Abstract
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 non-holographic microscope into a superresolved holographic one. Validation is presented for an Olympus BX-60 upright microscope with resolution test targets.
Original language | English |
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Pages (from-to) | 927-930 |
Number of pages | 4 |
Journal | Optics Letters |
Volume | 42 |
Issue number | 5 |
DOIs | |
State | Published - 1 Mar 2017 |
Bibliographical note
Publisher Copyright:© 2017 Optical Society of America.
Funding
Ministerio de Economía y Competitividad (MINECO) (FIS2013-47548-P); European Regional Development Fund (ERDF).
Funders | Funder number |
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Ministerio de Economía y Competitividad | FIS2013-47548-P |
European Regional Development Fund |