Sterilizing Activity Research Articles

Ketonized Carbonitride Assembled Face Mask with Long-Term Light Triggered Antimicrobial Ability for Bioprotective Applications.

The worldwide transmission of infectious respiratory pathogens has caused innumerable deaths and suffering, while wearing a face mask is still the most effective way to terminate the respiratory infections spread. However, the frequent mask replacement as a result of the lack of pathogen sterilization ability not only increases the cross-contamination risk but also, even worse, produces a large amount of medical waste. In this work, we report on a ketonized carbonitride functionalized bioprotective face mask with pathogen sterilization activity that can effectively produce biocidal singlet oxygen triggered by light irradiation. Ketonized carbonitride loading on the outer layer of the mask is found to be capable of generating singlet oxygen, enabling the mask with antibacterial ability. Thanks to its high pathogen inactivation activity, the as-prepared mask exhibits long-term light triggered health protection performance, which, in return, reduces medical waste production as a result of the decreased mask replacement frequency. The synthesis of a fascinating bioprotective mask provides a new viewpoint into the development of personal bioprotective devices for health protection.

A TBK1-independent primordial function of STING in lysosomal biogenesis

Stimulator of interferon genes (STING) is activated in many pathophysiological conditions, leading to TBK1-dependent interferon production in higher organisms. However, primordial functions of STING independent of TBK1 are poorly understood. Here, through proteomics and bioinformatics approaches, we identify lysosomal biogenesis as an unexpected function of STING. Transcription factor EB (TFEB), an evolutionarily conserved regulator of lysosomal biogenesis and host defense, is activated by STING from multiple species, including humans, mice, and frogs. STING-mediated TFEB activation is independent of TBK1, but it requires STING trafficking and its conserved proton channel. GABARAP lipidation, stimulated by the channel of STING, is key for STING-dependent TFEB activation. STING stimulates global upregulation of TFEB-target genes, mediating lysosomal biogenesis and autophagy. TFEB supports cell survival during chronic sterile STING activation, a common condition in aging and age-related diseases. These results reveal a primordial function of STING in the biogenesis of lysosomes, essential organelles in immunity and cellular stress resistance.

Antibacterial activity and mechanism of Ag2Cu2O3 mixed-metal oxide

Pure phase Ag2Cu2O3 mixed-metal oxides with homogeneous morphology of short rod-like structure were synthesized through simple co-precipitation methods. The efficacious antibacterial activities of the obtained Ag2Cu2O3 against both Gram positive and Gram negative bacteria were corroborated by the minimum inhibitory concentration (4.88 mg/L for both Escherichia coli and Staphylococcus lentus) and minimum bactericidal concentration (19.53 mg/L for E. coli and 9.76 mg/L for S. lentus). In shake flask inactivation experiments, more than 99 % of bactericidal rate was achieved for both test strains within 30 min using 250 mg/L of the Ag2Cu2O3. From the results of free radical quenching experiments and electron spin resonance spectroscopy, singlet oxygen in suspension played an important role in the sterilization of the Ag2Cu2O3, but some factors other than reactive oxygen species might also make a significant contribution. Through the simulated antibacterial experiments of the leached Cu2+ and Ag+ from Ag2Cu2O3, we found that trace Ag+ exhibits strong bactericidal ability against both strains. While, trace Cu2+ displayed a more pronounced sterilization activity against S. lentus than E. coli, which explains the higher antibacterial activity of Ag2Cu2O3 against Gram positive bacteria compared with Gram negative ones.

Sterile activation of RNA-sensing pathways in autoimmunity.

RNA-sensing pathways play a pivotal role in host defense against pathogenic infections to maintain cellular homeostasis. However, even in the absence of infection, certain endogenous self-RNAs still serve as the activators of RNA-sensing pathways. The inappropriate activation of RNA sensors by self-ligands leads to systemic inflammation and autoimmune diseases. In this review, we summarize current findings on the sterile activation of RNA sensors, as well as its implications in autoimmunity, inflammatory diseases, and therapeutics.

A Strategy of Killing Two Birds With One Stone for Blocking Drug Resistance Spread With Engineered Bdellovibrio bacteriovorus.

