pH-5.0) and 19.16 % (pH-7.4) in 72 h. The antibacterial performance of nanocarrier shows better zone of inhibition for E. coli [2.9 ± 0.2 cm(3)] as compared to B. subtilis [1.6 ± 0.3 cm(3)]. The antioxidant ability of nano-hybrid to scavenge DPPH and ABTS radicals were 53.18 % and 55.21 %, respectively. Thereafter, MTT cytotoxicity assay of nanohybrid on peripheral blood mononuclear cells) exhibited promising results for biomedical applications.

Dual metal centers within a water-stable Co/Ni bimetallic metal-triazolate framework contribute to durable photocatalysis for water treatment.

Bimetallic metal-organic frameworks (MOFs) have been studied extensively in various fields, including photocatalytic and electrocatalytic applications. The enhanced catalytic activity is typically attributed to the synergistic effect of the two metals, often without further explanation. Here, we demonstrate a CoNi-bimetallic triazolate MOF with fixed metal occupancy within the MOF's secondary building unit. Due to the difference in electronegativity and so on, the charge redistribution between the two metal centers could be responsible for the enhanced photocatalytic activity. In addition, the metal(II)-triazolate MOFs we synthesized exhibit unique metal-N coordination and a strong bond between the metal center and triazole ring. Therefore, their crystal structure and high porosity are highly retained even after exposure to humid environments for several months or stirring in water for several days. Overall, the CoNi-bimetallic triazolate MOF combines the excellent water stability and high surface area of its two monometallic counterparts. It can be further tailored to yield the highest colloidal stability during photocatalytic water treatment. As a result, the dual metal centers within the bimetallic MOF, combined with boosted colloidal stability, demonstrate the highest reactive oxygen species generation and promising antibacterial performance compared to their Ni- or Co-based counterparts. These findings shed light on the future design of robust MOF-based photocatalysts, particularly bimetallic ones.

Dipolar-hollowed α-Fe2O3@Au/Polydopamine nanospindle for photothermal-photodynamic coupling antibacterial and drug-delivery

With the prevalence of drug-resistant bacteria and the waning effects of antibiotics, nanoplatform has become an effective strategy for fighting infections. This work reports a dipolar-hollowed α-Fe2O3@Au/Polydopamine (PDA) nanospindle which possesses both photothermal-photodynamic (PTT-PDT) coupling antibacterial and drug carrying performance. Firstly, the spindle type α-Fe2O3@Au/PDA particle was prepared by a simple one-step strategy and then the dipolar-hollow structure was obtained by controlling etching the inside α-Fe2O3 core with hydrochloric acid. After further loading the photosensitizer zinc phthalocyanine (ZnPc), the dipolar-hollowed α-Fe2O3@Au/PDA-ZnPc nanospindles were obtained. Owing to the dipolar-hollowed interior, the nanospindles are also effective in carrying antitumor drug doxorubicin (DOX) and shows a good drug loading-release behavior. The dipolar-hollowed α-Fe2O3@Au/PDA nanospindles exhibits a high antibacterial performance against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) under near-infrared (NIR) and Xenon lamp irradiation. When α-Fe2O3@Au/PDA-ZnPc nanospindles concentration was increased to 100 μg/mL, the antibacterial rate was close to 100 %. In comparison to the original α-Fe2O3@Au/PDA nanospindles, the product achieved a lower effective antibacterial temperature. This triple-mode therapy (PTT/PDT/Drug) provides an interesting design idea for anisotropic therapeutic nanoplatform which can be applied in low-temperature antibacterial and drug delivery.

Double Layer SiO2-Coated Water-Stable Halide Perovskite as a Promising Antimicrobial Photocatalyst under Visible Light.

Halide perovskite nanocrystals (HPNCs) have emerged as promising materials for various light harvesting applications due to their exceptional optical and electronic properties. However, their inherent instability in water and biological fluids has limited their use as photocatalysts in the aqueous phase. In this study, we present highly water-stable SiO2-coated HPNCs as efficient photocatalysts for antimicrobial applications. The double SiO2 layer coating method confers long-term structural and optical stability to HPNCs in water, while the in situ synthesis of lead- and bismuth-based perovskite NCs into the SiO2 shell enhances their versatility and tunability. We demonstrate that the substantial generation of singlet oxygen via energy transfer from HPNCs enables efficient photoinduced antibacterial efficacy under aqueous conditions. More than 90% of Escherichia coli was inactivated under mild visible light irradiation for 6 h. The excellent photocatalytic antibacterial performance suggests that SiO2-coated HPNCs hold great potential for various aqueous phase photocatalytic applications.

