Amphiphilic phosphorous dendron micelles co-deliver microRNA inhibitor and doxorubicin for augmented triple negative breast cancer therapy

被引:8
作者
Chen, Liang [1 ,2 ,3 ]
Zhan, Mengsi [1 ]
Li, Jin [1 ]
Cao, Liu [1 ]
Sun, Huxiao [1 ]
Laurent, Regis [2 ,3 ]
Mignani, Serge [4 ,5 ]
Caminade, Anne-Marie [2 ,3 ]
Majoral, Jean-Pierre [2 ,3 ]
Shi, Xiangyang [1 ,5 ]
机构
[1] Donghua Univ, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai Engn Res Ctr Nanobiomat & Regenerat Med, Coll Biol Sci & Med Engn, Shanghai 201620, Peoples R China
[2] CNRS, Lab Chim Coordinat, 205 Route Narbonne,BP 44099, F-31077 Toulouse 4, France
[3] Univ Toulouse, UPS, INPT, F-31077 Toulouse 4, France
[4] Univ Paris 05, CNRS UMR 860, Lab Chim & Biochim Pharmacol & Toxicol, PRES Sorbonne Paris Cite, 45 rue St Peres, F-75006 Paris, France
[5] Univ Madeira, CQM Ctr Quim Madeira, Campus Penteada, P-9020105 Funchal, Portugal
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
ENTRAPPED GOLD NANOPARTICLES; DENDRIMERS; SIRNA; DRUG; NANOCARRIERS; ACID;
D O I
10.1039/d2tb02114e
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Combined chemo/gene therapy of cancer through different action mechanisms has been emerging to enhance the therapeutic efficacy towards cancer, and still remains a challenging task due to the lack of highly effective and biocompatible nanocarriers. In this work, we report a new nanosystem based on amphiphilic phosphorus dendron (1-C12G1) micelles to co-deliver microRNA-21 inhibitor (miR-21i) and doxorubicin (DOX) for combination therapy of triple negative breast cancer. The amphiphilic phosphorus dendron bearing a long linear alkyl chain and ten protonated pyrrolidine surface groups was prepared and was demonstrated to form micelles in water solution and have a hydrodynamic size of 103.2 nm. The micelles are shown to be stable, enable encapsulation of an anticancer drug DOX with optimal loading content (80%) and encapsulation efficiency (98%), and can compress miR-21i to form polyplexes to render it with good stability against degradation. The co-delivery system of 1-C12G1@DOX/miR-21i polyplexes has a pH-dependent DOX release profile, and can be readily phagocytosed by cancer cells to inhibit them due to the different anticancer mechanisms, which was further validated after intravenous injection to treat an orthotopic triple-negative breast tumor model in vivo. With the proven biocompatibility under the studied doses, the developed amphiphilic phosphorus dendron micelles could be developed as an effective nanomedicine formulation for synergistic cancer therapy.
引用
收藏
页码:5483 / 5493
页数:11
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