纳米载体
两亲性
药物输送
化学
天然聚合物
纳米技术
药品
靶向给药
毒品携带者
聚合物
材料科学
有机化学
药理学
共聚物
医学
作者
Sally Sabra,Mona A. Abdelmoneem,Mahmoud M. Abd-Elwakil,Moustafa T. Mabrouk,Doaa M. Anwar,Rania Hassan Mohamed,Sherine N. Khattab,Adnan A. Bekhit,Kadria A. Elkhodairy,May S. Freag,Ahmed O. Elzoghby
标识
DOI:10.2174/1381612823666170526111029
摘要
Micellization provides numerous merits for the delivery of water insoluble anti-cancer therapeutic agents including a nanosized 'core-shell' drug delivery system. Recently, hydrophobically-modified polysaccharides and proteins are attracting much attention as micelle forming polymers to entrap poorly soluble anti-cancer drugs.By virtue of their small size, the self-assembled micelles can passively target tumor tissues via enhanced permeation and retention effect (EPR). Moreover, the amphiphilic micelles can be exploited for active-targeted drug delivery by attaching specific targeting ligands to the outer micellar hydrophilic surface.Here, we review the conjugation techniques, drug loading methods, physicochemical characteristics of the most important amphiphilic polysaccharides and proteins used as anti-cancer drug delivery systems. Attention focuses on the mechanisms of tumor-targeting and enhanced anti-tumor efficacy of the encapsulated drugs. This review will highlight the remarkable advances of hydrophobized polysaccharide and protein micelles and their potential applications as anti-cancer drug delivery nanosystems.Micellar nanocarriers fabricated from amphiphilic natural polymers hold great promise as vehicles for anti-cancer drugs.
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