• Journal of Innovative Optical Health Sciences
  • Vol. 9, Issue 3, 1641003 (2016)
Guangyuan Zhao, Zihao Rong, Cuifang Kuang*, Cheng Zheng, and Xu Liu
Author Affiliations
  • State Key Laboratory of Modern Optical Instrumentation College of Optical Science and Engineering Zhejiang University, Hangzhou 310027, P. R. China
  • show less
    DOI: 10.1142/s1793545816410030 Cite this Article
    Guangyuan Zhao, Zihao Rong, Cuifang Kuang, Cheng Zheng, Xu Liu. 3D fluorescence emission difference microscopy based on spatial light modulator[J]. Journal of Innovative Optical Health Sciences, 2016, 9(3): 1641003 Copy Citation Text show less
    References

    [1] T. A. Klar, S. W. Hell, "Subdiffraction resolution in far-field fluorescence microscopy," Opt. Lett. 24(14), 954–956 (1999).

    [2] H. K€ohler, "On Abbe's theory of image formation in the microscope," J. Mod. Opt. 28(12), 1691–1701 (1981).

    [3] F. Bergermann et al., "2000-fold parallelized dualcolor STED fluorescence nanoscopy," Opt. Exp. 23 (1), 211–223 (2015).

    [4] T. Wilson, Confocal Microscopy, Vol. 426, pp. 1–64, Academic Press, London (1990).

    [5] T. Wilson, "Resolution and optical sectioning in the confocal microscope," J. Microsc. 244(2), 113–121 (2011).

    [6] Z. Rong et al., "Real-time super-resolution imaging by high-speed fluorescence emission difference microscopy," J. Mod. Opt. 61(16), 1364–1371 (2014).

    [7] C. Kuang et al., "Breaking the diffraction barrier using fluorescence emission difference microscopy," Sci. Rep. 3, 1441–1447 (2013).

    [8] Y. Fang et al., "Enhancing the resolution and contrast in CW-STED microscopy," Opt. Commun. 322, 169–174 (2014).

    [9] M. J. Rust, M. Bates, X. Zhuang, "Stochastic optical reconstruction microscopy (STORM) provides sub-diffraction-limit image resolution," Nat. Methods 3(10), 793 (2006).

    [10] E. Betzig et al., "Imaging intracellular fluorescent proteins at nanometer resolution," Science 313 (5793), 1642–1645 (2006).

    [11] S. W. Hell, J. Wichmann, "Breaking the diffraction resolution limit by stimulated emission: Stimulatedemission- depletion fluorescence microscopy," Opt. Lett. 19(11), 780–782 (1994).

    [12] R. Heintzmann, C. G. Cremer, Laterally modulated excitation microscopy: Improvement of resolution by using a diffraction grating, BiOS Europe'98, International Society for Optics and Photonics (1999).

    [13] M. G. Gustafsson, "Surpassing the lateral resolution limit by a factor of two using structured illumination microscopy," J. Microsc. 198(2), 82–87 (2000).

    [14] W. A. Carrington et al., "Superresolution three-dimensional images of fluorescence in cells with minimal light exposure," Science 268(5216), 1483–1487 (1995).

    [15] H. Kano et al., "Avalanche photodiode detection with object scanning and image restoration provides 2-4 fold resolution increase in two-photon fluorescence microscopy," Bioimaging 4(3), 187–197 (1996).

    [16] A. Sentenac et al., "High-resolution total-internalrefl ection fluorescence microscopy using periodically nanostructured glass slides," J. Opt. Soc. Am. A, Opt. Image Sci. 26(12), 2550–2557 (2009).

    [17] H. Dehez, M. Piche, Y. De Koninck, "Resolution and contrast enhancement in laser scanning microscopy using dark beam imaging," Opt. Exp. 21 (13), 15912–15925 (2013).

    [18] E. Rittweger, D. Wildanger, S. Hell, "Far-field fluorescence nanoscopy of diamond color centers by ground state depletion," Europhys. Lett. 86(1), 14001 (2009).

    [19] B. Harke et al., "Three-dimensional nanoscopy of colloidal crystals," Nano Lett. 8(5), 1309–1313 (2008).

    [20] S. Li et al., "Enhancing the performance of fluorescence emission difference microscopy using beam modulation," J. Opt. 15(12), 125708 (2013).

    [21] A. Gasecka et al., "Resolution and contrast enhancement in coherent anti-Stokes Raman-scattering microscopy," Opt. Lett. 38(21), 4510–4513 (2013).

    [22] Z. Rong et al., "Super-resolution microscopy based on fluorescence emission difference of cylindrical vector beams," Opt. Commun. 354, 71–78 (2015).

    [23] S. Segawa, Y. Kozawa, S. Sato, "Resolution enhancement of confocal microscopy by subtraction method with vector beams," Opt. Lett. 39(11), 3118–3121 (2014).

    [24] X. Hao et al., "Effects of polarization on the deexcitation dark focal spot in STED microscopy," J. Opt. 12(11), 115707 (2010).

    [25] D. Wildanger et al., "A compact STED microscope providing 3D nanoscale resolution," J. Microsc. 236(1), 35–43 (2009).

    [26] S. You et al., "Three-dimensional super-resolution imaging for fluorescence emission difference microscopy," AIP Adv. 5(8), 084901 (2015).

    [27] S. Segawa, Y. Kozawa, S. Sato, "Demonstration of subtraction imaging in confocal microscopy with vector beams," Opt. Lett. 39(15), 4529–4532 (2014).

    [28] N. Wang, T. Kobayashi, "Polarization modulation for fluorescence emission difference microscopy," Opt. Exp. 23(10), 13704–13712 (2015).

    [29] N. Wang, T. Kobayashi, "Numerical study of the subtraction threshold for fluorescence difference microscopy," Opt. Exp. 22(23), 28819–28830 (2014).

    Guangyuan Zhao, Zihao Rong, Cuifang Kuang, Cheng Zheng, Xu Liu. 3D fluorescence emission difference microscopy based on spatial light modulator[J]. Journal of Innovative Optical Health Sciences, 2016, 9(3): 1641003
    Download Citation