Jean-Christophe Brisset1,2, Monica Olivia Sigovan1,2, Fabien Chauveau1,2, Adrien Riou1,2, Norbert Nighoghossian1,2, Emmanuelle Canet-Soulas1,2, Yves Berthezene1,2, Marlene Wiart1,2
1University of lyon, Lyon, france, France; 2Creatis-LRMN, CNRS, UMR 5220; Inserm, U 630; Insa de Lyon, Lyon, France
The aim of this study was to compare 4 quantitative methods for estimating the number of iron-labelled cells injected in the mouse brain: T2, T2* relaxometry, and artefact volume measurement using negative and positive contrasts. Eight mice were stereotaxically injected with [500-7,500] iron-labelled cells and imaged at 4.7T. Bland-Altman and scatterplots were used to compare the T2 and T2*-based estimated number of cells, the artefact volumes, and the actual number of iron-labelled cells. T2 and T2* quantification failed to estimate the number of iron-labelled cell in-vivo, while measurement of the artefact volume gave promising results.