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A time-correlated single photon counting SPAD array camera with a bespoke data-processing algorithm for lightsheet fluorescence lifetime imaging (FLIM) and FLIM videos.
Nedbal, Jakub; Mattioli Della Rocca, Francesco; Ivanova, Iveta T; Allan, Andrew; Graham, Jeremy; Walker, Richard; Henderson, Robert K; Suhling, Klaus.
Afiliación
  • Nedbal J; Department of Physics, King's College London, Strand, London, WC2R 2LS, United Kingdom. jakub.nedbal@kcl.ac.uk.
  • Mattioli Della Rocca F; Occuity, The Blade, Abbey Square, Reading, RG1 3BE, United Kingdom. jakub.nedbal@kcl.ac.uk.
  • Ivanova IT; Institute for Integrated Micro and Nano Systems, The University of Edinburgh, Edinburgh, EH9 3FF, United Kingdom.
  • Allan A; Europe Technology Development Centre, Sony Semiconductor Solutions - Sony Europe B.V., Trento, Italy.
  • Graham J; Department of Physics, King's College London, Strand, London, WC2R 2LS, United Kingdom.
  • Walker R; Cairn Research, Graveney Road, Faversham, ME13 8UP, United Kingdom.
  • Henderson RK; Cairn Research, Graveney Road, Faversham, ME13 8UP, United Kingdom.
  • Suhling K; Photon Force, Max Born Crescent, Edinburgh, EH9 3BF, United Kingdom.
Sci Rep ; 14(1): 7247, 2024 03 27.
Article en En | MEDLINE | ID: mdl-38538638
ABSTRACT
A wide-field microscope with epi-fluorescence and selective plane illumination was combined with a single-photon avalanche diode (SPAD) array camera to enable live-cell fluorescence lifetime imaging (FLIM) using time-correlated single-photon counting (TCSPC). The camera sensor comprised of 192 × 128 pixels, each integrating a single SPAD and a time-to-digital converter. Jointly, they produced a stream of single-photon images of photon arrival times with ≈ 38 ps accuracy. The photon arrival times were subject to systematic delays and nonlinearities, which were corrected by a Monte-Carlo algorithm. The SPAD camera was then applied to FLIM where histogramming the resulting photon arrival times in each pixel resulted in decays compatible with common data processing pipelines for fluorescence lifetime analysis. The capabilities of the TCSPC camera-based FLIM microscope were demonstrated by imaging living unicellular photosynthetic algae and artificial lipid vesicles. Epi-fluorescence illumination enabled rapid fluorescence lifetime imaging of living cells and selective-plane illumination enabled 3-dimensional FLIM of stationary samples.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Algoritmos Idioma: En Revista: Sci Rep / Sci. rep. (Nat. Publ. Group) / Scientific reports (Nature Publishing Group) Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Algoritmos Idioma: En Revista: Sci Rep / Sci. rep. (Nat. Publ. Group) / Scientific reports (Nature Publishing Group) Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido