用于结肠靶向给药的抗寄生虫药物微球的制备与评估

Tushar Kumar G. Ingle, S. D. Pande, S. Atram, N. Bobade, Vikrant Wankhede
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引用次数: 0

摘要

本研究的目的是开发用于结肠靶向给药系统的缓释微球,以提高疗效,同时最大限度地减少全身副作用。在结肠中控制和延长药物释放可显著改善各种结肠相关疾病的治疗效果。微球是尺寸在 1 到 1000 微米之间的球形小颗粒,采用可生物降解的聚合物和天然材料配制,以确保生物相容性和药物的可控释放。配制过程包括选择合适的聚合物,如聚乳酸和聚乙醇酸,以及在微球中加入药物。对配制好的微球进行了广泛的评估,以评估它们是否适合用于持续释放结肠靶向给药。评估参数包括药物包封效率、粒度分布、表面形态和体外药物释放。体外药物释放研究使用模拟胃肠液进行,以模拟胃肠道内的情况。缓释微球在较长时间内表现出药物释放受控,特别是在结肠区域。这种缓释特性是通过优化聚合物成分和配方参数实现的,从而使微球逐渐降解,药物随之释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation and Evaluation of Microspheres for Colon Targeted Drug Delivery Using Anthelminthics Drugs
The objective of this study was to develop sustained release microspheres for colon-targeted drug delivery system to enhance therapeutic efficacy while minimizing systemic side effects. The controlled and prolonged release of drugs in the colon can significantly improve the treatment outcomes for various colon-related diseases. Microspheres, small spherical particles with sizes ranging from 1 to 1000 micrometers, were formulated using biodegradable polymers and natural materials to ensure biocompatibility and controlled drug release. The formulation process involved the selection of appropriate polymers, such as poly lactic acid and polyglycolic acid, and the incorporation of the drug within the microspheres. Various techniques, including solvent evaporation, coacervation, and spray drying, were employed to prepare the microspheres with the desired drug-loading efficiency and particle size distribution.The formulated microspheres were extensively evaluated to assess their suitability for sustained release colon-targeted drug delivery. Evaluation parameters included drug encapsulation efficiency, particle size distribution, surface morphology and in vitro.In vitro drug release studies were conducted using simulated gastrointestinal fluids to mimic the conditions in the gastrointestinal tract. The sustained release microspheres exhibited controlled drug release over an extended period, specifically in the colon region. This sustained release profile was achieved by optimizing the polymer composition and formulation parameters, which allowed for the gradual degradation of the microspheres and subsequent release of the drug.
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