The fibrous scaffolds for bone tissue engineering that mimic the extracellular matrix with bioactive and bactericidal properties could provide adequate conditions for regeneration of damaged bone. Electrospun ultrathin fiber covered with nano-hydroxyapatite is a favorable fibrous scaffold design. We developed a fast and reproducible strategy to produce polyvinylidene fluoride (PVDF)/nano-hydroxyapatite (nHAp) nanofibrous scaffolds with bactericidal and bioactive properties. Fibrous PVDF scaffolds were obtained first by the electrospinning method. Then, their surfaces were modified using oxygen plasma treatment followed by electrodeposition of nHAp. This process formed nanofibrous and superhydrophilic PVDF fibers (133.6 nm, fiber average diameter) covered with homogeneous nHAp (202.6 nm, average particle diameter) crystals. Energy-dispersive X-ray spectrometry demonstrated the presence of calcium phosphate, indicating a Ca/P molar ratio of approximately 1.64. X-ray diffraction, Fourier transform infrared spectroscopy, and Raman spectroscopy spectra identified β-phase of nHAp. Thermal analysis indicated a slight reduction in stability after nHAp electrodeposition. Bactericidal assays showed that nHAp exhibited 99.8% efficiency against Pseudomonas aeruginosa bacteria. The PVDF/Plasma and PVDF/nHAp groups had the highest cell viability, total protein, and alkaline phosphatase activity by 7 days after exposure of the scaffolds to MG63 cell culture. Therefore, the developed scaffolds are an exciting alternative for application in bone regeneration.

Membranes with special wettability have attracted increasing interest for oil/water separation. Herein, the cellulose-based nanofibrous membrane was fabricated in an aqueous system by an electrospinning technique. The membrane was then modified successively through coating polydopamine and polyethyleneimine on the surface, which endowed the membrane with superhydrophilic and underwater superoleophobic character. The composition and morphology of the resultant membrane were characterized by attenuated total reflectance Fourier transform infrared spectra, X-ray photoelectron spectroscopy, and field-emission scanning electron microscope, respectively. Surfactant-stabilized oil-in-water emulsions were used to evaluate the separation performance of the membrane at different pH values. It was found that the membrane displayed the excellent antifouling property and separation performance for all different emulsions, with separation efficiency above 99.1% due to the development of a hydration layer underwater on the membrane surface. The reusability study indicated that the modification coating was stable enough to effectively separate emulsions after recycling at least 20 times. The developed nanofibrous membrane, as well as the corresponding modification strategy, enriched the application of membranes with special wettability in the field of oil spills and oily wastewater treatments.

In this study, the surface morphology of electrospun polycaprolactone (PCL) fibers was investigated. PCL was dissolved in various solvent/nonsolvent systems (acetone/dimethylformamide (DMF), tetrahydrofuran (THF)/DMF, dichloromethane (DCM)/DMF, chloroform (CF)/DMF, acetone/dimethyl sulfoxide (DMSO), THF/DMSO, DCM/DMSO, CF/DMSO) at a fixed ratio of 80/20 v/v. PCL solutions from these solvent systems were electrospun under varying high relative humidity (60–90%), and also room humidity. Characterization of fibers was evaluated by a scanning electron microscope, an atomic force microscope, water contact angle measurements, the Brunauer–Emmett–Teller method, and a strain–stress test. Results revealed that the surface texture of individual fibers changed with the presence of different types of pores and surface roughness depending on both humidity and solvent/nonsolvent properties. Miscibility with water was another factor to be taken into account for understanding mechanisms that contributed to the formation of surface defects. Fibrous materials having such a surface architecture, especially the porous ones, are potential candidates for various applications such as tissue engineering, drug delivery, catalysis, and filtration.

