pH-Sensitive Poly(β-amino ester)s Nanocarriers Facilitate the Inhibition of Drug Resistance in Breast Cancer Cells

被引:51
|
作者
Zhou, Mengxue [1 ,2 ]
Zhang, Xingcai [3 ]
Xie, Jin [1 ]
Qi, Rongxiang [1 ]
Lu, Huiru [1 ]
Leporatti, Stefano [4 ]
Chen, Jun [1 ,2 ]
Hu, Yi [1 ,2 ]
机构
[1] Chinese Acad Sci, CAS Key Lab Biomed Effects Nanomat & Nanosafety, Multidisciplinary Res Div, Inst High Energy Phys, Beijing 100049, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Harvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[4] CNR, Nanotec Ist Nanotecnol, Polo Nanotecnol, I-73100 Lecce, Italy
来源
NANOMATERIALS | 2018年 / 8卷 / 11期
基金
中国国家自然科学基金;
关键词
nanoparticles; pH responsive; poly(beta-amino ester)s; doxorubicin; multidrug resistance; VITAMIN-E TPGS; MULTIDRUG-RESISTANCE; DOXORUBICIN DELIVERY; ANTICANCER DRUG; IN-VITRO; NANOPARTICLES; COPOLYMER; MICELLES; REVERSAL; METASTASIS;
D O I
10.3390/nano8110952
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multidrug resistance (MDR) remains an unmet challenge in chemotherapy. Stimuli-responsive nanocarriers emerge as a promising tool to overcome MDR. Herein, pH-sensitive poly(beta-amino ester)s polymers (PHP)-based micellar nanoparticles were synthesized for enhanced doxorubicin (DOX) delivery in drug resistant breast cancer MCF-7/ADR cells. DOX-loaded PHP micelles showed rapid cell-internalization and lysosomal escape in MCF-7/ADR cells. The cytotoxicity assays showed relatively higher cell inhibition of DOX-loaded PHP micelles than that of free DOX against MCF-7/ADR cells. Further mechanistic studies showed that PHP micelles were able to inhibit P-glycoprotein (P-gp) activity by lowering mitochondrial membrane potentials and ATP levels. These results suggested that the enhanced antitumor effect might be attributed to PHP-mediated lysosomal escape and drug efflux inhibition. Therefore, PHP would be a promising pH-responsive nanocarrier for enhanced intracellular drug delivery and overcoming MDR in cancer cells.
引用
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页数:16
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