急性肾损伤
氧化应激
谷胱甘肽
体内
肾毒性
肾
化学
对乙酰氨基酚
医学
药理学
内科学
生物化学
生物
酶
生物技术
作者
Yiteng Ding,Rongbin Zhong,Renfeng Jiang,Jing Wang,Longwei He,Lin Yuan,Dan Cheng
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2023-02-15
卷期号:8 (2): 914-922
被引量:17
标识
DOI:10.1021/acssensors.2c02610
摘要
Drug-induced acute kidney injury (DIAKI) is associated with high morbidity and mortality. It remains a diagnostic and therapeutic dilemma due to failure of providing unambiguous real-time feedback on nephrotoxicity, which is regarded as a serious problem in clinics. Herein, we report a reversible fluorescence probe, NRN, to monitor the ONOO–/GSH in an acute kidney injury model. The NRN near-infrared fluorescent probe features a big Stokes shift (83 nm), which was oxidized by ONOO– and reduced by succussive glutathione (GSH) with excellent selectivity and good sensitivity (detection limit: 418 nM and 0.28 mM, respectively). Taking the reversibility of NRN toward ONOO– and GSH, real-time evaluations in vivo with cisplatin (CP) alone and CP combined with acetaminophen-stimulated acute kidney injury and the following remedy process with l-carnitine were realized for the first time. The experiments revealed that acute kidney injury caused by combined drugs might be more serious and irreversible under certain conditions. Therefore, NRN could act as a potential tool for understanding oxidative stress-related DIAKI disease processes.
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