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Acyclovir-loaded PAN nanofiber membranes prepared using a special electrospinning process

机译:使用特殊的静电纺合过程制备Acyclovir负载锅纳米纤维膜

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A special electrospinning process was successfully developed for the preparation of acyclovir-loaded PAN nanofiber membrane in the present study. An additional apparatus for adjusting the temperature of the spinning solutions was fitted on the glass syringe for easy spinning and getting better performance of nanofibers. PAN nanofibers and acyclovir-loaded PAN nanofibers were prepared using this process with DMSO as solvent. The surface topographies of the as-prepared nanofiber membranes were observed using polarization optical microscope. The results demonstrated that the nanofibers were more uniform with very smooth surface when the electrospinning process was carried out at 80°C. However, the nanofibers were conglutinated together to form fiber mats with a poor structure when electrospinning was conducted at a normal ambient temperature. Electrospinning at 80°C was able to form drug-loaded nanofibers with uniform structure and well drug distribution, whereas electrospinning at 60°C resulted in a phase separation due to the poor solubility of acyclovir in DMSO at a lower temperature. Rising electrospinning temperature facilitates the preparation of drug-loaded nanofibers.
机译:成功开发了一种特殊的静电纺丝方法,用于制备本研究中的Acyclovir负载的锅纳纤维膜。用于调节纺丝溶液温度的附加装置安装在玻璃注射器上,以便于旋转并越好地性能纳米纤维。使用该方法使用该方法使用DMSO作为溶剂制备锅纳纤维和加载Acyclovir负载的锅纳米纤维。使用偏振光学显微镜观察由制备的纳米纤维膜的表面拓扑。结果表明,当在80℃下进行静电纺丝过程时,纳米纤维在非常光滑的表面上更均匀。然而,当在正常环境温度下进行静电纺丝时,纳米纤维将粘合在一起以形成具有差的结构差的纤维垫。在80℃下静电纺丝能够形成具有均匀结构和良好药物分布的药物负载纳米纤维,而在60℃下静电纺丝导致相分离,导致Acyclovir在DMSO中的较低温度下的溶解度差。静电纺丝温度上升有助于制备药物负载纳米纤维。

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