Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5223159 | Tetrahedron | 2009 | 6 Pages |
Abstract
A redox- and light-sensitive, T1-weighted magnetic resonance imaging (MRI) contrast agent, which tethers a spiropyran (SP)/merocyanine (MC) motif to a Gd-DO3A moiety was synthesized and characterized. When in the dark, the probe is in its MC form, which has an r1 relaxivity of 2.51 m Mâ1 sâ1 (60 MHz, 37 °C). After irradiation with visible light or mixing with NADH, the probe experiences an isomerization and the r1 relaxivity decreased 18% and 26%, respectively. Additionally, the signal intensity in MRI showed an observable decrease after the compound was mixed with NADH.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Chuqiao Tu, Elizabeth A. Osborne, Angelique Y. Louie,