共查询到18条相似文献,搜索用时 156 毫秒
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探头对共聚焦内窥成像系统层析能力的影响 总被引:2,自引:1,他引:1
根据透镜成像规律和单模光纤的传输特性,获得基于单模光纤的共聚焦内窥成像系统轴向光强分布,发现系统的成像过程由于单模光纤的介入呈现非线性,照明光路系统和接收光路系统仅影响系统接收信号的总强度,系统层析能力取决于探头和单模光纤性能.通过建立的共聚焦内窥成像实验装置,测量出在三组不同物镜组合情况下系统的归一化轴向光强分布.结果显示已建立的共聚焦内窥成像系统的理论模型是正确的,扫描光点的定位精度对系统层析能力影响很大,系统设计应该综合考虑光学、机械和电子方面的性能要求. 相似文献
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研制了一种激光共焦扫描显微内窥镜,采用望远式显微内窥光学系统,同时实现长距离的图像中继传输、远心f-theta光学扫描和显微内窥成像功能.二维共焦扫描由双振镜实现,低噪音扫描控制信号由嵌入式系统产生.为实现便携式应用,激光共焦扫描显微内窥镜采用小型化设计方案.首先,体内的显微内窥成像光学系统,外径尺寸为8 mm,工作长度为250.3 mm,可通过标准腹腔镜手术孔进行体内显微内窥成像;其次,采用3 mm通光孔径的小尺寸平面反射镜实现体外共焦扫描,摆动频率为100 Hz,实现快速共焦扫描;最后,激光控制和荧光探测仅通过电缆和光纤与共焦扫描显微内窥镜前端连接,减小了显微内窥镜的前端尺寸和重量.通过实验验证,本系统的成像视场为φ 600 μm,光学分辨率为2.2 μm,可采用手持式或者其他方式工作,进行体内组织的共焦扫描成像,实现微创、在体的荧光显微内窥术. 相似文献
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在共聚焦显微镜中,通过系统的归一化轴向光强半高宽与探测器有效半径和非相干光源有效半径的关系曲线,获得非相干光源照明下系统光学层析能力的变化规律.发现当探测器和光源的有效半径都小于3时,系统具有较好的光学层析能力;其他情况下,系统光学层析能力下降且会受入射光场分布的影响. 相似文献
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提出一种新的具有高空间分辨力的整形环形光式差动共焦测量方法。该方法通过整形环形光式共焦测量法和锐化爱里斑主瓣,改善系统横向分辨力;通过差动共焦测量法改善系统的轴向分辨力,最终达到提高系统空间分辨能力的目的。理论分析和实验表明:整形环形光内孔归一化半径ε越大,横向分辨力改善越明显,量程扩展范围越宽;当入射光波长λ=632.8nm,物镜数值孔径取NA=0.85,ε=0.5时,该系统的横向分辨力优于0.2μm,轴向分辨力优于2nm。该方法为光触针测量系统空间分辨力的提高提供了1种新的方法,可广泛应用于超精密三维微细结构工件的超精密测量。 相似文献
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《光谱学与光谱分析》2020,(6)
共焦布里渊光谱技术因其具有非接触、无损伤、高空间分辨等优点,在生物医学、物理化学以及材料科学中被广泛应用。由于布里渊散射频移较低、强度较弱,在弹性散射光没有被充分抑制的情况下,布里渊散射光容易受到弹性散射光的影响,导致光谱测量结果精度的下降,而且传统共焦布里渊光谱系统仍存在光谱轴向分辨力与层析能力不足等缺点,严重限制了共焦布里渊光谱探测系统在高散射样品以及长工作距离光谱探测领域中的应用。为改善共焦布里渊光谱探测系统的抗弹性散射能力、光谱轴向分辨力以及层析能力,构建了一种D形分光瞳共焦布里渊光谱探测系统。该系统通过侧向照明与侧向收集的方式消除背向散射,降低弹性散射强度,有效抑制弹性散射对布里渊散射的干扰,进而提高共焦布里渊光谱探测系统的抗弹性散射能力。通过D形光瞳对照明点扩散函数与收集点扩散函数进行调制,利用斜入射的方式使照明点扩散函数与收集点扩散函数仅在焦平面上发生重叠,在轴向上实现三维点扩散函数的压缩,有效去除离焦光谱信息对焦面光谱信息的干扰,降低轴向光谱强度响应曲线的半高全宽与全高全宽,进而达到提高共焦布里渊光谱探测系统的光谱轴向分辨力以及层析能力的效果。实验表明:相比于共焦布里渊光谱探测系统, D形分光瞳共焦布里渊光谱探测系统的抗弹性散射能力与层析能力得到大幅提升,通过优化光瞳参数,其光谱轴向分辨力可以提高30%以上,进而可以有效解决多层样品中的光谱串扰问题。D形分光瞳共焦布里渊光谱探测系统作为一种具有高层析能力、抗弹性散射能力强的布里渊光谱探测系统,为布里渊光谱技术在现代前沿基础学科领域中的进一步应用提供了有力保证。 相似文献
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We present a compact second-harmonic-generation (SHG) microscope based on a three-port single-mode fiber coupler. The fiber coupler is used to deliver a near-infrared ultrashort-pulsed laser beam as well as to collect the SHG signal in the visible wavelength range. The SHG microscope exhibits an axial resolution of 1.8 microm, which shows a slight enhancement of the optical sectioning effect compared with that for two-photon excitation at the same excitation wavelength. It is also demonstrated that SHG and two-photon fluorescence images under parallel and perpendicular laser excitation polarization can be simultaneously obtained. 相似文献
