2014
DOI: 10.1016/j.saa.2014.01.047
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Evaluation of glucose-linked nitroxide radicals for use as an in vivo spin-label probe

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Cited by 3 publications
(4 citation statements)
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“…As linking nitroxides to glucose seems to have a slight effect on the stability of the compounds, 22 radical stabilities of TEMPO-Glc and TEEPO-Glc were studied by T 1 -measurements as a function of time elapsed from the sample preparation. Human blood plasma was considered to be reasonable matrix to mimic in vivo conditions.…”
mentioning
confidence: 99%
“…As linking nitroxides to glucose seems to have a slight effect on the stability of the compounds, 22 radical stabilities of TEMPO-Glc and TEEPO-Glc were studied by T 1 -measurements as a function of time elapsed from the sample preparation. Human blood plasma was considered to be reasonable matrix to mimic in vivo conditions.…”
mentioning
confidence: 99%
“…Additionally, while stabilized nitroxide radicals are still relatively unstable, especially in an uncontrolled cellular environment where they are subject to reduction by radical scavengers, multiple studies have demonstrated use of nitroxide radicals as contrast agents for in vivo imaging. 22,32,33 These studies showed that pyrroline-based nitroxide radicals can remain stable for at least 20–30 minutes in vivo, which is sufficient time for injection, target hybridization, and imaging, though longer stability may be achieved by gadolinium chelates. 21 It has also been shown previously that molecular beacons can be modified for greater stability and resistance to nuclease degradation in cellular environments using 2′-o-methyl bases, peptide nucleic acids, locked nucleic acids, or phosphorothioate.…”
Section: Resultsmentioning
confidence: 99%
“…This compound was chosen for its stability in buffered systems, simple attachment chemistry to the oligonucleotide beacon, and the unique configuration of its single unpaired electron, which has a nearly isotropic g tensor that eliminates other paramagnetic effects like pseudocontact shifts. 18,22 With the oligonucleotide in its hairpin conformation, the radical is held within 6−12 Å of the fluorine compound, which enables PRE broadening of the 19 F resonance. However, in the linearized DNA conformation, the moieties have ∼100 Å separation, causing the effects of PRE to become negligible.…”
Section: ■ Introductionmentioning
confidence: 99%
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