药物小体作为囊状给药系统

R. R. Shinde, B. Chaudhari, A. Velhal, V. Redasani
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引用次数: 1

摘要

在提高溶解度方面,遇到了几个问题。药物小体是一种基于脂质药物载体的新技术。药物小体是胶体、囊泡、纳米大小的胶束或六边形排列的胶体药物分散体,共价附着在磷脂上。由于其具有载药活性强、体积小、包封效率高、亲和性好、稳定性好等特点,是一种精密的药物载体。它们有助于药物在作用部位的控制释放,降低治疗成本,提高难溶性药物的生物利用度,减少毒性和药物泄漏。除了大量的中草药外,这种递送系统的范围已经扩大到许多用于癌症、心脏病、炎症和蛋白质递送的药物。药物体为开发更有效的囊泡给药系统提供了新的机遇和挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacosome as a Vesicular Drug Delivery System
In the area of solubility enhancement, several problems are encountered. Pharmacosomes are a new technology based on lipid drug carriers. Pharmacosomes are colloidal, vesicles, nanometric size micelles or a hexagonal arrangement of colloidal drug dispersions covalently attached to the phospholipid. Because of their unique properties such as active drug loading, small size, high entrapment efficiency, amphiphilicity and stability, they act as a precise drug carrier. They contribute to the controlled release of medicament at the action site, as well as the reduction of therapy cost, increased bioavailability of poorly soluble drugs, decrease toxicity and drug leakage. There has been an advancement in the scope of this delivery system for a number of drugs used for cancer, heart diseases, inflammation and protein delivery besides with a large number of herbal drugs. Pharmacosomes offer new opportunities and challenges for developing a more effective new vesicular drug delivery system.
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