Superresolved spatially multiplexed interferometric microscopy

José Ángel Picazo-Bueno, Zeev Zalevsky, Javier García, Vicente Micó

Research output: Contribution to journalArticlepeer-review

28 Scopus citations

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 languageEnglish
Pages (from-to)927-930
Number of pages4
JournalOptics Letters
Volume42
Issue number5
DOIs
StatePublished - 1 Mar 2017

Bibliographical note

Publisher Copyright:
© 2017 Optical Society of America.

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