In vivo real-time epifluorescence imaging of mouse hindlimb vasculatures in
the second near-infrared region (NIR-II, 1.1~1.4 microns) is performed using
single-walled carbon nanotubes (SWNTs) as fluorophores. Both high spatial
resolution (~30 microns) and temporal resolution (<200 ms/frame) for small
vessel imaging are achieved 1-3 mm deep in the tissue owing to the beneficial
NIR-II optical window that affords deep anatomical penetration and low
scattering. This spatial resolution is unattainable by traditional NIR imaging
(NIR-I, 0.75~0.9 microns) or microscopic computed tomography (micro-CT), while
the temporal resolution far exceeds scanning microscopic imaging techniques.
Arterial and venous vessels are unambiguously differentiated using a dynamic
contrast-enhanced NIR-II imaging technique based on their distinct
hemodynamics. Further, the deep tissue penetration, high spatial and temporal
resolution of NIR-II imaging allow for precise quantifications of blood
velocity in both normal and ischemic femoral arteries, which are beyond the
capability of ultrasonography at lower blood velocity.Comment: 33 pages, 5 main text figures, 6 supporting figures and 2 tables;
Published online at Nature Medicine, 201