Drug-resistant pathogens significantly threaten human health and life. Simply killing drug-resistant pathogens cannot effectively eliminate their threat since the drug-resistant genes (DRGs) released from dead drug-resistant pathogens are difficult to eliminate and can further spread via horizontal gene transfer, leading to the spread of drug resistance. The development of antibacterial materials with sterilization and DRGs cleavage activities is highly crucial. Herein, a living system, Ce-PEA@Bdello, is fabricated with bacterial killing and DRGs cleavage activities for blocking bacterial drug resistance dissemination by engineered Bdellovibrio bacteriovorus (Bdello). Ce-PEA@Bdello is obtained by engineering Bdello with dopamine and a multinuclear cerium (IV) complex. Ce-PEA@Bdello can penetrate and eliminate kanamycin-resistant P. aeruginosa (KanR) biofilms via the synergistic effect of predatory Bdello and photothermal polydopamine under near-infrared light. Additionally, the DNase-mimicking ability of Ce-PEA@Bdello endows it with genome and plasmid DNA cleavage ability. An in vivo study reveals that Ce-PEA@Bdello can eliminate P. aeruginosa (KanR) and cleave DRGs in scald/burn infected wounds to block the spread of drug resistance and accelerate wound healing. This bioactive system constructed from natural living materials offers a promising means for blocking the spread of drug resistance.

Investigating the treatment shortening potential of a combination of bedaquiline, delamanid and moxifloxacin with and without sutezolid, in a murine tuberculosis model with confirmed drug exposures.

New and shorter regimens against multi-drug resistant tuberculosis (TB) remain urgently needed. To inform treatment duration in clinical trials, this study aimed to identify human pharmacokinetic equivalent doses, antimycobacterial and sterilizing activity of a novel regimen, containing bedaquiline, delamanid, moxifloxacin and sutezolid (BDMU), in the standard mouse model (BALB/c) of Mycobacterium tuberculosis (Mtb) infection. Treatment of mice with B25D0.6M200U200, B25D0.6M200, B25D0.6M200(U2003) or H10R10Z150E100 (isoniazid, rifampicin, pyrazinamide, ethambutol, HRZE), started 3 weeks after Mtb infection. Bactericidal activity was assessed after 1, 2, 3 and 4 months of treatment and relapse rates were assessed 3 months after completing treatment durations of 2, 3 and 4 months. B25D0.6M200U200 generated human equivalent exposures in uninfected BALB/c mice. After 1 month of treatment, a higher bactericidal activity was observed for the B25D0.6M200U200 and the B25D0.6M200 regimen compared to the standard H10R10Z150E100 regimen. Furthermore, 3 months of therapy with both BDM-based regimens resulted in negative lung cultures, whereas all H10R10Z150E100 treated mice were still culture positive. After 3 months of therapy 7% and 13% of mice relapsed receiving B25D0.6M200U200 and B25D0.6M200, respectively, compared to 40% for H10R10Z150E100 treatment showing an increased sterilizing activity of both BDM-based regimens. BDM-based regimens, with and without sutezolid, have a higher efficacy than the HRZE regimen in the BALB/c model of TB, with some improvement by adding sutezolid. By translating these results to TB patients, this novel BDMU regimen should be able to reduce treatment duration by 25% compared to HRZE therapy.

PCN-222/H3PW12O40/graphene oxide@cotton cloth with improved photocatalytic/photothermal properties for water decontamination

In this study, a novel visible-light-driven PCN-222/H3PW12O40/graphene oxide@cotton cloth (PCN-222/HPW/GO@Cot) photocatalytic platform was developed for efficient water sterilization and purification. PCN-222/HPW/GO ternary photocatalyst was prepared via one-pot solvothermal method, and anchored onto cotton cloth though catechol-amine reaction. By introducing HPW as the quasi-semiconductor co-catalyst and efficient electron trap, the photocatalytic activity of PCN-222 was boosted. Besides, the addition of GO further enhanced electron transfer capability and photothermal properties. PCN-222/HPW/GO@Cot exhibited significantly improved organic dye photodegradation and sterilization efficiencies compared to PCN-222 and PCN-222/HPW coated cotton cloths. It also maintained consistent organic dye removal efficiency over reuse cycles and retained high sterilization activity after repeated washings, indicating its remarkable durability and coating stability. The band positions and the enhanced photocatalytic/photothermal mechanisms were investigated in depth. This research suggests the great potential of PCN-222/HPW/GO@Cot photocatalytic platform for practical water purification and sterilization applications, and the potential to become multifunctional textiles.

