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Signal enhancement in multiphoton imaging by the use of coated glass substrates

机译:通过使用镀膜玻璃基板增强多光子成像中的信号

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摘要

In nonlinear optical imaging of biological specimens, more than half of the generated luminescence signal is lost, when signal collection is performed in the epi-illuminated geometry. In this study, we enhanced the collected luminescence signal by the use of alternating multiply-coated layers of tantalum pentoxide (Ta2O5) and silicon dioxide (SiO2) on standard microscope cover glasses that has high transmission in the near-infrared wavelength region and high reflection of the visible, luminescence signal. Our coating is biocompatible, allows visual examination of the specimens and optimize collection of the luminescence signal. We demonstrated this approach on a number of specimens including sulforhodamine solution, fluorescence microspheres, and labeled 3T3 cells. In all cases, the use of coated cover glass enhanced signal, optimally by a factor of about 2. Image analysis of labeled 3T3 cells also shows signal enhancement did not contribute to additional photobleaching. Our results show that properly designed coated cover glass can enhance detected signal in multiphoton microscopy and result in improved image quality.
机译:在生物样本的非线性光学成像中,当在落射照明的几何体中执行信号收集时,会丢失一半以上的发光信号。在这项研究中,我们通过在标准的显微镜盖玻片上使用五氧化钽(Ta2O5)和二氧化硅(SiO2)的交替多层涂层来增强收集的发光信号,该显微镜在近红外波长区域具有高透射率并且具有高反射率可见的发光信号。我们的涂层具有生物相容性,可以目检样品并优化发光信号的收集。我们在包括硫磺罗丹明溶液,荧光微球和标记3T3细胞在内的许多标本上证明了这种方法。在所有情况下,使用带涂层的盖玻片均可以将信号增强,最理想的情况约为2倍。对标记的3T3细胞的图像分析还表明,信号增强并不会增加光漂白。我们的结果表明,经过适当设计的镀膜防护玻璃可以增强多光子显微镜检测到的信号,并改善图像质量。

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