Functional micro-imaging of soft and hard tissue using synchrotron light

被引:7
作者
Thurner, PJ [1 ]
Wyss, P [1 ]
Voide, R [1 ]
Stauber, M [1 ]
Müller, B [1 ]
Stampanoni, M [1 ]
Hubbell, JA [1 ]
Müller, R [1 ]
Sennhauser, U [1 ]
机构
[1] Swiss Fed Labs Mat Testing & Res EMPA, Dubendorf, Switzerland
来源
DEVELOPMENTS IN X-RAY TOMOGRAPHY IV | 2004年 / 5535卷
关键词
imaging; image processing. micro-computed tomography; synchrotron radiation; soft tissue; cell cultures; contrast agents; bone; image guided failure assessment; microdamage;
D O I
10.1117/12.559515
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
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.
引用
收藏
页码:112 / 128
页数:17
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