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MXenes are gaining popularity in biomedicine, energy storage, electronics, and environmental applications. When combined with electrospun polymers, their simple and large‐scale manufacturing potential makes them ideal for obtaining multifunctional, photothermally active hybrid nanofibers. Here, a combination of biodegradable and biocompatible polymers, poly(L‐lactide‐co‐ε‐caprolactone) (PLCL) and polyethylene glycol (PEG), was used to fabricate nanofibers loaded with MXenes. Various weight ratios of MXene were incorporated into nanofibers, and the photothermal response of the resulting hybrid materials was studied using a low‐power NIR‐LED light source. Additionally, physicochemical properties of the nanofibers were studied to identify their fundamental properties, such as morphology, thermal, and surface characteristics. The incorporation of MXene enabled the nanofibers to function as highly efficient photothermal receptive materials. A direct correlation between photothermal activity and MXene concentration was observed. Significant photothermal activity, with a temperature difference of up to 20°C in heating performance, was demonstrated for nanofibers containing 10% of MXenes. The photothermal stability, demonstrated through multiple irradiation cycles, makes it an attractive, low‐cost, and low‐energy platform for biomedical purposes such as photothermal therapy. Biocompatible, photothermally active nanofibers were fabricated by electrospinning of Ti3C2Tx‐MXene with poly(L‐lactide‐co‐ε‐caprolactone) and polyethylene glycol. Photothermal heating can be activated by a low‐power NIR‐LED and tuned by varying the amount of incorporated MXene. Temperature increases of up to 20°C within 3 min were observed. Fast response times and fiber stability were achieved over consecutive on/off irradiation cycles.

This study investigates the impact of hydroxyapatite (HA) nanoparticles (NPs) on the cellular responses of poly(L-lactide-co-ε-caprolactone) (PLCL) scaffolds in bone tissue engineering applications. Three types of PLCL scaffolds were fabricated, varying in HANPs content. Saos-2 osteoblast-like cells (OBs) and THP-1-derived osteoclast-like cells (OCs) were co-cultured on the scaffolds, and cell proliferation was assessed using the MTS assay. The amount of double-stranded DNA (dsDNA) was quantified to evaluate cell proliferation. Expression levels of OBs and OCs markers were analyzed via quantitative polymerase chain reaction (qPCR) and the production of Collagen type I was visualized using confocal microscopy. Additionally, enzymatic activity of alkaline phosphatase (ALP) and tartrate-resistant acid phosphatase (TRAP or ACP5) was measured to assess OB and OC function, respectively. Interestingly, despite the scaffold’s structured character supporting the growth of the Saos-2 OBs and THP-1-derived OCs coculture, the incorporation of HANPs did not significantly enhance cellular responses compared to scaffolds without HANPs, except for collagen type I production. These findings suggest the need for further investigation into the potential benefits of HANPs in bone tissue engineering applications. Nevertheless, our study contributes valuable insights into optimizing biomaterial design for bone tissue regeneration, with implications for drug screening and material testing protocols.

Electrospun hybrid nanofibers, based on functional agents immobilized in polymeric matrix, possess a unique combination of collective properties. These are beneficial for a wide range of applications, which include theranostics, filtration, catalysis, and tissue engineering, among others. The combination of functional agents in a nanofiber matrix offer accessibility to multifunctional nanocompartments with significantly improved mechanical, electrical, and chemical properties, along with better biocompatibility and biodegradability. This review summarizes recent work performed for the fabrication, characterization, and optimization of different hybrid nanofibers containing varieties of functional agents, such as laser ablated inorganic nanoparticles (NPs), which include, for instance, gold nanoparticles (Au NPs) and titanium nitride nanoparticles (TiNPs), perovskites, drugs, growth factors, and smart, inorganic polymers. Biocompatible and biodegradable polymers such as chitosan, cellulose, and polycaprolactone are very promising macromolecules as a nanofiber matrix for immobilizing such functional agents. The assimilation of such polymeric matrices with functional agents that possess wide varieties of characteristics require a modified approach towards electrospinning techniques such as coelectrospinning and template spinning. Additional focus within this review is devoted to the state of the art for the implementations of these approaches as viable options for the achievement of multifunctional hybrid nanofibers. Finally, recent advances and challenges, in particular, mass fabrication and prospects of hybrid nanofibers for tissue engineering and biomedical applications have been summarized.

