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

页码：927 / 930

页数：4

共 39 条

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