Polyphenol-based nanoplatform for MRI/PET dual-modality imaging guided effective combination chemotherapy

被引:19
|
作者
Wang, Jingjing [1 ,2 ]
Sang, Wei [3 ,4 ]
Yang, Zhen [2 ]
Shen, Zheyu [2 ]
Wang, Zhantong [2 ]
Jacobson, Orit [2 ]
Chen, Yundai [1 ]
Wang, Yong [5 ]
Shao, Mingyan [5 ]
Niu, Gang [2 ]
Dai, Yunlu [3 ,4 ]
Chen, Xiaoyuan [2 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Cardiol, Beijing 100853, Peoples R China
[2] NIBIB, LOMIN, NIH, Bethesda, MD 20892 USA
[3] Univ Macau, Fac Hlth Sci, Canc Ctr, Macau 999078, Peoples R China
[4] Univ Macau, Fac Hlth Sci, Inst Translat Med, Macau 999078, Peoples R China
[5] Beijing Univ Chinese Med, Sch Life Sci, Beijing 100029, Peoples R China
基金
美国国家卫生研究院;
关键词
TOPOISOMERASE-II; SIMVASTATIN; CHALLENGES; MICELLES; THERAPY;
D O I
10.1039/c9tb01597c
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
Combination therapy with multiple chemotherapeutic agents is the main approach for cancer treatment in the clinic. Polyphenol-based materials are found in our diet, demonstrate good biocompatibility, and prevent numerous diseases. In this study, we encapsulate two drugs in a single polyphenol-based polymer with Fe3+ or Mn2+ ions as the cross-linker for cancer therapy. The combination index of two drugs is an essential parameter to evaluate drug combinations. The amphiphilic polymer poly(ethylene glycol)-block-polydopamine (PEG-PDA) was prepared by RAFT polymerization. The nanoparticles were prepared via self-assembly with Fe3+ or Mn2+ ions. Both doxorubicin (DOX) and simvastatin (SV) were encapsulated in the core of the nanoparticles. The cell viability and combination index were evaluated in vitro. The tumor accumulation of the nanoparticles was investigated by positron-emission tomography (PET) and magnetic resonance (MR) imaging. The as-prepared nanoparticles exhibited high drug loading capacity. The drug loaded nanoparticles could kill cancer cells effectively with a combination index via intravenous injection of nanoparticles. The polyphenol-based nanoplatform may serve as a promising theranostic candidate for clinical application.
引用
收藏
页码:5688 / 5694
页数:7
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