Elson Dan, Requejo-Isidro Jose, Munro Ian, Reavell Fred, Siegel Jan, Suhling Klaus, Tadrous Paul, Benninger Richard, Lanigan Peter, McGinty James, Talbot Clifford, Treanor Bebhinn, Webb Stephen, Sandison Ann, Wallace Andrew, Davis Dan, Lever John, Neil Mark, Phillips David, Stamp Gordon, French Paul
Photonics Group, Physics Department, Imperial College London, London, UK.
Photochem Photobiol Sci. 2004 Aug;3(8):795-801. doi: 10.1039/b316456j. Epub 2004 Jun 4.
Fluorescence lifetime imaging (FLIM) is a functional imaging methodology that can provide information, not only concerning the localisation of specific fluorophores, but also about the local fluorophore environment. It may be implemented in scanning confocal or multi-photon microscopes, or in wide-field microscopes and endoscopes. When applied to tissue autofluorescence, it reveals intrinsic excellent contrast between different types and states of tissue. This article aims to review our recent progress in developing time-domain FLIM technology for microscopy and endoscopy and applying it to biological tissue.
荧光寿命成像(FLIM)是一种功能成像方法,它不仅可以提供有关特定荧光团定位的信息,还能提供关于局部荧光团环境的信息。它可以在扫描共聚焦显微镜或多光子显微镜中实现,也可以在宽视场显微镜和内窥镜中实现。当应用于组织自发荧光时,它能揭示不同类型和状态的组织之间固有的出色对比度。本文旨在综述我们在开发用于显微镜和内窥镜的时域FLIM技术并将其应用于生物组织方面的最新进展。