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Fluorescence Lifetime Macro Imager for Biomedical Applications.
Sen, Rajannya; Zhdanov, Alexander V; Devoy, Ciaran; Tangney, Mark; Hirvonen, Liisa M; Nomerotski, Andrei; Papkovsky, Dmitri B.
Affiliation
  • Sen R; School of Biochemistry and Cell Biology, University College Cork; rajannya.sen@ucc.ie.
  • Zhdanov AV; School of Biochemistry and Cell Biology, University College Cork.
  • Devoy C; Cancer Research@UCC, University College Cork.
  • Tangney M; Cancer Research@UCC, University College Cork.
  • Hirvonen LM; Centre for Microscopy, Characterisation and Analysis (CMCA), The University of Western Australia.
  • Nomerotski A; Physics Department, Brookhaven National Laboratory.
  • Papkovsky DB; School of Biochemistry and Cell Biology, University College Cork.
J Vis Exp ; (194)2023 04 07.
Article in En | MEDLINE | ID: mdl-37092825
This paper presents a new photoluminescence lifetime imager designed to map the molecular oxygen (O2) concentration in different phosphorescent samples ranging from solid-state, O2-sensitive coatings to live animal tissue samples stained with soluble O2-sensitive probes. In particular, the nanoparticle-based near-infrared probe NanO2-IR, which is excitable with a 625 nm light-emitting diode (LED) and emits at 760 nm, was used. The imaging system is based on the Timepix3 camera (Tpx3Cam) and the opto-mechanical adaptor, which also houses an image intensifier. O2 phosphorescence lifetime imaging microscopy (PLIM) is commonly required for various studies, but current platforms have limitations in their accuracy, general flexibility, and usability. The system presented here is a fast and highly sensitive imager, which is built on an integrated optical sensor and readout chip module, Tpx3Cam. It is shown to produce high-intensity phosphorescence signals and stable lifetime values from surface-stained intestinal tissue samples or intraluminally stained fragments of the large intestine and allows the detailed mapping of tissue O2 levels in about 20 s or less. Initial experiments on the imaging of hypoxia in grafted tumors in unconscious animals are also presented. We also describe how the imager can be re-configured for use with O2-sensitive materials based on Pt-porphyrin dyes using a 390 nm LED for the excitation and a bandpass 650 nm filter for emission. Overall, the PLIM imager was found to produce accurate quantitative measurements of lifetime values for the probes used and respective two-dimensional maps of the O2 concentration. It is also useful for the metabolic imaging of ex vivo tissue models and live animals.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxygen / Hypoxia Type of study: Diagnostic_studies Limits: Animals Language: En Journal: J Vis Exp Year: 2023 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxygen / Hypoxia Type of study: Diagnostic_studies Limits: Animals Language: En Journal: J Vis Exp Year: 2023 Document type: Article Country of publication: United States