Two-color in vivo dynamic contrast-enhanced pharmacokinetic imaging

被引:12
作者
Hama, Yukihiro [1 ]
Koyama, Yoshinori [1 ]
Choyke, Peter L. [1 ]
Kobayashi, Hisataka [1 ]
机构
[1] NCI, NIH, Mol Imaging Program, Canc Res Ctr, Bethesda, MD 20892 USA
关键词
pharmacokinetics; near infrared (NIR); fluorescence imaging; in vivo dynamic imaging; two-color imaging;
D O I
10.1117/1.2745306
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Optical imaging is unique among in vivo imaging methods because it is possible to simultaneously resolve two or more probes emitting at different wavelengths of light. We employed two near-infrared (NIR) fluorescent optical probes each labeled with a different, protein, to simultaneously evaluate the pharmacokinetics of each probe. Dynamic optical imaging was performed in live mice after the coinjection of bovine serum albumin (BSA) and galactosamine-conjugated bovine serum albumin (GmSA) labeled with either Cy5.5 or Cy7 NIR dyes. The pharmacokinetics of BSA and GmSA were independently and simultaneously visualized. Next, two-color dynamic imaging of biotinylated BSA (b-BSA) and BSA labeled with Cy5.5 or Cy7 was performed before and after an avidin "chase." Following avidin injection, fluorescently labeled b-BSA rapidly accumulated in the liver, while minimal liver uptake of BSA was noted. Thus, multicolor dynamic contrast-enhanced optical imaging can be performed to noninvasively track the pharmacokinetics of different proteins. This imaging technique can be applied to a wide variety of optically labeled proteins in order to simultaneously track their biodistribution. (C) 2007 Society of Photo-Optical Instrumentation Engineers.
引用
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页数:7
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