Photochromically-controlled, reversibly-activated MRI and optical contrast agent - PubMed (original) (raw)
. 2007 Apr 7:(13):1331-3.
doi: 10.1039/b616991k. Epub 2007 Jan 18.
Affiliations
- PMID: 17377672
- PMCID: PMC2556594
- DOI: 10.1039/b616991k
Photochromically-controlled, reversibly-activated MRI and optical contrast agent
Chuqiao Tu et al. Chem Commun (Camb). 2007.
Abstract
The contrast agent which tethers a spiropyran group to a Gd-DO3A moiety has higher relaxivity and fluorescence intensity in the dark; the relaxivity and fluorescence intensity decrease after irradiation with visible light.
Figures
Fig. 1
Absorption spectrum of compound 5 (7.665 × 10-5 M) in water. 1: in the dark; 2: irradiated with visible light for 1 minute; 3: irradiated with UV at 365 nm for 10 minutes after being irradiated with visible light for 1 minute; 4: in the dark for 20 minutes after being irradiated with visible light for 1 minute.
Fig. 2
Emission spectrum of compound 5 (7.665 × 10-5 M) in water with excitation at 500 nm.
Scheme 1
Synthesis of compound 5.
Scheme 2
Proposed isomerization of Gd-SPDO3A (left) and Gd- MCDO3A (right).
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