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Optical fiber based ultrashort pulse multispectral nonlinear optical microscopy

机译:基于光纤的超短脉冲多光谱非线性光学显微镜

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摘要

Nonlinear optical microscopy (NLOM) utilizing femtosecond laser pulses is well suited for imaging living tissues. This work reports on the design and development of an optical fiber based multispectral NLOM developed around a laser generating broadband sub-10-fs pulses. An all-mirror dispersion-compensation setup is used to correct for quadratic and cubic phase distortions induced within the NLOM. Mouse tail tendon was used to characterize sub-10-fs pulses by interferometric autocorrelation. This is an effective method for characterizing dispersion from the optical system, immersion medium, and wet biological sample. The generation of very short autocorrelations demonstrates the ability to compensate for phase distortions within the imaging system and efficient second-harmonic upconversion of the ultrashort pulse spectrum within collagen. Reconstruction of ultrashort pulses at the focal plane of the objective allows the excitation of multiple fluorescent probes simultaneously. Multiple fluorescent probe excitation and spectral discrimination is demonstrated using mixtures of fluorescent dye solutions and an in-vitro angiogenesis model containing human umbilical vein endothelial cells (HUVEC?s) expressing multiple fluorescent proteins. Sub-10-fs pulses can be propagated through polarization-maintaining single mode fiber (PMF) for use in NLOM. We demonstrate delivery of near transform-limited, 1 nJ pulses from a Ti:Al2O3 oscillator via PMF to the NLOM focal plane while maintaining 120 nm of bandwidth. Negative group delay dispersion (GDD) introduced to pre-compensate normal dispersion of the optical fiber and microscope optics ensured linear pulse propagation through the PMF. Nonlinear excitation of multiple fluorophores simultaneously and polarization sensitive NLOM imaging using second harmonic generation in collagen was demonstrated using PMF delivered pulses. Two-photon excited fluorescence spectra and second harmonic images taken with and without the fiber indicates that the fiber based system is capable of generating optical signals that are within a factor of two to three of our traditional NLOM.
机译:利用飞秒激光脉冲的非线性光学显微镜(NLOM)非常适合对活组织成像。这项工作报告了基于光纤的多光谱NLOM的设计和开发,该NLOM是围绕产生宽带sub-10-fs脉冲的激光而开发的。全镜面色散补偿设置用于校正NLOM中引起的二次和三次相位失真。小鼠尾部肌腱用于通过干涉自相关来表征低于10 fs的脉冲。这是表征来自光学系统,浸没介质和湿生物样品的色散的有效方法。非常短的自相关的产生证明了能够补偿成像系统内的相位畸变以及对胶原蛋白内的超短脉冲谱进行有效的二次谐波上转换的能力。在物镜焦平面上重建超短脉冲可以同时激发多个荧光探针。使用荧光染料溶液的混合物和包含表达多种荧光蛋白的人脐静脉内皮细胞(HUVEC?s)的体外血管生成模型,证明了多种荧光探针激发和光谱区分。 Sub-10-fs脉冲可以通过用于NLOM的保偏单模光纤(PMF)传播。我们演示了从Ti:Al2O3振荡器通过PMF向NLOM焦平面传递近变换限制的1 nJ脉冲,同时保持120 nm的带宽。负组延迟色散(GDD)用来预补偿光纤和显微镜光学器件的正常色散,从而确保了线性脉冲传播通过PMF。演示了使用PMF传递脉冲同时激发多个荧光团的非线性激发和使用胶原蛋白中二次谐波产生的偏振敏感NLOM成像。使用和不使用光纤而获得的双光子激发荧光光谱和二次谐波图像表明,基于光纤的系统能够生成光信号,该光信号在传统NLOM的2到3倍之内。

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    Larson Adam Michael;

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  • 年度 2009
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  • 原文格式 PDF
  • 正文语种 en_US
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