Three dimensional mapping of strontium in bone by dual energy K-edge subtraction imaging

被引:28
作者
Cooper, D. M. L. [1 ]
Chapman, L. D. [1 ]
Carter, Y. [1 ]
Wu, Y. [2 ]
Panahifar, A. [2 ]
Britz, H. M. [3 ]
Bewer, B. [4 ]
Zhouping, W. [1 ]
Duke, M. J. M. [2 ,5 ]
Doschak, M. [2 ]
机构
[1] Univ Saskatchewan, Dept Anat & Cell Biol, Saskatoon, SK, Canada
[2] Univ Alberta, Fac Pharm & Pharmaceut Sci, Edmonton, AB T6G 2N8, Canada
[3] Univ Calgary, Calgary, AB, Canada
[4] Canadian Light Source, Saskatoon, SK, Canada
[5] Univ Alberta, SLOWPOKE Nucl Reactor Facil, Edmonton, AB, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
RANELATE; RESORPTION; ANGIOGRAPHY; AGENT; WOMEN; RISK; RAT;
D O I
10.1088/0031-9155/57/18/5777
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The bones of many terrestrial vertebrates, including humans, are continually altered through an internal process of turnover known as remodeling. This process plays a central role in bone adaptation and disease. The uptake of fluorescent tetracyclines within bone mineral is widely exploited as a means of tracking new tissue formation. While investigation of bone microarchitecture has undergone a dimensional shift from 2D to 3D in recent years, we lack a 3D equivalent to fluorescent labeling. In the current study we demonstrate the ability of synchrotron radiation dual energy K-edge subtraction (KES) imaging to map the 3D distribution of elemental strontium within rat vertebral samples. This approach has great potential for ex vivo analysis of preclinical models and human tissue samples. KES also represents a powerful tool for investigating the pharmokinetics of strontium-based drugs recently approved in many countries around the globe for the treatment of osteoporosis.
引用
收藏
页码:5777 / 5786
页数:10
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