Morais Maria S, Bonfim Daniela P F, Aguiar Mônica L, Oliveira Wanderley P
Laboratory of Pharmaceutical Processes, LAPROFAR, Faculty of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, 14040-903 Brazil.
Department of Chemical Engineering, University Federal of São Carlos, Rod. Washington Luiz, km 235, São Carlos, SP Brazil.
J Pharm Innov. 2022 Aug 30:1-15. doi: 10.1007/s12247-022-09681-7.
The objective of this work was to produce and characterise biodegradable poly (vinyl alcohol) (PVA) nanofibre loaded with green propolis extract (GPE), chitosan (CS) and nystatin (NYS) alone and in mixtures as a potential wound dressing material.
The GPE, NYS and CS1% were loaded in electrospinning compositions based on PVA 7%, 8% and 12% solubilised in milli-Q water or a mixture of water and glacial acetic acid. The electrospinning compositions without actives (blank) and those loaded with actives were characterised by determining the pH, electrical conductivity and rheological properties. An image analysis procedure applied to photomicrographs obtained by scanning electronic microscopy (SEM) allowed the determination of the nanofibres' diameter distribution and average surface porosity. The disintegration time and swelling ratio of the nanofibre mats were also determined.
The physicochemical parameters of the electrospinning compositions (pH, electrical conductivity and rheology) and the incorporated active ingredients (GPE, CS and NYS) affected the electrospun nanofibre mats properties. The electrospun nanofibres' mean diameters and surface porosity ranged from 151.5 to 684.5 nm and from 0.29 ± 0.04 to 0.50 ± 0.05. The PVA/CS electrospun nanofibres fibres exhibited the smallest diameters, high surface porosity, water absorption capacity and disintegration time. The characteristics of the PVA/CS nanofibres mat associated with the biodegradability of the polymers make them a novel material with the potential to be applied as wound and burn dressings.
本研究的目的是制备并表征负载绿蜂胶提取物(GPE)、壳聚糖(CS)和制霉菌素(NYS)的可生物降解聚乙烯醇(PVA)纳米纤维,单独或混合使用,作为潜在的伤口敷料材料。
将GPE、NYS和1%的CS加入到基于7%、8%和12% PVA的静电纺丝组合物中,PVA溶解在超纯水或水与冰醋酸的混合物中。通过测定pH值、电导率和流变学性质,对不含活性成分的静电纺丝组合物(空白)和负载活性成分的组合物进行表征。应用图像分析程序对扫描电子显微镜(SEM)获得的显微照片进行分析,以确定纳米纤维的直径分布和平均表面孔隙率。还测定了纳米纤维垫的崩解时间和溶胀率。
静电纺丝组合物的物理化学参数(pH值、电导率和流变学)以及所含活性成分(GPE、CS和NYS)影响了静电纺纳米纤维垫的性能。静电纺纳米纤维的平均直径和表面孔隙率范围分别为151.5至684.5 nm和0.29±0.04至0.50±0.05。PVA/CS静电纺纳米纤维的直径最小,表面孔隙率高,吸水性强,崩解时间短。PVA/CS纳米纤维垫的特性与聚合物的生物降解性使其成为一种有潜力应用于伤口和烧伤敷料的新型材料。