Volume 64, Issue 6 pp. 1607-1615
Preclinical and Clinical Imaging-Full Papers

Intracellular and extracellular T1 and T2 relaxivities of magneto-optical nanoparticles at experimental high fields

Gert Klug

Corresponding Author

Gert Klug

Medizinische Klinik und Poliklinik I, Universitätsklinik Würzburg, Würzburg, Germany

Universitätsklinik für Innere Medizin III, Medizinsche Universität Innsbruck, Austria===Search for more papers by this author
Thomas Kampf

Thomas Kampf

Experimentelle Physik 5, Universität Würzburg, Würzburg, Germany

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Steffen Bloemer

Steffen Bloemer

Institut für Anorganische Chemie, Universität Würzburg, Würzburg, Germany

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Johannes Bremicker

Johannes Bremicker

Medizinische Klinik und Poliklinik I, Universitätsklinik Würzburg, Würzburg, Germany

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Christian H. Ziener

Christian H. Ziener

Experimentelle Physik 5, Universität Würzburg, Würzburg, Germany

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Andrea Heymer

Andrea Heymer

Division of Tissue Engineering, König-Ludwig-Haus, Würzburg, Germany

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Uwe Gbureck

Uwe Gbureck

Department of Functional Materials in Medicine and Dentistry, Universität Würzburg, Würzburg, Germany

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Eberhard Rommel

Eberhard Rommel

Experimentelle Physik 5, Universität Würzburg, Würzburg, Germany

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Ulrich Nöth

Ulrich Nöth

Division of Tissue Engineering, König-Ludwig-Haus, Würzburg, Germany

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Wolfdieter A. Schenk

Wolfdieter A. Schenk

Institut für Anorganische Chemie, Universität Würzburg, Würzburg, Germany

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Peter M. Jakob

Peter M. Jakob

Experimentelle Physik 5, Universität Würzburg, Würzburg, Germany

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Wolfgang R. Bauer

Wolfgang R. Bauer

Medizinische Klinik und Poliklinik I, Universitätsklinik Würzburg, Würzburg, Germany

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First published: 23 November 2010
Citations: 35

Abstract

This study reports the T1 and T2 relaxation rates of rhodamine-labeled anionic magnetic nanoparticles determined at 7, 11.7, and 17.6 T both in solution and after cellular internalization. Therefore cells were incubated with rhodamine-labeled anionic magnetic nanoparticles and were prepared at decreasing concentrations. Additionally, rhodamine-labeled anionic magnetic nanoparticles in solution were used for extracellular measurements. T1 and T2 were determined at 7, 11.7, and 17.6 T. T1 times were determined with an inversion-recovery snapshot-flash sequence. T2 times were obtained from a multispin-echo sequence. Inductively coupled plasma-mass spectrometry was used to determine the iron content in all samples, and r1 and r2 were subsequently calculated. The results were then compared with cells labeled with AMI-25 and VSOP C-200. In solution, the r1 and r2 of rhodamine-labeled anionic magnetic nanoparticles were 4.78/379 (7 T), 3.28/389 (11.7 T), and 2.00/354 (17.6 T). In cells, the r1 and r2 were 0.21/56 (7 T), 0.19/37 (11.7 T), and 0.1/23 (17.6 T). This corresponded to an 11- to 23-fold decrease in r1 and an 8- to 15-fold decrease in r2. A decrease in r1 was observed for AMI-25 and VSOP C-200. AMI-25 and VSOP exhibited a 2- to 8-fold decrease in r2. In conclusion, cellular internalization of iron oxide nanoparticles strongly decreased their T1 and T2 potency. Magn Reson Med, 2010. © 2010 Wiley-Liss, Inc.

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