首页> 外文期刊>Journal of Microencapsulation: Microcapsules Liposomes Nanoparticles Microcells Microspheres >Ibuprofen-loaded ethylcellulose/polystyrene microspheres: an approach to get prolonged drug release with reduced burst effect and low ethylcellulose content
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Ibuprofen-loaded ethylcellulose/polystyrene microspheres: an approach to get prolonged drug release with reduced burst effect and low ethylcellulose content

机译:布洛芬负载的乙基纤维素/聚苯乙烯微球:一种延长药物释放的方法,具有降低的破裂效应和较低的乙基纤维素含量

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摘要

The aim of this study ws to develop ethylcellulose micropheres for prolonged drug delivery with reduced burst effect. Ethylcellulose microspheres loaded with ibuprofen were prepared with and without polystyrene, which was used to retard drug release from ethylcellulose microspheres. Ibuprofen-loaded ethylcellulose microspheres with a polystyrene content of 0-25% were prepared by the solvent evaporation technique and characterized by drug loading, infrared spectroscopy, differential scanning calorimetry and scanning electron microscopy. The in vitro release studies were performed to study the influence of polystyrene on ibuprofen release from ethylcellulose microspheres. The microspheres showed 28-46% of drug loading and 80-92% of entrapment, depending on polymer/drug ratio. The infrared spectrum and thermogram showed stable character of ibuprofen in the microspheres and revealed an absence of drug polymer interaction. The prepared microspheres were spherical in shape and had a size range of 0.1-4 mum. Ethylcellulose/polystyrene micro-spheres showed prolonged drug release and less burst effect when compared to microspheres prepared with ethylcullulose alone. Microspheres prepared with an ethylcellulose/polstyrene ratio of 80:20 gave a required release pattern for oral durg delivery. The presence of polystyrene above this ratio gave release over 24 h. To find out the mechanism of drug release from ethylcellulose/polystyrene microspheres, the data obtained from in vitro release were fitted in various kinetic models. High correlation was obtained in Higuchi and Korsmeyer-Peppas models. The drug release from ethylcellulose/polystyrene microspheres was found to be diffusion controlled.
机译:这项研究的目的是开发乙基纤维素微球,以延长药物的输送,降低突释作用。在有和没有聚苯乙烯的情况下,制备了装载有布洛芬的乙基纤维素微球,该聚苯乙烯用于阻止药物从乙基纤维素微球中释放。通过溶剂蒸发技术制备了聚苯乙烯含量为0-25%的布洛芬负载乙基纤维素微球,并通过载药,红外光谱,差示扫描量热法和扫描电子显微镜进行了表征。进行了体外释放研究以研究聚苯乙烯对布洛芬从乙基纤维素微球中释放的影响。根据聚合物/药物的比例,微球显示出28-46%的载药量和80-92%的包封物。红外光谱和热谱图显示了布洛芬在微球中的稳定特性,并且表明没有药物聚合物相互作用。制备的微球为球形,尺寸范围为0.1-4μm。与仅用乙基海藻糖制备的微球相比,乙基纤维素/聚苯乙烯微球显示出延长的药物释放和较小的破裂作用。乙基纤维素/聚苯乙烯比例为80:20制备的微球具有口服药物递送所需的释放方式。高于该比例的聚苯乙烯的存在在24小时内释放。为了找出药物从乙基纤维素/聚苯乙烯微球中释放的机理,将体外释放获得的数据拟合到各种动力学模型中。在Higuchi和Korsmeyer-Peppas模型中获得了高度相关性。发现从乙基纤维素/聚苯乙烯微球释放的药物是受扩散控制的。

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