纳米载体
脂质体
药物输送
生物利用度
医学
药理学
食品药品监督管理局
口服途径
药品
纳米技术
材料科学
作者
Eric Mühlberg,Mira Burtscher,Florian Umstätter,Gert Fricker,Walter Mier,Philipp Uhl
出处
期刊:Nanomedicine
[Future Medicine]
日期:2021-08-01
卷期号:16 (20): 1813-1832
被引量:7
标识
DOI:10.2217/nnm-2021-0177
摘要
The number of approved macromolecular drugs such as peptides, proteins and antibodies steadily increases. Since drugs with high molecular weight are commonly not suitable for oral delivery, research on carrier strategies enabling oral administration is of vital interest. In past decades, nanocarriers, in particular liposomes, have been exhaustively investigated as oral drug-delivery platform. Despite their successful application as parenteral delivery vehicles, liposomes have up to date not succeeded for oral administration. However, a plenitude of approaches aiming to increase the oral bioavailability of macromolecular drugs administered by liposomal formulations has been published. Here, we summarize the strategies published in the last 10 years (vaccine strategies excluded) with a main focus on strategies proven efficient in animal models.
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