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In vitro and in vivo NIR fluorescence lifetime imaging with a time-gated SPAD camera.
Smith, Jason T; Rudkouskaya, Alena; Gao, Shan; Gupta, Juhi M; Ulku, Arin; Bruschini, Claudio; Charbon, Edoardo; Weiss, Shimon; Barroso, Margarida; Intes, Xavier; Michalet, Xavier.
Afiliação
  • Smith JT; Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York 12180, USA.
  • Rudkouskaya A; Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York 12208, USA.
  • Gao S; Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York 12180, USA.
  • Gupta JM; Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York 12180, USA.
  • Ulku A; AQUA Lab, Ecole Polytechnique Fédérale de Lausanne (EPFL), Neuchâtel, Switzerland.
  • Bruschini C; AQUA Lab, Ecole Polytechnique Fédérale de Lausanne (EPFL), Neuchâtel, Switzerland.
  • Charbon E; AQUA Lab, Ecole Polytechnique Fédérale de Lausanne (EPFL), Neuchâtel, Switzerland.
  • Weiss S; Department of Chemistry & Biochemistry, University of California at Los Angeles, Los Angeles, California 90095, USA.
  • Barroso M; Department of Molecular and Cellular Physiology, Albany Medical College, Albany, New York 12208, USA.
  • Intes X; Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, New York 12180, USA.
  • Michalet X; Department of Chemistry & Biochemistry, University of California at Los Angeles, Los Angeles, California 90095, USA.
Optica ; 9(5): 532-544, 2022 May.
Article em En | MEDLINE | ID: mdl-35968259
ABSTRACT
Near-infrared (NIR) fluorescence lifetime imaging (FLI) provides a unique contrast mechanism to monitor biological parameters and molecular events in vivo. Single-photon avalanche diode (SPAD) cameras have been recently demonstrated in FLI microscopy (FLIM) applications, but their suitability for in vivo macroscopic FLI (MFLI) in deep tissues remains to be demonstrated. Herein, we report in vivo NIR MFLI measurement with SwissSPAD2, a large time-gated SPAD camera. We first benchmark its performance in well-controlled in vitro experiments, ranging from monitoring environmental effects on fluorescence lifetime, to quantifying Förster resonant energy transfer (FRET) between dyes. Next, we use it for in vivo studies of target-drug engagement in live and intact tumor xenografts using FRET. Information obtained with SwissSPAD2 was successfully compared to that obtained with a gated intensified charge-coupled device (ICCD) camera, using two different approaches. Our results demonstrate that SPAD cameras offer a powerful technology for in vivo preclinical applications in the NIR window.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Optica Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Optica Ano de publicação: 2022 Tipo de documento: Article