Photoacoustic tomography of joints aided by an Etanercept-conjugated gold nanoparticle contrast agent -: an ex vivo preliminary rat study

被引:100
作者
Chamberland, David L. [3 ]
Agarwal, Ashish [2 ]
Kotov, Nicholas [2 ]
Fowlkes, J. Brian [1 ]
Carson, Paul L. [1 ]
Wang, Xueding [1 ]
机构
[1] Univ Michigan, Sch Med, Dept Radiol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[3] Rheumatol Associates, Medford, OR 97504 USA
关键词
D O I
10.1088/0957-4484/19/9/095101
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Monitoring of anti-rheumatic drug delivery in experimental models and in human diseases would undoubtedly be very helpful for both basic research and clinical management of inflammatory diseases. In this study, we have investigated the potential of an emerging hybrid imaging technology-photoacoustic tomography-in noninvasive monitoring of anti-TNF drug delivery. After the contrast agent composed of gold nanorods conjugated with Etanercept molecules was produced, ELISA experiments were performed to prove the conjugation and to show that the conjugated anti-TNF-alpha drug was biologically active. PAT of ex vivo rat tail joints with the joint connective tissue enhanced by intra-articularly injected contrast agent was conducted to examine the performance of PAT in visualizing the distribution of the gold-nanorod-conjugated drug in articular tissues. By using the described system, gold nanorods with a concentration down to 1 pM in phantoms or 10 pM in biological tissues can be imaged with good signal-to-noise ratio and high spatial resolution. This study demonstrates the feasibility of conjugating TNF antagonist pharmaceutical preparations with gold nanorods, preservation of the mechanism of action of TNF antagonist along with preliminary evaluation of novel PAT technology in imaging optical contrast agents conjugated with anti-rheumatic drugs. Further in vivo studies on animals are warranted to test the specific binding between such conjugates and targeted antigen in joint tissues affected by inflammation.
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页数:7
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