Search Results (115)

Bone grafting remains limited, and the strategies to design even more structurally complex scaffolds—able to reproduce the hierarchical architecture of bone extracellular matrix—are rapidly growing. In this study, we report the fabrication of a hierarchically structured scaffold produced by layering poly(ε-caprolactone)/gelatin (PCL/Gt) or poly(lactic acid)/gelatin (PLA/Gt) electrospun nanofibers via coaxial electrospinning onto 3D-printed poly(lactic acid) (PLA) scaffolds via fused deposition modeling (FDM). After the printing process, PLA disks (10 × 1 mm, 20% infill, ~80% porosity, pore size ~1.57 mm) were coated with core/shell (PCL/Gt, PLA/Gt) fibers to investigate the in vitro interfacial response of osteoblasts in comparison with monocomponent fibrous coatings (PCL, PLA, Gt). SEM and TEM confirmed that core/shell fibers exhibited bead-free morphologies, with a significant reduction in fiber diameter (≈287–316 nm) and higher interfibrillar porosity compared to monocomponent fibers. FTIR and thermogravimetric analyses indicated the presence of hydrogen bonding between the polyester and gelatin, and the absence of residual solvent after deposition. At the same time, water contact angle measurements confirmed an increase in hydrophilic properties from 80–86° to 120° ascribable to the presence of gelatin. Accordingly, in vitro response of human fetal osteoblasts (hFOB 1.19) exhibited an evident improvement in the case of Gt-based fibrous coatings (i.e., PCL/Gt and PLA/Gt) in terms of early adhesion (4–24 h) and metabolic activity from 3 to 21 days, cell spreading into star-shaped morphologies, formation of extracellular matrix, and mineral phase deposition. In more detail, a remarkable increase in alkaline phosphatase activity was observed in Gt-based coaxial coatings from day 7 onward, with the highest values recorded for PLA/Gt. Overall, we demonstrated that the Gt-based coaxial fibrous coating provided a mix of topological and biochemical cues that synergistically promoted key osteoblast activities at the interface, supporting the regeneration of new bone tissue in highly tailored 3D-printed scaffolds, thus suggesting a promising strategy for personalized regenerative medicine. Full article

Coaxial electrospinning technology enables the fabrication of nanofibers with a core-shell structure, thereby facilitating the encapsulation of functional materials. Its efficacy lies in the precise regulation of mass transfer behavior at the sensing interface. However, achieving the controllable preparation of core-shell fiber structures in complex environments and quantitatively predicting their mass transfer kinetics remain challenging. This study aims to establish a predictive framework combining simulation and experiment. Firstly, finite element simulations using COMSOL clarified that increasing the shell thickness or decreasing its effective diffusion coefficient can significantly delay analyte transport. A model incorporating time-varying parameters further revealed the influence of polymer swelling on the initial release kinetics. Using the diffusion of an aqueous KCl solution as a model system, experiments confirmed that increasing the shell solution concentration is an effective processing strategy for enhancing the mass transfer barrier. Based on the Box-Behnken design and response surface methodology (RSM), a quantitative model linking key process parameters to release kinetic parameters was established. Model diagnostics indicated that the regression equation is significant and reliable. Validation experiments demonstrated that the model possesses good predictive capability for the key release kinetic parameters, with prediction errors within an acceptable range. The framework established in this study indicates that active design of the mass transfer behavior of core-shell fibers can be achieved through process control, providing a quantitative predictive tool and methodological reference for the preparation of controllable mass transfer interfaces for sensing applications. Full article

Semiconductor miniaturization demands stricter material uniformity. Core-shell nanofibers, promising for semiconductor packaging and flexible circuits, face application limits due to traditional coaxial electrospinning’s electric field instability—causing poor fiber diameter uniformity and challenges with high-viscosity and low-conductivity solutions. To address this, airflow-assisted coaxial electrospinning leveraged airflow-electric field synergy to enhance fiber stretching. COMSOL Multiphysics 6.4 simulated the influence of different inner diameters of the air flow nozzles on the air flow field, while the response surface method optimized parameters. At 10 kPa air pressure, 16.71 kV voltage, and a gas nozzle inner diameter of 3.42 mm, nanofibers showed regular morphology with a diameter coefficient of variation as low as 9.2%. This study enables stable preparation of highly uniform core-shell nanofibers, providing key process support for their large-scale semiconductor application and advancing flexible electronics and photodetection. Full article

