Conjugation to Biocompatible Dendrimers Increases Lanthanide T(2) Relaxivity of Hydroxypyridinone (HOPO) Complexes for Magnetic Resonance Imaging (MRI).
Conjugation to Biocompatible Dendrimers Increases Lanthanide T(2) Relaxivity of Hydroxypyridinone (HOPO) Complexes for Magnetic Resonance Imaging (MRI).
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DOI:
10.1002/ejic.201101167
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发表时间:
2012-04
影响因子:
2.3
通讯作者:
Raymond, Kenneth N.
中科院分区:
文献类型:
--
作者:
Klemm, Piper J.;Floyd, William C., III;Andolina, Christopher M.;Frechet, Jean M. J.;Raymond, Kenneth N.
Magnetic resonance imaging (MRI) contrast agents represent a worldwide billion-dollar market annually. While T1 relaxivity enhancement contrast agents receive greater attention and a significantly larger market share, the commercial potential for T2 relaxivity enhancing contrast agents remains a viable diagnostic option due to their increased relaxivity at high field strengths. Improving the contrast and biocompatibility of T2 MRI probes may enable new diagnostic prospects for MRI. Paramagnetic lanthanides have the potential to decrease T1 and T2 proton relaxation times, but are not commercially used in MRI diagnostics as T2 agents. In this article, oxygen donor chelates (hydroxypyridinone, HOPO, and terephthalamide, TAM) of various lanthanides are demonstrated as biocompatible macromolecular dendrimer conjugates for the development of T2 MRI probes. These conjugates have relaxivities up to 374 mm−1s−1 per dendrimer, high bioavailability, and low in vitro toxicity.
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