Table 1.
Probe | Basic imaging principle | Main advantage | Main disadvantage | Detection sensitivity (number of cells)f | Used for cell tracking in human subjects |
---|---|---|---|---|---|
Iron oxide nanoparticles | Shortening T2 relaxation of surrounding water protons | High sensitivity | Lack of specific signal; i.e. signal loss | 1 cella,18,19 | Yes20–29 |
Gd-based nanoparticles | Shortening T1 relaxation of surrounding water molecules | Giving rise to signal enhancement | Issues regarding toxicity | 300–3000 cellsb,30–32 | No |
Manganese-based nanoparticles | Shortening T1 relaxation of surrounding water molecules | Natural body mineral | Issues regarding toxicity | 1000–100,000 cellsc,33–35 | No |
Chemical exchange saturation transfer agents | Transfer of selectively saturated, exchangeable spins to surrounding bulk water via chemical exchange | Multispectral imaging | Requires specialized imaging techniques | 10,000 cellsd,36 | No |
19F-based nanoparticles | Magnetic spin of 19F nuclei | Not naturally present in body, therefore providing unique signal | Requires specialized imaging techniques | 2000–9000 cellse,37,38 | Yes39 |
19F, fluorine-19.
at intracellular concentrations of 9–50 pg/cell; voxel size 0.26–1 × 10−3 mm3.
at intracellular Gd concentrations of 0.05–70 pg/cell; voxel size 2.24–10.3 × 10−3 mm3.
at intracellular Mn concentrations of 0.35–0.7 pg/cell; voxel size 160 × 10−-3 mm3 (only specified by Letourneau et al.35).
at intracellular CEST agent concentrations of 3–4 mM/cell; voxel size 24–73 × 10−3 mm3.
at intracellular 19F concentrations of 0.35–0.7 pg/cell; voxel size 660–2000 × 10−3 mm3.
Detection sensitivity is highly dependent of various conditions, such as the cell type, intracellular loading, imaging parameters including voxel size, and magnetic field strength.