Gd-BOPTA demonstrates the highest longitudinal r1 at all field strengths, which is ascribable to weak protein interaction. The R2/R1 ratio increases at higher field strength only for Gd-BOPTA, hence very short echo times are required for Gd-BOPTA to benefit from the higher longitudinal relaxivity.

SPIO or USPIO labeling without TAs has an influence on gene expression of MSCs upregulating transferrin receptor. Furthermore, SPIO labeling with a TA will coat the cellular surface.

The ability of magnetic resonance imaging (MRI) to visualize magnetically labelled cells has attracted much attention for revealing cellular events. The present study addressed the geometry and the extension of signal voids in static signal dephasing MRI induced by aggregations of magnetically labelled cells by means of a three-dimensional numerical model. The magnetic field distortions around spherical cell aggregations were treated as equivalent to those of a magnetic dipole. Intravoxel signal dephasing and respective signal voids attributed to these field inhomogeneities were computed. Effects of cell concentration on the signal void in the plane of view were evaluated in terms of dipole magnetization. Signal void characteristics were scrutinized systematically for fundamental sequence parameters including echo time, voxel size and plane-of-view orientation. For all variables examined, significant changes in geometry as well as extension of signal voids were demonstrated. The results are of crucial importance to optimize and interpret MR images with regard to spatial accuracy as well as sensitivity to detect aggregations of labelled cells in vitro or even in vivo. It is anticipated that the dependence of the extension of signal voids on the local magnetization may be valuable for quantifying labelled cells.

The objective of this study was to demonstrate the feasibility of 3D proton MR spectroscopic imaging (MRSI) of the prostate using a standard spine instead of a dedicated endorectal coil at 1.5 T. Twenty-eight patients (25 with biopsy proven prostate cancers and three patients with a benign prostate hyperplasia) were examined. MRI and MRSI were conducted with commercial array surface coils at 1.5 T. Ratios of choline (Cho), creatine (Cr) and citrate (Ci) were calculated for tumour, central and peripheral zone retrospectively, based on axial T2 weighed MR images and histology reports. Prostate cancer was characterized by significantly elevated (Cho+Cr)/Ci ratio compared with non-tumourous prostate tissue. The quality of all proton MR spectra was considered to be good or acceptable in 17/28 patients (61%) and poor in 11/28 (39%) examinations. In 20/25 patients with proven malignancy (80%), MRSI was considered to be helpful for the detection of prostate cancer. In 4/25 patients with proven malignancy (16%) who underwent seed implantation, radiotherapy or hormone deprivation before MR examination spectroscopy was of poor and non-diagnostic quality. MRSI of the prostate is feasible within clinical routine using the spine array surface coil at 1.5 T. It can consequently be applied to patients even with contraindications for endorectal coils. However, spectral quality and signal-to-noise ratio is clearly inferior to 3D MRSI examinations with endorectal coils.

The proposed preparation strategy with a well defined spatial distribution of the magnetic material in an agar gel phantom produced reliable results and appears clearly superior compared to set-ups with randomly distributed material in glass tubes. The diameter of the signal extinction in gradient echo images was significantly affected by the choice of echo time and spatial resolution. The calibration of signal cancellation versus iron concentrations may be valuable to assess SPIO concentrations and possibly numbers of labeled cells under specific conditions in vitro or even in vivo.