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Construction of a lysosome-targetable ratiometric fluorescent probe for H(2)O(2) tracing and imaging in living cells and an inflamed model
Hydrogen peroxide (H(2)O(2)), an important reactive oxygen species (ROS) with unique destructive oxidation properties, can be produced in lysosomes to fight off pathogens. Although many fluorescent probes have been developed for the detection and imaging of H(2)O(2), the development of a ratiometric...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9036682/ https://www.ncbi.nlm.nih.gov/pubmed/35479027 http://dx.doi.org/10.1039/d1ra04026j |
Sumario: | Hydrogen peroxide (H(2)O(2)), an important reactive oxygen species (ROS) with unique destructive oxidation properties, can be produced in lysosomes to fight off pathogens. Although many fluorescent probes have been developed for the detection and imaging of H(2)O(2), the development of a ratiometric fluorescent probe for H(2)O(2) detection and imaging in lysosomes and an inflammation model remains rather scarce. Therefore, it is important to develop an efficient tool for monitoring H(2)O(2) in inflamed tissues to evaluate the physiological and pathological relationship between inflammation and lysosomal H(2)O(2). In this work, a new naphthalimide-based lysosome-targeting fluorescent probe (NPT-H(2)O(2)) for ratiometric detection and imaging was developed in vitro and in vivo. The probe exhibited two well-resolved emission peaks separated by 125 nm, rapid response (<40 s), and high selectivity and sensitivity toward H(2)O(2), as well as low cytotoxicity in vitro. Inspired by prominent features of these results, we further successfully applied NPT-H(2)O(2) for H(2)O(2) imaging with a dual-channel in living cells, demonstrating that our probe NPT-H(2)O(2) was targeted in the lysosomes. Finally, NPT-H(2)O(2) was used for H(2)O(2) detection in inflamed tissues and achieved satisfactory results. We predict that our probe can be used as a powerful tool to reveal the relationship between physiology and pathology of inflammation and lysosomal H(2)O(2). |
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