Literature DB >> 21381109

19F-lanthanide complexes with increased sensitivity for 19F-MRI: optimization of the MR acquisition.

Kirsten H Chalmers1, Alan M Kenwright, David Parker, Andrew M Blamire.   

Abstract

Fluorine-19 magnetic resonance methods offer advantages for molecular or cellular imaging in vivo due to the absence of radioactivity, lack of naturally occurring background signal, and the ability to easily combine measurements with anatomical MRI. Previous studies have shown that (19) F-MRI sensitivity is limited to millimolar concentrations by slow longitudinal relaxation. In this study, a new class of macrocyclic fluorinated lanthanide complexes is investigated where relaxation rates are significantly shortened by proximity of the fluorine group to a paramagnetic lanthanide ion located within the same molecule. Longitudinal and transverse relaxation rates are field dependent and in the range 50-150 s(-1) and 70-200 s(-1), respectively, at 7 T. Relaxation rates in these complexes are a function of the molecular structure and are independent of concentration at biologically relevant levels, so can be used as criteria to optimize imaging acquisition. Phantom experiments at 7 T indicate a lower limit for detection by imaging of 20 μM.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21381109     DOI: 10.1002/mrm.22881

Source DB:  PubMed          Journal:  Magn Reson Med        ISSN: 0740-3194            Impact factor:   4.668


  17 in total

1.  Cell tracking using (19)F magnetic resonance imaging: technical aspects and challenges towards clinical applications.

Authors:  Houshang Amiri; Mangala Srinivas; Andor Veltien; Mark J van Uden; I Jolanda M de Vries; Arend Heerschap
Journal:  Eur Radiol       Date:  2014-11-06       Impact factor: 5.315

Review 2.  New frontiers and developing applications in 19F NMR.

Authors:  Jian-Xin Yu; Rami R Hallac; Srinivas Chiguru; Ralph P Mason
Journal:  Prog Nucl Magn Reson Spectrosc       Date:  2012-11-02       Impact factor: 9.795

Review 3.  Overcoming the concentration-dependence of responsive probes for magnetic resonance imaging.

Authors:  Levi A Ekanger; Matthew J Allen
Journal:  Metallomics       Date:  2015-03       Impact factor: 4.526

4.  Functional Imaging Using Fluorine (19F) MR Methods: Basic Concepts.

Authors:  Sonia Waiczies; Christian Prinz; Ludger Starke; Jason M Millward; Paula Ramos Delgado; Jens Rosenberg; Marc Nazaré; Helmar Waiczies; Andreas Pohlmann; Thoralf Niendorf
Journal:  Methods Mol Biol       Date:  2021

5.  Exploiting the Fluxionality of Lanthanide Complexes in the Design of Paramagnetic Fluorine Probes.

Authors:  Randall K Wilharm; Mandapati V Ramakrishnam Raju; John C Hoefler; Carlos Platas-Iglesias; Valérie C Pierre
Journal:  Inorg Chem       Date:  2022-02-23       Impact factor: 5.165

Review 6.  Chemistry of MRI Contrast Agents: Current Challenges and New Frontiers.

Authors:  Jessica Wahsner; Eric M Gale; Aurora Rodríguez-Rodríguez; Peter Caravan
Journal:  Chem Rev       Date:  2018-10-16       Impact factor: 60.622

Review 7.  Enhancing magnetic resonance imaging with contrast agents for ultra-high field strengths.

Authors:  Akhila N W Kuda-Wedagedara; Matthew J Allen
Journal:  Analyst       Date:  2014-09-21       Impact factor: 4.616

8.  Copper(ii) complexes for cysteine detection using 19F magnetic resonance.

Authors:  José S Enriquez; Meng Yu; Bailey S Bouley; Da Xie; Emily L Que
Journal:  Dalton Trans       Date:  2018-10-30       Impact factor: 4.390

9.  A systematic optimization of 19F MR image acquisition to detect macrophage invasion into an ECM hydrogel implanted in the stroke-damaged brain.

Authors:  Harmanvir Ghuman; T Kevin Hitchens; Michel Modo
Journal:  Neuroimage       Date:  2019-08-10       Impact factor: 6.556

10.  Characterisation and evaluation of paramagnetic fluorine labelled glycol chitosan conjugates for (19)F and (1)H magnetic resonance imaging.

Authors:  Elena De Luca; Peter Harvey; Kirsten H Chalmers; Anurag Mishra; P Kanthi Senanayake; J Ian Wilson; Mauro Botta; Marianna Fekete; Andrew M Blamire; David Parker
Journal:  J Biol Inorg Chem       Date:  2013-08-17       Impact factor: 3.358

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