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Mapping the subcellular localization of Fe3O4@TiO2 nanoparticles by X-ray Fluorescence Microscopy.
Yuan, Y; Chen, S; Gleber, S C; Lai, B; Brister, K; Flachenecker, C; Wanzer, B; Paunesku, T; Vogt, S; Woloschak, G E.
Afiliación
  • Yuan Y; Department of Radiation Oncology, Northwestern University, Chicago, IL 60611, USA.
  • Chen S; X-ray Sciences Division, Argonne National Laboratory, Argonne, IL 60439, USA.
  • Gleber SC; X-ray Sciences Division, Argonne National Laboratory, Argonne, IL 60439, USA.
  • Lai B; X-ray Sciences Division, Argonne National Laboratory, Argonne, IL 60439, USA.
  • Brister K; Life Sciences Collaborative Access Team, Argonne National Laboratory, Argonne, IL 60439, USA.
  • Flachenecker C; Xradia, Pleasanton, CA 94588, USA.
  • Wanzer B; Department of Radiation Oncology, Northwestern University, Chicago, IL 60611, USA.
  • Paunesku T; Department of Radiation Oncology, Northwestern University, Chicago, IL 60611, USA.
  • Vogt S; X-ray Sciences Division, Argonne National Laboratory, Argonne, IL 60439, USA.
  • Woloschak GE; Department of Radiation Oncology, Northwestern University, Chicago, IL 60611, USA.
Article en En | MEDLINE | ID: mdl-26413134
ABSTRACT
The targeted delivery of Fe3O4@TiO2 nanoparticles to cancer cells is an important step in their development as nanomedicines. We have synthesized nanoparticles that can bind the Epidermal Growth Factor Receptor, a cell surface protein that is overexpressed in many epithelial type cancers. In order to study the subcellular distribution of these nanoparticles, we have utilized the sub-micron resolution of X-ray Fluorescence Microscopy to map the locationof Fe3O4@TiO2 NPs and other trace metal elements within HeLa cervical cancer cells. Here we demonstrate how the higher resolution of the newly installed Bionanoprobe at the Advanced Photon Source at Argonne National Laboratory can greatly improve our ability to distinguish intracellular nanoparticles and their spatial relationship with subcellular compartments.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Phys Conf Ser Año: 2013 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Phys Conf Ser Año: 2013 Tipo del documento: Article País de afiliación: Estados Unidos