The development of cost-effective and highly efficient electrocatalysts for the hydrogen evolution reaction (HER) is pivotal for sustainable hydrogen energy production. Herein, coaxial electrospinning one-dimensional (1D) hollow carbon nanofiber (HCNF) in situ-grown MoS₂/CoS₂ nanosheets were impregnated with a NaBH₄ solution to obtain a HCNF-loaded sulfur-vacancy-rich MoS₂/CoS₂ heterojunction nanosheets catalyst of Vs-MoS₂/CoS₂-0.1@HCNFs. The unique hollow architecture afforded by electrospinning facilitates rapid electron transport and effectively mitigates the agglomeration of active 2D nanosheets, ensuring maximum exposure of catalytic sites. Furthermore, NaBH₄ impregnation introduces abundant sulfur vacancies into the heterojunction lattice, synergistically modulating the electronic structure. Benefiting from the structural advantages of the electrospun framework and defect engineering, the optimized catalyst (Vs-MoS₂/CoS₂-0.1@HCNFs) exhibits superior HER activity in 1.0 M KOH, requiring an overpotential of only 115 mV to achieve a current density of 10 mA cm⁻², along with a low Tafel slope of 83.3 mV dec⁻¹ and excellent long-term stability. This study demonstrates the efficacy of electrospinning in designing high-performance, self-supported electrocatalysts for sustainable energy applications. Full article

Post-harvest deterioration in strawberries is an urgent and critical issue that requires significant attention. Glycerol monolaurate (GML), a broad-spectrum food-grade antimicrobial agent, faces limited applicability due to its poor water solubility. In this study, a confined encapsulation strategy was employed to encapsulate GML within hydroxypropyl-γ-cyclodextrin (HPγCD), which improved the physicochemical properties of GML and enhanced its stability in the environment. The fiber morphology was observed through scanning electron microscopy (SEM) and transmission electron microscopy (TEM), confirming the presence of a uniform, non-nodular core–shell structure. The Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) validated the successful encapsulation of GML within the cavity of HPγCD. Thermogravimetric analysis (TGA) demonstrated that the thermal stability of the core–shell system was significantly improved. In vitro release followed first-order kinetics (R² = 0.9842), with 79.5% of GML released over 68 h. The DPPH and ABTS assays demonstrated that PLA/GML-HPγCD NF exhibited sustained radical scavenging activity (p < 0.05, ANOVA). Compared to GML-HPγCD NF, PLA/GML-HPγCD NF exhibited prolonged antibacterial activity against Escherichia coli and superior antifungal efficacy in strawberry preservation. Meanwhile, PLA/GML-HPγCD NF significantly reduced lesion diameter and weight loss while maintaining hardness, total soluble solids, and vitamin C content over 8 days of storage. In conclusion, these characteristics highlighted the potential of P/G-HPγCD NF as a promising active packaging material for extending the shelf life of perishable fruits. Full article

To overcome the limitations of traditional motion sickness medications—slow onset of action, short duration of efficacy, and poor patient compliance—this study employed coaxial electrospinning technology. Poly(lactic acid) (PLA) and polyvinylpyrrolidone K90 (PVP K90) were used as composite carrier materials. The sheath layer is composed of highly hydrophilic PVP K90, loaded with the antihistamine diphenhydramine (DPH). The core layer, composed of biodegradable PLA with excellent sustained-release properties, carries the anticholinergic drug scopolamine hydrobromide (SH). This core–sheath nanostructured nanofiber sublingual film delivers dual anti-motion sickness drugs. A series of characterization tests revealed that the sublingual membrane exhibits a linear morphology with a distinct core–shell nanostructure. The drugs DPH and SH are distributed in an amorphous state within the sheath and core layers, respectively. Wetting performance tests indicate that the membrane’s wettability falls between those of monofilament membranes. In vitro drug release experiments revealed that DPH exhibited a “rapid onset + sustained release” biphasic profile, with cumulative release reaching 60% within 2 h and approaching complete release by 10 h, primarily via Fickian diffusion (n = 0.30). SH exhibited prolonged sustained release, approaching complete release at 12 h via non-Fickian diffusion (n = 0.55). Cytotoxicity and vital/necrotic staining experiments mutually corroborated that cell viability remained above 80%, further validating the safety and efficacy of PLA/PVP as a combined drug delivery carrier. This study provides a novel delivery system for motion sickness treatment, offering significant theoretical value and broad clinical application prospects. Full article

