磷光
持续发光
猝灭(荧光)
材料科学
光化学
限制
纳米颗粒
激发态
纳米技术
化学
发光
光电子学
热释光
光学
荧光
物理
原子物理学
机械工程
工程类
作者
Juqing Gu,Wentao Yuan,Kai Chang,Cheng Zhong,Yufeng Yuan,Jinghua Li,Yufeng Zhang,Tian Deng,Yuanyuan Fan,Likai Yuan,Siwei Liu,Yong‐Zhen Xu,Sisi Ling,Chunyan Li,Zhaoke Zheng,Qianqian Li,Zhen Li,Ben Zhong Tang
标识
DOI:10.1002/anie.202415637
摘要
In contrast to the high efficiency of room temperature phosphorescence in crystal states, the generally utilized nanoparticles of organic materials in bioimaging demonstrated sharply decreased performance by orders of magnitude under physiological conditions, badly limiting the realization of their unique advantages. This case, especially for organic red/near‐infrared (NIR) phosphorescence materials, is not only the challenge present in reality but more importantly, for the theoretical problem of deeply understanding and avoiding the quenching effect by oxygen and water toward excited triplet states. Herein, thanks to the intelligent molecular design by the introduction of abundant hydrophobic chains and highly‐branched structures, bright and persistent red/NIR phosphorescence under physiological conditions has been realized, which demonstrated the shielding effect towards oxygen, and strengthened the intermolecular interactions to suppress the non‐radiative transitions. Accordingly, the record phosphorescence intensity of nanoparticles in bioimage, up to 8.21 ± 0.36 × 108 p s−1 cm−2 sr−1, was achieved, to realize the clear phosphorescence imaging of liver and tumors in living mice, even lymph nodes in rabbit models with high SBRs. This work afforded an efficient way to achieve the bright red/NIR phosphorescence nanoparticles, guiding their further applications in biology and medicine.
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