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提出了一种基于偏振滤波图像增强和动态散斑照明的新型宽场荧光层析显微镜. 该显微镜采用了一种新型的偏振滤波图像增强技术, 基于激发光与荧光偏振态的差异, 利用偏振器件滤除激发光; 并利用动态散斑照明实现宽场层析. 该荧光层析显微镜具有结构简单、低成本、响应速度快、容易操作等特点. 实验研究结果表明, 本文提出的滤波方案能够显著地提高图像质量, 利用动态散斑照明实现宽场层析具有较高的纵向分辨能力. 研究丰富了在荧光显微镜中, 从强激发光中提取弱荧光信号的技术手段, 为今后发展具有快速响应, 波长可调谐的多光谱荧光层析等高端的显微镜具有重要参考意义. 相似文献
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We describe a method of obtaining optical sectioning with a standard wide-field fluorescence microscope. The method involves acquiring two images, one with nonuniform illumination (in our case, speckle) and another with uniform illumination (in our case, randomized speckle). An evaluation of the local contrast in the speckle-illumination image provides an optically sectioned image with low resolution. This is complemented with high-resolution information obtained from the uniform-illumination image. A fusion of both images leads to a full resolution image that is optically sectioned across all spatial frequencies. This hybrid illumination method is fast, robust, and generalizable to a variety of illumination and imaging configurations. 相似文献
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We present a simple modification to a conventional wide-field fluorescence microscope that provides depth discrimination in thick tissues. The technique consists of illuminating a sample with a sequence of independent speckle patterns and displaying the rms of the resultant sequence of fluorescence images. The advantage of speckle illumination is that it provides diffraction-limited illumination granularity that is highly contrasted even in scattering media. We demonstrate quasi-confocal imaging in a mouse olfactory bulb labeled with green fluorescent protein. 相似文献
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Two-photon excitation provides efficient optical sectioning in three-dimensional fluorescence microscopy, independently of a confocal detection. In two-photon laser-scanning microscopy, the image resolution is governed by the volume of the excitation light spot, which is obtained by focusing the incident laser beam through the objective lens of the microscope. The light spot being strongly elongated along the optical axis, the axial resolution is much lower than the transverse one. In this Letter we show that it is possible to strongly reduce the axial size of the excitation spot by shaping the incident beam and using a mirror in place of a standard glass slide to support the sample. Provided that the contribution of sidelobes can be removed through deconvolution procedures, this approach should allow us to achieve similar axial and lateral resolution. 相似文献