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首页> 外文期刊>Journal of Applied Physics >One-photon and two-photon excited fluorescence microscopies based on polarization-control: Applications to tip-enhanced microscopy
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One-photon and two-photon excited fluorescence microscopies based on polarization-control: Applications to tip-enhanced microscopy

机译:基于偏振控制的单光子和双光子激发荧光显微镜:在尖端增强显微镜中的应用

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摘要

One-photon and two-photon excited fluorescence microscopies using either radial or azimuthal polarization have been developed and applied to the imaging of quantum dots. In both cases (one-photon and two-photon excitations), the fluorescence image profile of each quantum dot is in good agreement with the electric field intensity distribution of a tightly focused spot using a high numerical aperture objective lens. While this polarization dependence of the absorption/emission of quantum dots (or other dye molecules) is useful for characterizing the orientation of the quantum dots, most of the biological applications that employ quantum dots or dye molecules as labels require the information describing not only the orientation but also the precise position of each dot. In order to improve the sensing accuracy of the dot's position, we employ a modified near-field fluorescence microscopy system that utilizes a tip-enhancement technique and radially polarized two-photon excitations. For the tip enhancement, a commercially available silicon cantilever tip has been successfully utilized instead of metallic tips, as the latter tip can drastically quench the near-field fluorescence. Our tip-enhanced two-photon excited fluorescence microscopy technique enables visualization of the quantum dots distributed on a cover slip beyond the diffraction limit of light. We demonstrate that our approach is advantageous not only due to its high spatial resolution but also due to its high sensitivity by showing that the fluorescence signal is not detectable without the aid of the tip enhancement in some cases.
机译:已经开发出使用径向或方位极化的单光子和双光子激发荧光显微镜,并将其应用于量子点的成像。在两种情况下(单光子和双光子激发),每个量子点的荧光图像轮廓与使用高数值孔径物镜的紧密聚焦点的电场强度分布非常吻合。虽然量子点(或其他染料分子)的吸收/发射的极化相关性可用于表征量子点的方向,但大多数采用量子点或染料分子作为标记的生物学应用都需要信息,不仅描述方向以及每个点的精确位置。为了提高点位置的感测精度,我们采用了改进的近场荧光显微镜系统,该系统利用尖端增强技术和径向极化的两个光子激发。对于尖端的增强,已经成功地利用了市场上可买到的硅悬臂尖端来代替金属尖端,因为后者可以彻底淬灭近场荧光。我们的尖端增强型双光子激发荧光显微镜技术可以使分布在盖玻片上的量子点可视化,而超出光的衍射极限。通过证明在某些情况下如果没有尖端增强的帮助,荧光信号是无法检测到的,我们证明了我们的方法不仅由于其高空间分辨率而且还由于其高灵敏度而具有优势。

著录项

  • 来源
    《Journal of Applied Physics》 |2009年第11期|113103.1-113103.8|共8页
  • 作者单位

    NanoPhotonics Laboratory, RIKEN, Wako, Saitama 351-0198, Japan Near-field NanoPhotonics Research Team, RIKEN, Wako, Saitama 351-0198, Japan and CREST, Japan Corporation of Science and Technology, Kawaguchi, Saitama 332-0012, Japan;

    NanoPhotonics Laboratory, RIKEN, Wako, Saitama 351-0198, Japan;

    NanoPhotonics Laboratory, RIKEN, Wako, Saitama 351-0198, Japan;

    NanoPhotonics Laboratory, RIKEN, Wako, Saitama 351-0198, Japan Near-field NanoPhotonics Research Team, RIKEN, Wako, Saitama 351-0198, Japan CREST, Japan Corporation of Science and Technology, Kawaguchi, Saitama 332-0012, Japan and Department of Applied Physics, Osaka University, Suita, Osaka 565-0871, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
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