化学发光
发光
光化学
发光测量
材料科学
持续发光
费斯特共振能量转移
过氧化氢
临床前影像学
化学
体内
纳米技术
荧光
活性氧
光电子学
光学
物理化学
生物化学
生物技术
物理
热释光
生物
作者
Zhen Xu,Chengwu Zhang,Chen Xie,Qingqing Miao,Kah Leong Lim,Kanyi Pu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2016-06-14
卷期号:10 (6): 6400-6409
被引量:332
标识
DOI:10.1021/acsnano.6b02908
摘要
Detection of reactive oxygen species (ROS), a hallmark of many pathological processes, is imperative to understanding, detection and treatment of many life-threatening diseases. However, methods capable of real-time in situ imaging of ROS in living animals are still very limited. We herein report the development and optimization of chemiluminescent semiconducting polymer nanoparticles (SPNs) for ultrasensitive in vivo imaging of hydrogen peroxide (H2O2). The chemiluminescence is amplified by adjusting the energy levels between the luminescence reporter and the chemiluminescence substrate to facilitate intermolecular electron transfer in the process of H2O2-activated luminescence. The optimized SPN can emit chemiluminescence with the quantum yield up to 2.30 × 10(-2) einsteins/mol and detect H2O2 down to 5 nM, which substantially outperforms the previous probes. Further doping of this SPN with a naphthalocyanine dye creates intraparticle chemiluminescence resonance energy transfer (CRET), leading to the near-infrared (NIR) luminescence responding to H2O2. By virtue of high brightness and ideal NIR optical window, SPN-NIR permits ultrasensitive imaging of H2O2 in the mouse models of peritonitis and neuroinflammation with the minute administration quantity. Thus, this study not only provides a category of optical probes that eliminates the need of external light excitation for imaging of H2O2, but also reveals the underlying principle to enhance the brightness of chemiluminescence systems.
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