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Simultaneous quantification of SPIO and gadolinium contrast agents using MR fingerprinting
Anna Marriott1, Chris Bowen1, James Rioux1
1Biomedical Translational Imaging Centre (BIOTIC), Halifax, NS, Canada; Dalhousie University, Halifax, NS, Canada.
Magnetic Resonance Imaging
|March 28, 2021
Summary
This study introduces an advanced magnetic resonance fingerprinting (MRF) method for simultaneous R1, R2, and R2* quantification. The technique enables dual contrast agent mapping, including gadolinium and iron-labeled cells, for enhanced molecular imaging.
Area of Science:
- Biomedical Imaging
- Quantitative MRI
- Molecular Imaging
Background:
- Magnetic Resonance Fingerprinting (MRF) is a powerful technique for quantitative MRI.
- Simultaneous mapping of multiple contrast agents is crucial for advanced molecular imaging applications.
Purpose of the Study:
- To develop an MRF methodology capable of R2* quantification.
- To enable simultaneous contrast agent concentration mapping, specifically for gadolinium (Gd) and iron-labeled CD8+ T cells.
Main Methods:
- Variable-density spiral SSFP MRF was modified for variable TE and dictionary modulation.
- In vitro phantoms with SPIO-labeled cells and Gd were used for validation.
- In vivo imaging in mice demonstrated feasibility at 8x undersampling for a 25-min scan.
Main Results:
- High agreement between conventional and MRF-derived R1, R2, and R2* values.
- Successful quantification of iron-loaded CD8+ T cells using expanded MRF.
- Robustness to 8x undersampling, enabling simultaneous relaxation profile recreation for Gd and iron-labeled cells.
Conclusions:
- Expanded MRF allows R1, R2, and R2* mapping for simultaneous Gd and SPIO quantification.
- This methodology supports future in vivo studies using dual MR contrast agents.
- Potential for molecular imaging of labeled cells with enhanced dual contrast agent tracking.

