Stable J-Aggregation of an aza-BODIPY-Lipid in a Liposome for Optical Cancer Imaging

被引:136
作者
Cheng, Miffy H. Y. [1 ]
Harmatys, Kara M. [1 ]
Charron, Danielle M. [1 ,2 ]
Chen, Juan [1 ]
Zheng, Gang [1 ,2 ,3 ]
机构
[1] Univ Hlth Network, Princess Margaret Canc Ctr, 101 Coll St,PMCRT 5-354, Toronto, ON M5G 1L7, Canada
[2] Univ Toronto, Inst Biomat & Biomed Engn, 64 Coll St, Toronto, ON M5S 3G9, Canada
[3] Univ Toronto, Dept Med Biophys, 101 Coll St, Toronto, ON M5G 1L7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
aza-BODIPY; photoacoustic imaging; J-aggregation; lipid nanoparticles; self-assembly; NANOPARTICLES; CHEMISTRY; DIMERS; PROBES; DYES;
D O I
10.1002/anie.201907754
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Organic building blocks are the centerpieces of "one-for-all" nanoparticle development. Herein, we report the synthesis of a novel aza-BODIPY-lipid building block and its self-assembly into a liposomal nanoparticle (BODIPYsome). We observed optically stable NIR J-aggregation within the BODIPYsome that is likely attributed to J-dimerization. BODIPYsomes with cholesterol showed enhanced colloidal stability while maintaining a high extinction coefficient (128 mm(-1) cm(-1)) and high fluorescence quenching (99.70 +/- 0.09 %), which enables photoacoustic (PA) properties from its intact structure and recovered NIR fluorescence properties when it is disrupted in cancer cells. Finally, its capabilities for optical imaging (PA/fluorescence) were observed in an orthotopic prostate tumor mouse model 24 h after intravenous administration. Overall, the BODIPYsome opens the door for engineering new building blocks in the design of optically stable biophotonic imaging agents.
引用
收藏
页码:13394 / 13399
页数:6
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