金黄色葡萄球菌
体内
荧光
荧光寿命成像显微镜
活性氧
体外
纳米颗粒
微生物学
化学
材料科学
生物
纳米技术
细菌
生物化学
光学
物理
生物技术
遗传学
作者
Lingling Xu,Wenjun Zhan,Yu Deng,Xiaoyang Liu,Ge Gao,Xianbao Sun,Gaolin Liang
标识
DOI:10.1002/adhm.202200453
摘要
Abstract Direct, noninvasive, and real‐time imaging of Staphylococcus aureus ( S. aureus ) infection is of great value for quick diagnosis of related disease in clinic, but remains challenging. Herein, employing a rationally designed near‐infrared fluorescence probe Cys(StB u)‐EDA‐Thioketal‐Lys(Cy5.5)‐CBT (TK‐CBT) and a CBT‐Cys click reaction, the fluorescence‐quenched nanoparticles TK‐CBT‐NPs are facilely prepared. Upon oxidation by the abundant reactive oxygen species in S. aureus ‐infected macrophages, TK‐CBT‐NPs are fractured, turning the fluorescence “on” for imaging infections in vitro and in vivo. Specifically, TK‐CBT‐NPs show a 6.1‐fold fluorescence imaging signal enhancement of the macrophages that are infected by S. aureus for 20 h in vitro. At 4 h postinjection, TK‐CBT‐NPs show a 2.8‐fold fluorescence imaging signal enhancement of the sites in mice that are infected by S. aureus for 24 h. It is anticipated that TK‐CBT‐NPs could be applied for diagnosis of S. aureus infections in clinic in the near future.
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