The use of chitosan in the preparation of bioadhesive buccal films: Film-forming ability and sustaining ibuprofen release

Fadia Mussa, Haytham Mousi, Mahmud S. Treki
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引用次数: 1

Abstract

Aim: Different polymers were introduced into Chitosan bioadhesive buccal films to achieve substantial success in sustaining Ibuprofen release for few hours, with reasonable bioadhesion strength. Design: Thin, isolatable, transparent, and elastic films of these copolymers were prepared. Nineteen formulations have been classified as six systems according to the percentages of hydrocolloids used. Materials and Methods: The films were prepared using the solvent casting technique. Bioadhesion study was conducted using the stomach mucosa of a sacrificed albino rabbit. Hydrocolloids such as Hydroxy Propyl Cellulose (HPC), Chitosan, and Methyl Cellulose (MC), in addition to other polymers, were used in addition to Ibuprofen as a model drug. Results: The mechanical strength and flexibility of the films were confirmed with no signs of breaking down. Selected films composed of about 60% (w/w) HPC were found to show higher tendency to adhere to the stomach mucosa than lower percentages of the same polymer. Chitosan films have released more than 78% of Ibuprofen content in the 1st h of release study. The introduction of MC in these films has led to a slow but continuous increase in the percentage of drugs released, reaching the climax of 82% after 4 h. Conclusion: Films made of formulation (L17) were found to be the most ideal for both releasing appreciable amount of drug (about 98% in 4 h), and their high tendency to adhering to the rabbit mucosa (71.00 Mn/m) giving enough time to exert the drug's effect locally. The mechanism of drug release was found to follow Higuchi's diffusion model for some systems and the classical first-order kinetics for others.
壳聚糖在生物黏附口腔膜制备中的应用:成膜能力和布洛芬的持续释放
目的:在壳聚糖生物黏附口腔膜中引入不同的聚合物,使布洛芬在合理的生物黏附强度下持续释放数小时。设计:制备了这些共聚物的薄、可隔离、透明和有弹性的薄膜。根据所使用的胶体百分比,19种配方被分为6种体系。材料与方法:采用溶剂铸造技术制备薄膜。以白化兔胃黏膜为材料,进行了生物黏附研究。除布洛芬外,还使用了羟基丙基纤维素(HPC)、壳聚糖和甲基纤维素(MC)等水胶体以及其他聚合物作为模型药物。结果:薄膜的机械强度和柔韧性得到证实,无破裂迹象。我们发现,由约60% (w/w)的HPC组成的膜比低百分比的相同聚合物具有更高的粘附胃粘膜的倾向。壳聚糖薄膜在释放实验的第1 h内释放了78%以上的布洛芬。在这些膜中引入MC后,药物释放率缓慢而持续地增加,在4 h后达到82%的高潮。结论:由制剂(L17)制成的膜最理想,既能释放一定量的药物(4 h约98%),又具有较高的粘附兔黏膜的倾向(71.00 Mn/m),有足够的时间局部发挥药物作用。发现药物释放机制在一些系统中遵循Higuchi扩散模型,而在另一些系统中遵循经典的一级动力学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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