生物光子学
光热治疗
菁
材料科学
生物医学中的光声成像
吸收(声学)
紧身衣
近红外光谱
纳米技术
荧光
光化学
光电子学
化学
光学
光子学
物理
复合材料
作者
Xiaoqing Wang,Zhiyong Jiang,Zhaolun Liang,Tianzhu Wang,Yuncong Chen,Zhipeng Liu
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2022-12-02
卷期号:8 (48)
被引量:39
标识
DOI:10.1126/sciadv.add5660
摘要
Organic dyes with absorption maxima in the second near-infrared window (NIR-II; 1000 to 1700 nm) are of great interest in biophotonics. However, because of the lack of appropriate molecular scaffolds, current research in this field is limited to cyanine dyes, and developing NIR-II-absorbing organic dyes for biophotonics remains an immense challenge. Here, we rationally designed an ethenylene-bridged BODIPY scaffold featuring excellent J-aggregation capabilities and revealed that the bridging ethylene unit is crucial for intermolecular J-coupling regulation. By integrating the electron-donating groups into the scaffold, we obtained a BODIPY dye, BisBDP2, with a J-aggregate absorption maximum of around 1300 nm. BisBDP2 J-aggregates show excellent photothermal performance, including intense photoacoustic response, and a high photothermal conversion efficiency value of 63%. In vivo results demonstrate the potential of J-aggregates for photoacoustic imaging and photothermal ablation of deep-seated tumors. This study will speed up the exploration of NIR-II-absorbing J-aggregates for future biophotonic applications.
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