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Multi-photon near-infrared emission saturation nanoscopy using upconversion nanoparticles

机译:使用上转换纳米粒子的多光子近红外发射饱和纳米技术

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摘要

Multiphoton fluorescence microscopy (MPM), using near infrared excitation light, provides increased penetration depth, decreased detection background, and reduced phototoxicity. Using stimulated emission depletion (STED) approach, MPM can bypass the diffraction limitation, but it requires both spatial alignment and temporal synchronization of high power (femtosecond) lasers, which is limited by the inefficiency of the probes. Here, we report that upconversion nanoparticles (UCNPs) can unlock a new mode of near-infrared emission saturation (NIRES) nanoscopy for deep tissue super-resolution imaging with excitation intensity several orders of magnitude lower than that required by conventional MPM dyes. Using a doughnut beam excitation from a 980 nm diode laser and detecting at 800 nm, we achieve a resolution of sub 50 nm, 1/20th of the excitation wavelength, in imaging of single UCNP through 93 μm thick liver tissue. This method offers a simple solution for deep tissue super resolution imaging and single molecule tracking.
机译:使用近红外激发光的多光子荧光显微镜(MPM)可以增加穿透深度,降低检测背景,并降低光毒性。使用受激发射损耗(STED)方法,MPM可以绕过衍射限制,但是它需要高功率(飞秒)激光器的空间对准和时间同步,这受探针效率低下的限制。在这里,我们报告上转换纳米粒子(UCNPs)可以解锁一种新模式的近红外发射饱和(NIRES)纳米技术,用于深层组织超分辨率成像,其激发强度比传统MPM染料所需的激发强度低几个数量级。使用从980 nm二极管激光器发出的甜甜圈光束激发并在800 nm处检测,在通过93μm厚的肝组织成像单个UCNP时,我们获得了低于50 nm的分辨率,是激发波长的1/20。该方法为深组织超分辨率成像和单分子跟踪提供了简单的解决方案。

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