In recent years, tissue engineering has helped to reduce hospital stays and deaths caused by skin wounds. Scaffolds are one of the main factors that influence the success of any tissue graft. Collagen is one of the main components of the extracellular matrix, and there has been much interest in new sources for application as a biomaterial. In this work, a tissue engineering scaffold was developed using the electrospinning technique. The chicken skin was used as an alternative source to obtain collagen. The combination of this collagen with elastin was successfully electrospun, and a distribution of diameters was obtained, less than 100 nm. In vitro tests showed the adhesion and proliferation of the cells, as well as an absence of cytotoxicity from non–cross-linked scaffolds and scaffolds that were cross-linked with carbonyldiimidazole. The structure and composition of the developed scaffolding provide a favorable environment for cell growth and generating a skin substitute.

As distinctive spontaneous polarization and far-infrared radiation characteristics, the natural mineral tourmaline (TM) has the regulatory effect on crystallization behavior, which possesses potential application in biomimetic mineralization and bone regeneration. In this study, polyurethane (PU) and gelatin (GE) membranes with different adding proportion of TM nanoparticles were prepared via electrospinning. Additionally, the effect of TM nanoparticles on the mineralization process of hydrophobic PU and hydrophilic GE was investigated by immersing the composite TM/PU and TM/GE electrospun membranes in the 10× simulated body fluid (10SBF) at 37 °C for varying periods of time. SEM images confirmed the well-dispersed TM nanoparticles in the PU and GE electrospun fibers. The mineralization deposition was characterized by the SEM, EDS, XRD, and FTIR, and it indicated that two types of calcium phosphate deposits with different Ca/P molar ratios were obtained when TM/PU membranes and TM/GE membranes were incubated in 10SBF. Honeycomb-like hydroxyapatite crystals nucleated and grew faster on TM/PU and TM/GE membranes than the pure PU and GE membranes, respectively. Furthermore, with the increase of the added TM nanoparticles in the composite membranes, more calcium phosphate crystals were precipitated. These results showed that the added TM nanoparticles were able to improve the mineralization of polymer fibrous membranes, which is potential for the composite bone scaffold.

Compared with commercial polyolefin membranes, polyacrylonitrile (PAN) membrane prepared by electrostatic spinning has higher porosity, electrolyte uptake, thermal stability, and lithium-ion conductivity, etc. However, poor mechanical performance has largely limited the application of electrospun PAN separators. In this study, PAN/polyimide (PI) composite membrane is prepared by electrostatic spinning to improve the mechanical and electrochemical performances. Scanning electron microscopy, thermal analysis method, and electrochemical methods were used for evaluation of the electrospun composite membrane. The results show that the composite membrane possesses good thermal stability and exhibits better mechanical performance than pristine PAN membrane (increasing by 1.1 times in tension strength). The addition of PI can increase porosity and fluid absorption rate obviously. In addition, the composite membrane has high ionic conductivity (18.77 × 10−4 S/cm), wide electrochemical window (about 4.0 V), and excellent cycling performance. It can retain a discharge specific capacity of 153 mA h/g even after 50 cycles at 0.5 C. The electrospun PAN/PI membrane may be a promising candidate for lithium-ion battery separators.

Carbon nanofibers are prepared via the electrospinning method accompanied by the phase-separation process using polyacrylonitrile as a carbon precursor. Effects of preoxidation and carbonation temperatures on electrochemical performance are studied and optimized in detail. The morphology and porous structure are characterized by scanning electron microscope, transmission electron microscope, and nitrogen adsorption and desorption measurements, respectively; the electrochemical performances are measured by the CHI660E workstation. The results show that the diameter of carbon nanofibers is about 150–200 nm with a uniform and smooth surface. The optimized preoxidation temperature is 280 °C with a carbonation temperature of 700 °C. The highest capacitance is up to 155 F/g, and the symmetric supercapacitor delivers a maximum energy density of 7.78 W h/kg with a power density of 400 W/kg and a maximum power density of 4000 W/kg with an energy density of 2.0 W h/kg. The symmetric supercapacitor also exhibits good cycle stability 91.0% of initial specific capacitance after 5000 cycles.

