Abstract
Aims: To investigate various protocols for magnetic labeling of human cancer cells with ferumoxides with a view to developing an effective and fast technique for potential clinical use in MRI. Materials & methods: Transfection methods utilizing poly-L-lysine and protamine sulfate (PS), electroporation, and combination of PS with electroporation were evaluated in this in vitro study. Results: Although transfection was more effective in terms of uptake rates (95-100%) and intracellular iron concentrations (4.01-7.34 pg/cell), all transfection agents required prolonged incubation. By contrast, electroporation yielded fast labeling but with a lower efficacy (68-75%, 1.63-2.59 pg/cell). The addition of PS to electroporation increased the labeling efficacy (80-91%, 2.84-4.16 pg/cell) and protected cell viability. This combined method also resulted in the best T-2*-shortening effect in the in vitro cellular MRI. Conclusion: The combined PS-electroporation method provides a fast and efficient protocol for ferumoxide-based cellular imaging and therapeutic procedure.
Original language | English |
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Pages (from-to) | 305-315 |
Number of pages | 11 |
Journal | Nanomedicine |
Volume | 4 |
Issue number | 3 |
DOIs | |
Publication status | Published - Apr 2009 |
Keywords
- electroporation
- magnetic cell labeling
- MRI
- protamine sulfate
- SPION
- transfection
- IN-VIVO TRACKING
- MAGNETIC NANOPARTICLES
- STEM-CELLS
- SMALL MOLECULES
- IRON-OXIDE
- GENE
- THERAPY
- MODEL
- ELECTROPERMEABILIZATION
- FERUMOXIDES