Bactericidal and sterilizing activity of sudapyridine-clofazimine-TB47 combined with linezolid or pyrazinamide in a murine model of tuberculosis.

As an obligate aerobe, Mycobacterium tuberculosis relies on its branched electron transport chain (ETC) for energy production through oxidative phosphorylation. Regimens targeting ETC exhibit promising potential to enhance bactericidal activity against M. tuberculosis and hold the prospect of shortening treatment duration. Our previous research demonstrated that the bacteriostatic drug candidate TB47 (T) inhibited the growth of M. tuberculosis by targeting the cytochrome bc1 complex and exhibited synergistic activity with clofazimine (C). Here, we found synergistic activities between C and sudapyridine (S), a structural analog of bedaquiline (B). S has shown similar anti-tuberculosis efficacy and may share a mechanism of action with B, which inhibits ATP synthesis and the energy metabolism of bacteria. We evaluated the efficacy of SCT in combination with linezolid (L) or pyrazinamide (Z) using a well-established murine model of tuberculosis. Compared to the BPa(pretomanid)L regimen, SCT and SCTL demonstrated similar bactericidal and sterilizing activities. There was no significant difference in activity between SCT and SCTL. In contrast, SCZ and SCTZ showed much higher activities, with none of the 15 mice experiencing relapse after 2 months of treatment with either SCZ or SCTZ. However, T did not contribute to the activity of the SCZ. Our findings emphasize the efficacy and the potential clinical significance of combination therapy with ETC inhibitors. Additionally, cross-resistance exists not only between S and B but also between S/B and C. This is supported by our findings, as spontaneous S-resistant mutants exhibited mutations in Rv0678, which are associated with cross-resistance to B and C.

The Stimulation of Chemical Male Sterility for F1 Hybrid Lettuce (Lactuca Sativa Var. Longifolia) Production

Male sterility is a unique application in the production of F1 hybrid seeds of some important species. Today, while F1 hybrid lettuce varieties of abroad origin take their place in the Türkiye seed market, unfortunately, we do not have a native F1 hybrid variety. Besides, F1 hybrid seed production has become a prestige for multi-national companies regardless of the type of vegetable. Within this perspective, the effects of some chemical hybridizing agents (CHAs) such as E4FO, Ethrel and GA3 on male sterilizing activity in lettuce cultivars (Maylight352 F1, Presidential and Yedikule) were evaluated. Therefore, pollen presence in the early bud stage, seed formation and seed viability (germination) were examined. The applications had different effects on pollen presence, seed formation and seed germination, and thus male sterility. Ethrel was not effective at low doses, but at high doses, it caused flower bud deformation and growth retardation. E4FO is partially effective, but the application doses are low. Therefore, E4FO should be used at higher than 1500 ppm and 2000 ppm. GA3 applications produced the best results in stimulating male sterility, and full sterility (% 100) was achieved from 200, 250 and 300 ppm in all cultivars. As a result, 200 ppm GA3 was determined as the recommendable dose in the production of Fı hybrid lettuce.

Visible-Light-Driven Inactivation of Bacteria and H2 Generation Catalyzed by Oxygen-Vacancy-Rich One-Dimensional/Two-Dimensional W18O49/g-C3N4 Z-Scheme Heterostructures.

Z-scheme heterostructure-based photocatalysts consist of a reduction photocatalyst and an oxidation photocatalyst, enabling them to possess a high capacity for both reduction and oxidation. However, the coupling reaction between photocatalytic H2 generation through water reduction and sterilization using Z-scheme systems has been rarely reported. Herein, 1D W18O49 nanowires embedded over 2D g-C3N4 nanosheets are well-constructed as an integrated Z-scheme heterojunction. Experimental results and density functional theory calculations not only demonstrate the achievement of efficient interfacial charge separation and transport, leading to prolonged lifetime of photogenerated charge carriers, but also directly confirm the mechanism of Z-scheme charge transfer. As expected, the optimized W18O49/g-C3N4 nanostructure exhibits superior photocatalytic sterilization activity against Staphylococcus aureus as well as excellent H2 generation performance under visible-light irradiation (λ ≥ 420 nm). Due to its nontoxic nature, W18O49/g-C3N4 holds great potential in eradicating bacterial infections in living organisms.

