The distribution and degradation of radiolabeled superparamagnetic iron oxide nanoparticles and quantum dots in mice

Denise Bargheer, Artur Giemsa, Barbara Freund, Markus Heine, Christian Waurisch, Gordon M. Stachowski, Stephen G. Hickey, Alexander Eychmüller, Jörg Heeren and Peter Nielsen
Beilstein J. Nanotechnol. 2015, 6, 111–123. https://doi.org/10.3762/bjnano.6.11

Cite the Following Article

The distribution and degradation of radiolabeled superparamagnetic iron oxide nanoparticles and quantum dots in mice
Denise Bargheer, Artur Giemsa, Barbara Freund, Markus Heine, Christian Waurisch, Gordon M. Stachowski, Stephen G. Hickey, Alexander Eychmüller, Jörg Heeren and Peter Nielsen
Beilstein J. Nanotechnol. 2015, 6, 111–123. https://doi.org/10.3762/bjnano.6.11

How to Cite

Bargheer, D.; Giemsa, A.; Freund, B.; Heine, M.; Waurisch, C.; Stachowski, G. M.; Hickey, S. G.; Eychmüller, A.; Heeren, J.; Nielsen, P. Beilstein J. Nanotechnol. 2015, 6, 111–123. doi:10.3762/bjnano.6.11

Download Citation

Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window below.
Citation data in RIS format can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Zotero.

