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Highly sensitive benzothiazole-based chemosensors for detection and bioimaging of peroxynitrite in living cells

It is well accepted that peroxynitrite (ONOO(−)) plays a crucial role in various physiological and pathological processes. Thus, the detection and imaging of ONOO(−)in vitro and in vivo with high selectivity and sensitivity is of great significance. Here we report two simple benzothiazole-based fluo...

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Detalles Bibliográficos
Autores principales: Kong, Yaqiong, Wu, Rong, Wang, Xiaodong, Qin, Guoxu, Wu, Fengyi, Wang, Chunyu, Chen, Minmin, Wang, Nannan, Wang, Qian, Cao, Duojun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9523762/
https://www.ncbi.nlm.nih.gov/pubmed/36320233
http://dx.doi.org/10.1039/d2ra04549d
Descripción
Sumario:It is well accepted that peroxynitrite (ONOO(−)) plays a crucial role in various physiological and pathological processes. Thus, the detection and imaging of ONOO(−)in vitro and in vivo with high selectivity and sensitivity is of great significance. Here we report two simple benzothiazole-based fluorescent chemosensors, BS1 and BS2. Under physiological pH, both probes could quickly sense ONOO(−) with a remarkable “turn-on” fluorescence signal at 430 nm. The limit of detection (LOD) of BS1 and BS2 toward ONOO(−) was 12.8 nM and 25.2 nM, respectively, much lower than the reported values. Experimental results indicated that BS1 with a diphenyl phosphonate unit presented higher selectivity for ONOO(−) than BS2. Furthermore, based on the advantages of lower cytotoxicity and pH-stabilities of BS1, probe BS1 was successfully employed to detect and image ONOO(−) in HepG2 cells. More importantly, we used BS1 to successfully showcase drug-induced hepatotoxicity via imaging ONOO(−) upregulated by acetaminophen (APAP), and also evaluated the remediation effect of GSH. All the results illustrated that the fluorescent probe BS1 has great potential for the detection of ONOO(−) and to further uncover the roles of ONOO(−) during the drug-induced liver injury (DILI) process.