2013
DOI: 10.1038/srep01280
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Visualizing Brain Inflammation with a Shingled-Leg Radio-Frequency Head Probe for 19F/1H MRI

Abstract: Magnetic resonance imaging (MRI) provides the opportunity of tracking cells in vivo. Major challenges in dissecting cells from the recipient tissue and signal sensitivity constraints albeit exist. In this study, we aimed to tackle these limitations in order to study inflammation in autoimmune encephalomyelitis. We constructed a very small dual-tunable radio frequency (RF) birdcage probe tailored for 19F (fluorine) and 1H (proton) MR mouse neuroimaging. The novel design eliminated the need for extra electrical … Show more

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Cited by 41 publications
(58 citation statements)
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“…More recently, it was also shown that leukocytes infiltrate periventricular tissue as well as perivascular spaces prior to clinical symptom onset [36]. In agreement with this study, we have also recently shown an extensive accumulation of inflammatory cells on the ventral side of the forebrain, midbrain and brainstem as shown by fluorine/proton MRI [37]. …”
Section: Discussionsupporting
confidence: 89%
“…More recently, it was also shown that leukocytes infiltrate periventricular tissue as well as perivascular spaces prior to clinical symptom onset [36]. In agreement with this study, we have also recently shown an extensive accumulation of inflammatory cells on the ventral side of the forebrain, midbrain and brainstem as shown by fluorine/proton MRI [37]. …”
Section: Discussionsupporting
confidence: 89%
“…Although the migration capability of DCs labeled with DPPE-enriched fluorine nanoparticles is diminished when compared to non-enriched nanoparticles, when given at the same PFCE labeling concentration, lower concentrations of DPPE-enriched fluorine nanoparticles still resulted in a higher 19 F signal per million cells and minimal decrease in migration, implying a possible threshold for aminophospholipid enriched nanoparticle labelling concentration that increases the 19 F MRS signal without influencing DC migration ability. The order of magnitude increase in 19 F signal we observed with 19 F spectroscopy could be translated into two advantages: (i) we could decrease the concentration of the 19 F label (PFCE) from 20 μmol (employed in our original studies5612) to 5 μmol per 10 7 DCs and thus decrease the impact of the 19 F label on cell migration and (ii) the sensitivity gain considerably improved the cell detection limit to enable imaging and quantification of DCs within specific anatomical regions in vivo.…”
Section: Discussionmentioning
confidence: 99%
“…For the 47 mmol/L FA sample, TE values of 5. 5,9,15,20,30,40, 50 and 60 ms were employed. For both FA concentrations, TR was set to 4000 ms with number of averages = 128 and total scan time = 512 s. To calculate the T 1 and T 2 relaxation times for each sample, data were fitted to T 1 and T 2 relaxation equations using MATLAB.…”
Section: F Mr Spectroscopymentioning
confidence: 99%