Abstract
In this paper, we propose a new method to obtain the improvement of lateral axial resolution of confocal fluorescence microscopy. In this method, we employ two different beams to illuminate the sample: (1) the Gaussian beam; (2) the donut beam. Two different images are produced from these two illumination beams. A higher resolution image is generated by a multi-relationship between these two image. A set of simulation and experimental results are employed to compare the effectiveness of proposed method with the traditional confocal fluorescence microscopy. These results demonstrated that our method can be employed to achieve the resolution-enhancement of confocal fluorescence microscopy.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Wan, C., et al.: Three-dimensional visible-light capsule enclosing perfect supersized darkness via antiresolution. Laser Photonic Rev. 5, 743–749 (2014)
Pawley, J.: Handbook of Biological of Confocal Microscopy, 3rd edn. Springer, New York (2006)
Wilson, T.: Confocal Microscopy, vol. 426, pp. 1–64. Academic Press, London (1990)
Gu, M.: Principles of Three Dimensional Imaging in Confocal Microscopies. World Scientific, Singapore (1996)
Segawa, S., Kozawa, Y., Sato, S.: Resolution enhancement of confocal microscopy by subtraction method with vector beams. Opt. Lett. 39(11), 3118–3121 (2014)
So, S., et al.: Overcoming diffraction limit: from microscopy to nanoscopy. Appl. Spectros. Rev. 53(1) (2017)
Le, V., Wang, X., Kuang, C., Liu, X.: Resolution enhancement of confocal fluorescence microscopy via two illumination beams. Optics Lasers Eng. 122, 8–13 (2019)
Hell, S.W., Wichmann, J.: Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy. Opt. Lett. 19, 780–782 (1994)
Gao, P., Prunsche, B., Zhou, L., Nienhaus, K., Nienhaus, G.U.: Background suppression in fluorescence nanoscopy with stimulated emission double depletion. Nature photonic. 11, 163–169 (2017)
Wang, S., Chen, X., Chang, L., Xue, R., Duan, H., Sun, Y.: GMars-Q Enables long-term live-cell parallelized reversible saturable optical fluorescence transitions nanoscopy. ACS Nano 10(10), 9136–9144 (2016)
Sharma, Reena., Singh, Manjot, Sharma, Rajesh: Recent advances in STED and RESOLFT super-resolution imaging techniques. Spectrochim. Acta Part A Mol. Biomol. Spectrosc. 231(15), 117715 (2020)
Dixon, Rose E., Vivas, Oscar., Hannigan, Karen I., Dickson, Eamonn J.: Ground state depletion super-resolution imaging in mammalian cells. J. Vis. Exp. 129, 56239 (2017)
Chen, X., Zou, C., Gong, Z., Dong, C., Guo, G., Sun, F.: Sub-diffraction optical manipulation of the chargestate of nitrogen vacancy center in diamond. arXiv:1410.4668
Trebbia, J.-B., Baby, R., Tamarat, P., Lounis, B.: 3D optical nanoscopy with excited state saturation at liquid helium temperatures. Opt. Express 27(16), 23486–23496 (2019)
Li, Y., et al.: Image scanning fluorescence emission difference microscopy based on a detector array. J. Microsc. 266, 288–297 (2017)
Rust, M.J., et al.: Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM). Nat. Methods 3, 793–796 (2006)
Huang, B., et al.: Three-dimensional super-resolution imaging by stochastic optical reconstruction microscopy. Science 319, 810–813 (2008)
Betzig, E., et al.: Imaging intracellular fluorescent proteins at nanometer resolution. Science 313, 1642–1645 (2006)
Hess, S.T., et al.: Ultra-high resolution imaging by fluorescence photoactivation localization microscopy. Biophys. J. 91(11), 4258–4272 (2006)
Classen, A., et al.: Superresolution via structured illumination quantum correlation microscopy. Optica 4(6), 480 (2017)
Gustafsson, M.G.L.: Nonlinear structured-illumination microscopy: wide-field fluorescence imaging with theorycally unlimited resolution. PNAS 102(37), 13081–13086 (2005)
Acknowledgment
This work is supported by Vietnam National Foundation for Science and Technology Development (NAFOSTED) under Grant number (103.03-2018.08).
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2020 ICST Institute for Computer Sciences, Social Informatics and Telecommunications Engineering
About this paper
Cite this paper
Hoang, X., Le, V., Pham, M. (2020). Resolution-Improvement of Confocal Fluorescence Microscopy via Two Different Point Spread Functions. In: Vo, NS., Hoang, VP. (eds) Industrial Networks and Intelligent Systems. INISCOM 2020. Lecture Notes of the Institute for Computer Sciences, Social Informatics and Telecommunications Engineering, vol 334. Springer, Cham. https://doi.org/10.1007/978-3-030-63083-6_6
Download citation
DOI: https://doi.org/10.1007/978-3-030-63083-6_6
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-63082-9
Online ISBN: 978-3-030-63083-6
eBook Packages: Computer ScienceComputer Science (R0)