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  Comparison of 2 Different Tumor Cell Labeling Techniques for in Vitro MRI Characterization with New Iron Oxide Particles

Saborowski, O., Santini, F., Fani, M., Robert, P., Ballet, S., Raynaud, J., et al. (2008). Comparison of 2 Different Tumor Cell Labeling Techniques for in Vitro MRI Characterization with New Iron Oxide Particles. Poster presented at 16th Scientific Meeting and Exhibition of the International Society of Magnetic Resonance in Medicine (ISMRM 2008), Toronto, Canada.

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Item Permalink: http://hdl.handle.net/21.11116/0000-0003-9330-0 Version Permalink: http://hdl.handle.net/21.11116/0000-0003-9331-F
Genre: Poster

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 Creators:
Saborowski, O, Author
Santini, F, Author
Fani, M, Author
Robert, P, Author
Ballet, S, Author
Raynaud, JS, Author
Santus, R, Author
Froehlich, J, Author
Scheffler, K1, Author              
Bongartz, G, Author
Maecke, HR, Author
Affiliations:
1External Organizations, ou_persistent22              

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 Abstract: Iron oxide particles (SPIO and USPIO) are widely used for MRI-based cell labeling and tracking because they can be loaded on cells by simple protocols and provide high image contrast due to their large susceptibility effect. We compared 2 different cell labeling models (AGAR and Ficoll) in human KB cells. Both presented cell labeling methods (AGAR and Ficoll model) are feasible for in vitro MR characterization of KB tumor cells at 1.5, 2.35 and 3T. Ficoll method is easier to perform because it does not need a heating procedure for preparation without air bubbles as compared to AGAR method.

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 Dates: 2008-05
 Publication Status: Published in print
 Pages: -
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Title: 16th Scientific Meeting and Exhibition of the International Society of Magnetic Resonance in Medicine (ISMRM 2008)
Place of Event: Toronto, Canada
Start-/End Date: 2008-05-03 - 2008-05-09

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Title: 16th Scientific Meeting and Exhibition of the International Society of Magnetic Resonance in Medicine (ISMRM 2008)
Source Genre: Proceedings
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Publ. Info: -
Pages: - Volume / Issue: - Sequence Number: 3233 Start / End Page: 522 Identifier: -