Recent advances in nanomedicine-based delivery of histone deacetylase inhibitors for cancer therapy

被引:7
作者
Hafez, Dina A. [1 ,2 ]
Hassanin, Islam A. [1 ,3 ]
Teleb, Mohamed [1 ,4 ]
Khattab, Sherine N. [1 ,5 ]
Elkhodairy, Kadria A. [1 ,2 ]
Elzoghby, Ahmed O. [1 ,2 ]
机构
[1] Alexandria Univ, Canc Nanotechnol Res Lab CNRL, Fac Pharm, Alexandria 21521, Egypt
[2] Alexandria Univ, Dept Ind Pharm, Fac Pharm, Alexandria 21521, Egypt
[3] Alexandria Univ, Inst Grad Studies & Res, Dept Biotechnol, Alexandria 21526, Egypt
[4] Alexandria Univ, Dept Pharmaceut Chem, Fac Pharm, Alexandria 21521, Egypt
[5] Alexandria Univ, Dept Chem, Fac Sci, Alexandria 21321, Egypt
关键词
cancer drug resistance; drug delivery; epigenetics; HDAC inhibitors; nanoparticles; SOLID LIPID NANOPARTICLES; ZINC-BINDING GROUPS; DRUG-DELIVERY; CO-DELIVERY; UNIMOLECULAR MICELLES; ANTICANCER ACTIVITY; POOR-PROGNOSIS; HDAC; VORINOSTAT; CELLS;
D O I
10.2217/nnm-2021-0196
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
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.
引用
收藏
页码:2305 / 2325
页数:21
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