Photothermal-Induced Multimodal Antibacterial Dressing Comprising N-Halamine Hydrogel Loaded with Cow Dung Biochar for Infected Wound Healing.

Disposal of the cow dung pollutants arising from cattle farming threatens the environment and public safety in diverse ways. To date, researchers have worked on developing new pathways to control and manage cattle farming wastes, but most do not involve the reuse of these wastes. Herein, a cow dung biochar-modulated photothermal N-halamine hydrogel (i.e., PAN/CA/CoBC/pMAG-Cl) was designed for converting cow dung into biochar (CoBC), which was then coupled with a 3D interpenetrating hydrogel network to treat infected wounds. The PAN/CA/CoBC/pMAG-Cl hydrogel exhibited excellent synergistic antibacterial performance against 106 CFU·mL-1 Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) within 60 min. The bactericidal effect was multimodal, involving CoBC-based photothermal killing (i.e., temperature as high as 80.5 °C) after 808 nm near-infrared light irradiation for 10 min, contact killing through the strong oxidative characteristic of N-halamine (pMAG-Cl), and release killing via active halogens (i.e., Cl+) reinforced by the photothermal action of CoBC. The S. aureus-infected wound model in vivo demonstrated that the PAN/CA/CoBC/pMAG-Cl hydrogel worked as an ideal wound dressing, capable of resisting bacterial infection, accelerating the healing process, and promoting epithelial regeneration. This proposed strategy could indicate a new way for the disposal of cow dung pollutant and its reuse in antibacterial-associated applications.

Developing high elongation of Ca-containing Zn alloys with superior osteogenic and antibacterial properties

The development of high-strength zinc (Zn) alloys significantly contributes to the field of orthopedics by enhancing their osteogenic properties. Calcium (Ca) is pivotal for bone composition; however, its incorporation into the Zn matrix often hampers elongation due to the formation of large-sized CaZn13 phases. In this study, two Zn alloys with different Ca contents were prepared, and their microstructures, mechanical properties, corrosion behavior and biocompatibility were investigated. Results indicate that the Zn alloy with high Ca content exhibits large-sized and high-volume-fraction CaZn13 phases, which do not significantly change during equal channel angular pressing (ECAP). The grain sizes of ECAPed Zn alloys decreased from 36.75 μm and 35.81 μm of as-cast state to 4.32 μm and 1.71 μm, respectively. Refined microstructures contributed to the improvement of mechanical properties of Zn alloys, which have elongation over 15 % higher than that of all Zn-Mg-Ca alloys reported so far. The high elongation of Zn alloys originates from the inhibition of the propagation of microcracks which generated from the Zn/CaZn13 interphase. Moreover, the formation of large-sized CaZn13 phases leads to the severe local corrosion through enhancing galvanic effect, finally increasing corrosion rate. During degradation, the release of metallic ions, such as Zn2+, Mg2+, and Ca2+, are beneficial to the cell viability and osteogenic properties. And the accelerated release of Zn2+ plays a role in antibacterial performance. These results are very helpful for promoting the application of biodegradable Zn alloys in the field of orthopedics.

Murexide retention and antibacterial performance of semiconductor copolymer/magnetic iron oxide hybrid nanocomposites synthesized via one pot in-situ chemical oxidative polymerization

