# Fluorescence Imaging of DMDG-ICG Across NIR-I and NIR-II Windows Using a Single-Camera System

**Authors:** Bonghwan Chon, Mukesh P. Yadav, William Ghann, Stuart S. Martin, Jamal Uddin, Ananth Annapragada, Vikas Kundra

PMC · DOI: 10.3390/ijms27041857 · International Journal of Molecular Sciences · 2026-02-14

## TL;DR

This study shows that using a single-camera system for both NIR-I and NIR-II imaging improves image quality and resolution in nanoparticle-based imaging.

## Contribution

The novel use of a single InGaAs camera system enables direct comparison of NIR-I and NIR-II imaging performance.

## Key findings

- NIR-II imaging showed better spatial resolution and higher CNR than NIR-I at depths up to 10 mm in Intralipid.
- In vivo imaging of the mouse femoral artery demonstrated higher CNR with NIR-II compared to NIR-I.

## Abstract

Near-infrared (NIR) imaging, including NIR-I (800–1000 nm) and NIR-II (1000–1700 nm), has been primarily evaluated using separate cameras with different detectors, limiting comparison. We investigated whether using a single-camera system capable of both NIR-I and NIR-II acquisition, NIR-II improves spatial resolution and contrast-to-noise ratio (CNR) for nanoparticle-based imaging. Dual-mode, dual-Gd ICG (DMDG-ICG) nanoparticles were characterized for absorption and fluorescence. A custom NIR imaging system using a single InGaAs camera enabled visualizing both NIR-I and -II windows. In vitro, capillary tubes containing nanoparticles in water, in tissue-mimicking Intralipid, or covered with mouse skin were imaged, and full-width-half maximum (FWHM) and CNR were measured. In vivo, the mouse femoral artery was imaged after IV nanoparticle delivery. DMDG-ICG showed strong fluorescence at both NIR-I and NIR-II. Scatter greater at NIR-I than NIR-II increased with depth and tissue layers. FWHM was lower and CNR higher at NIR-II versus NIR-I for up to 10 mm depth (p < 0.05, n = 3) in Intralipid. In vivo, femoral artery CNR was also higher at NIR-II (p < 0.05, n = 3). Using a single-camera system allowing direct comparison, NIR-II imaging provided greater penetration, spatial resolution, and CNR compared to NIR-I. The findings support the utility of NIR-II for vascular and molecular imaging applications.

## Linked entities

- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Twist1 (twist basic helix-loop-helix transcription factor 1) [NCBI Gene 22160] {aka M-Twist, Pde, Ska10, Ska<m10Jus>, Twist, bHLHa38}
- **Diseases:** ovarian cancer (MESH:D010051), tumor (MESH:D009369), injury to (MESH:D014947)
- **Chemicals:** ICG (MESH:D007208), Gd-DTPA (MESH:D019786), DMDG (-), silicon (MESH:D012825), Gd (MESH:D005682), Intralipid (MESH:C545823), histidine (MESH:D006639), nitrogen (MESH:D009584), fat (MESH:D005223), gadobenate dimeglumine (MESH:C064572), saline (MESH:D012965), Chol (MESH:D002784), Water (MESH:D014867)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940706/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12940706/full.md

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Source: https://tomesphere.com/paper/PMC12940706