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  Quantitative assessment of xenon exchange kinetics with Cucurbit[6]uril in physiological saline.

Korchak, S., Riemer, T., Kilian, W., & Mitschang, L. (2018). Quantitative assessment of xenon exchange kinetics with Cucurbit[6]uril in physiological saline. ChemPhysChem, 19(15), 1859-1865. doi:10.1002/cphc.201800048.

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Item Permalink: http://hdl.handle.net/21.11116/0000-0002-0112-8 Version Permalink: http://hdl.handle.net/21.11116/0000-0003-7A44-8
Genre: Journal Article

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Korchak, S.1, Author              
Riemer, T., Author
Kilian, W., Author
Mitschang, L., Author
Affiliations:
1Research Group of NMR Signal Enhancement, MPI for Biophysical Chemistry, Max Planck Society, ou_2396691              

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Free keywords: cucurbituril; host-guest system; hyperpolarized xenon; kinetics; NMR spectroscopy
 Abstract: Cucurbit[6]uril and xenon form supramolecular complexes that are of great potential for biosensing by NMR. This host-guest system acts alike a signaler in sensors facilitating the ultrasensitive detection of biomarkers by saturation transfer of chemically exchanging, hyperpolarized Xe-129. Here, the exchange process is evaluated by NMR exchange spectroscopy utilizing the preparation of anti-parallel longitudinal magnetization with respect to free and host-bound xenon and the variation of xenon concentration. Evidence for dissociative as well as degenerate exchange mechanisms is revealed by a linear regression analysis of the determined exchange rates resulting in rate coefficients of 1131 +/- 11s(-1) (2390 +/- 70s(-1)) and 108500 +/- 4900M(-1)s(-1) (174200 +/- 13900M(-1)s(-1)), respectively, and an affinity constant of 289 +/- 8M(-1) (278 +/- 14M(-1)) in physiological saline at 298K (310K). The results elucidate the supramolecular exchange and underpin the high efficacy for biosensing of this host-guest system. The approach is generally applicable to enhanced host-xenon exchange dynamics, yet slow on the NMR timescale, for quantitative kinetics and biosensing analyses.

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Language(s): eng - English
 Dates: 2018-06-012018-08-07
 Publication Status: Published in print
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 Rev. Method: Peer
 Identifiers: DOI: 10.1002/cphc.201800048
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Title: ChemPhysChem
Source Genre: Journal
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Pages: - Volume / Issue: 19 (15) Sequence Number: - Start / End Page: 1859 - 1865 Identifier: -