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Enhancing the Isotropy of Lateral Resolution in Coherent Structured Illumination Microscopy

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Specialty Radiology
Date 2014 Jun 19
PMID 24940548
Citations 2
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Abstract

We present a method to improve the isotropy of spatial resolution in a structured illumination microscopy (SIM) implemented for imaging non-fluorescent samples. To alleviate the problem of anisotropic resolution involved with the previous scheme of coherent SIM that employs the two orthogonal standing-wave illumination, referred to as the orthogonal SIM, we introduce a hexagonal-lattice illumination that incorporates three standing-wave fields simultaneously superimposed at the orientations equally divided in the lateral plane. A theoretical formulation is worked out rigorously for the coherent image formation with such a simultaneous multiple-beam illumination and an explicit Fourier-domain framework is derived for reconstructing an image with enhanced resolution. Using a computer-synthesized resolution target as a 2D coherent sample, we perform numerical simulations to examine the imaging characteristics of our three-angle SIM compared with the orthogonal SIM. The investigation on the 2D resolving power with the various test patterns of different periods and orientations reveal that the orientation-dependent undulation of lateral resolution can be reduced from 27% to 8% by using the three-angle SIM while the best resolution (0.54 times the resolution limit of conventional coherent imaging) in the directions of structured illumination is slightly deteriorated by 4.6% from that of the orthogonal SIM.

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References
1.
Frohn J, Knapp H, Stemmer A . True optical resolution beyond the Rayleigh limit achieved by standing wave illumination. Proc Natl Acad Sci U S A. 2000; 97(13):7232-6. PMC: 16528. DOI: 10.1073/pnas.130181797. View

2.
Gustafsson M . Surpassing the lateral resolution limit by a factor of two using structured illumination microscopy. J Microsc. 2000; 198(Pt 2):82-7. DOI: 10.1046/j.1365-2818.2000.00710.x. View

3.
Hell S, Wichmann J . Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy. Opt Lett. 2009; 19(11):780-2. DOI: 10.1364/ol.19.000780. View

4.
Sun P, Leith E . Superresolution by spatial-temporal encoding methods. Appl Opt. 2010; 31(23):4857-62. DOI: 10.1364/AO.31.004857. View

5.
Gustafsson M . Nonlinear structured-illumination microscopy: wide-field fluorescence imaging with theoretically unlimited resolution. Proc Natl Acad Sci U S A. 2005; 102(37):13081-6. PMC: 1201569. DOI: 10.1073/pnas.0406877102. View