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High resolution whole-field three-dimensional fluorescence lifetime imaging

ReferenceE11178
Principal Investigator / Supervisor Professor Tony Wilson
Co-Investigators /
Co-Supervisors
Professor Paul Michael William French, Professor M. John Lever
Institution University of Oxford
DepartmentEngineering Science
Funding typeResearch
Value (£) 137,653
StatusCompleted
TypeResearch Grant
Start date 01/12/1999
End date 30/06/2002
Duration30 months

Abstract

The aim of this project is to investigate the use of structured excitation in fluorescence microscopy, pioneered at Oxford University, to provide whole-field 3-D sectioning with comparable resolution to confocal microscopy, combined with fluorescence lifetime imaging to map the local chemical and physical fluorophore environment. This novel imaging modality will be implemented using state-of-the-art diode-pumped ultrafast laser technology pioneered at Imperial College. Single and multi-photon excitation of fluorophores with ultrashort pulses in the visible and near infrared spectral region will be applied to standard phantoms and biological tissue in vitro. (Joint with grant E11253).

Summary

unavailable
Committee Closed Committee - Engineering & Biological Systems (EBS)
Research TopicsX – not assigned to a current Research Topic
Research PriorityX – Research Priority information not available
Research Initiative BioImaging (BI) [1998]
Funding SchemeX – not Funded via a specific Funding Scheme
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