Responsive MR-imaging probes for N-methyl-D-aspartate receptors and direct 
visualisation of the cell-surface receptors by optical microscopy

Sim, N; Gottschalk, S; Pal, R; Engelmann, J; Parker, D; Mishra, A

doi:10.1039/C3SC50903F

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Responsive MR-imaging probes for N-methyl-D-aspartate receptors and direct visualisation of the cell-surface receptors by optical microscopy

Sim, N., Gottschalk, S., Pal, R., Engelmann, J., Parker, D., & Mishra, A. (2013). Responsive MR-imaging probes for N-methyl-D-aspartate receptors and direct visualisation of the cell-surface receptors by optical microscopy. Chemical Science, 4(8), 3148-3153. doi:10.1039/C3SC50903F.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-001A-136B-5 Version Permalink: https://hdl.handle.net/21.11116/0000-0001-3EC0-1

Genre: Journal Article

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http://pubs.rsc.org/en/content/articlepdf/2013/sc/c3sc50903f (Publisher version) Open Access status unknown

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Creators:
Sim, N, Author
Gottschalk, S^{1, 2}, Author
Pal, R, Author
Engelmann, J^{1, 2}, Author
Parker, D, Author
Mishra, A, Author

Affiliations:
1Department High-Field Magnetic Resonance, Max Planck Institute for Biological Cybernetics, Max Planck Society, ou_1497796
2Max Planck Institute for Biological Cybernetics, Max Planck Society, Spemannstrasse 38, 72076 Tübingen, DE, ou_1497794

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Abstract: A series of N-methyl-D-aspartate (NMDA) receptor-targeted MRI contrast agents has been developed, based on the known competitive NMDA antagonist, 3,4-diamino-3-cyclobutene-1,2-dione. Their use as responsive MR imaging probes has been evaluated in vitro and two contrast agents showed 170–176 enhancements in relaxation rate, following incubation with a neuronal cell line model. A derivative of the lead compound was prepared containing a biotin moiety, and both the specificity and reversibility of binding to the NMDA cell surface receptors demonstrated using confocal microscopy.

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Dates: Date issued: 2013-08

Publication Status: Issued

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Identifiers: DOI: 10.1039/C3SC50903F
BibTex Citekey: SimGPEPM2014

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Title: Chemical Science

Source Genre: Journal

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Pages: - Volume / Issue: 4 (8) Sequence Number: - Start / End Page: 3148 - 3153 Identifier: -