This research developed an active food packaging system featuring a tailored controlled-release mechanism. The system was fabricated using temperature-responsive poly(N-vinylcaprolactam) (PNVCL) nanofibers with a core-shell architecture. The resulting film incorporated cinnamon essential oil (CEO) as a natural preservative within a composite structure consisting of PNVCL, polyvinyl alcohol (PVA), polylactic acid (PLA) and CEO. The nanofiber film obtained via coaxial electrospinning exhibited a sandwich-like structure; the obtained fiber membrane is abbreviated as PP/PC, and the number represents the essential oil content. The PP/PC-4 composite demonstrated exceptional physical barrier properties and mechanical strength, with a WVP as high as 5.74 ± 0.37 (g·mm)/(m²·h·kPa). It also achieved the highest maximum force, elastic modulus, and tensile strength, recorded at 3.08 ± 0.31 N, 228.86 ± 15.46 MPa, and 5.26 ± 0.72 MPa, respectively, along with superior thermal stability. FTIR spectroscopy confirmed molecular interactions, specifically through C–H bonding, between the PLA/CEO core and the PNVCL shell layers. After 5 d of storage at 40 °C, the PP/PC-4 film retained substantial antibacterial efficacy. The antifungal efficacy demonstrated the highest performance, exceeding the control group by 32%. The weight loss rate on day four was 28%, significantly lower than other groups, while the hardness retention rate was 73% higher than the control group and 44% higher than PLA/CEO (4%). Application of this material prolonged the shelf life of Chinese bayberry (Myrica rubra) by 4 d while enhancing key preservation metrics. Owing to its advanced barrier properties, mechanical performance and temperature-modulated release characteristics, this PNVCL-based nanofiber film demonstrated strong potential as an intelligent packaging material for prolonging the freshness of perishable food products. Full article

Gas-assisted coaxial electrospinning (GACES), a simple and versatile technique for the large-scale fabrication of coaxial nanofiber membranes, possesses significant industrial potential across advanced manufacturing sectors including semiconductors—particularly for fabricating high-precision dielectric layers, high-uniformity encapsulation materials, and flexible semiconductor substrates requiring tailored core-shell architectures. However, there is still a lack of relevant studies on the effective regulation of the core-shell structures of coaxial fibers based on GACES, which greatly limits the batch preparation and wide application of coaxial fibers. Finite element simulation analysis of the flow field and development of the coaxial jet mechanics model with a gas-driven flow field—two key methodologies in this study—successfully uncovered the influence mechanism of gas-assisted flow fields on the core-shell structures of coaxial nanofibers. By adjusting the gas-assisted flow fields parameters, we reduced the total diameter of coaxial fibers by 47.33% (average fiber diameter: 334.12 ± 16.29 nm → 175.98 ± 1.18 nm), decreased the shell thickness by 72.98%, increased the core-shell ratio by 289% (core-shell ratio: 0.49 → 1.91), and improved the uniformity of the total diameter distribution of coaxial fibers by 30.64%. This study delivers a practical conceptual framework and robust experimental underpinnings for the scalable fabrication of coaxial nanofiber membranes with controllable core-shell structures, thereby promoting their practical application in semiconductor devices such as ultra-thin dielectric layers, precisely structured encapsulation materials, and high-uniformity templates for nanoscale circuit patterning. Full article

In this work, hollow-structured nanofibers with densely and uniformly distributed ZnO nanorods were successfully prepared by a combination of coaxial electrospinning, heat treatment, and hydrothermal synthesis, exhibiting excellent photocatalytic degradation performance. The morphological and structural characteristics of hollow ZnO nanofibers obtained at different heat treatment temperatures were systematically investigated, and their photocatalytic degradation performances were compared through degrading methylene blue (MB) under ultraviolet (UV) irradiation. It was found that the hollow ZnO nanofibers obtained by heat treatment at 280 °C exhibited the best photocatalytic degradation performance due to their optimal morphology and structure. Their photocatalytic degradation efficiencies for MB under 3 h of UV light and natural sunlight were 94.70% and 92.95%, respectively. Furthermore, cyclic stability tests were conducted on the optimal sample, revealing that its degradation efficiency remained at 89.96% after three cycles, demonstrating its excellent reusability. Full article

