Super-resolution structured illumination in optically thick specimens without fluorescent tagging

被引:1
作者
Hoffman, Zachary R. [1 ,2 ]
DiMarzio, Charles A. [1 ]
机构
[1] Northeastern Univ, Dept Elect & Comp Engn, Boston, MA 02115 USA
[2] Charles Stark Draper Lab, Cambridge, MA 02139 USA
基金
美国国家科学基金会;
关键词
structured Illumination; optical sectioning; super-resolution; incoherent; random; DYNAMIC SPECKLE ILLUMINATION; MICROSCOPY; LIGHT; PATTERNS; LIMIT;
D O I
10.1117/1.JBO.22.11.116003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This research extends the work of Hoffman et al. to provide both sectioning and super-resolution using random patterns within thick specimens. Two methods of processing structured illumination in reflectance have been developed without the need for a priori knowledge of either the optical system or the modulation patterns. We explore the use of two deconvolution algorithms that assume either Gaussian or sparse priors. This paper will show that while both methods accomplish their intended objective, the sparse priors method provides superior resolution and contrast against all tested targets, providing anywhere from similar to 1.6 x to similar to 2x resolution enhancement. The methods developed here can reasonably be implemented to work without a priori knowledge about the patterns or point spread function. Further, all experiments are run using an incoherent light source, unknown random modulation patterns, and without the use of fluorescent tagging. These additional modifications are challenging, but the generalization of these methods makes them prime candidates for clinical application, providing super-resolved noninvasive sectioning in vivo. (c) 2017 Society of Photo-Optical Instrumentation Engineers (SPIE)
引用
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页数:11
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