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Imaging of 3D Engineered Tissues
Reference
BB/D524983/1
Principal Investigator / Supervisor
Professor John Haycock
Co-Investigators /
Co-Supervisors
Professor Ian Brook
,
Professor Nicola Brown
,
Professor Freddie Hamdy
,
Professor Paul Hatton
,
Professor Sheila MacNeil
,
Professor Stephen Rimmer
,
Professor Anthony Ryan
,
Dr Andrew Scutt
,
Professor Nicholas Williams
Institution
University of Sheffield
Department
Materials Science and Engineering
Funding type
Research
Value (£)
184,000
Status
Completed
Type
Research Grant
Start date
01/02/2006
End date
31/10/2006
Duration
9 months
Abstract
The current proposal outlines research themes on tissue engineering at Sheffield University where a laser scanning confocal microscope with META multichannel confocal detection is requested (with the potential for multiphoton upgrade in the future). The model is for a confocal system to be located in the new interdisciplinary Kroto Research Institute at Sheffield University. This facility will have a suite of GMP accredited clean rooms to enable tissue engineered construct formation under sterile conditions for clinical use. Multidisciplinary research laboratories located immediately next to the clean rooms will support core research and further development of reconstructed tissues. Location of an on-site confocal microscope in the research laboratories will therefore enable the in-depth study of cells in synthetic scaffolds across a number of research programmes. Confocal microscopy is a leading-edge technology and a powerful research tool, enabling the capture of unrivalled high resolution of cells within 3 dimensional constructs as well as in-depth penetration of specimens tagged with very specific fluorophores. This leading edge technology is now becoming a method of choice for the dynamic imaging of cells, tissues and biological systems not otherwise possible by other optical systems. Such a technology is essential for driving the research of our team, understanding a range of interconnected problems spanning the life sciences-engineering interface. Each member of our team has programmes that rely heavily on the need for high resolution microscopy which presently is only partially met by existing fluorescence systems. META confocal technology advances the quality of imaging and flexibility of analysis by such a high degree over standard fluorescence that it is now the new benchmark from visualising cells in vitro or in 3 dimension structures in vivo. It therefore has wide applicability in biology, chemistry and engineering and this is represented by our team ofapplicants. A central imaging facility will also be essential for maintaining research of an internationally competitive standard and will act as a potent catalyst for attracting high quality collaborations with investigators in the UK and abroad.
Summary
unavailable
Committee
Closed Committee - Engineering & Biological Systems (EBS)
Research Topics
X – not assigned to a current Research Topic
Research Priority
X – Research Priority information not available
Research Initiative
Research Equipment Initiative 2005 (RE5) [2005]
Funding Scheme
X – not Funded via a specific Funding Scheme
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