PET imaging and optical imaging with D-luciferin [11C]methyl ester and D-luciferin [11C]methyl ether of luciferase gene expression in tumor xenografts of living mice

被引:15
作者
Wang, JQ
Pollok, KE
Cai, SB
Stantz, KM
Hutchins, GD
Zheng, QH [1 ]
机构
[1] Indiana Univ, Sch Med, Dept Radiol, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Herman B Wells Ctr Pediat Res, Indianapolis, IN 46202 USA
关键词
D-luciferin [C-11]methyl ester ([C-11]LMEster; C-11]1); D-luciferin [C-11]methyl ether ([C-11]LMEther; C-11]2); luciferase; gene expression; positron emission tomography (PET) imaging; optical imaging; tumor xenografts;
D O I
10.1016/j.bmcl.2005.09.082
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
New carbon-11 labeled D-luciferin analogs D-luciferin [C-11]methyl ester ([C-11]LMEster, [C-11]1) and D-luciferin [C-11]methyl ether ([C-11]LMEther, [C-11]2) were synthesized in 25-55% radiochemical yield. PET studies with [C-11]LMEster and [C-11]LMEther demonstrate a lower retention of the C-11 label at 45 min post-injection in luciferase expression tumor. Optical imaging with unlabeled substrate D-luciferin and radiotracers [C-11]LMEster and [C-11]LMEther gave tumor luciferase images within a few minutes of photon counting. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:331 / 337
页数:7
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