Deregulated protein homeostasis constrains fetal hematopoietic stem cell pool expansion in Fanconi anemia

Demand-adjusted and cell type specific rates of protein synthesis represent an important safeguard for fate and function of long-term hematopoietic stem cells. Here, we identify increased protein synthesis rates in the fetal hematopoietic stem cell pool at the onset of hematopoietic failure in Fanconi Anemia, a prototypical DNA repair disorder that manifests with bone marrow failure. Mechanistically, the accumulation of misfolded proteins in Fancd2−/− fetal liver hematopoietic stem cells converges on endoplasmic reticulum stress, which in turn constrains midgestational expansion. Restoration of protein folding by the chemical chaperone tauroursodeoxycholic acid, a hydrophilic bile salt, prevents accumulation of unfolded proteins and rescues Fancd2−/− fetal liver long-term hematopoietic stem cell numbers. We find that proteostasis deregulation itself is driven by excess sterile inflammatory activity in hematopoietic and stromal cells within the fetal liver, and dampened Type I interferon signaling similarly restores fetal Fancd2−/− long-term hematopoietic stem cells to wild type-equivalent numbers. Our study reveals the origin and pathophysiological trigger that gives rise to Fanconi anemia hematopoietic stem cell pool deficits. More broadly, we show that fetal protein homeostasis serves as a physiological rheostat for hematopoietic stem cell fate and function.

Bactericidal and sterilizing activity of novel regimens combining bedaquiline or TBAJ-587 with GSK2556286 and TBA-7371 in a mouse model of tuberculosis.

The combination of bedaquiline, pretomanid, and linezolid (BPaL) has become a preferred regimen for treating multidrug- and extensively drug-resistant tuberculosis (TB). However, treatment-limiting toxicities of linezolid and reports of emerging bedaquiline and pretomanid resistance necessitate efforts to develop new short-course oral regimens. We recently found that the addition of GSK2556286 increases the bactericidal and sterilizing activity of BPa-containing regimens in a well-established BALB/c mouse model of tuberculosis. Here, we used this model to evaluate the potential of new regimens combining bedaquiline or the more potent diarylquinoline TBAJ-587 with GSK2556286 and the DprE1 inhibitor TBA-7371, all of which are currently in early-phase clinical trials. We found the combination of bedaquiline, GSK2556286, and TBA-7371 to be more active than the first-line regimen and nearly as effective as BPaL in terms of bactericidal and sterilizing activity. In addition, we found that GSK2556286 and TBA-7371 were as effective as pretomanid and the novel oxazolidinone TBI-223 when either drug pair was combined with TBAJ-587 and that the addition of GSK2556286 increased the bactericidal activity of the TBAJ-587, pretomanid, and TBI-223 combination. We conclude that GSK2556286 and TBA-7371 have the potential to replace pretomanid, an oxazolidinone, or both components, in combination with bedaquiline or TBAJ-587.

Chlorella-Loaded Antibacterial Microneedles for Microacupuncture Oxygen Therapy of Diabetic Bacterial Infected Wounds.

Hypoxia and infection are urgent clinical problems in chronic diabetic wounds. Herein, living Chlorella-loaded poly(ionic liquid)-based microneedles (PILMN-Chl) are constructed for microacupuncture oxygen and antibacterial therapy against methicillin-resistant Staphylococcus aureus (MRSA)-infected chronic diabetic wounds. The PILMN-Chl can stably and continuously produce oxygen for more than 30h due to the photosynthesis of the loaded self-supported Chlorella. By combining the barrier penetration capabilities of microneedles, the continuous and sufficient oxygen supply of Chlorella, and the sterilization activities of PIL, the PILMN-Chl can accelerate chronic diabetic wounds in vivo by topical targeted sterilization and hypoxia relief in deep parts of wounds. Thus, the self-oxygen produced microneedles modality may provide a promising and facile therapeutic strategy for treating chronic, hypoxic, and infected diabetic wounds.

Construction of Fe3O4/MoS2-O/biochar heterostructure with visible light-driven photodegradation of levofloxacin and sterilization activity: efficiency, reaction pathway, and mechanism

Construction of Fe3O4/MoS2-O/biochar heterostructure with visible light-driven photodegradation of levofloxacin and sterilization activity: efficiency, reaction pathway, and mechanism

Preparation and characterization of Fe-ZnO cellulose-based nanofiber mats with self-sterilizing photocatalytic activity to enhance antibacterial applications under visible light.

