In Vivo Time-Resolved Fluorescence Imaging of a NIR FRET Probe in Live Mice

Lingling Zhao, K. Abe, Margarida M Barroso, X. Intes
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Abstract

One of the key challenges in anti-cancer drug validation is to quantitatively discriminate in vivo non-specific receptor-independent tumor accumulation from receptor-mediated uptake into the tumor cells. To overcome this challenge, we develop a new near-infrared Förster resonance energy transfer fluorescence lifetime imaging (NIR FRET FLIM) technique. We apply herein this novel approach to monitor and characterize cellular uptake in both cancer cells and normal cells in vitro and in vivo. Our results demonstrate that NIR FRET FLIM can quantitatively distinguish receptor-bound from unbound donor in live animals with high sensitivity and high accuracy. Thus, it has a great potential for the quantitative detection of targeted delivery systems for diagnostic and therapeutic use.
近红外FRET探针在活体小鼠体内时间分辨荧光成像
抗癌药物验证的关键挑战之一是定量区分体内非特异性受体非依赖型肿瘤积累和受体介导的肿瘤细胞摄取。为了克服这一挑战,我们开发了一种新的近红外Förster共振能量转移荧光寿命成像(NIR FRET FLIM)技术。我们在此应用这种新方法来监测和表征癌细胞和正常细胞在体外和体内的细胞摄取。我们的研究结果表明,近红外FRET FLIM可以定量区分活体动物的受体结合和非结合供体,具有高灵敏度和高精度。因此,它在诊断和治疗用途的靶向递送系统的定量检测方面具有很大的潜力。
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