# HOCl and viscosity dual-responsive fluorescent probe for accurate discrimination between early hepatocellular carcinoma and acute liver injury

**Authors:** Jiakang Sun, Lidong Cao, Mengmeng Dong, Yumeng Liu, Yun Wang, Yong Zhan

PMC · DOI: 10.1016/j.mtbio.2026.102816 · Materials Today Bio · 2026-01-16

## TL;DR

A new fluorescent probe can accurately tell early liver cancer from liver injury by detecting two specific signals in a key cell part.

## Contribution

First AIE-NIR probe for dual-channel imaging of viscosity and HOCl in lipid droplets to distinguish HCC and ALI.

## Key findings

- Probe shows 1532-fold fluorescence enhancement in response to viscosity and 363-fold response to HOCl.
- Red-to-green signal ratio clearly discriminates HCC from ALI in multiple models.
- High specificity confirmed with PCC of 0.8773 in lipid droplet-targeted imaging.

## Abstract

The accurate differentiation between early-stage hepatocellular carcinoma (HCC) and acute liver injury (ALI) remains a critical yet unresolved challenge in clinical practice, as these conditions share overlapping symptoms and biomarkers, often leading to misdiagnosis with conventional techniques. Although fluorescent probes offer potential for high-sensitivity imaging, existing designs typically detect only a single parameter and lack subcellular targeting precision. Consequently, a methodology that simultaneously visualizes multiple pathology-specific biomarkers within a key organelle for precise discrimination is urgently needed. Here, we present a lipid droplet-targeted, dual-channel fluorescent probe, TPA-DCN-TPE, which independently monitors microenvironmental viscosity and hypochlorous acid (HOCl). This probe exhibits a remarkable 1532-fold fluorescence enhancement in response to viscosity (red channel) and a 363-fold turn-on response to HOCl (green channel). Crucially, we discovered a distinct red-to-green signal ratio that clearly discriminates HCC (high ratio) from ALI (low ratio) in vivo, ex vivo, and in tissue sections. Our work establishes a quantifiable optical criterion for differentiating these liver pathologies, thereby addressing a major diagnostic gap. We anticipate this dual-parameter imaging strategy will advance the precision diagnosis of liver diseases and provide a versatile platform for studying organelle-specific microenvironments in other metabolic and inflammatory disorders.

Image 1

•First AIE-NIR probe to distinguish between early hepatocellular carcinoma and acute liver injury.•Dual-channel imaging of viscosity and HOCl with orthogonal signal responses.•Lipid droplet-targeted imaging demonstrates high specificity (PCC = 0.8773).•Allows for real-time monitoring of ferroptosis and inflammation processes.•Validates the Red-to-Green (R/G) fluorescence ratio as a robust, quantitative diagnostic criterion.

First AIE-NIR probe to distinguish between early hepatocellular carcinoma and acute liver injury.

Dual-channel imaging of viscosity and HOCl with orthogonal signal responses.

Lipid droplet-targeted imaging demonstrates high specificity (PCC = 0.8773).

Allows for real-time monitoring of ferroptosis and inflammation processes.

Validates the Red-to-Green (R/G) fluorescence ratio as a robust, quantitative diagnostic criterion.

## Linked entities

- **Chemicals:** hypochlorous acid (PubChem CID 24341), HOCl (PubChem CID 24341)
- **Diseases:** hepatocellular carcinoma (MONDO:0007256)

## Full-text entities

- **Diseases:** liver diseases (MESH:D008107), ALI (MESH:D017114), inflammatory disorders (MESH:D007249), metabolic (MESH:D008659), HCC (MESH:D006528)
- **Chemicals:** HOCl (MESH:D006997), lipid (MESH:D008055), DCN (-)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12858355/full.md

## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC12858355/full.md

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Source: https://tomesphere.com/paper/PMC12858355