自体荧光
化学
体内
临床前影像学
发光
共焦
光子上转换
荧光
荧光寿命成像显微镜
分子成像
光学
材料科学
光电子学
生物
物理
生物技术
作者
Liqin Xiong,Zhigang Chen,Qiwei Tian,Tianye Cao,Congjian Xu,Fuyou Li
摘要
Fluorescence targeted imaging in vivo has proven useful in tumor recognition and drug delivery. In the process of in vivo imaging, however, a high autofluorescence background could mask the signals from the fluorescent probes. Herein, a high contrast upconversion luminescence (UCL) imaging protocol was developed for targeted imaging of tumors based on RGD-labeled upconversion nanophosphors (UCNPs) as luminescent labels. Confocal Z-scan imaging of tissue slices revealed that UCL imaging showed no autofluorescence signal even at high penetration depth (∼600 μm). More importantly, region of interest (ROI) analysis of the UCL signal in vivo showed that UCL imaging achieved a high signal-to-noise ratio (∼24) between the tumor and the background. These results demonstrate that the UCL imaging technique appears particularly suited for applications in tracking and labeling components of complex biological systems.
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