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High resolution whole-field three dimensional fluorescence lifetime imaging

ReferenceE11253
Principal Investigator / Supervisor Professor Paul Michael William French
Co-Investigators /
Co-Supervisors
Professor M. John Lever, Professor Tony Wilson
Institution Imperial College London
DepartmentBiological Sciences
Funding typeResearch
Value (£) 271,572
StatusCompleted
TypeResearch Grant
Start date 01/02/1999
End date 01/11/2001
Duration33 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 E11178).

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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