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UNMIX-ME: spectral and lifetime fluorescence unmixing via deep learning.
Smith, Jason T; Ochoa, Marien; Intes, Xavier.
Afiliação
  • Smith JT; Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY 12180, USA.
  • Ochoa M; These authors contributed equally.
  • Intes X; Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY 12180, USA.
Biomed Opt Express ; 11(7): 3857-3874, 2020 Jul 01.
Article em En | MEDLINE | ID: mdl-33014571
ABSTRACT
Hyperspectral fluorescence lifetime imaging allows for the simultaneous acquisition of spectrally resolved temporal fluorescence emission decays. In turn, the acquired rich multidimensional data set enables simultaneous imaging of multiple fluorescent species for a comprehensive molecular assessment of biotissues. However, to enable quantitative imaging, inherent spectral overlap between the considered fluorescent probes and potential bleed-through must be considered. Such a task is performed via either spectral or lifetime unmixing, typically independently. Herein, we present "UNMIX-ME" (unmix multiple emissions), a deep learning-based fluorescence unmixing routine, capable of quantitative fluorophore unmixing by simultaneously using both spectral and temporal signatures. UNMIX-ME was trained and validated using an in silico framework replicating the data acquisition process of a compressive hyperspectral fluorescent lifetime imaging platform (HMFLI). It was benchmarked against a conventional LSQ method for tri and quadri-exponential simulated samples. Last, UNMIX-ME's potential was assessed for NIR FRET in vitro and in vivo preclinical applications.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biomed Opt Express Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biomed Opt Express Ano de publicação: 2020 Tipo de documento: Article