Applied Physics B

, Volume 84, Issue 3, pp 379–383

Simultaneous time- and spectrum-resolved multifocal multiphoton microscopy

Authors

    • Key Laboratory of Optoelectronic Devices and Systems, Ministry of EducationInstitute of Optoelectronics, Shenzhen University
  • J. Qu
    • Key Laboratory of Optoelectronic Devices and Systems, Ministry of EducationInstitute of Optoelectronics, Shenzhen University
  • Z. Lin
    • Key Laboratory of Optoelectronic Devices and Systems, Ministry of EducationInstitute of Optoelectronics, Shenzhen University
  • L. Wang
    • Key Laboratory of Optoelectronic Devices and Systems, Ministry of EducationInstitute of Optoelectronics, Shenzhen University
  • Z. Fu
    • Key Laboratory of Optoelectronic Devices and Systems, Ministry of EducationInstitute of Optoelectronics, Shenzhen University
  • B. Guo
    • Key Laboratory of Optoelectronic Devices and Systems, Ministry of EducationInstitute of Optoelectronics, Shenzhen University
    • Key Laboratory of Optoelectronic Devices and Systems, Ministry of EducationInstitute of Optoelectronics, Shenzhen University
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DOI: 10.1007/s00340-006-2314-y

Cite this article as:
Liu, L., Qu, J., Lin, Z. et al. Appl. Phys. B (2006) 84: 379. doi:10.1007/s00340-006-2314-y

Abstract

We present a novel multifocal multiphoton microscope that is based on a sampling imaging technique using a microlens array, a prism for two-dimensionalspectral dispersion, and a specially designed streak camera to provide simultaneous time- and spectrum-resolved fluorescence microscopy. We split the near-infrared light of a mode-locked titanium:sapphire femtosecond laser into an array of beams that are transformed into an array of high-aperture foci at the sample. A time- and spectrum-resolved image of 3×3 foci on the sample can be obtained with a snapshot. By translating the sample stage laterally and axially and implementing a dedicated image reconstruction algorithm in the control system of the instrument, we demonstrate the acquisition of a five-dimensional data set combining lifetime and spectral resolutions in biological fluorescence imaging.

Copyright information

© Springer-Verlag 2006