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • Pan, X.; Ni, S.; Hu, K. Nanomedicines for reversing immunosuppressive microenvironment of hepatocellular carcinoma. Biomaterials 2024, 306, 122481. doi:10.1016/j.biomaterials.2024.122481
  • Nasiri-Ansari, N.; Androutsakos, T.; Flessa, C.-M.; Kyrou, I.; Siasos, G.; Randeva, H. S.; Kassi, E.; Papavassiliou, A. G. Endothelial Cell Dysfunction and Nonalcoholic Fatty Liver Disease (NAFLD): A Concise Review. Cells 2022, 11, 2511. doi:10.3390/cells11162511
  • Niu, Y.; Tang, M. In vitro review of nanoparticles attacking macrophages: Interaction and cell death. Life sciences 2022, 307, 120840. doi:10.1016/j.lfs.2022.120840
  • Nowak-Jary, J.; Machnicka, B. Pharmacokinetics of magnetic iron oxide nanoparticles for medical applications. Journal of nanobiotechnology 2022, 20, 305. doi:10.1186/s12951-022-01510-w
  • Zelepukin, I. V.; Mashkovich, E. A.; Lipey, N. A.; Popov, A. A.; Shipunova, V. O.; Griaznova, O. Y.; Deryabin, M. S.; Kurin, V. V.; Nikitin, P. I.; Kabashin, A. V.; Bakunov, M. I.; Deyev, S. M.; Zvyagin, A. V. Direct photoacoustic measurement of silicon nanoparticle degradation promoted by a polymer coating. Chemical Engineering Journal 2022, 430, 132860. doi:10.1016/j.cej.2021.132860
  • Curcio, A.; Van de Walle, A.; Péchoux, C.; Abou-Hassan, A.; Wilhelm, C. In Vivo Assimilation of CuS, Iron Oxide and Iron Oxide@CuS Nanoparticles in Mice: A 6-Month Follow-Up Study. Pharmaceutics 2022, 14, 179. doi:10.3390/pharmaceutics14010179
  • Kappel, C.; Seidl, C.; Medina-Montano, C.; Schinnerer, M.; Alberg, I.; Leps, C.; Sohl, J.; Hartmann, A.-K.; Fichter, M.; Kuske, M.; Schunke, J.; Kuhn, G.; Tubbe, I.; Paßlick, D.; Hobernik, D.; Bent, R.; Haas, K.; Montermann, E.; Walzer, K. C.; Diken, M.; Schmidt, M.; Zentel, R.; Nuhn, L.; Schild, H.; Tenzer, S.; Mailänder, V.; Barz, M.; Bros, M.; Grabbe, S. ACS Nano - Density of Conjugated Antibody Determines the Extent of Fc Receptor Dependent Capture of Nanoparticles by Liver Sinusoidal Endothelial Cells. ACS nano 2021, 15, 15191–15209. doi:10.1021/acsnano.1c05713
  • Curcio, A.; Van de Walle, A.; Benassai, E.; Serrano, A.; Luciani, N.; Menguy, N.; Manshian, B. B.; Sargsian, A.; Soenen, S. J.; Espinosa, A.; Abou-Hassan, A.; Wilhelm, C. Massive Intracellular Remodeling of CuS Nanomaterials Produces Nontoxic Bioengineered Structures with Preserved Photothermal Potential. ACS nano 2021, 15, 9782–9795. doi:10.1021/acsnano.1c00567
  • Pan, J.; Xu, Y.; Wu, Q.; Hu, P.; Shi, J. Mild Magnetic Hyperthermia-Activated Innate Immunity for Liver Cancer Therapy. Journal of the American Chemical Society 2021, 143, 8116–8128. doi:10.1021/jacs.1c02537
  • Van de Walle, A.; Perez, J. E.; Abou-Hassan, A.; Hémadi, M.; Luciani, N.; Wilhelm, C. Magnetic nanoparticles in regenerative medicine: what of their fate and impact in stem cells?. Materials Today Nano 2020, 11, 100084. doi:10.1016/j.mtnano.2020.100084
  • Kermanizadeh, A.; Powell, L. G.; Stone, V. A review of hepatic nanotoxicology - summation of recent findings and considerations for the next generation of study designs. Journal of toxicology and environmental health. Part B, Critical reviews 2020, 23, 137–176. doi:10.1080/10937404.2020.1751756
  • Lafoz, E.; Ruart, M.; Anton, A.; Oncins, A.; Hernández-Gea, V. The Endothelium as a Driver of Liver Fibrosis and Regeneration. Cells 2020, 9, 929. doi:10.3390/cells9040929
  • Akhtar, K.; Javed, Y.; Shad, N. A.; Shrivastava, N.; Sharma, S. K. Persistence, Toxicity, and Biodegradation of Gold- and Iron Oxide-Based Nanoparticles in the Living Systems. Magnetic Nanoheterostructures; Springer International Publishing, 2020; pp 447–478. doi:10.1007/978-3-030-39923-8_14
  • Van de Walle, A.; Fromain, A.; Sangnier, A. P.; Curcio, A.; Lenglet, L.; Motte, L.; Lalatonne, Y.; Wilhelm, C. Real-time in situ magnetic measurement of the intracellular biodegradation of iron oxide nanoparticles in a stem cell-spheroid tissue model. Nano Research 2020, 13, 467–476. doi:10.1007/s12274-020-2631-1
  • Liu, Z.; Escudero, A.; Carrillo-Carrión, C.; Chakraborty, I.; Zhu, D.; Gallego, M.; Parak, W. J.; Feliu, N. Biodegradation of Bi-Labeled Polymer-Coated Rare-Earth Nanoparticles in Adherent Cell Cultures. Chemistry of Materials 2019, 32, 245–254. doi:10.1021/acs.chemmater.9b03673
  • Yoshida, S.; Duong, C. P.; Oestergaard, M.; Fazio, M.; Chen, C.; Peralta, R.; Guo, S.; Seth, P. P.; Li, Y.; Beckett, L. A.; Nitin, N.; Satake, N. MXD3 antisense oligonucleotide with superparamagnetic iron oxide nanoparticles: A new targeted approach for neuroblastoma. Nanomedicine : nanotechnology, biology, and medicine 2019, 24, 102127. doi:10.1016/j.nano.2019.102127
  • Naumenko, V.; Nikitin, A.; Kapitanova, K.; Mel’nikov, P. A.; Vodopyanov, S.; Garanina, A. S.; Valikhov, M. P.; Ilyasov, A.; Vishnevskiy, D. A.; Markov, A.; Golyshev, S. A.; Zhukov, D. G.; Alieva, I. B.; Abakumov, M. A.; Chekhonin, V. P.; Majouga, A. G. Intravital microscopy reveals a novel mechanism of nanoparticles excretion in kidney. Journal of controlled release : official journal of the Controlled Release Society 2019, 307, 368–378. doi:10.1016/j.jconrel.2019.06.026
  • Frey, A.; Ramaker, K.; Röckendorf, N.; Wollenberg, B.; Lautenschläger, I.; Gébel, G.; Giemsa, A.; Heine, M.; Bargheer, D.; Nielsen, P. Fate and Translocation of (Nano)Particulate Matter in the Gastrointestinal Tract. Biological Responses to Nanoscale Particles; Springer International Publishing, 2019; pp 281–327. doi:10.1007/978-3-030-12461-8_12
  • Hwang, E.; Song, J.; Zhang, J. Integration of Nanomaterials and Bioluminescence Resonance Energy Transfer Techniques for Sensing Biomolecules. Biosensors 2019, 9, 42. doi:10.3390/bios9010042
  • Ferreira, C. A.; Goel, S.; Cai, W. Exogenous Radionanomedicine: Inorganic Nanomaterials. Radionanomedicine; Springer International Publishing, 2018; pp 13–47. doi:10.1007/978-3-319-67720-0_2
Other Beilstein-Institut Open Science Activities