Polysaccharide-Based Nanoparticles for Colon-Targeted Drug Delivery Systems

Y. De Anda-Flores, E. Carvajal‐Millan, A. Campa-Mada, J. Lizardi‐Mendoza, A. Rascón-Chu, J. Tánori-Córdova, A. Martínez-López
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引用次数: 20

Abstract

Polysaccharide biomaterials have gained significant importance in the manufacture of nanoparticles used in colon-targeted drug delivery systems. These systems are a form of non-invasive oral therapy used in the treatment of various diseases. To achieve successful colonic delivery, the chemical, enzymatic and mucoadhesive barriers within the gastrointestinal (GI) tract must be analyzed. This will allow for the nanomaterials to cross these barriers and reach the colon. This review provides information on the development of nanoparticles made from various polysaccharides, which can overcome multiple barriers along the GI tract and affect encapsulation efficiency, drug protection, and release mechanisms upon arrival in the colon. Also, there is information disclosed about the size of the nanoparticles that are usually involved in the mechanisms of diffusion through the barriers in the GI tract, which may influence early drug degradation and release in the digestive tract.
用于结肠靶向药物递送系统的多糖纳米颗粒
多糖生物材料在制造用于结肠靶向药物输送系统的纳米颗粒方面具有重要意义。这些系统是非侵入性口服疗法的一种形式,用于治疗各种疾病。为了实现成功的结肠输送,必须分析胃肠道(GI)内的化学、酶和黏附屏障。这将允许纳米材料穿过这些屏障并到达结肠。本文综述了由多种多糖制成的纳米颗粒的研究进展,这些纳米颗粒可以克服胃肠道中的多种屏障,影响包封效率、药物保护和到达结肠后的释放机制。此外,还有关于纳米颗粒大小的信息,这些纳米颗粒通常参与胃肠道屏障扩散机制,这可能影响药物在消化道中的早期降解和释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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