Bacterial infections and antibiotic resistance have posed a severe threat to public health in recent years. One emerging and promising approach to this issue is the photocatalytic sterilization of nanohybrids. By utilizing ZnO photocatalytic sterilization, the drawbacks of conventional antibacterial treatments can be efficiently addressed. This study examines the enhanced photocatalytic sterilizing effectiveness of Fe-doped ZnO nanoparticles (Fe-ZnO nanohybrids) incorporated into polymer membranes that are active in visible light. Using the co-precipitation procedure, Fe-ZnO nanohybrids (Fe x Zn100-x O) have been generated using a range of dopant ratios (x = 0, 3, 5, 7, and 10) and characterized. The ability to scavenge free radicals was assessed and the IC50 value was calculated using the DPPH test at different catalytic concentrations. PXRD patterns showed a hexagonal wurtzite structure, which indicated that the particle size of the nanohybrid decreased as the dopant concentration rose. It was demonstrated by UV-vis diffuse reflectance experiments that the band gap of the nanohybrid decreased (redshifted) with Fe doping. The photocatalytic activity under sunlight increased steadily to 87% after Fe was added as a dopant. The Fe 5%-ZnO nanohybrid exhibited the lowest IC50 value of 81.44 μg mL-1 compared to ZnO, indicating the highest radical scavenging activity and the best antimicrobial activity. The Fe 5%-ZnO nanohybrid, which is proven to have the best photocatalytic sterilization activity, was then incorporated into a cellulose acetate polymer membrane by electrospinning. Disc diffusion assay confirmed the highest antimicrobial activity of the Fe 5%-ZnO nanohybrid incorporated electrospun membrane against Staphylococcus aureus (ATCC 25923), Streptococcus pneumoniae (ATCC 49619), Escherichia coli (ATCC 25922), Pseudomonas aeruginosa (ATCC 27853), and Candida albicans (ATCC 10231) under visible light. As a result, Fe 5%-ZnO nanofiber membranes have the potential to be employed as self-sterilizing materials in healthcare settings.

Protein-based coating strategy for preparing durable sunlight-driven rechargeable antibacterial, super hydrophilic, and UV-resistant textiles

With the improvement of the hygiene awareness and pathogen prevention awareness of patients and medical staff, textiles with efficient and long-lasting pathogen inactivation effects are urgently needed. Photodynamic therapy (PDT) has rapidly developed into a new type of antibacterial technology due to its high antibacterial activity and has received widespread attention. However, the commonly used photosensitizers are mostly inorganic nanomaterials, which have poor adhesion to textiles and are not environmentally or human friendly. Here, we report a strategy of preparation of a sunlight-driven rechargeable antibacterial textiles based on natural antibacterial agents, which can work in light and dark conditions. The prepared BD-PTL@wool has long-lasting antibacterial properties, can rapidly produce ROS, and can store sterilization activity under light irradiation, ensuring all-day bacterial killing (>99.95 % under light irradiation and >99.80 % under dark conditions after light irradiation). BD-PTL@wool has excellent reusability, and the antibacterial rate can still above 95 % after repeated use for 5 times. In addition, BD-PTL@wool has excellent hydrophilic, UV resistance, biocompatibility and can withstand 50 washing cycles. The successful application of this strategy in textile preparation broadens the research idea for exploring the application of green photosensitive antibacterial materials in textile field.

Photothermocatalytic sterilization activity enhancement and mechanism evaluation of WO3/TpPa-1/N-Nb2CTx constructed with a 2D Z-type heterojunction WO3/TpPa-1 and 2D co-catalyst Nb2CTx

Foodborne pathogens are the main factors causing food poisoning, and it is of great significance to develop novel nanocomposites to obtain efficient and stable photothermal-assisted photocatalysts for killing foodborne pathogens. In this paper, Z-type heterojunction WO3/TpPa-1 with a core-shell structure was constructed by in-situ synthesis, and the Nb2CTx was used as a co-catalyst to obtain an efficient ternary composite WO3/TpPa-1/N-Nb2CTx. Compared to the monomers, the ternary composites improved light trapping, interfacial separation effectiveness, and the mobility of photogenerated carriers. The WO3/TpPa-1/15% N-Nb2CTx has the best sterilization efficiency of 99.69% under visible-infrared light irradiation for 30 min. The construction of WO3/TpPa-1/N-Nb2CTx promoted the separation of electron and hole pairs, which improved the electron transport efficiency and the generation of reactive oxygen species. In addition, the excellent photothermal effect of Nb2CTx improves the sterilization performance of WO3/TpPa-1/N-Nb2CTx. The WO3/TpPa-1/N-Nb2CTx has a broad application prospect in photothermal-assisted photocatalytic sterilization.