A versatile, straightforward approach for direct fabrication of three‐dimensional (3D) nanofibrous sponges via electrospinning is reported. The fabrication of porous 3D nanofibrous sponges is facilitated due to the protonation of dimethylamino ethyl (DMAE) groups in Eudragit E100 (EE). The generated 3D sponges are characterized by microscopy, thermal analysis, light scattering, and contact angle measurements to reveal their physicochemical properties. Additionally, antibacterial properties are confirmed via a colony‐forming unit assay. Microscopy analysis demonstrated that the obtained nanofibers possessed uniform conformation without beads, and their overall diameter varies depending on the fraction of the blend composition. The protonation of DMAE groups is investigated via infrared spectroscopy and further confirmed via zeta potential measurements. The charged electrospun 3D sponges exhibited significant antibacterial properties, effectively combating E. coli even at a diluted extract of samples. Owing to their morphology, electrostatically charged surface, and significant antibacterial properties, these 3D nanofibrous sponges present themselves as an effective material for integration in filtering membranes or cartridges, which may minimize harmful substances suspended in the air. This work introduces a versatile and straightforward approach for directly fabricating electrospun 3D nanofibrous sponge using a selection of solvents, avoiding potentially toxic additives or additional steps. The most important novelty in this study is a one‐step electrospinning process that simultaneously imparts three‐dimensionality and antimicrobial properties to nanofibrous matrices via in situ protonation of the polymer blend.

Metallic nanoparticles (NPs) are highly exploited in manufacturing and medical processes in a broad spectrum of industrial applications and in the academic sectors. Several studies have suggested that many metallic nanomaterials including those derived by silver (Ag) are entering the ecosystem to cause significant toxic consequences in cell culture and animal models. However, ecotoxicity studies are still receiving limited attention when designing functionalized and non.-functionalized AgNPs. This study aimed to investigate different ecotoxicological profiles of AgNPs, which were analyzed in two different states: in pristine form uncoated AgNPs and coated AgNPs with the antimicrobial peptide indolicidin. These two types of AgNPs are exploited for a set of different tests using and , which are representatives of two different levels of the aquatic trophic chain, and seeds of and . Ecotoxicological studies showed that the most sensitive organism to AgNPs was crustacean followed by and plant seeds, while AgNPs coated with indolicidin (IndAgNPs) showed a dose-dependent decreased toxicity for all three. The obtained results demonstrate that high ecotoxicity induced by AgNPs is strongly dependent on the surface chemistry, thus the presence of the antimicrobial peptide. This finding opens new avenues to design and fabricate the next generation of metallic nanoparticles to ensure the biosafety and risk of using engineered nanoparticles in consumer products.

Fabrication and characterization of hybrid nanomats containing quantum dots can play a prominent role in the development of advanced biosensors and bio-based semiconductors. Owing to their size-dependent properties and controlled nanostructures, quantum dots (QDs) exhibit distinct optical and electronic characteristics. However, QDs include heavy metals and often require stabilizing agents which are toxic for biological applications. Here, to mitigate the use of toxic ligands, cadmium selenide quantum dots (CdSe QDs) were synthesized in situ with polyvinylpyrrolidone (PVP) at room temperature. The addition of PVP polymer provided size regulation, stability, and control over size distribution of CdSe QDs. The characterization of the optical properties of the CdSe QDs was performed using fluorescence and ultraviolet–visible (UV-Vis) spectroscopy. CdSe QDs exhibited a typical absorbance peak at 280 nm and a photoluminescence emission peak at 580 nm. Transmission electron microscopy (TEM) micrographs demonstrated that CdSe QDs having an average size of 6 ± 4 nm were obtained via wet chemistry method. CdSe QDs were immobilized in a blend of PVP and poly(L-lactide-co-ε-caprolactone) (PL-b-CL) copolymer that was electrospun to produce nanofibers. Scanning electron microscopy (SEM), thermal analyses and attenuated total reflectance Fourier-transform infrared spectroscopy (ATR-FTIR) were used to characterize properties of fabricated nanofibers. Both pristine and hybrid nanofibers possessed cylindrical geometry and rough surface features, facilitating increased surface area. Infrared absorption spectra showed a slight shift in absorbance peaks due to interaction of PVP-coated CdSe QDs and nanofiber matrix. The presence of CdSe QDs influenced the fiber diameter and their thermal stability. Further, in vitro biological analyses of hybrid nanofibers showed promising antibacterial effect and decline in cancer cell viability. This study offers a simple approach to obtain hybrid nanomats immobilized with size-controlled PVP-coated CdSe QDs, which have potential applications as biosensors and antibacterial and anticancer cell agents.