Herein, semiconductor-magnetic hybrid nanocomposites, poly(vanillin-co-thiophene)/magnetic iron oxide (PVTO-Fe3O4), were successfully synthesized via single-step in situ chemical oxidative polymerization in the presence of different weight percentages of magnetic iron oxide nanoparticles Fe3O4 NPs (3, 6, and 9 wt%). Whereas the Fe3O4 NPs were prepared via an environmentally friendly, modified co-precipitation method, and their physicochemical characteristics were comprehensively analyzed using various analytical techniques. The adsorption behavior of the resulting samples towards murexide dye in aqueous solutions was investigated, along with their antibacterial efficacy against both gram-positive (Staphylococcus aureus and Bacillus) and gram-negative (Escherichia coli and Pseudomonas aeruginosa) bacteria. The adsorption study revealed that the nanocomposite containing 9 wt% Fe3O4 NPs achieved the highest removal efficiency for MX (approximately 87.41 %) and exhibited a maximum adsorption capacity of approximately 100.7 mg/g, surpassing many adsorbents reported in the literature. Optimization experiments identified the optimal conditions as 40 mg of adsorbent dose, 40 mL of MX solution (125 mg/L), pH 5, and 160 min contact time. The adsorption kinetics followed pseudo-second-order kinetics, and the adsorption isotherm fitted well with the Freundlich model. Moreover, the nanocomposite was efficiently recovered from the solution using an external magnet, highlighting its potential for practical applications. Antibacterial testing revealed significant antibacterial effectiveness of PVTO and its nanocomposites against both gram-positive and gram-negative bacteria, with a minimum inhibition zone of 20 mm.

Fabrication and photocatalysis of novel Z-scheme Cu2O/Cu-Ag/AgCl heterojunction possessed broad-spectrum antibacterial performance and degradation capabilities

The construction of nanostructured Z-heterostructures is a potent strategy for achieving efficient photocatalyst synthesis. Herein, a novel Cu2O/Cu-Ag/AgCl (CCAA) Z-scheme heterostructure was created via photoreduction precipitation and utilized for pollutant decomposition and microorganism inactivation. Subject to visible light (λ > 420 nm) illumination, specimen CCAA-2 demonstrated superior photodegradation competence for Congo Red (CR), achieving a degradation rate of 92.6 % within 60 min. The superior removal performance is attributed to the Z-scheme heterostructure, featuring precise interfacial contact, and the combined effect of adsorption and photocatalytic activity. Meanwhile, the optimal sample, CCAA-2, was able to achieve 100 % inactivation of Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) within 15 min under visible light. The photocatalytic performance of CCAA nanocomposites is primarily attributed to the surface plasmon resonance (SPR) effect of the noble metal Ag and the fabrication of Z-Scheme heterostructures to improve the utilization efficiency of electrons (e-) and holes (h+). Particularly, the photocatalytic mechanism was scrutinized via active substance capture experiments and electron spin resonance (ESR) analysis, uncovering that •O2ˉ and h+ served as key active constituents. Hence, this research presents a feasible approach for designing and constructing Z-Scheme heterojunctions for efficacious removal of contaminants from water.

Semi-Interpenetrating Hydrogel with Long-Term Intrinsic Antibacterial Properties Promotes Healing of Infected Wounds In Vivo.

Bacterial infections significantly deteriorate the process of wound healing. The wound dressings loaded with antimicrobials are widely used to reduce bacterial infections. However, release-based sterilization may increase the risk of drug resistance of bacteria and complicate translation. Thus, the development of long-term intrinsic antibacterial wound dressings is highly desirable. In this study, an intrinsic antibacterial hydrogel (PVA/PPG-HBPL) consisting of poly(vinyl alcohol) (PVA), poly(polyethylene glycol methyl ether methacrylate-co-glycidyl methacrylate) (PPG), and hyperbranched poly-l-lysine (HBPL) was designed and fabricated. The mechanical properties of the PVA/PPG-HBPL hydrogel were enhanced by hydrogen bonding and semi-interpenetrating networks. It also possessed a favorable ability to absorb the wound exudates. The release of antibacterial HBPL was significantly decreased by the methods of cyclic freeze-thawing and covalent cross-linking during hydrogel fabrication, enabling the PVA/PPG-HBPL hydrogel with intrinsic and long-term antibacterial performance. The PVA/PPG-HBPL hydrogel dressing killed 99.9% of methicillin-resistant Staphylococcus aureus (MRSA) cultured on its surface without observable cytotoxicity in vitro. It observably shortened the healing process by 2 orders of magnitude of MRSA colonies compared with the control in the MRSA-infected full-thickness skin wound of rats in vivo even after being soaked in phosphate-buffered saline (PBS) for 21 days (PBS was changed every 3 days). The antibacterial hydrogels could kill wound bacteria in a timely manner, significantly reduce inflammatory cell infiltration, and promote neovascularization and collagen deposition.