A wide-field time-domain fluorescence lifetime imaging microscope with optical sectioning
2002; American Institute of Physics; Volume: 73; Issue: 4 Linguagem: Inglês
10.1063/1.1458061
ISSN1527-2400
AutoresS Webb, Yuchen Gu, Sandrine Lévêque‐Fort, Jan Siegel, Mary J. Cole, K. Dowling, Richard W. Jones, P. M. W. French, Mark A. A. Neil, R. Juškaitis, L. O. D. Sucharov, T. Wilson, M. J. Lever,
Tópico(s)Photodynamic Therapy Research Studies
ResumoThis article describes a wide-field time-domain fluorescence lifetime imaging (FLIM) microscope with optical sectioning. The FLIM system utilizes a wide-field time-gated optical image intensifier, with a minimum gate width of 85 ps, to achieve high temporal resolution of fluorescence decays induced by ultrashort laser pulses. Different configurations, using excitation pulses of picojoule energy at 80 MHz repetition rate and of nanojoule energy at 10 kHz, are compared. The instrument has a temporal dynamic range spanning from 100 ps to tens of μs and is shown to have a temporal discrimination better than 10 ps. When applied to laser dye samples, it has produced FLIM maps demonstrating sensitivity to variations in both chemical species and local environment, e.g., viscosity. Wide-field optical sectioning is achieved using the technique of structured illumination, which is applied to remove out-of-focus light that can result in lifetime artifacts. The sectioning strength, which may be adjusted by choosing an appropriate spatial modulation frequency, is characterized and shown to be comparable to that of a confocal microscope. Practical considerations concerned with improving the quality of sectioned fluorescence lifetime maps, including using a large bit depth camera, are discussed.
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