DocumentCode :
2752554
Title :
Spatial light interference microscopy (SLIM)
Author :
Popescu, Gabriel
Author_Institution :
Dept. of Electr. & Comput. Eng., Univ. of Illinois at Urbana-Champaign, Urbana, IL, USA
fYear :
2011
fDate :
9-13 Oct. 2011
Firstpage :
797
Lastpage :
797
Abstract :
Spatial light interference microscopy (SLIM) is 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.
Keywords :
holography; light interference; optical microscopy; transparency; Gabor holography; atomic force microscopy; light imaging; light microscopy; optical microscopy technique; phase contrast microscope; phase information; primary cell cultures; quantitative optical path length maps; spatial light interference microscopy; topographic accuracy; transparent specimens; Holography; Microscopy; Optical imaging; Optical interferometry; Optical microscopy; Optical variables measurement;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Photonics Conference (PHO), 2011 IEEE
Conference_Location :
Arlington, VA
Print_ISBN :
978-1-4244-8940-4
Type :
conf
DOI :
10.1109/PHO.2011.6110797
Filename :
6110797
Link To Document :
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