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) [CrossRef]  , J. Biomed. Opt. 21, 106007 (2016) [CrossRef]  ] 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.

© 2017 Optical Society of America

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Supplementary Material (1)

NameDescription
» Visualization 1: AVI (4685 KB)      Whole set of recorded slightly off-axis holograms from which phase-shifting algorithm is applied.

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