Collagen functionalized thermoplastic polyurethane nanofibers (TPU/collagen) were successfully produced by coaxial electrospinning technique with a goal to develop biomedical scaffold. A series of tests were conducted to characterize the compound nanofiber and its membrane in this study. Surface morphology and interior structure of the ultrafine fibers were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and atomic force microscopy (AFM), whereas the fiber diameter distribution was also measured. The crosslinked membranes were also characterized by SEM. Porosities of different kinds of electrospun mats were determined. The surface chemistry and chemical composition of collagen/TPU coaxial nanofibrous membranes were verified by X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectrometry (FTIR). Mechanical measurements were carried out by applying tensile test loads to samples which were prepared from electrospun ultra fine non-woven fiber mats. The coaxial electrospun nanofibers were further investigated as a promising scaffold for PIECs culture. The results demonstrated that coaxial electrospun composite nanofibers had the characters of native extracellular matrix and may be used effectively as an alternative material for tissue engineering and functional biomaterials. 相似文献
Electrospinning is a simple and effective technology for fabricating nanofibers and polymer blending provides strength and minimal defects of electrospun ones. Therefore, in the present study, fabrication, and characterization of nylon-6/gelatin electrospun nanofibers using low-toxic solvents was investigated as means to improve the morphological deficiencies of gelatin nanofibers and facilitate its electrospinnability. The morphology of electrospun nylon-6/gelatin nanofibers were characterized using scanning electron microscope (SEM). SEM results showed that electrospun blend nanofibers had smooth surface with average diameter of from 40 to 100 nm; while, the miscibility of the blend and thermal behavior of nanofibers were determined using Fourier transform-infrared spectroscopy (FTIR) and differential scanning calorimeter (DSC). Water contact-angle measurement (WCA) was employed to investigating the wettability of nanofibers. 相似文献
Carboxymethyl starch (CMS) is a natural polymer derived from sago starch that is obtained from sago palm (Metroxylon spp.). Herein, CMS was used as a polysaccharide source in preparations of composite nanofibers with poly(L‐lactide acid) (PLLA). The incorporation of CMS with PLLA in nanofiber form has great potential to be used in biomedical applications. The composite PLLA/CMS nanofibers were fabricated by electrospinning technique at various ratios of CMS, which were 5, 10, 15, and 20% vol/vol. The composite nanofibers were characterized according to their physical morphology, chemical interaction, wettability, water uptake, and thermal and mechanical behaviors. The result showed that uniform and bead‐free nanofibers were produced at the low ratio of CMS while fractal and discontinuing fiber was observed at a high ratio of CMS. A better mechanical strength was obtained at low CMS ratio as compared with higher one. Fourier transform infrared results showed that there was an interaction between CMS and PLLA after electrospinning. The surface hydrophilicity and water uptake increased with increasing ratio of CMS. The results from the differential scanning calorimeter analysis showed the decrease of the glass transition (Tg) and cold crystallization temperature (Tcc) of the nanofiber after addition of CMS in PLLA. 相似文献
Polysulfone nanofibers were prepared by electrospinning. The electrospinning equipment was designed in a new way, wherein
the spinneret was combined with a gas jet device. The intrinsic viscosity of the used polysulfone was 0.197 dL/g in dimethyl
acetamide, which was also the solvent in electrospinning. The gas used in this gas jet/electrostatic spinning was nitrogen.
The relationship between the process parameters and the average diameter of polysulfone nanofibers was investigated. The main
process parameters studied in this work were the voltage, the flow rate of the spinning fluid, the distance between the spinneret
and the nanofiber collector and the temperature in the spinning chamber. The other important factors determining the nanometer
diameter were the spinning fluid properties including its viscosity, surface tension and electrical conductivity. The average
diameter and the diameter distribution of electrospinning nanofibers were measured experimentally by using scanning electron
microscopy. The diameter of polysulfone nanofibers prepared by the gas jet/electrostatic spinning was in the range 50–500
nm. It was found that the diameter of nanofibers mainly depended on high voltage, the gap between the spinneret and the collector
and the concentration of polymer solutions. It is concluded that the gas-jet/electrospinning is a better method than the conventional
electrospinning, in that it makes the nanofibers finer and more uniform and exhibits higher efficiency in the process of electrospinning.
