Deep-Tissue Anatomical Imaging of Mice Using Carbon Nanotube Fluorophores in the Second Near Infrared Window

TL;DR

This study demonstrates that using carbon nanotube fluorophores in the second near infrared window enables high-resolution, real-time deep-tissue imaging in mice, surpassing traditional NIR I imaging in clarity and organ discrimination.

Contribution

The paper introduces biocompatible carbon nanotubes as effective NIR II fluorescent agents for dynamic, high-resolution deep-tissue imaging, enhanced by principal component analysis.

Findings

SWNTs enable real-time imaging of mouse organs post-injection.

PCA significantly improves organ resolution and discriminates otherwise indistinguishable tissues.

NIR II imaging shows superior feature contrast and tissue penetration compared to NIR I.

Abstract

Fluorescent imaging in the second near infrared window (NIR II, 1-1.4 {\mu}m) holds much promise due to minimal autofluorescence and tissue scattering. Here, using well functionalized biocompatible single-walled carbon nanotubes (SWNTs) as NIR II fluorescent imaging agents, we performed high frame rate video imaging of mice during intravenous injection of SWNTs and investigated the path of SWNTs through the mouse anatomy. We observed in real-time SWNT circulation through the lungs and kidneys several seconds post-injection, and spleen and liver at slightly later time points. Dynamic contrast enhanced imaging through principal component analysis (PCA) was performed and found to greatly increase the anatomical resolution of organs as a function of time post-injection. Importantly, PCA was able to discriminate organs such as the pancreas which could not be resolved from real-time raw images. Tissue phantom studies were performed to compare imaging in the NIR II region to the traditional NIR I biological transparency window (700- 900 nm). Examination of the feature sizes of a common NIR I dye (indocyanine green, ICG) showed a more rapid loss of feature contrast and integrity with increasing feature depth as compared to SWNTs in the NIR II region. The effects of increased scattering in the NIR I versus NIR II region were confirmed by Monte Carlo simulation. In vivo fluorescence imaging in the NIR II region combined with PCA analysis may represent a powerful approach to high resolution optical imaging through deep tissues, useful for a wide range of applications from biomedical research to disease diagnostics.