结肠靶向微珠:治疗NDDS的新方法

Piyush Mahajan
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引用次数: 0

摘要

在口服结肠特异性给药系统中,结肠有大量的淋巴瘤组织(有利于直接吸收到血液中),与小肠相比,结肠的刷壁膜活性可以忽略不计,胰腺酶活性也低得多。结肠特异性药物递送已变得越来越重要,这不仅是因为用于治疗与结肠相关的局部疾病的药物递送,而且还因为它具有递送蛋白质和治疗性肽的潜力。根据前药配方、ph敏感性、时间依赖性(滞后时间)、微生物降解和渗透压等设计不同的方法,以配制不同的剂型,如片剂、胶囊、多颗粒、微球、微珠、脂质体用于结肠靶向。通过不同的体外和体内释放研究来评估药物传递系统的效率。本文综述了结肠特异性给药系统(CDDS)的制备和评价方法的最新研究进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
COLON TARGETED MICROBEADS: A NOVEL APPROACH IN NDDS
In oral colon-specific drug delivery system, colon has a large amount of lymphoma tissue (facilitates direct absorption in to the blood), negligible brush boarder membrane activity, and much less pancreatic enzymatic activity as compared with the small intestine. Colon-specific drug delivery has gained increased importance not just for the delivery of the drugs for treatment of local diseases associated with the colon but also for its potential for the delivery of proteins and therapeutic peptides. Different approaches are designed based on prodrug formulation, pH-sensitivity, time-dependency (lag time), microbial degradation and osmotic pressure etc to formulate the different dosage forms like tablets, capsules, multiparticulates, microspheres, microbeads, liposome for colon targeting. The efficiency of drug delivery system is evaluated using different in vitro and in vivo release studies. This review updated the research on different approaches for formulation and evaluation of colon-specific drug delivery systems (CDDS).
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