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相关概念视频

Imaging Biological Samples with Optical Microscopy01:18

Imaging Biological Samples with Optical Microscopy

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Optical microscopy uses optic principles to provide detailed images of samples. Antonie van Leeuwenhoek designed the first compound optical microscope in the 17th century to visualize blood cells, bacteria, and yeast cells. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes with enhanced magnification and resolution.
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Total internal reflection fluorescence microscopy or TIRF is an advanced microscopic technique used to visualize fluorophores in samples close to a solid surface with a higher refractive index, such as a glass coverslip. TIRF only allows fluorophores in proximity to the solid surface to be excited. When light from a medium with a lower refractive index (such as air) hits the glass coverslip at a critical angle, the light undergoes total internal reflection stead of passing through the glass.
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Confocal microscopy is an advanced microscopic technique. The prime advantage of the confocal microscope over other microscopy techniques is its ability to block the out-of-focus light from the illuminated samples using pinholes. It is widely used with fluorescence optics to obtain high-resolution, sharp contrast images. Unlike optical microscopes, confocal microscopes use a focused beam of light laser to scan the entire sample surface at different z-planes. These microscopes are, therefore,...
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Three-dimensional imaging techniques are essential in cell biology, allowing researchers to visualize intricate cellular structures with high resolution. Two prominent methods, Differential Interference Contrast Microscopy (DIC) and Confocal Scanning Laser Microscopy (CSLM), provide distinct advantages for imaging live and thick specimens, respectively.Differential Interference Contrast MicroscopyDIC microscopy enhances contrast in transparent, unstained samples by converting phase...
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相关实验视频

Updated: Oct 10, 2025

Simultaneous Brightfield, Fluorescence, and Optical Coherence Tomographic Imaging of Contracting Cardiac Trabeculae Ex Vivo
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通过多模光纤进行飞行时间3D成像

Daan Stellinga1, David B Phillips2, Simon Peter Mekhail1

  • 1School of Physics and Astronomy, University of Glasgow, Glasgow G12 8QQ, UK.

Science (New York, N.Y.)
|December 9, 2021
PubMed
概括
此摘要是机器生成的。

这项研究提出了一种通过微小光纤进行3D成像的新方法, 这一突破使得在狭窄的空间中具有先进的检查能力.

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科学领域:

  • 光学和光学
  • 三维成像技术
  • 生物医学工程

背景情况:

  • 飞行时间 (ToF) 3D成像依赖于测量激光脉冲往返时间.
  • 传统的ToF系统使用大光学 (直径为厘米).
  • 在需要小型化或灵活的成像系统的应用中,现有的方法是有限的.

研究的目的:

  • 通过多模光纤展示近视频速率的3D成像.
  • 为了实现超薄微内镜的深度分辨能力.
  • 探索临床和远程检查中的应用.

主要方法:

  • 使用波面造型用于与脉冲激光源同步的偏差校正.
  • 实施扫描技术以捕获每秒约23,000个点.
  • 使用的多模纤维的核心直径小 (50微米),总孔径为几百微米.

主要成果:

  • 通过光纤实现近视频速率的3D成像.
  • 成功拍摄了离纤维端几米远的移动物体.
  • 通过长度为40厘米,核心直径为50微米的纤维,证明了约5Hz的率.

结论:

  • 这种技术通过微型光学系统显著提升了3D成像.
  • 开发的方法为微内镜提供了远场深度分辨能力.
  • 预计可以实现新的临床和远程检查应用.