Antimicrobial function in protective and medical textiles is an essential safety feature since textiles can become breeding grounds for microorganisms. Ideally, the antimicrobial function in textiles should be non-toxic, stable, and durable. This study explores a core–shell nanofiber with a core of the cationic biopolymer ε-poly-L-lysine (PL) and shell of structurally similar and biocompatible polyamide-6 (PA). The core–shell structure is expected to have a more stable antimicrobial function than its monolithic counterpart. Further, thermal crosslinking is expected to prevent rapid diffusion of the water-soluble PL. Therefore, this study establishes a comparison between a monolithic (control), a core–shell (CS), and a thermally crosslinked core–shell (CL-CS) nanofiber of PL and PA. Morphological analysis confirmed the successful generation of the core–shell nanofibers. All the samples exhibited hydrophilic behavior and antimicrobial function. However, the control sample showcased significantly reduced zones of inhibition in antimicrobial testing with 21 days of bacterial exposure (1.027 ± 0.072 cm²), as compared to 24 h bacterial exposure (1.347 ± 0.151 cm²). On the other hand, the zones of inhibition for 24 h vs. 21 days for CS (1.265 ± 0.042 cm² vs. 1.052 ± 0.235 cm²) and CL-CS (1.128 ± 0.161 cm² vs. 1.106 ± 0.047 cm²) showed no significant differences. Therefore, the core–shell structure allowed for sustainable and durable antimicrobial action. Lastly, the CL-CS sample exhibited reusable antimicrobial function owing to the core–shell structure paired with thermal crosslinking. This study showcases a fiber system with non-toxic, durable, and reusable antimicrobial function. This study builds grounds for the development and multifaceted holistic characterization of safe, stable, and scalable antimicrobial textiles. Full article

Background/Objectives: Skin wounds interrupt the natural anatomy and function of the skin. The body passes through four physiological phases to repair wounds after injury. Since the fibers are more closely related to the extracellular matrix structure, they can be used as scaffolds to accelerate wound closure. Shikonin is a botanical herbal remedy used as an anti-inflammatory agent and for its wound-healing characteristics. Cresols are known for their bactericidal and fungicidal properties, which promote their utilization as a disinfectant in soap. Therefore, this study aimed to formulate shikonin and cresol-loaded nanofibers for a dual wound-healing and antibacterial wound dressing in vitro. Methods: This study demonstrated the effectiveness of the drug-loaded nanofibers against diverse Gram-positive and Gram-negative bacteria using the minimum inhibitory concentration (MIC) and zone of inhibition assays. Results: Scanning electron microscopy images showed successful formulation of shikonin/cresol fibers with an average diameter of 772 ± 152 nm. The encapsulation efficiency and drug loading for the dual drug-loaded fibers were 44 ± 1% and 25 ± 1 µg/mg, respectively, for shikonin, and 38 ± 1% and 21 ± 0.5 µg/mg, respectively, for cresol, with a full release of both drugs achieved after 180 min. The combination of both compounds exhibited a safe concentration of ≤6 µg/mL, with cell viability of >50% in human dermal fibroblasts (HFF-1) after 24 h. The MIC results indicated that the combination was efficient as an antibacterial agent against Gram-positive bacteria at a safe concentration. The shikonin/cresol-loaded fibrous system showed an inhibition zone close to that of the control drugs, suggesting that the drugs have retained their antibacterial activity after electrospinning. Conclusions: This dual drug-loaded fiber system showed a high potential as an antibacterial wound dressing for skin infection injuries. However, in vivo studies are required to assess the safety and efficacy in an animal model of the dual drug-loaded fiber system. Full article

Emerging organic contaminants (EOCs), including polychlorinated bisphenyls (PCBs), pharmaceuticals, personal care products, pesticides, polycyclic aromatic hydrocarbons (PAH), and dyes, are among the most hazardous pollutants found in water bodies and sediments. These substances pose serious threats to the environment and human health due to their high toxicity, long-range mobility, and bioaccumulation potential. Although various methods for degradation of organic pollutants exist, photocatalysis using ultraviolet (UV) and visible light (VIS) has emerged as a promising approach. However, its practical applications remain limited due to challenges such as the use of powdered photocatalysts, which complicates their removal and recycling in industrial settings, and the restricted solar availability of UV light (~4% of the solar spectrum). This review investigates the effectiveness of hybrid electrospun conductive polymer nanofibers on metal oxide photocatalysts such as TiO₂ and ZnO (including doped and co-doped forms) and fabricated via mono- or coaxial electrospinning, in the degradation of EOCs in water under visible light. Furthermore, strategies to enhance the fabrication of these hybrid electrospun conductive nanofibers as visible-light-responsive photocatalysts, such as the inclusion of dopants and/or plasmonic materials, are discussed. Finally, the current challenges and future research directions related to electrospun nanofibers combined with photocatalysts for the degradation of EOCs in water treatment applications are outlined. Full article

