Evidence map›Paper›PMID 42084765›Full record

ArticleAnalytical and bioanalytical chemistry2026

An ICT + ESIPT synergistic NIR ratiometric probe for mitochondrial MAOs imaging in vivo and in vitro.

Ting Cao, Mengjin Li, Hong Ma, Zhefeng Fan

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Article in Analytical and bioanalytical chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ting CaoKey Laboratory of Magnetic Molecules & Magnetic Information Materials Ministry of Education, The School of Chemistry and Chemical Engineering, Shanxi Normal University, Taiyuan, 030031, PR China.
Mengjin LiKey Laboratory of Magnetic Molecules & Magnetic Information Materials Ministry of Education, The School of Chemistry and Chemical Engineering, Shanxi Normal University, Taiyuan, 030031, PR China.
Hong MaCollege of Chemistry and Materials, Taiyuan Normal University, Jinzhong, 030619, PR China.
Zhefeng FanKey Laboratory of Magnetic Molecules & Magnetic Information Materials Ministry of Education, The School of Chemistry and Chemical Engineering, Shanxi Normal University, Taiyuan, 030031, PR China. zhefengfan@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The liver is a vital metabolic and detoxification organ in the body, yet the diagnosis of drug-induced liver injury (DILI) remains challenging due to the limitations of traditional detection methods. Monoamine oxidases (MAOs), which are highly expressed on the mitochondrial membrane of hepatic tissues, are closely associated with DILI. In this study, a near-infrared ratiometric fluorescent probe Mito-1 was developed based on the intramolecular charge transfer (ICT) and excited-state intramolecular proton transfer (ESIPT) mechanisms. This probe could precisely target mitochondria, exhibiting high sensitivity (DL = 0.14 μg/mL), a wide linear detection range (10-150 μg/mL), excellent selectivity towards MAOs, and good biocompatibility. Cellular experiments confirmed its ability to distinguish MAO activity between normal and liver cancer cells. In an acetaminophen (APAP)-induced DILI zebrafish model, Mito-1 enabled in vivo dynamic visualization of MAO activity in hepatic tissues. Collectively, this work provides a novel visual tool for the early diagnosis of DILI and the mechanistic study of MAOs.

Indexed as

Chemical and Drug Induced Liver InjuryFluorescent DyesMitochondriaMonoamine OxidaseAcetaminophenAnimalsFluorescent Chemosensor CompoundsHumansProtonsZebrafishAcetaminophenFluorescent Chemosensor CompoundsFluorescent DyesMonoamine OxidaseProtonsDILI imaging“ICT + ESIPT” mechanismMitochondrial MAOsNIR ratiometric fluorescent probeNormal/cancer cells distinguish

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.