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Design and characterization of dual drug delivery based on in-situ assembled PVA/PAN core-shell nanofibers for wound dressing application

机译:基于原位组装的PVA / PAN核壳纳米纤维的双重药物递送的设计和表征用于伤口敷料应用

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摘要

Core-shell nanofibers with the ability to carry multiple drugs are attracting the attention to develop appropriate drug delivery systems for wounds dressing applications. In this study, biocompatible core-shell nanofibers have been designed as a promising dual-drug carrier with the capability of delivering both water-soluble and organic solvent-soluble drugs simultaneously. With the aim of fabricating the core-shell nanofibers, the dipping method has been employed. For this propose, core nanofibers made from polyvinyl alcohol (PVA) were immersed in various concentrations of polyacrylonitrile (PAN) and cross-linked by dipping into ethanol. Diclofenac sodium salt (DSs) and gentamicin sulfate (GENs) have been loaded into the core and shell nanofibers as models of the drug, respectively. The morphology study of core-shell nanofibers showed that the concentrations between 1% w/w up to 2% w/w PAN/GENs, with deep penetration into the internal layers of PAV/DSs nanofibers could lead to the core-shell structure. The cytotoxicity results showed the competency of designed core-shell nanofibers for wound dressing application. Also, the release profile exhibits the controllable behavior of drug release.
机译:具有携带多种药物能力的核壳纳米纤维吸引了人们的注意力,以开发适合伤口敷料应用的药物递送系统。在这项研究中,生物相容性核壳纳米纤维已被设计为一种有前途的双重药物载体,具有同时递送水溶性和有机溶剂可溶性药物的能力。为了制造核-壳纳米纤维,已采用浸渍法。对于此建议,将聚乙烯醇(PVA)制成的核心纳米纤维浸入各种浓度的聚丙烯腈(PAN)中,并通过浸入乙醇中进行交联。双氯芬酸钠盐(DSs)和硫酸庆大霉素(GENs)已分别装载到核和壳纳米纤维中,作为该药物的模型。核-壳纳米纤维的形态研究表明,浓度在1%w / w至2%w / w PAN / GENs之间,并深入渗透到PAV / DSs纳米纤维的内层中可能导致核-壳结构。细胞毒性结果表明,设计的核壳纳米纤维具有用于伤口敷料的能力。而且,释放曲线表现出药物释放的可控行为。

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