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1.
Gallic acid (GA)–loaded cellulose acetate (CA) nanofiber mats with 10 to 40 wt.% GA contents (based on the weight of CA) were fabricated by electrospinning. The effects of GA contents and applied potential on the morphology and the average diameters of fibers were studied. The electrospun fiber mats containing 20 and 40 wt.% GA were investigated for their potential use as carrier of GA in wound dressing application. The GA‐loaded CA films were prepared by solvent casting technique for use in comparative studies. Determination of the release characteristics of GA from the GA‐loaded fiber mats and films was carried out by the total immersion and the transdermal diffusion through a pig skin method in acetate buffer solution (pH 5.5) or normal saline (pH 7.0) at either 32 or 37°C, respectively. In the total immersion method, the maximum amounts of the GA released from the fiber mats containing 20 and 40 wt.% GA in the acetate buffer were approximately 97% and 71% (based on the weight of initial GA), while those of the GA released into the normal saline were approximately 96% and 81%, respectively. Lower values were observed in the experiments of the transdermal diffusion through a pig skin method. The corresponding GA‐loaded CA films showed the lower amounts of GA released into media. The as‐loaded and the as‐released GA remained its antioxidant activity as investigated by 1,1‐diphenyl‐2‐picrylhydrazyl (DPPH) assay. Lastly, the GA‐loaded CA fiber mats exhibited antibacterial activity against Staphylococcus aureus, which showed the potential for use as wound dressing materials.  相似文献   

2.
Fabrication and characterization of chitosan/poly(vinyl alcohol) electrospun nanofibers for adsorption of phenol from water were investigated. The effects of voltage (15–30 kV), solution injection flow rate (0.5–1.5 ml/hr), distance of needle and collector (10–20 cm) and chitosan/poly(vinyl alcohol) ratio (25/75, 50/50, 75/25) were studied to obtain the optimum electrospinning conditions for the maximum adsorption capacity of phenol. Central composite design (CCD) was used to investigate and optimize the processing factors for production of chitosan/poly(vinyl alcohol) nanofibers from aqueous solutions. The nanofibers were characterized using scanning electron microscopy and Fourier transform infrared spectroscopy (FTIR). Uniform beadless nanofibers with the minimum diameters of 3–11 nm were obtained at chitosan/poly(vinyl alcohol) ratio of 50/50, voltage of 22.5 kV, distance of 15 cm and injection flow rate of 1.99 ml hr?1. Fourier transform infrared spectrum of chitosan/poly(vinyl alcohol) exhibited the existence of relevant functional groups of both poly(vinyl alcohol) and chitosan in the blends. Results of CCD show that among all processing factors, rate of electrospinning will highly affect the nanofiber adsorption. The response surface quadratic order model presented correlation coefficient explaining 69.5% of the variability in the adsorption. Copyright © 2017 John Wiley & Sons, Ltd.  相似文献   

3.
A novel heterogenized organometallic catalyst was synthesized by coordinating palladium with polyvinyl alcohol‐functionalized Fe3O4@SiO2 nanospheres. This novel catalyst was characterized using Fourier transform infrared spectroscopy, X‐ray diffraction, transmission electron microscope, field emission scanning electron microscope, dynamic light scattering, UV–vis spectroscopy, X‐ray photoelectron spectroscopy, energy dispersive X‐ray analysis, thermogravimetric analysis and inductively coupled plasma analysis. The prepared palladium nanoparticles supported on polyvinyl alcohol functionalized Fe3O4@SiO2 nanoparticles were successfully applied as a magnetically recyclable catalyst in Heck and Sonogashira coupling reactions in water. They showed remarkable activity toward aryl halides (I, Br, Cl) using very low palladium loading in excellent yields and demonstrated high TONs (mmol of product per mmol of catalyst). Also, the catalyst could be magnetically separated and reused seven times without any appreciable loss of catalytic activity.  相似文献   

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