Functional micro-imaging of soft and hard tissue using synchrotron light
Functional micro-imaging of soft and hard tissue using synchrotron light
In current biological and biomedical research, quantitative endpoints have become an important factor of success. Classically, such endpoints were investigated with 2D imaging, which is usually destructive and the 3D character of tissue gets lost. 3D imaging has gained in importance as a tool for both, qualitative and quantitative assessment of biological systems. In this context synchrotron radiation based tomography has become a very effective tool for opaque 3D tissue systems. Cell cultures and adherent scaffolds are visualized in 3D in a hydrated environment, even uncovering the shape of individual cells. Advanced morphometry allows to characterize the differences between the cell cultures of two distinct phenotypes. Moreover, a new device is presented enabling the 3D investigation of trabecular bone under mechanical load in a time-lapsed fashion. Using the highly brilliant X-rays from a synchrotron radiation source, bone microcracks and an indication for un-cracked ligament bridging are uncovered. 3D microcrack analysis proves that the classification of microcracks from 2D images is ambiguous. Fatigued bone was found to fail in burst-like fashion, whereas non-fatigued bone exhibited a distinct failure band. Additionally, a higher increase in microcrack volume was detected in fatigued in comparison to non-fatigued bone. The developed technologies prove to be very effective tools for advanced 3D imaging of both hard and soft tissue.
112-128
SPIE - The International Society for Optical Engineering
Thurner, Philipp J.
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Wyss, Peter
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Voide, Romain
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Stauber, Martin
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Müller, Bert
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Stampanoni, Marco
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Hubbell, Jeffrey A.
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Müller, Ralph
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Sennhauser, Urs
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October 2004
Thurner, Philipp J.
ab711ddd-784e-48de-aaad-f56aec40f84f
Wyss, Peter
37835676-2f92-4df7-bc35-97b2c80c1104
Voide, Romain
8859d4cc-c065-4034-b350-0538997ce8fe
Stauber, Martin
f69dbdc0-ebca-41eb-aab7-0679e6b78874
Müller, Bert
acba4294-b684-4a09-81ac-32de31d39923
Stampanoni, Marco
bfedb3b0-01e8-4e1b-9163-41295b4ceeb1
Hubbell, Jeffrey A.
c9b5c639-f582-43a8-b82f-0d5da8a0d9f8
Müller, Ralph
f881853a-540f-48f1-bb6d-e0cf1894e036
Sennhauser, Urs
3c0e14aa-da0a-48da-bb7b-c65401b1d01b
Thurner, Philipp J., Wyss, Peter, Voide, Romain, Stauber, Martin, Müller, Bert, Stampanoni, Marco, Hubbell, Jeffrey A., Müller, Ralph and Sennhauser, Urs
(2004)
Functional micro-imaging of soft and hard tissue using synchrotron light.
Bonse, Ulrich
(ed.)
In Developments in X-ray Tomography IV.
vol. 5535,
SPIE - The International Society for Optical Engineering.
.
(doi:10.1117/12.559515).
Record type:
Conference or Workshop Item
(Paper)
Abstract
In current biological and biomedical research, quantitative endpoints have become an important factor of success. Classically, such endpoints were investigated with 2D imaging, which is usually destructive and the 3D character of tissue gets lost. 3D imaging has gained in importance as a tool for both, qualitative and quantitative assessment of biological systems. In this context synchrotron radiation based tomography has become a very effective tool for opaque 3D tissue systems. Cell cultures and adherent scaffolds are visualized in 3D in a hydrated environment, even uncovering the shape of individual cells. Advanced morphometry allows to characterize the differences between the cell cultures of two distinct phenotypes. Moreover, a new device is presented enabling the 3D investigation of trabecular bone under mechanical load in a time-lapsed fashion. Using the highly brilliant X-rays from a synchrotron radiation source, bone microcracks and an indication for un-cracked ligament bridging are uncovered. 3D microcrack analysis proves that the classification of microcracks from 2D images is ambiguous. Fatigued bone was found to fail in burst-like fashion, whereas non-fatigued bone exhibited a distinct failure band. Additionally, a higher increase in microcrack volume was detected in fatigued in comparison to non-fatigued bone. The developed technologies prove to be very effective tools for advanced 3D imaging of both hard and soft tissue.
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More information
Published date: October 2004
Venue - Dates:
SPIE Medical Imaging, Denver, USA, 2004-08-04 - 2004-08-04
Identifiers
Local EPrints ID: 49340
URI: http://eprints.soton.ac.uk/id/eprint/49340
PURE UUID: c3443e23-f58a-4cc0-9108-09e69769644a
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Date deposited: 01 Nov 2007
Last modified: 15 Mar 2024 09:55
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Contributors
Author:
Peter Wyss
Author:
Romain Voide
Author:
Martin Stauber
Author:
Bert Müller
Author:
Marco Stampanoni
Author:
Jeffrey A. Hubbell
Author:
Ralph Müller
Author:
Urs Sennhauser
Editor:
Ulrich Bonse
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