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Gold nanoparticles as multimodality imaging agents for brain gliomas.
Lai, Sheng-Feng; Ko, Bai-Hung; Chien, Chia-Chi; Chang, Chia-Ju; Yang, Shun-Ming; Chen, Hsiang-Hsin; Petibois, Cyril; Hueng, Dueng-Yuan; Ka, Shuk-Man; Chen, Ann; Margaritondo, G; Hwu, Y.
Afiliação
  • Lai SF; Department of Engineering Science, National Cheng Kung University, Tainan, 701, Taiwan. sflai@phys.sinica.edu.tw.
  • Ko BH; Department of Engineering Science, National Cheng Kung University, Tainan, 701, Taiwan. bhko@phys.sinica.edu.tw.
  • Chien CC; Institute of Physics, Academia Sinica, Nankang, Taipei, 115, Taiwan. bhko@phys.sinica.edu.tw.
  • Chang CJ; Institute of Physics, Academia Sinica, Nankang, Taipei, 115, Taiwan. chiachi.chien@gmail.com.
  • Yang SM; Institute of Physics, Academia Sinica, Nankang, Taipei, 115, Taiwan. echo826@gate.sinica.edu.tw.
  • Chen HH; Institute of Physics, Academia Sinica, Nankang, Taipei, 115, Taiwan. smyang@phys.sinica.edu.tw.
  • Petibois C; Inserm U1029 LMMA, University of Bordeaux, 33600, Pessac Cedex, France. hhchen@phys.sinica.edu.tw.
  • Hueng DY; Inserm U1029 LMMA, University of Bordeaux, 33600, Pessac Cedex, France. cyril.petibois@u-bordeaux.fr.
  • Ka SM; Department of Biochemistry, School of Medicine, National Defense Medical Center, Taipei, 114, Taiwan. hondy2195@gmail.com.
  • Chen A; Department of Neurological Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei, 114, Taiwan. hondy2195@gmail.com.
  • Margaritondo G; Institute of Aerospace and Undersea Medicine, School of Medicine, National Defense Medical Center, Taipei, 114, Taiwan. shukmanka@gmail.com.
  • Hwu Y; Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei, 114, Taiwan. Aannchen31717@gmail.com.
J Nanobiotechnology ; 13: 85, 2015 Nov 20.
Article em En | MEDLINE | ID: mdl-26589283
ABSTRACT

BACKGROUND:

Nanoparticles can be used for targeted drug delivery, in particular for brain cancer therapy. However, this requires a detailed analysis of nanoparticles from the associated microvasculature to the tumor, not easy because of the required high spatial resolution. The objective of this study is to demonstrate an experimental solution of this problem, based in vivo and post-mortem whole organ imaging plus nanoscale 3-dimensional (3D) X-ray microscopy.

RESULTS:

The use of gold nanoparticles (AuNPs) as contrast agents paved the way to a detailed high-resolution three dimensional (3D) X-ray and fluorescence imaging analysis of the relation between xenografted glioma cells and the tumor-induced angiogenic microvasculature. The images of the angiogenic microvessels revealed nanoparticle leakage. Complementary tests showed that after endocytotic internalization fluorescent AuNPs allow the visible-light detection of cells.

CONCLUSIONS:

AuNP-loading of cells could be extended from the case presented here to other imaging techniques. In our study, they enabled us to (1) identify primary glioma cells at inoculation sites in mice brains; (2) follow the subsequent development of gliomas. (3) Detect the full details of the tumor-related microvasculature; (4) Finding leakage of AuNPs from the tumor-related vasculature, in contrast to no leakage from normal vasculature.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Neoplasias Encefálicas / Meios de Contraste / Nanopartículas Metálicas / Glioma / Ouro Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Neoplasias Encefálicas / Meios de Contraste / Nanopartículas Metálicas / Glioma / Ouro Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2015 Tipo de documento: Article