临床前影像学
荧光寿命成像显微镜
分子成像
吲哚青绿
光学成像
医学
化学
离体
生物物理学
作者
Guosong Hong,Jerry C Lee,Joshua T Robinson,Uwe Raaz,Liming Xie,Ngan F Huang,John P Cooke,Hongjie Dai
出处
期刊:Nature Medicine
[Springer Nature]
日期:2012-11-18
卷期号:18 (12): 1841-1846
被引量:951
摘要
In vivo real-time epifluorescence imaging of mouse hind limb vasculatures in the second near-infrared region (NIR-II) is performed using single-walled carbon nanotubes as fluorophores. Both high spatial (∼30 μm) and temporal (<200 ms per frame) resolution for small-vessel imaging are achieved at 1-3 mm deep in the hind limb 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) or microscopic computed tomography, and 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 on the basis of their distinct hemodynamics. Further, the deep tissue penetration and 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 capabilities of ultrasonography at lower blood velocities.
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