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Quantitative MR imaging of targeted SPIO particles on the cell surface and comparison to flow cytometry
Authors:Kersten Peldschus  Alexander Schultze  Peter Nollau  Michael Kaul  Udo Schumacher  Christoph Wagener  Gerhard Adam  Harald Ittrich
Institution:1. Department of Diagnostic and Interventional Radiology, University Cancer Center Hamburg-Eppendorf (UCCH), 20246 Hamburg, Germany;2. Department of Hematology and Oncology, University Cancer Center Hamburg-Eppendorf (UCCH), 20246 Hamburg, Germany;3. Department of Clinical Chemistry, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany;4. Department of Anatomy II: Experimental Morphology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany
Abstract:

Purpose

To detect anti-CEACAM5 targeted superparamagnetic iron oxide (SPIO) particles in vitro on the cell surface by quantitative magnetic resonance (MR) imaging and to compare with flow cytometry.

Materials and Methods

The monoclonal mouse antibody T84.1 and an appropriate IgG isotype antibody were conjugated to dextran-coated SPIO particles. HT29 cells expressing carcinoembryonic antigen (CEACAM5) were treated with antibody-conjugated SPIO particles. Purified cell samples were examined on a 3.0-T MR scanner using a multi-echo spin-echo sequence for MR relaxometry. Aliquots of the cell samples were further treated with a fluorescein isothiocyanate (FITC) anti-dextran antibody and an Alexa Fluor 488 anti-mouse antibody for the corresponding flow cytometry.

Results

MR relaxometry revealed a dose-dependent binding of T84.1-conjugated SPIO particles with a positive correlation between R2 relaxation rate of cell samples and SPIO particle concentration during incubation (r=0.993, P<.01). Positive correlations were also observed between R2 relaxation rate and flow cytometry (geometric mean) with both fluorescent antibodies (r=0.972 and r=0.953, both P<.01), respectively.

Conclusion

The study revealed the feasibility of quantitative MR imaging of targeted SPIO particles on the cell surface comparable to flow cytometry.
Keywords:Superparamagnetic iron oxide particle  Magnetic resonance relaxometry  Flow cytometry  Carcinoembryonic antigen
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