An Activatable NIR-II Nanoprobe for In Vivo Early Real-Time Diagnosis of Traumatic Brain Injury.
Chunyan LiWanfei LiHuanhuan LiuYejun ZhangGuangcun ChenZijing LiQiangbin WangPublished in: Angewandte Chemie (International ed. in English) (2019)
Traumatic brain injury (TBI) is one of the most dangerous acute diseases resulting in high morbidity and mortality. Current methods remain limited with respect to early diagnosis and real-time feedback on the pathological process. Herein, a targeted activatable fluorescent nanoprobe (V&A@Ag2 S) in the second near-infrared window (NIR-II) is presented for in vivo optical imaging of TBI. Initially, the fluorescence of V&A@Ag2 S is turned off owing to energy transfer from Ag2 S to the A1094 chromophore. Upon intravenous injection, V&A@Ag2 S quickly accumulates in the inflamed vascular endothelium of TBI based on VCAM1-mediated endocytosis, after which the nanoprobe achieves rapid recovery of the NIR-II fluorescence of Ag2 S quantum dots (QDs) owing to the bleaching of A1094 by the prodromal biomarker of TBI, peroxynitrite (ONOO- ). The nanoprobe offers high specificity, rapid response, and high sensitivity toward ONOO- , providing a convenient approach for in vivo early real-time assessment of TBI.
Keyphrases
- traumatic brain injury
- quantum dots
- energy transfer
- fluorescent probe
- living cells
- fluorescence imaging
- sensitive detection
- severe traumatic brain injury
- photodynamic therapy
- high resolution
- single molecule
- drug release
- nitric oxide
- liver failure
- loop mediated isothermal amplification
- highly efficient
- hydrogen peroxide
- parkinson disease
- low dose
- high dose
- respiratory failure
- acute respiratory distress syndrome
- high speed
- drug induced