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The Controlled Release of Dexamethasone Sodium Phosphate from Bioactive Electrospun PCL/Gelatin Nanofiber Scaffold

机译:从生物活性电纺PCL /明胶纳米纤维支架中控制地塞米松磷酸钠的释放

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摘要

In this study, a system of dexamethasone sodium phosphate (DEXP)-loaded chitosan nanoparticles embedded in poly-ε-caprolacton (PCL) and gelatin electrospun nanofiber scaffold was introduced with potential therapeutic application for treatment of the nervous system. Besides anti-inflammatory properties, DEXP act through its glucocorticoid receptors, which are involved in the inhibition of astrocyte proliferation and microglial activation. Bovine serum albumin (BSA) was used to improve the encapsulation efficiency of DEXP within chitosan nanoparticles and to overcome its initial burst release. BSA incorporation within the chitosan nanoparticles increased the encapsulation efficiency of DEXP from 30% to 77%. The comparison between DEXP release profile from PCL/gelatin scaffold with and without chitosan nanoparticles revealed that the system of DEXP-BSA-loaded chitosan nanoparticles embedded in electrospun PCL nanofiber scaffold provided a more controlled release pattern of the loaded drug. The scaffolds properties in terms of structure, hydrophilicity, cell compatibility, mechanical property, and biodegradability were further investigated, which might show its potential application for the repair of spinal cord injury.
机译:在这项研究中,介绍了一种嵌入地塞米松磷酸钠(DEXP)的壳聚糖纳米粒子嵌入聚ε-己内酰胺(PCL)和明胶电纺纳米纤维支架的系统,具有治疗神经系统的潜在治疗应用。除了具有抗炎特性外,DEXP还通过其糖皮质激素受体发挥作用,该受体参与抑制星形胶质细胞的增殖和小胶质细胞的活化。牛血清白蛋白(BSA)用于提高DEXP在壳聚糖纳米粒子中的封装效率并克服其最初的爆发释放。壳聚糖纳米粒子中BSA的掺入将DEXP的封装效率从30%提高到77%。具有和不具有壳聚糖纳米颗粒的PCL /明胶支架的DEXP释放曲线之间的比较表明,嵌入电纺PCL纳米纤维支架中的DEXP-BSA负载的壳聚糖纳米颗粒系统提供了负载药物的更受控释放模式。从结构,亲水性,细胞相容性,机械性能和生物降解性等方面对支架的性质进行了进一步研究,这可能表明其在修复脊髓损伤中的潜在应用。

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