Capparis spinosa L. (CSL) is a medicinal plant with high antibacterial activity against a variety of pathogens and antioxidation properties. In this paper, for the first time, nanofiber membranes of polylactic acid (PLA) containing 0, 4, 7,and 10 wt% CSL ethyl acetate extract were fabricated by electrospinning. Scanning electron microscopy showed that the fiber diameter decreased after adding CSL to the PLA nanofibers. Fourier transform infrared spectroscopy confirmed that CSL was successfully incorporated in the matrix. The water contact angle test proved that the addition of CSL improved the hydrophilic properties of the material. Moreover, the addition of CSL improved the oxidation resistance of the composite fiber membrane. A burst drug release from the composite nanofibers occurred within the first 12 hr, followed by slow release over a prolonged period of time. As the concentration of CSL increased, the inhibition ability of nanofibers against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) gradually increased. In summary, due to their good mechanical, antioxidant, and antibacterial properties, CSL/PLA nanofiber membranes may possess potential applications as wound dressing materials. 相似文献
To endow nanofibers with the desirable antibacterial and mechanical properties, a facile strategy using Pickering emulsion (PE) electrospinning is proposed to prepare functional nanofibers with core/shell structure for the first time. The water‐in‐oil (W/O) Pickering emulsion stabilized by oleic acid (OA)‐coated magnetite iron oxide nanoparticles (OA‐MIONs) is comprised of aqueous vancomycin hydrochloride (Van) solution and poly(lactic acid) (PLA) solution. The core/shell structure of the electrospun Van/OA‐MIONs‐PLA nanofibers is confirmed by scanning electron microscopy and transmission electron microscopy observation. Sustained release of Van from the PE electrospun nanofiber membrane is achieved within the time of 600 h. Compared with the neat PLA electrospun nanofiber membrane, 57% increase of tensile strength and 36% elevation of elongation at break are achieved on PE electrospun nanofiber membrane. In addition, the PE electrospun nanofiber membrane demonstrates excellent antibacterial property stemming from the combinational antibacterial activities of OA‐MIONs and Van. The Van‐loaded PE electrospinning nanofibers with sustained antibacterial performance possess potential applications in tissue engineering and drug delivery.
In this paper, PLA/RSF with different mass ratios and aspirin-loaded PLA/RSF composite nanofiber membranes were prepared via electrospinning. Polylactic acid (PLA) and regenerated silk fibroin (RSF) were dissolved in trifluoroacetic acid and dichloromethane at a volume ratio of 70/30. The structure analysis made by Fourier transform infrared spectroscopy (FTIR) suggested that PLA and RSF blended very well in the composite membranes. In addition, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) revealed that the average diameters of composite nanofibers were between 80 and 210 nm. Furthermore, the composite nanofibers had better uniformity in the range of the experiment, and the average diameter of composite nanofibers decreased with the increase of aspirin content. Wettability performance was investigated via contact water angle meter; the hydrophilic property of composite membranes had been improved with the existence of SF. Drug release property was tested by detecting the absorbency of drug in PBS solution via UV–visible spectroscopy, and the results showed that drug release rate reached the maximum when the mass ratio of PLA/RSF was 8/3. With the raise of aspirin content, the drug release rate increased. The in vitro anticoagulation behavior was studied by static platelet adhesion test. The results revealed that the anticoagulation property of composite membranes was superior to that of pure PLA nanofiber membranes. The anticoagulation property significantly improved in the presence of aspirin. 相似文献
In this paper, we fabricate ZnO nanofibers and nanoparticles through electrospinning precursor solution zinc acetate(ZnAc)/cellulose acetate(CA) in mixed-solvent N , N -dimethylformamide/acetone. Depending on the posttreatment of precursor ZnAc/CA composite nanofibers, both ZnO nanofibers and nanoparticles were synthesized after calcination of precursor nanofibers. The morphology and crystal structure of the ZnO nanofiber and nanoparticle were characterized by scanning electron microscopy, transmission electron microscopy, atomic force microscopy, and X-ray diffraction. It was found that the mean diameter of the ZnO nanofiber and nanoparticle was ca. 78 and 30 nm, respectively. The photo-degradation of dye molecules such as Rhodamine B and acid fuchsin catalyzed by the ZnO nanofiber and nanoparticle was evaluated under the irradiation of visible light. Both morphological ZnO species showed strong photocatalytic activity. However, the ZnO nanofiber in the form of nanofibrous mats showed much higher efficiency than the nanoparticle although the latter has a smaller size than the former. The porous structure of ZnO nanofibrous mats is believed to improve the contacting surface areas between the catalyst and the dye molecules, while the aggregation of ZnO nanoparticle in the solution lowers the photocatalytic efficiency. 相似文献
