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Spray-dried chitosan/ethylcellulose microspheres for nasal drug delivery:Swelling study and evaluation of in vitro drug release properties

机译:喷雾干燥的壳聚糖/乙基纤维素微球用于鼻腔给药:溶胀研究和体外药物释放特性评估

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The aim of this study was to develop spray-dried chitosan-based microspheres,suitable for nasal delivery of loratadine,and to evaluate their potential of modifying loratadine release.The microspheres were composed with ethylcellulose (EC) and chitosan (CM) in two different weight ratios,1:2 and 1:3.One-phase systems (dispersions) and two-phase systems (emulsions and suspensions) were subjected to spray-drying,resulting in conventional and composed microspheres,respectively.The microspheres were evaluated with respect to the yield,particle size,encapsulation efficiency,physical state of the drug in the polymer matrix,swelling properties and in vitro drug release profile.It was shown that particle size,swelling ability and loratadine release from spray-dried microspheres were significantly affected by the polymeric composition and feed concentration in spray-drying process.Emulsifying method to produce composed EC/CM microspheres resulted in improved loratadine entrapment and moderate swelling,when compared to conventional chitosan microspheres.It seems like better formation of EC cores and chitosan coating were obtained when higher feed concentration and ultrasonic homogenization were employed in the preparation of emulsion systems and when EC to CM weight ratio was 1:3.
机译:这项研究的目的是开发适合于鼻腔输送氯雷他定的喷雾干燥的壳聚糖基微球,并评估其修饰氯雷他定释放的潜力。该微球由乙基纤维素(EC)和壳聚糖(CM)组成,两种不同的形式重量比为1:2和1:3。分别对一相体系(分散体)和两相体系(乳液和悬浮液)进行喷雾干燥,分别制成常规微球和组成微球。聚合物基质中药物的收率,粒径,包封效率,物理状态,溶胀特性和体外药物释放曲线。研究表明,喷雾干燥微球的粒径,溶胀能力和氯雷他定的释放受到显着影响。通过乳化法生产组成的EC / CM微球,改善了氯雷他定的包封性和适度的悬浮当在乳液体系的制备中采用较高的进料浓度和超声均质化,并且当EC与CM的重量比为1:3时,似乎可以更好地形成EC核和壳聚糖涂层。

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