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Translated from Acta Polymerica Sinica, 2005, (5) (in Chinese) 相似文献
Chitosan/gelatin blend nanofibers were electrospun and the focus of this study was on the chitosan and gelatin concretions and on morphology of resulting nanofibers. The morphology of electrospun chitosan/gelatin blend nanofibers were characterized using scanning electron microscope (SEM). The miscibility of blend was determined using a SEM and Fourier transform infrared spectrometer/attenuated total reflectance (FTIR/ATR). Antibacterial property and stability of samples was also investigated. Water contact angle measurement (WCA) was employed to investigate the wettability of nanofibers. 相似文献
This work was focused on preparation and characterizations of chitosan blended polyamide-6 nanofibers by a new single solvent system via electrospinning process for human osteoblastic (HOB) cell culture applications. The morphological, structural and thermal properties of the polyamide-6/chitosan nanofibers were analyzed by using field-emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), Fourier transform-infrared (FT-IR) spectroscopy, Raman spectroscopy, differential scanning calorimetry (DSC) and thermogravimetry (TGA). SEM images revealed that the nanofibers were well-oriented and had good incorporation of chitosan. FT-IR results indicated that the amino groups of chitosan existed in the blended nanofibers. TGA analysis revealed that the onset degradation temperature was decreased with increasing chitosan content in the blended nanofibers. The morphological features of the cells attached on nanofibers were confirmed by SEM. The adhesion, viability and proliferation properties of osteoblast cells on the polyamide-6/chitosan blended nanofibers were analyzed by in vitro cell compatibility test. 相似文献
We report a simple method to produce stable chitosan derivative nanofibers via electrospinning. A chitosan solution with lactate salt was electrospun to produce nanofibers, followed by thermal treatment to enhance fiber stability. Chemical and morphological analyses demonstrated that the resulting nanofibers were crosslinked via amidation between chitosan and lactate salt. These fibers exhibited sustained morphological and structural stabilities to serve as a scaffold for biomedical applications. 相似文献
Core-shell nanofibers are of great interest in the field of tissue engineering and cell biology. We fabricated porous core-shell fiber networks using an electrospinning system with a water-immersed collector. We hypothesized that the phase separation and solvent evaporation process would enable the control of the pore formation on the core-shell fiber networks. To synthesize porous core-shell fiber networks, we used polycaprolactone (PCL) and gelatin. Quantitative analysis showed that the sizes of gelatin-PCL core-shell nanofibers increased with PCL concentrations. We also observed that the shapes of the pores created on the PCL fiber networks were elongated, whereas the gelatin-PCL core-shell fiber networks had circular pores. The surface areas of porous nanofibers were larger than those of the nonporous nanofibers due to the highly volatile solvent and phase separation process. The porous core-shell fiber network was also used as a matrix to culture various cell types, such as embryonic stem cells, breast cancer cells, and fibroblast cells. Therefore, this porous core-shell polymeric fiber network could be a potentially powerful tool for tissue engineering and biological applications. 相似文献
Ultrafine fibers were spun from polyacrylonitrile (PAN)/N,N-dimethyl formamide (DMF) solution as a precursor of carbon nanofibers using a homemade electrospinning set-up. Fibers with diameter ranging from 200 nm to 1200 nm were obtained. Morphology of fibers and distribution of fiber diameter were investigated varying concentration and applied voltage by scanning electric microscopy (SEM). Average fiber diameter and distribution were determined from 100 measurements of the random fibers with an image analyzer (SemAfore 5.0, JEOL). A more systematic understanding of process parameters was obtained and a quantitative relationship between electrospinning parameters and average fiber diameter was established by response surface methodology (RSM). It was concluded that concentration of solution played an important role to the diameter of fibers and standard deviation of fiber diameter. Applied voltage had no significant impact on fiber diameter and standard deviation of fiber diameter. 相似文献
