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
Full Article | PDF ArticleMore Like This
José Ángel Picazo-Bueno, Maciej Trusiak, Javier García, Krzysztof Patorski, and Vicente Micó
Opt. Lett. 43(5) 1007-1010 (2018)
Vicente Mico, Carlos Ferreira, Zeev Zalevsky, and Javier García
Opt. Express 22(12) 14929-14943 (2014)
Alejandro Calabuig, Javier Garcia, Carlos Ferreira, Zeev Zalevsky, and Vicente Micó
J. Opt. Soc. Am. A 28(11) 2346-2358 (2011)