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In Vivo Time-gated Fluorescence Imaging with Biodegradable Luminescent Porous Silicon Nanoparticles

机译:生物可降解的发光多孔硅纳米粒子的体内时间门控​​荧光成像。

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摘要

Fluorescence imaging is one of the most versatile and widely used visualization methods in biomedical research. However, tissue autofluorescence is a major obstacle confounding interpretation of in vivo fluorescence images. The unusually long emission lifetime (5-13 μs) of photoluminescent porous silicon nanoparticles can allow the time-gated imaging of tissues in vivo, completely eliminating shorter-lived (< 10 ns) emission signals from organic chromophores or tissue autofluorescence.Here, using a conventional animal imaging system not optimized for such long-lived excited states, we demonstrate improvement of signal to background contrast ratio by > 50-fold in vitro and by > 20-fold in vivo when imaging porous silicon nanoparticles. Time-gated imaging of porous silicon nanoparticles accumulated in a human ovarian cancer xenograft following intravenous injection is demonstrated in a live mouse. The potential for multiplexing of images in the time domain by using separate porous silicon nanoparticles engineered with different excited state lifetimes is discussed.
机译:荧光成像是生物医学研究中功能最广泛,使用最广泛的可视化方法之一。然而,组织自发荧光是混淆体内荧光图像解释的主要障碍。光致发光多孔硅纳米粒子具有异常长的发射寿命(5-13μs),可以在体内对组织进行时间门控成像,从而完全消除了来自有机发色团或组织自发荧光的寿命较短(<10 ns)的发射信号。传统的动物成像系统未针对此类长寿命激发态进行优化,当对多孔硅纳米粒子成像时,我们证明了其信号与背景对比度之比在体外提高了50倍,在体内提高了20倍。在活小鼠中证实了静脉注射后在人类卵巢癌异种移植物中积累的多孔硅纳米粒子的时间门控成像。讨论了通过使用设计有不同激发态寿命的单独的多孔硅纳米粒子在时域中复用图像的潜力。

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