In this work, the optimal electrospinning conditions of trans-polyisoprene (TPI) solutions were evaluated nevertheless its lower glass transition temperature than the room temperature. Subsequently, chemical crosslinking of TPI nonwovens was firstly investigated by vulcanizing at high temperatures in the case of the persistence of nanofiber structure. For this purpose, curing agents of TPI were embedded in TPI nanofibers by co-electrospinning, and then a protect layer was coated on TPI nanofibers by filtering gelatin solution going through TPI nonwoven before the vulcanization at 140?160 °C. The results showed that the vulcanization of TPI fibrous nonwoven at high temperatures did not destroy the fiber morphology. Interestingly, TPI fibrous nonwovens after vulcanization showed excellent mechanical properties (~17 MPa of tensile strength) that could be comparable to or even higher than that of some bulk rubber materials. 相似文献
A kind of water-stable phosphotungstic acid/polyvinyl alcohol(PW12/PVA) fiber was prepared by thermal or chemical crosslinking treatments with the help of electrospinning, and silver nanoparticles(NPs) modified fibrous precursor was successfully obtained by photoreduced method. The nanocomposites were characterized by transformation infrared spectroscopy(FTIR), UV-Vis diffuse reflection spectroscopy(DRS), field environmental scanning electron microscopy(FE-SEM), transmission electron microscopy(TEM) and X-ray photoelectron spectroscopy(XPS). The results indicate that the sizes of silver NPs are about 20 or 40 nm on thermally or glutaraldehyde(GA) vapor crosslinked PW12/PVA fiber, respectively. As a photocatalyst, PW12/PVA fiber possesses high surface area to volume ratio, stable recyclability, and efficient transportation of electrons under visible light. The nanohybrids exhibit excellent photocatalytic activity for the degradation of Rhodamin B than PW12/PVA nanofiber. 相似文献
The potential of polarizing-interference Pluta microscope for determination of optical birefringence of individual nanofibers formed by electrospinning was shown. This technique can be applied for measurements of fiber birefringence, practically at diameter above 300 nm. The molecular orientation of individual polycaprolactone (PCL) nanofibers was determined from birefringence assuming the same orientation of both phases, crystal and amorphous. The molecular orientation was determined using DSC crystallinity, crystal intrinsic birefringence calculated for the first time for PCL from bond polarizabilities as well as estimated value of amorphous intrinsic birefringence. Our results indicate that the birefringence and thus molecular orientation are strongly inhomogeneous along the nanofibers, reflecting a complex nature of forces acting during electrospinning process. The average molecular orientation is weak if any, being dependent together with fiber thickness and crystallinity on electrospinning parameters, like applied voltage, concentration and type of solvent. The obtained results indicate that the average molecular orientation displays similar dependence on applied voltage as fiber diameter. Relatively low melting temperature of electrospun nanofibers suggests low crystal size and/or high concentration of defects in crystals. This observation corresponds with low crystallinity and molecular orientation, indicating together relatively low degree of crystal ordering due to high rate of cooling and solvent evaporation during electrospinning, limiting thus crystallization process. 相似文献
We have successfully fabricated poly(ethylene oxide) (PEO) nanofibers containing embedded multi‐wall carbon nanotubes (MWCNTs). An initial dispersion of the MWCNTs in distilled water was achieved using sodium dodecyl sulfate. Subsequently, the dispersion was decanted into a PEO solution, which enabled separation of the MWCNTs and their individual incorporation into the PEO nanofibers on subsequent electrospinning. Initially, the carbon nanotube (CNT) rods were randomly oriented, but owing to the sink‐like flow in the electrospinning wedge, they became gradually oriented along the streaming direction, in order that oriented CNTs were obtained on entering the electrospun jet. Individual MWCNTs became embedded in the nanofibers, and were mostly aligned along the fiber axis. Evidence of load transfer to the nanotubes in the composite nanofiber was observed from the field‐emission scanning electron microscopy, transmission electron microscopy and conductivity data. 相似文献
Composite nanofibers of poly(caprolactone) (PCL) and gelatin crosslinked with genipin are prepared. The contact angles and mechanical properties of crosslinked PCL‐gelatin nanofibers decrease as the gelatin content increases. The proliferation of myoblasts is higher in the crosslinked PCL‐gelatin nanofibers than in the PCL nanofibers, and the formation of myotubes is only observed on the crosslinked PCL‐gelatin nanofibers. The expression level of myogenin, myosin heavy chain, and troponin T genes is increased as the gelatin content is increased. The results suggest that PCL‐gelatin nanofibers crosslinked with genipin can be used as a substrate to modulate proliferation and differentiation of myoblasts, presenting potential applications in muscle tissue engineering.