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A fast multislice sequence for 3D MRI-CEST pH imaging.
Villano, Daisy; Romdhane, Feriel; Irrera, Pietro; Consolino, Lorena; Anemone, Annasofia; Zaiss, Moritz; Dastrù, Walter; Longo, Dario Livio.
Affiliation
  • Villano D; Molecular Imaging Center, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.
  • Romdhane F; Molecular Imaging Center, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.
  • Irrera P; National Engineering School of Tunis (ENIT), University al Manar, Tunis, Tunisia.
  • Consolino L; Molecular Imaging Center, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.
  • Anemone A; Institute of Biostructures and Bioimaging, University of Campania "Luigi Vanvitelli," Italian National Research Council, Napoli, Italy.
  • Zaiss M; Molecular Imaging Center, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.
  • Dastrù W; Molecular Imaging Center, Department of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy.
  • Longo DL; Department of Neuroradiology, Friedrich-Alexander Universität Erlangen-Nürnberg, University Hospital Erlangen, Erlangen, Germany.
Magn Reson Med ; 85(3): 1335-1349, 2021 03.
Article de En | MEDLINE | ID: mdl-33031591
ABSTRACT

PURPOSE:

Chemical exchange saturation transfer MRI can provide accurate pH images, but the slow scan time (due to long saturation periods and multiple offsets sampling) reduce both the volume coverage and spatial resolution capability, hence the possibility to interrogate the heterogeneity in tumors and organs. To overcome these limitations, we propose a fast multislice CEST-MRI sequence with high pH accuracy and spatial resolution.

METHODS:

The sequence first uses a long saturation pulse to induce the steady-state CEST contrast and a second short saturation pulse repeated after each image acquisition to compensate for signal losses based on an uneven irradiation scheme combined with a single-shot rapid acquisition with refocusing echoes readout. Sequence sensitivity and accuracy in measuring pH was optimized by simulation and assessed by in vitro studies in pH-varying phantoms. In vivo validation was performed in two applications by acquiring multislice pH images covering the whole tumors and kidneys after iopamidol injection.

RESULTS:

Simulated and in vivo data showed comparable contrast efficiency and pH responsiveness by reducing saturation time. The experimental data from a homogeneous, pH-varying, iopamidol-containing phantom show that the sequence produced a uniform CEST contrast across slices and accurate values across slices in less than 10 minutes. In vivo measurements allowed us to quantify the 3D pH gradients of tumors and kidneys, with pH ranges comparable with the literature.

CONCLUSION:

The proposed fast multislice CEST-MRI sequence allows volumetric acquisitions with good pH sensitivity, accuracy, and spatial resolution for several in vivo pH imaging applications.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Iopamidol / Imagerie par résonance magnétique Langue: En Journal: Magn Reson Med Sujet du journal: DIAGNOSTICO POR IMAGEM Année: 2021 Type de document: Article Pays d'affiliation: Italie

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Iopamidol / Imagerie par résonance magnétique Langue: En Journal: Magn Reson Med Sujet du journal: DIAGNOSTICO POR IMAGEM Année: 2021 Type de document: Article Pays d'affiliation: Italie
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