微秒
体内
临床前影像学
荧光
光学
材料科学
成像体模
循环肿瘤细胞
分子成像
纳秒
斯托克斯位移
荧光寿命成像显微镜
发光
自体荧光
物理
癌症
光电子学
激光器
医学
生物
转移
生物技术
内科学
作者
Xu Cao,Cuiping Yao,Shudong Jiang,Jason R. Gunn,Austin C Van Namen,Petr Brůža,Brian W. Pogue
出处
期刊:Optics Letters
[The Optical Society]
日期:2020-06-30
卷期号:45 (13): 3761-3761
被引量:4
摘要
Fluorescence imaging is severely limited by the background and autofluorescence of tissues for in vivo detection of circulating tumor cells (CTCs). Time-gated luminescence (TGL) imaging, in combination with luminescent probes that possess hundreds of microsecond emission lifetimes, can be used to effectively suppress this background, which has predominantly nanosecond lifetimes. This Letter demonstrates the feasibility of TGL imaging using luminescent probes for the in vivo real time imaging and tracking of single CTCs circulating freely in the blood vessels with higher accuracy given by substantially higher signal-to-noise ratio. The luminescent probe used in this Letter was a commercial E u 3 + chelate (EuC) nanosphere with a super-long lifetime of near 800 µs, which enabled TGL imaging to achieve background-free detection with ∼ 5 times higher SNR versus steady state. Phantom and in vivo mouse studies indicated that EuC labeled tumor cells moving in medium or bloodstream at the speed of 1–2 mm/s could be captured in real time.
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