The global crisis concerning multidrug-resistant microorganisms necessitates the development of innovative antimicrobial strategies that avoid conventional antibiotics and overcome the toxicity and environmental persistence associated with traditional metal-based biocides. This work aims to develop safe and sustainable antibacterial filtration materials by integrating cationic hyperbranched polymer dendrimers (HBP) into electrospun nanofibers. Cationic HBPs were successfully embedded into recycled polyamide 6 nanofibers using industrial needleless electrospinning. Filtration efficiency, assessed against a 0.3 µm paraffin oil aerosol according to EN 149:2001, consistently exceeded 99.8%, meeting and surpassing the FFP3 classification threshold while maintaining low air resistance. The HBP-functionalized nanofibers exhibited pronounced contact-active antibacterial activity against Staphylococcus aureus and Escherichia coli. Quantitative plate count assays confirmed viability reductions of up to 74.1% after 2 h of co-incubation. Crucially, the absence of inhibition zones in agar diffusion tests confirmed that the active polymer was stably embedded within the nanofiber matrix and did not leach. Comprehensive toxicological tests, including cell line and 3D human skin and airway tissue models, confirmed the material’s safety for both dermal and respiratory contact. This study presents a scalable, metal-free, and environmentally responsible next-generation filtration system that combines high mechanical efficiency with active antimicrobial functionality.

(1) Background: In dentistry, silver nanoparticles (AgNPs) have progressively earned great interest as antimicrobial drugs and are widely used in several biomedical fields. Recent progress in the analysis of complex bacterial communities has demonstrated the richness of the oral microbiota and the presence of numerous previously unexplained strains. Several efforts have been dedicated to the investigation of antimicrobial peptides (AMPs). Those peptides are a widespread group of small peptides against invading microbes. We report the production of a hybrid molecule composed of AgNPs and indolicidin, a well-known antibacterial peptide. (2) Methods: Spectroscopy and microscopy were used to analyze the optical features and to determine the size of the generated AgNPs. The AgNP antibacterial activity was evaluated versus oral Gram-positive and Gram-negative bacteria. (3) Results: The coated nanoparticles’ antibacterial activity strongly inhibited the growth of microorganisms, with very low minimum inhibitory concentration (MIC) values in the range of 5–12.5 μg/mL. We hypothesize that this effect depended on the specific characteristics of the metal surface coated with indolicidin. The second result was that the coated nanoparticles observed cellular toxicity, was lower with respect to the toxicity of peptide and the naked AgNPs when used individually. (4) New investigations regarding antimicrobial effect of AgNPs coated with AMPs in oral infections are an urgent task.

As bacterial resistance to antibiotics increases, there is an urgent need to identify alternative antibacterial agents and improve antibacterial materials. One is the controlled transport of antibacterial agents that prevents infection with drug-resistant bacteria, especially in the treatment of difficult-to-heal wounds. This work presents the use of electrospun PLCL/PVP (poly(L-lactide-co-ε-caprolactone/polyvinylpyrrolidone) nanofibers modified with two agents with antibacterial properties but with different mechanisms of action, that is, dendritic silver nanoparticles (Dend-AgNPs) and endolysin. The nanomat prepared in this manner showed significant antibacterial activity against antibiotic-resistant Pseudomonas aeruginosa strains, inhibiting their growth and production of key pigments and virulence factors. Moreover, the use of nanofibers as carriers of the selected factors significantly reduced their cytotoxicity towards human fibroblasts. The results confirmed the possibility of using the presented product as an innovative dressing material, opening new perspectives for the treatment of wounds and combating bacterial infections with drug-resistant bacteria.

Herein, we report the fabrication and characterization of novel polycaprolactone (PCL)-based nanofibers functionalized with bare (ligand-free) titanium nitride (TiN) nanoparticles (NPs) for tissue engineering applications. Nanofibers were prepared by a newly developed protocol based on the electrospinning of PCL solutions together with TiN NPs synthesized by femtosecond laser ablation in acetone. The generated hybrid nanofibers were characterised using spectroscopy, microscopy, and thermal analysis techniques. As shown by scanning electron microscopy measurements, the fabricated electrospun nanofibers had uniform morphology, while their diameter varied between 0.403 ± 0.230 µm and 1.1 ± 0.15 µm by optimising electrospinning solutions and parameters. Thermal analysis measurements demonstrated that the inclusion of TiN NPs in nanofibers led to slight variation in mass degradation initiation and phase change behaviour (Tm). In vitro viability tests using the incubation of 3T3 fibroblast cells in a nanofiber-based matrix did not reveal any adverse effects, confirming the biocompatibility of hybrid nanofiber structures. The generated hybrid nanofibers functionalized with plasmonic TiN NPs are promising for the development of smart scaffold for tissue engineering platforms and open up new avenues for theranostic applications.