Ultrasound-enhanced theranostics of orthotopic breast cancer through a multifunctional core-shell tecto dendrimer-based nanomedicine platform

被引:7
作者
Gong, Junli [1 ,2 ]
Song, Cong [3 ]
Li, Gaoming [2 ]
Guo, Yunqi [2 ]
Wang, Zhiqiang [2 ]
Guo, Honghua [4 ]
Xia, Jindong [4 ]
Tao, Yuchen [5 ]
Shi, Qiusheng [5 ]
Shi, Xiangyang [2 ]
Shen, Mingwu [2 ]
机构
[1] Donghua Univ, Coll Chem & Chem Engn, Shanghai Engn Res Ctr Nanobiomat & Regenerat Med, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
[2] Donghua Univ, Coll Biol Sci & Med Engn, Shanghai 201620, Peoples R China
[3] Shandong First Med Univ, Med Sci & Technol Innovat Ctr, Jinan 250117, Shandong, Peoples R China
[4] Shanghai Songjiang Dist Cent Hosp, Dept Radiol, Shanghai 201600, Peoples R China
[5] Shanghai Jiao Tong Univ, Shanghai Gen Hosp, Dept Ultrasound, Sch Med, Shanghai 200080, Peoples R China
基金
中国国家自然科学基金;
关键词
MICROBUBBLE DESTRUCTION; OXIDE NANOPARTICLES; TARGETED DELIVERY; DOXORUBICIN; INHIBITOR;
D O I
10.1039/d3bm00375b
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
Design of multifunctional nanoplatforms combined with ultrasound-targeted microbubble destruction (UTMD) technology for enhanced tumor accumulation is feasible to solve the bottleneck of theranostics. Herein, we present the development of zwitterion-modified gadolinium (Gd)-chelated core-shell tecto dendrimers (CSTDs) as a nanomedicine platform (PCSTD-Gd) for enhanced magnetic resonance (MR) imaging-guided chemo-gene therapy of orthotopic breast cancer with the assistance of UTMD. In our design, CSTDs synthesized via supramolecular recognition of beta-cyclodextrin and adamantane were covalently linked with tetraazacyclododecane tetraacetic acid-Gd(iii) chelators, modified with 1,3-propane sultone to achieve good protein-resistance property, and used for co-delivery of an microRNA 21 inhibitor (miR 21i) and an anticancer drug doxorubicin (DOX). The overall design is quite advantageous and cooperative. The CSTDs with a greater size than single-generation core dendrimers have amplified the enhanced permeability and retention effect for better passive tumor targeting, with a larger r(1) relaxivity for sensitive MR imaging and serum-enhanced gene delivery efficiency due to the better compaction ability as well as the protein resistance ability, and with larger interior space for improved drug loading. Through the unique design and the assistance of UTMD, the obtained PCSTD-Gd/DOX/miR 21i polyplexes enable enhanced MR imaging-guided combined chemo-gene therapy of an orthotopic breast cancer model in vivo.
引用
收藏
页码:4385 / 4396
页数:12
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