Superresolved spatially multiplexed interferometric microscopy

被引：30
作者：
Angel Picazo-Bueno, Jose [1 ]
Zalevsky, Zeev [2 ]
Garcia, Javier [1 ]
Mico, Vicente [1 ]
机构：
[1] Univ Valencia, Fac Fis, Dept Opt & Optometria & Ciencias Vis, C Doctor Moliner 50, E-46100 Burjassot, Spain
[2] Bar Ilan Univ, Sch Engn, IL-52900 Ramat Gan, Israel
来源：
OPTICS LETTERS | 2017年 / 42卷 / 05期
关键词：
DIGITAL HOLOGRAPHIC MICROSCOPY; QUANTITATIVE PHASE MICROSCOPY; STRUCTURED ILLUMINATION; RESOLUTION IMPROVEMENT; SAMPLES; LIMITS;
D O I：
10.1364/OL.42.000927
中图分类号：
O43 [光学];
学科分类号：
070207 ; 0803 ;
摘要：
Superresolution capability by angular and time multiplexing is implemented onto a regular microscope. The technique, named superresolved spatially multiplexed interferometric microscopy (S2MIM), follows our previously reported SMIM technique [Opt. Express 22, 14929 (2014), J. Biomed. Opt. 21, 106007 (2016)] improved with superresolved imaging. All together, S2MIM updates a commercially available nonholographic microscope into a superresolved holographic one. Validation is presented for an Olympus BX-60 upright microscope with resolution test targets. (C) 2017 Optical Society of America
引用
收藏
页码：927 / 930
页数：4
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