Cellular delivery of MRI contrast agents

被引:71
|
作者
Allen, MJ
MacRenaris, KW
Venkatasubramanian, PN
Meade, TJ
机构
[1] Northwestern Univ, Dept Chem Biochem & Mol & Cell Biol, Evanston, IL 60208 USA
[2] Northwestern Univ, Dept Neurobiol & Physiol, Evanston, IL 60208 USA
[3] Northwestern Univ, Dept Radiol, Evanston, IL 60208 USA
[4] ENH Res Inst, Ctr Basic MR Res, Evanston, IL 60201 USA
来源
CHEMISTRY & BIOLOGY | 2004年 / 11卷 / 03期
关键词
D O I
10.1016/j.chembiol.2004.03.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Magnetic resonance imaging (MRI) is a powerful tool for acquiring images of opaque living animals with the benefit of tracking events over extended periods of time on the same specimen. Contrast agents are used to enhance regions, tissues, and cells that are magnetically similar but histologically distinct. A principal barrier to the development of MRI contrast agents for investigating biological questions is the delivery of agents across cellular membranes. Here, we describe the synthesis and in vitro testing of Gd(III)-based MRI contrast agents containing varying length polyarginine oligomers capable of permeating cell membranes. We examine the effect of the length of oligomer on T-1 enhancement and cellular uptake. Furthermore, the effect of incubation time, concentration, and cell type on uptake is explored. Toxicity and washout studies are performed in addition to MRI phantom studies.
引用
收藏
页码:301 / 307
页数:7
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