Department of Chemistry, College of Science, King Saud University, Riyadh 11451, Saudi Arabia; PG and Research Department of Chemistry, Jamal Mohamed College, Bharathidasan University, Tiruchirapalli 620 024, Tamilnadu, India.
PG and Research Department of Chemistry, Jamal Mohamed College, Bharathidasan University, Tiruchirapalli 620 024, Tamilnadu, India.
Int J Biol Macromol. 2018 Sep;116:1250-1259. doi: 10.1016/j.ijbiomac.2018.05.130. Epub 2018 May 20.
A green electrospinning was used for the fabrication of PVA/Dex (dextran sulfate) nanofibers as a carrier for drug delivery. Core-shell nanofibers were fabricated by emulsion electrospinning from PVA/Dex loaded with ciprofloxacin (Cipro) as a model drug. The ratio of the PVA/Dex mixture was optimized and nanofibers were stabilized against disintegration in water by thermal treatment at 120 °C. The morphology of the prepared nanofibers was observed by scanning electron microscopy (SEM) and the core-shell structure of the nanofibers was confirmed by transmission electron microscopy (TEM). Drug entrapment was confirmed by Fourier-transform infrared spectroscopy (FT-IR) and thermogravimetric analysis (TGA). The interaction between PVA and Dex was affirmed by differential scanning calorimetry (DSC). In vitro drug release was monitored by UV-vis spectrophotometer and its associated mechanism was studied using diverse kinetic models. The release study demonstrated that the core-shell nanofibers can sustain the Cipro release compared with the blending electrospinning nanofibers. Moreover, the drug release mechanism is controlled by the Dex content of the polymer blends and can occur by diffusion within the delivery system. It is anticipated that Cipro@PVA/Dex nanofibers are promising eco-friendly drug delivery system which can be prepared by a green method.
绿色静电纺丝被用于制备 PVA/Dex(硫酸葡聚糖)纳米纤维作为药物输送的载体。通过乳液静电纺丝从负载环丙沙星(Cipro)的 PVA/Dex 中制备核壳纳米纤维作为模型药物。优化了 PVA/Dex 混合物的比例,并通过在 120°C 下进行热处理使纳米纤维在水中稳定,防止其崩解。通过扫描电子显微镜 (SEM) 观察了制备的纳米纤维的形态,并通过透射电子显微镜 (TEM) 证实了纳米纤维的核壳结构。通过傅里叶变换红外光谱 (FT-IR) 和热重分析 (TGA) 证实了药物包封。通过差示扫描量热法 (DSC) 证实了 PVA 和 Dex 之间的相互作用。通过紫外可见分光光度计监测体外药物释放,并使用多种动力学模型研究其相关机制。释放研究表明,与共混静电纺丝纳米纤维相比,核壳纳米纤维可以持续释放 Cipro。此外,药物释放机制受聚合物共混物中 Dex 含量的控制,并且可以通过输送系统内的扩散发生。预计 Cipro@PVA/Dex 纳米纤维是一种有前途的环保药物输送系统,可通过绿色方法制备。