In vivo risk evaluation of carbon-coated iron carbide nanoparticles based on short- and long-term exposure scenarios

Author:

Herrmann Inge K123,Beck-Schimmer Beatrice12,Schumacher Christoph M4,Gschwind Sabrina5,Kaech Andres6,Ziegler Urs6,Clavien Pierre-Alain7,Günther Detlef5,Stark Wendelin J4,Graf Rolf7,Schlegel Andrea A7

Affiliation:

1. Institute of Anesthesiology, University Hospital Zurich, Rämistrasse 100, CH-8091 Zurich, Switzerland

2. Institute of Physiology & Zurich Center for Integrative Human Physiology, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland

3. Department Materials Meet Life, Swiss Federal Laboratories for Materials Science & Technology (Empa), Lerchenfeldstrasse 5, 9014 St. Gallen, Switzerland

4. ETH Zurich, Institute for Chemical & Bioengineering, Vladimir-Prelog-Weg 1-5/10, CH-8093 Zurich, Switzerland

5. ETH Zurich, Laboratory of Inorganic Chemistry, Vladimir-Prelog-Weg 1-5/10, CH-8093 Zurich, Switzerland

6. Center for Microscopy & Image Analysis, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland

7. Swiss HPB & Transplant Center, Department of Surgery, University Hospital Zurich, Rämistrasse 100, CH-8091 Zurich, Switzerland

Abstract

Background: While carbon-encapsulated iron carbide nanoparticles exhibit strong magnetic properties appealing for biomedical applications, potential side effects of such materials remain comparatively poorly understood. Here, we assess the effects of iron-based nanoparticles in an in vivo long-term study in mice with observation windows between 1 week and 1 year. Materials & methods: Functionalized (PEG or IgG) carbon-encapsulated platinum-spiked iron carbide nanoparticles were injected intravenously in mice (single or repeated dose administration). Results: One week after administration, magnetic nanoparticles were predominantly localized in organs of the reticuloendothelial system, particularly the lung and liver. After 1 year, particles were still present in these organs, however, without any evident tissue alterations, such as inflammation, fibrosis, necrosis or carcinogenesis. Importantly, reticuloendothelial system organs presented with normal function. Conclusion: This long-term exposure study shows high in vivo compatibility of intravenously applied carbon-encapsulated iron nanoparticles suggesting continuing investigations on such materials for biomedical applications.

Publisher

Future Medicine Ltd

Subject

Development,General Materials Science,Biomedical Engineering,Medicine (miscellaneous),Bioengineering

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