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Development of Bioadhesive Chitosan Superporous Hydrogel Composite Particles Based Intestinal Drug Delivery System

机译:生物粘附性壳聚糖超孔水凝胶复合颗粒肠内给药系统的开发

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摘要

Bioadhesive superporous hydrogel composite (SPHC) particles were developed for an intestinal delivery of metoprolol succinate and characterized for density, porosity, swelling, morphology, and bioadhesion studies. Chitosan and HPMC were used as bioadhesive and release retardant polymers, respectively. A 32 full factorial design was applied to optimize the concentration of chitosan and HPMC. The drug loaded bioadhesive SPHC particles were filled in capsule, and the capsule was coated with cellulose acetate phthalate and evaluated for drug content, in vitro drug release, and stability studies. To ascertain the drug release kinetics, the drug release profiles were fitted for mathematical models. The prepared system remains bioadhesive up to eight hours in intestine and showed Hixson-Crowell release with anomalous nonfickian type of drug transport. The application of SPHC polymer particles as a biomaterial carrier opens a new insight into bioadhesive drug delivery system and could be a future platform for other molecules for intestinal delivery.
机译:开发了生物粘附性超多孔水凝胶复合物(SPHC)颗粒,用于琥珀酸美托洛尔的肠内递送,并针对密度,孔隙率,溶胀,形态和生物粘附性研究进行了表征。壳聚糖和HPMC分别用作生物粘附和释放延迟聚合物。应用3 2 全因子设计优化壳聚糖和HPMC的浓度。将装载有药物的生物粘附性SPHC颗粒填充到胶囊中,并在该胶囊上涂上邻苯二甲酸醋酸纤维素,并评估药物含量,体外药物释放和稳定性研究。为了确定药物释放动力学,将药物释放曲线拟合为数学模型。所制备的系统在肠道中最多可保持8个小时的生物粘附性,并显示出Hixson-Crowell释放,并带有异常的非菲克式药物转运。 SPHC聚合物颗粒作为生物材料载体的应用为生物粘附性药物输送系统打开了新的视野,并可能成为其他分子用于肠道输送的未来平台。

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