Authors
Yuxun Lu, Wenyi He, Yinuo Li, Yingping Liu, Zhenhui Li, Ruqiu Zhang, Fanyi Kong, Fan Li, Ying Zhou
Published in
Analytica chimica acta. Volume 1424. Pages 346241. Nov 22, 2026. Epub Sep 09, 2026.
Abstract
Hydrogen peroxide (H2O2) is a key mediator of oxidative stress in neuroinflammation-related brain injury, yet brain H2O2 imaging remains challenging because of the blood-brain barrier (BBB) and tissue autofluorescence. In addition, most reported probes have been evaluated in only one or a few disease models, limiting cross-model comparison. Here, we developed MH-1, an H2O2-responsive near-infrared (NIR) fluorescent probe for brain-section optical mapping after systemic administration.
MH-1 exhibited an approximately 60-fold fluorescence turn-on at 667 nm, enabled H2O2 detection over 0.107-1000 μmol/L, and reached a stable response within approximately 30 min, with high selectivity, interference resistance, pH stability, and low cytotoxicity. Its fluorescence quantum yield increased from 0.72% to 2.45% upon activation. CD31 co-staining confirmed MH-1-associated fluorescence in extravascular brain parenchyma after systemic administration. Ex vivo brain-section imaging further revealed model-dependent H2O2-associated fluorescence in LPS-induced neonatal neuroinflammation, hypoxic-ischemic encephalopathy (HIE), and Alzheimer's disease (AD), with an effective imaging window of approximately 12 h.
Rather than relying on a single best-in-class analytical parameter, MH-1 integrates NIR emission, a large fluorescence turn-on, BBB access, and applicability across three mechanistically distinct brain-injury models. This combined performance enables region-resolved, cross-model comparison of H2O2-associated oxidative stress in preclinical brain tissue.
PMID:
42887984
Bibliographic data and abstract were imported from PubMed on 17 Oct 2026.
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