PLGA-PEG nano-delivery system for epigenetic therapy

被引:22
作者
Naz, Asia [1 ,2 ,3 ]
Cui, Yi [1 ,2 ,5 ]
Collins, Christopher J. [4 ]
Thompson, David H. [4 ]
Irudayaraj, Joseph [1 ,2 ]
机构
[1] Purdue Univ, Dept Agr & Biol Engn, Bindley Biosci Ctr, W Lafayette, IN 47907 USA
[2] Purdue Univ, Dept Agr & Biol Engn, Purdue Ctr Canc Res, W Lafayette, IN 47907 USA
[3] Univ Karachi, Dept Pharmaceut Chem, Karachi 75270, Pakistan
[4] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
[5] Pacific Northwest Natl Lab, Earth & Biol Sci Directorate, Richland, WA 99354 USA
关键词
Azacitidine; Nanomedicine; Drug delivery; DNA methylation; Single-molecule fluorescence; CELL-CYCLE ARREST; DNA METHYLATION; MYELODYSPLASTIC SYNDROME; CANCER-CELLS; SOLID TUMORS; PHASE-I; DECITABINE; METHYLTRANSFERASE; 5-AZACYTIDINE; INHIBITOR;
D O I
10.1016/j.biopha.2017.03.093
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Efficient delivery of cytidine analogues such as Azacitidine (AZA) into solid tumors constitutes a primary challenge in epigenetic therapies. We developed a di-block nano-vector based on poly(lactic-co-glycolic acid) (PLGA) and poly(ethylene glycol) (PEG) for stabilization of the conjugated AZA under physiological conditions. With equimolar drug content, our nano-conjugate could elicit a better anti-proliferative effect over free drug in breast cancer both in vitro and in vivo, through reactivation of p21 and BRCA1 to restrict cell proliferation. In addition, we applied single-molecule fluorescence tools to characterize the intracellular behavior of the AZA-PLGE-PEG nano-micelles at a finer spatiotemporal resolution. Our results suggest that the nano-micelles could effectively enrich in cancer cells and may not be limited by nucleoside transporters. Afterwards, the internalized nano-micelles exhibit pH-dependent release and resistance to active efflux. Altogether, our work describes a delivery strategy for DNA demethylating agents with nanoscale tunability, providing a cost-effective option for pharmaceutics. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:586 / 597
页数:12
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