H3PW12O40/polymethylmethacrylate (PMMA)/polycaprolactam (PA6) nanofibrous membrane with a sandwich structure was prepared by electrospinning. Characterization with Fourier transformation infrared spectroscopy (FT-IR), energy-dispersive x-ray spectroscopy (EDX), and x-ray photoelectron spectroscopy (XPS) indicated that H3PW12O40 has been successfully loaded into the upper and bottom layers of the sandwich membrane and its Keggin structure was not destroyed. The photocatalytic efficiency of the sandwich membranes were much higher (≥87.2%) than that of H3PW12O40 only (15.6%) and H3PW12O40/PMMA composite nanofibrous membrane (11.6%) in the degradation of methyl orange (MO) under ultraviolet irradiation. It may be caused by two factors: one was the photoreduction mechanism induced by the electron donating from PA6 to H3PW12O40, the other was the double contact area between H3PW12O40 and MO due to the sandwich structure of the laminated membrane. What is noteworthy is that the sandwich membranes were stable in water, so that they could be easily separated from the aqueous MO solution and reused without appreciable losses in photocatalytic activity after three photocatalytic cycles. In view of this, H3PW12O40/PMMA/PA6 sandwich nanofibrous membrane is promising as a photocatalyst to remove organic pollutants from practical wastewater.

Magnetic Fe3O4–polyhedral oligomeric silsesquioxanes (POSS) particles with Si-OH were prepared by hydrosilylation reaction between the Fe3O4–SiH and POSS with hydroxyl and vinyl groups. The magnetic Fe3O4–POSS particles were characterized by using transmission electron microscopy, scanning electron microscopy, Fourier transform infrared absorption spectroscopy, thermogravimetry, and vibrating sample magnetometry. The magnetic saturation value of Fe3O4–POSS particles was 18.77 emu/g. Polyacrylonitrile (PAN)/Fe3O4–POSS nanofibers mats were subsequently fabricated by electrospinning technique. The electret properties of PAN/Fe3O4–POSS nanofibers mats and their aerosol filtration property as electrets filter media were characterized. The stability of the surface potential was remarkably improved and the surface potential retention reached 50% for PAN/Fe3O4–POSS mats with 1 wt% Fe3O4–POSS. Compared with pure PAN, the charge retention of PAN/Fe3O4–POSS was increased by 21% and reached 52.40%. Moreover, the collection efficiency increased and the filter resistance decreased when the PAN nanofibers with Fe3O4–POSS were used as electrets filter media. Our study provided an effective method to prepare novel filter materials with high efficiency and low resistance.

The work was intended to explore the effect of the widely available cationic polymer polyethylenimine (PEI) on small diameter poly(ɛ-caprolactone) (PCL) blood vessel grafts. PEI was blended with PCL and electrospun into nanofibrous vascular scaffolds. The morphologies, wettabilities, mechanical properties, and biological activities of the PCL/PEI electrospun nanofibers were investigated. It was found that by increasing the content of PEI to 5% within the scaffolds, the fiber diameters decreased from 469.7 ± 212.1 to 282.5 ± 107.1 nm, the water contact angle was reduced from 126.6 ± 1.1° to 27.6 ± 3.9°, while the Young's modulus increased from 2.0 ± 0.2 to 4.1 ± 0.1 MPa, the suture retention strength increased from 4.2 ± 0.4 to 6.1 ± 0.7 N, and the burst pressure increased from 801.2 ± 14.1 to 926.2 ± 22.8 mmHg. The in vitro evaluations demonstrated that the nanofibers containing 2% PEI promoted the attachment and proliferation of human umbilical vein endothelial cells (HUVECs).