Background: Although electrohydrodynamic atomization (EHDA) consistently provides drug-encapsulation efficiencies (DEE) far above those of conventional bottom-up nanotechnologies, the question of how to systematically push that efficiency even higher remains largely unexplored. Methods: This study introduces a modified triaxial electrospinning protocol tailored to the application and benchmarks it against two conventional techniques: single-fluid blending and coaxial electrospinning. Ethylcellulose (EC) served as the polymeric matrix, while curcumin (Cur) was chosen as the model drug. In the triaxial setup, an electrospinnable, drug-free EC solution was introduced as an intermediate sheath to act as a molecular barrier, preventing Cur diffusion from the core fluid. Ethanol alone was used as the outermost fluid to guarantee a stable and continuous jet. Results: This strategy provided a DEE value of 98.74 ± 6.45%, significantly higher than the 93.74 ± 5.39% achieved by coaxial electrospinning and the 88.63 ± 7.36% obtained with simple blending. Sustained-release testing revealed the same rank order: triaxial fibers released Cur the most slowly and exhibited the smallest initial burst release effect, followed by coaxial and then blended fibers. Mechanistic models for both fiber production and drug release are proposed to clarify how the tri-layer core–shell structure translates into superior performance. Conclusions: The modified triaxial electrospinning was able to open a new practical route to produce core-sheath nanofibers. These nanofibers could provide a higher DEE and a better sustained drug release profile than those from the coaxial and blending processes. Full article

Co-axial electrospinning is one of the facile methods for the fabrication of core–shell metal oxides for environmental applications. Indeed, core–shell architectures featuring a magnetic core and a photocatalytic shell represent a novel approach to catalytic nanostructures in applications such as water treatment and pollutant removal via magnetic separation. This study focuses on the fabrication of novel Fe₃O₄-Fe₂NiO₄/NiO core–shell nanofibers with enhanced optical and magnetic properties using co-axial electrospinning. The aim is to optimize the fabrication parameters, particularly the amount of metal precursor in the starting solutions, to achieve well-defined core and shell structures (rather than single-phase spinels), and to investigate phase transitions, structural characteristics, as well as the optical and magnetic properties of the resulting nanofibers. Raman, XRD, and XPS results show several phases and high defect concentration in the NiO shell. The Fe₃O₄-Fe₂NiO₄/NiO core–shell nanofibers exhibit strong visible-light absorption and significant magnetization. These advanced properties highlight their potential in photocatalytic applications. Full article

To address mass transport limitations in carbon nanofiber membrane electrodes for overall water splitting, a self-supporting nitrogen-doped hollow carbon nanofiber membrane embedded with Co/Co₂P heterojunctions (Co/Co₂P-NCNFs-H) was fabricated via continuous coaxial electrospinning. The architecture features uniform hollow channels (200–250 nm diameter, 30–50 nm wall thickness) and a high specific surface area (254 m² g⁻¹), as confirmed by SEM, TEM, and BET analysis. The Co/Co₂P heterojunction was uniformly dispersed on nitrogen-doped hollow carbon nanofibers through electrospinning, leverages interfacial electronic synergy to accelerate charge transfer and optimize the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). Electrochemical tests demonstrated exceptional catalytic activity, achieving current densities of 100 mA cm⁻² at ultralow overpotentials of 405.6 mV (OER) and 247.9 mV (HER) in 1.0 M KOH—surpassing most reported transition metal catalysts for both half-reactions. Moreover, the electrode exhibited robust long-term stability, maintaining performance for nearly 20 h at 0.6 V (vs. Ag/AgCl) (OER) and over 250 h at −1.5 V (vs. Ag/AgCl) (HER), attributed to the mechanical integrity of the hollow architecture and strong metal–carbon interactions. This work demonstrates that integrating hollow nanostructures (enhanced mass transport) and heterojunction engineering (optimized electronic configurations) creates a scalable strategy for designing efficient bifunctional catalysts, offering significant promise for sustainable hydrogen production via water electrolysis. Full article