返回
Spatial light interference microscopy (SLIM)
DOI:10.1364/OE.19.001016.png)
摘要
En 中文
We present spatial light interference microscopy (SLIM) as a new optical microscopy technique, capable of measuring nanoscale structures and dynamics in live cells via interferometry. SLIM combines two classic ideas in light imaging: Zernike's phase contrast microscopy, which renders high contrast intensity images of transparent specimens, and Gabor's holography, where the phase information from the object is recorded. Thus, SLIM reveals the intrinsic contrast of cell structures and, in addition, renders quantitative optical path-length maps across the sample. The resulting topographic accuracy is comparable to that of atomic force microscopy, while the acquisition speed is 1,000 times higher. We illustrate the novel insight into cell dynamics via SLIM by experiments on primary cell cultures from the rat brain. SLIM is implemented as an add-on module to an existing phase contrast microscope, which may prove instrumental in impacting the light microscopy field at a large scale. (C) 2011 Optical Society of America
Keyword:
DIGITAL HOLOGRAPHIC MICROSCOPY
PHASE MICROSCOPY
DIFFRACTION TOMOGRAPHY
COMPUTED-TOMOGRAPHY
DYNAMICS
REFRACTOMETRY
CONTRAST
AI总结
对已上传原文的论文进行重点信息的提取,主要内容包括:简要概述、研究摘要、背景介绍、关键亮点、图文解析、展望与总结。
期刊
IF:
3.3
论文数:
6.1W
被引数:
14.3W