ZnO/TiO2 heterojunction composite fibers were prepared via a physical route, i.e., first electrospinning titanium dioxide (TiO2) fibers, then pulse plating zinc (Zn) on the fibers, and at last thermal treating the fibers. The morphologies, phase structures, and photocatalytic property of the composite fibers were characterized by using field-emission gun scanning electron microscope, x-ray diffractometer, high-resolution transmission electron microscope, and ultraviolet–visible spectrophotometer. It was found that a full or partial lattice coherent heterojunction was formed between the TiO2 fibers and zinc oxide (ZnO) particles, due to thermal treatment at 400 °C, which simultaneously resulted in the phase transformations including Zn to ZnO and amorphous TiO2 to anatase TiO2. The experimental results demonstrated that the photocatalytic activity of the composite fibers was improved and exhibited a value more than two times higher than that of TiO2 fibers.

One of the many obstacles to spinal cord repair following trauma is the formation of a cyst that impedes axonal regeneration. Accordingly, we examined the potential use of electrospinning to engineer an implantable polarized matrix for axonal guidance. Polydioxanone, a resorbable material, was electrospun to fabricate matrices possessing either aligned or randomly oriented fibers. To assess the extent to which fiber alignment influences directional neuritic outgrowth, rat dorsal root ganglia (DRGs) were cultured on these matrices for 10 days. Using confocal microscopy, neurites displayed a directional growth that mimicked the fiber alignment of the underlying matrix. Because these matrices are generated from a material that degrades with time, we next determined whether a glial substrate might provide a more stable interface between the resorbable matrix and the outgrowing axons. Astrocytes seeded onto either aligned or random matrices displayed a directional growth pattern similar to that of the underlying matrix. Moreover, these glia-seeded matrices, once co-cultured with DRGs, conferred the matrix alignment to and enhanced outgrowth exuberance of the extending neurites. These experiments demonstrate the potential for electrospinning to generate an aligned matrix that influences both the directionality and growth dynamics of DRG neurites.

Cellulose acetate (CA) thin, porous membranes were produced by electrospinning precursor polymer solutions in acetone at room temperature. During this process, CA nanofibers were produced when a high electric field of 12 kV was applied to the precursor solution. The diameters of fibers obtained varied from 100 nm to 1.2 μm while the average diameter was approximately 500 nm. The electrospinning parameters used to control the morphology of the fibers and their membranes are flow rate, the distance between the syringe needle that ejects fluid and the collector, and the voltage applied. These membranes were used as scaffolds for microvascular cells growth. The structure of the membranes that were produced mimic the topography and porosity of extracellular matrix (ECM) in two key ways. The fiber diameter mimics extracellular protein fiber diameter, thus enabling cellular attachment and facilitating cellular migration. The porosity mimics that of extracellular matrix such that microvascular capillary tube formation is enhanced. The non-woven fiber mats were examined by means of electron microscopy and the nanofibers were seen to be oriented randomly. The issue of strengthening the CA scaffold is currently studied by adding ceramic nano-structured component (carbon nanotubes) in the polymer membranes.

Biodegradable polymeric nanofibers are of great interest as scaffolds for tissue engineering and drug delivery due to their extremely high surface area, high aspect ratio and similarity in structure to the extracellular matrix (ECM). Polyphosphazenes due to their synthetic flexibility, wide range of physico-chemical properties, non-toxic and neutral degradation products and excellent biocompatibility are suitable candidates for biomedical applications. The objective of the present study was to develop and evaluate composite nanofibers of a biodegradable polyphosphazene, poly[bis(ethyl alanato)phosphazene] (PNEA) and nanocrystals of hydroxyapatite (nHAp) via electrospinning. A suspension of nHAp in dimethyl formamide (DMF) sonicated with PNEA solution in tetrahydrofuran (THF) was used to develop composite nanofiber matrices via electrospinning at ambient conditions. In the present study the theoretical loading of nHAp was varied from 50%-90% (w/w) to PNEA. The nHAp content (actual loading of nHAp) of the composite nanofibers was determined by gravimetric estimation. The composite nanofibers were characterized by transmission electron microscopy (TEM), gravimetry and energy dispersive X-ray mapping. This study demonstrated the feasibility of developing novel composite nanofibers of biodegradable polyphosphazenes with more than 50% (w/w) loading of nHAp on and within the nanofibers.