纳米医学
纳米载体
药物输送
表观遗传学
组蛋白脱乙酰基酶
癌症治疗
药理学
药品
靶向给药
癌症
组蛋白脱乙酰酶抑制剂
伏立诺他
医学
化学
组蛋白
癌症研究
纳米技术
纳米颗粒
材料科学
内科学
生物化学
基因
作者
Dina Ashraf Hafez,Islam A. Hassanin,Mohamed Teleb,Sherine N. Khattab,Kadria A. Elkhodairy,Ahmed O. Elzoghby
出处
期刊:Nanomedicine
日期:2021-10-01
卷期号:16 (25): 2305-2325
被引量:4
标识
DOI:10.2217/nnm-2021-0196
摘要
Histone deacetylase inhibitors (HDACi) are cancer therapeutics that operate at the epigenetic level and which have recently gained wide attention. However, the applications of HDACi are generally hindered by their poor physicochemical characteristics and unfavorable pharmacokinetic profile. Inspired by the approved nanomedicine-based drugs in the market, nanocarriers could provide a resort to circumvent the limitations imposed by HDACi. Enhanced tumor targeting, improved cellular uptake and reduced toxicity are major advantages offered by HDACi-loaded nanoparticles. More importantly, site-specific drug delivery can be achieved via engineered stimuli-responsive nanosystems. In this review we elucidate the anticancer mechanisms of HDACi and their structure–activity relationships, with a special focus on their nanomedicine-based delivery, different drug loading concepts and their implications.
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