# From the Clinic, to the Clinic: Improving the Fluorescent Imaging Quality of ICG via Amphiphilic NIR-IIa AIE Probe

**Authors:** Anjun Zhu, Zhibo Xiao, Aihui Sun, Feng Lu, Haozhou Tang, Xuekun Zhang, Ran Ren, Wei Yu, Andong Shao, Ninghan Feng, Shouyu Wang, Jianming Ni, Yaxi Li

PMC · DOI: 10.3390/bios16020090 · Biosensors · 2026-02-01

## TL;DR

This paper introduces a new method combining a special fluorescent probe and AI to improve the quality of clinical imaging, enabling clearer and faster imaging for better diagnostics and surgery.

## Contribution

A novel 'probe-plus-AI' approach using an amphiphilic NIR-IIa AIE probe and a deep learning model to enhance fluorescence imaging quality and speed.

## Key findings

- TCP probe provides 2.6-fold higher signal-to-background ratio in the NIR-IIa region compared to ICG in the NIR-I region.
- Deep learning model successfully converts low-quality ICG images into high-resolution NIR-IIa-like images.
- The method enables rapid, high-quality fluorescence imaging suitable for clinical diagnostics and image-guided surgery.

## Abstract

Fluorescence imaging is crucial for providing detailed information in clinical practice. However, traditional first near-infrared (NIR-I) dyes such as indocyanine green (ICG) exhibit limitations such as shallow penetration depth, low contrast, and suboptimal clarity due to light scattering and autofluorescence. To overcome these drawbacks, we utilized a novel amphiphilic second near-infrared (NIR-II) aggregation-induced emission (AIE) probe (TCP) with an emission range beyond 1300 nm (NIR-IIa). Using approximately 200 co-registered NIR-I/NIR-IIa image pairs acquired with TCP, we trained a SwinUnet-based deep learning model to transform low-quality NIR-I ICG images into high-resolution NIR-IIa-like images. Owing to its superior brightness and photostability, TCP enhances in vivo fluorescent angiography, offering clearer vascular details and a higher signal-to-background ratio (SBR) in the NIR-IIa region, 2.6-fold higher than that of ICG in the NIR-I region. The deep learning model successfully converted blurred NIR-I images into high-SBR NIR-IIa-like images, achieving rapid imaging speeds without compromising quality. This work introduces a synergistic “probe-plus-AI” paradigm that substantially improves both the quality and speed of clinical fluorescence imaging, providing a pathway that is immediately translatable to enhanced diagnostics and image-guided surgery.

## Linked entities

- **Chemicals:** indocyanine green (PubChem CID 5282412)

## Full-text entities

- **Genes:** Scgb1b27 (secretoglobin, family 1B, member 27) [NCBI Gene 11354] {aka Abp, Abpa, Abpa27, Sal-1, Tcp}
- **Diseases:** tumor (MESH:D009369), injury to (MESH:D014947), Hemolysis (MESH:D006461), Cytotoxicity (MESH:D064420), vascular-related disorders (MESH:D002561)
- **Chemicals:** DCM (MESH:D008752), PEG (MESH:D011092), acetonitrile (MESH:C032159), methanol (MESH:D000432), salt (MESH:D012492), TC (MESH:D013667), HBTU (MESH:C074712), chloride (MESH:D002712), 13C (MESH:C000615229), water (MESH:D014867), isoflurane (MESH:D007530), MTT (MESH:C070243), TFA (MESH:D014269), ICG (MESH:D007208), 6H (-), 2H (MESH:D003903), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MESH:C022616), H&amp;E (MESH:D006371), hematoxylin (MESH:D006416), sodium (MESH:D012964), PBS (MESH:D007854), eosin (MESH:D004801), Hydrogen (MESH:D006859), DIPEA (MESH:C027070), TCP (MESH:C049563), thiophene (MESH:D013876), DMF (MESH:D004126)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** 293 — Homo sapiens (Human), Transformed cell line (CVCL_0045), /6N — Mus musculus (Mouse), Transformed cell line (CVCL_D461), /6NJ — Mus musculus (Mouse), Hybridoma (CVCL_KS11)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938000/full.md

## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938000/full.md

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Source: https://tomesphere.com/paper/PMC12938000