Hyaluronic Acid Modified Tantalum Oxide Nanoparticles Conjugating Doxorubicin for Targeted Cancer Theranostics

被引:41
|
作者
Jin, Yushen [1 ]
Ma, Xibo [4 ]
Feng, Shanshan [2 ]
Liang, Xiao [4 ]
Dai, Zhifei [3 ]
Tian, Jie [4 ]
Yue, Xiuli [2 ]
机构
[1] Harbin Inst Technol, Sch Life Sci & Technol, Harbin 150001, Peoples R China
[2] Harbin Inst Technol, Sch Municipal & Environm Engn, Harbin 150001, Peoples R China
[3] Peking Univ, Coll Engn, Dept Biomed Engn, Beijing 100871, Peoples R China
[4] Chinese Acad Sci, Inst Automat, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
MESOPOROUS SILICA NANOPARTICLES; BREAST-CANCER; ANTICANCER DRUG; CHEMOTHERAPY; CD44; THERAPY; PARTICLES; MOLECULES; MIGRATION; RELEASE;
D O I
10.1021/acs.bioconjchem.5b00551
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Theranostic tantalum oxide nanoparticles (TaO(x)NPs) of about 40 nm were successfully developed by conjugating functional molecules including polyethylene glycol (PEG), near-infrared (NIR) fluorescent dye, doxorubicin (DOX), and hyaluronic acid (HA) onto the surface of the nanopartides (TaOx@Cy7-DOX-PEG-HA NPs) for actively targeting delivery, pH-responsive drug release, and NIR fluorescence/X-ray CT bimodal imaging. The obtained nanoagent exhibits good biocompatibility, high cumulative release rate in the acidic microenvironments, long blood circulation time, and superior tumor-targeting ability. Both in vitro and in vivo experiments show that it can serve as an excellent contrast agent to simultaneously enhance fluorescence imaging and CT imaging greatly. Most importantly, such a nanoagent could enhance the therapeutic efficacy of the tumor greatly and the tumor growth inhibition was evaluated to be 87.5%. In a word, multifunctional TaOx@Cy7-DOX-PEG-HA NPs can serve as a theranostic nanomedicine for fluorescence/X-ray CT bimodal imaging, remote-controlled therapeutics, enabling personalized detection, and treatment of cancer with high efficacy.
引用
收藏
页码:2530 / 2541
页数:12
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