前药
吉西他滨
脂质体
微泡
药物输送
胰腺癌
外体
药品
毒品携带者
靶向给药
化学
生物制药
药理学
癌症研究
纳米技术
材料科学
癌症
医学
生物化学
内科学
生物
小RNA
遗传学
基因
作者
Bora Kim,Heewon Park,H.‐J. LIU,Sejin Kim,Yong-Kyu Lee,Yeu‐Chun Kim
出处
期刊:ACS applied bio materials
[American Chemical Society]
日期:2024-09-04
卷期号:7 (9): 6025-6033
标识
DOI:10.1021/acsabm.4c00658
摘要
Liposomes are applied to various anticancer treatments as representative drug delivery carriers. However, liposomes do not have their own targeting properties; therefore, there are limitations in drug delivery to specific tissues or cells. High targetability in drug delivery is an important factor in improving bioavailability and drug efficacy and reducing side effects; recent research has been actively investigated to modify the surface of liposomes to give them specific functions. In this study, we studied a drug delivery system for anticancer treatment that enhances targeting ability through fusion with exosomes on the surface of liposomes. We designed exosome-liposome hybrid nanoparticles loaded with a gemcitabine prodrug as a treatment for pancreatic ductal adenocarcinoma (PDAC). Membrane fusion with exosomes shows excellent targeting ability to pancreatic cancer cells due to intrinsic targeting ability and expansion of the macropinocytosis pathway.
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