Gold nanoprisms as a hybrid in vivo cancer theranostic platform for in situ photoacoustic imaging, angiography, and localized hyperthermia

被引:69
作者
Bao, Chenchen [1 ]
Conde, Joao [2 ,3 ]
Pan, Fei [1 ]
Li, Chao [1 ]
Zhang, Chunlei [1 ]
Tian, Furong [4 ]
Liang, Shujing [1 ]
de la Fuente, Jesus M. [1 ,5 ]
Cui, Daxiang [1 ]
机构
[1] Shanghai Jiao Tong Univ, Collaborat Innovat Ctr Syst Biol, Natl Ctr Translat Med,Dept Instrument Sci & Engn, Sch Elect Informat & Elect Engn,Inst Nano Biomed, Shanghai 200240, Peoples R China
[2] MIT, Inst Med Engn & Sci, Harvard MIT Div Hlth Sci & Technol, E25-449, Cambridge, MA USA
[3] Queen Mary Univ London, Sch Engn & Mat Sci, London E1 4NS, England
[4] Dublin Inst Technol, Coll Sci & Hlth, Sch Food Sci & Environm Hlth, Camden Row, Dublin 4, Ireland
[5] Univ Zaragoza, INA, Zaragoza 50018, Spain
基金
中国国家自然科学基金;
关键词
gold nanoprisms; in situ gastric cancer; photoacoustic imaging; photothermal therapy; MAGNETIC NANOPARTICLES; BRCAA1; TOMOGRAPHY; ANTIBODY; THERAPY;
D O I
10.1007/s12274-016-0996-y
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The development of high-resolution nanosized photoacoustic contrast agents is an exciting yet challenging technological advance. Herein, antibody (breast cancer-associated antigen 1 (Brcaa1) monoclonal antibody)- and peptide (RGD)-functionalized gold nanoprisms (AuNprs) were used as a combinatorial methodology for in situ photoacoustic imaging, angiography, and localized hyperthermia using orthotopic and subcutaneous murine gastric carcinoma models. RGD-conjugated PEGylated AuNprs are available for tumor angiography, and Brcaa1 monoclonal antibody-conjugated PEGylated AuNprs are used for targeting and for in situ imaging of gastric carcinoma in orthotopic tumor models. In situ photoacoustic imaging allowed for anatomical and functional imaging at the tumor site. In vivo tumor angiography imaging showed enhancement of the photoacoustic signal in a time-dependent manner. Furthermore, photoacoustic imaging demonstrated that tumor vessels were clearly damaged after localized hyperthermia. This is the first proof-of-concept using two AuNprs probes as highly sensitive contrasts and therapeutic agents for in situ tumor detection and inhibition. These smart antibody/peptide AuNprs can be used as an efficient nanotheranostic platform for in vivo tumor detection with high sensitivity, as well as for tumor targeting therapy, which, with a single-dose injection, results in tumor size reduction and increases mice survival after localized hyperthermia treatment.
引用
收藏
页码:1043 / 1056
页数:14
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