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A novel ESIPT fluorescent probe for early detection and assessment of ferroptosis-mediated acute kidney injury via peroxynitrite fluctuation.

Authors :
Chen M
Lin S
Tang B
Tian T
Leng Y
Liu D
Wang K
Geng Y
Luo Z
Shen L
Chen T
Source :
Analytica chimica acta [Anal Chim Acta] 2024 Jun 15; Vol. 1308, pp. 342611. Date of Electronic Publication: 2024 Apr 16.
Publication Year :
2024

Abstract

Background: Acute kidney injury (AKI) poses a severe risk to public health, mostly manifested by damage and death of renal tubular epithelial cells. However, routine blood examination, a conventional approach for clinical detection of AKI, is not available for identifying early-stage AKI. Plenty of reported methods were lack of early biomarkers and real time evaluation tools, which resulted in a vital challenge for early diagnosis of AKI. Therefore, developing novel probes for early detection and assessment of AKI is exceedingly crucial.<br />Results: Based on ESIPT mechanism, a new fluorescent probe (MEO-NO) with 2-(2'-hydroxyphenyl) benzothiazole (HBT) derivatives as fluorophore has been synthesized for dynamic imaging peroxynitrite (ONOO <superscript>-</superscript> ) levels in ferroptosis-mediated AKI. Upon the addition of ONOO <superscript>-</superscript> , MEO-NO exhibited obvious fluorescence changes, a significant Stokes shift (130 nm) and rapid response (approximately 45 s), and featured exceptional sensitivity (LOD = 7.28 nM) as well as high selectivity from the competitive species at physiological pH. In addition, MEO-NO was conducive to the biological depth imaging ONOO <superscript>-</superscript> in cells, zebrafish, and mice. Importantly, MEO-NO could monitor ONOO <superscript>-</superscript> levels during sorafenib-induced ferroptosis and CP-induced AKI. With the assistance of MEO-NO, we successfully visualized and tracked ONOO <superscript>-</superscript> variations for early detection and assessment of ferroptosis-mediated AKI in cells, zebrafish and mice models.<br />Significance and Novelty: Benefiting from the superior performance of MEO-NO, experimental results further demonstrated that the levels of ONOO <superscript>-</superscript> was overexpressed during ferroptosis-mediated AKI in cells, zebrafish, and mice models. The developed novel probe MEO-NO provided a strong visualization tool for imagining ONOO <superscript>-</superscript> , which might be a potential method for the prevention, diagnosis, and treatment of ferroptosis-mediated AKI.<br />Competing Interests: Declaration of competing interest The authors declare that there are no conflicts of interest.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1873-4324
Volume :
1308
Database :
MEDLINE
Journal :
Analytica chimica acta
Publication Type :
Academic Journal
Accession number :
38740450
Full Text :
https://doi.org/10.1016/j.aca.2024.342611