Ultraviolet-C light at 222 nm has a high disinfecting spectrum in environments contaminated by infectious pathogens, including SARS-CoV-2.

Ultraviolet light (UV) acts as a powerful disinfectant and can prevent contamination of personal hygiene from various contaminated environments. The 222-nm wavelength of UV-C has a highly effective sterilization activity and is safer than 275-nm UV-C. We investigated the irradiation efficacy of 222-nm UV-C against contaminating bacteria and viruses in liquid and fabric environments. We conducted colony-forming unit assays to determine the number of viable cells and a 50% tissue culture infectious dose assay to evaluate the virus titration. A minimum dose of 27 mJ/cm2 of 222-nm UV-C was required for >95% germicidal activity for gram-negative and -positive bacteria. A 25.1 mJ/cm2 dose could ensure >95% virucidal activity against low-pathogenic avian influenza virus and severe acute respiratory syndrome coronavirus (SARS-CoV-2). In addition, this energy dose of 222-nm UV-C effectively inactivated SARS-CoV-2 variants, Delta and Omicron. These results provide valuable information on the disinfection efficiency of 222-nm UV-C in bacterial and virus-contaminated environments and can also develop into a powerful tool for individual hygiene.

The activation of carbon materials to control airborne pathogenic bacteria in the pig house by efficient adsorption

The presence of pathogenic bacteria at high levels in the air of concentrated animal production building aggravates cross transmission and impedes the biosafety of animal husbandry. Carbon material shows great potential in microbial adsorption to reduce the misuse of chemical disinfectants in livestock and poultry houses, but the complex environmental conditions and low efficiency in gas phase pose significant challenges to its practical implementation. A novel modified method of carbon felts, acidified and then ammoniated, was developed in simulated experiments. An intensive field study in a pig house was conducted to deploy carbon felts and adsorb airborne microorganisms efficiently. They had above 90% sterilizing activity against a broad spectrum of pathogenic bacteria in the laboratory. And the highest sterilization rate was 75.52% with operation of carbon felts in the pig house and could be maintained below 3 × 104 CFU m−3 for 18 d. Specifically, the relative abundance of several major pathogenic bacteria was significantly reduced in the air of pig house. Our research activates the antibacterial activity of carbon materials in the gas phase and further provides a promising strategy to improve animal health and welfare by purifying the air in livestock and poultry houses.

Preparation of polyvinyl alcohol/chitosan nanofibrous films incorporating graphene oxide and lanthanum chloride by electrospinning method for potential photothermal and chemical synergistic antibacterial applications in wound dressings

Electrospun fibres have been widely used as skin dressings due to their unique structur. However, due to the lack of intrinsic antimicrobial activity, it is easy for the wound to become infected. Bacterial infection, which leads to chronic inflammation, severely hinders the normal process of skin regeneration. In this study, a polyvinyl alcohol/chitosan (PVA/CS) composite films with chemical sterilization and near-infrared (NIR) photothermal antibacterial activity was fabricated by electrospinning. Graphene oxide (GO), a photosensitiser, was incorporated into the films, and lanthanum chloride (Lacl3) as a chemical antibacterial agent was also doped in the electrospun films. The structure, morphology, mechanical properties, wettability, and antimicrobial and photothermal antibacterial activity of the PVA/CS-based fibre films were investigated. The results showed that the addition of Lacl3 to the PVA/CS/GO nanofibres (PVA/CS/GO-La) improved the hydrophilicity, tensile strength and resistance to elastic deformation of the nanofibres. The PVA/CS/GO-La12.5 mM sample exhibited the best antibacterial performance, showing high inhibition against Staphylococcus aureus (82% antibacterial efficacy) and Escherichia coli (99.7% antibacterial efficacy). Furthermore, the antibacterial efficacy of the films surface was further enhanced after exposure to NIR light (808 nm, 0.01 W) for 20 min. In addition, the nanofibre films showed no cytotoxicity against human skin fibroblasts (HSFs), indicating its potential application in the field of broad-spectrum antibacterial materials.