| Literature DB >> 25921808 |
Andrea Bianchi1, Damien Moncelet1, François Lux2, Marie Plissonneau2,3, Silvia Rizzitelli1, Emeline Julie Ribot1, Nawal Tassali1, Véronique Bouchaud1, Olivier Tillement2, Pierre Voisin1, Yannick Crémillieux1.
Abstract
The development of new non-invasive diagnostic and therapeutic approaches is of paramount importance in order to improve the outcome of patients with glioblastoma (GBM). In this work we investigated a completely non-invasive pre-clinical protocol to effectively target and detect brain tumors through the orotracheal route, using ultra-small nanoparticles (USRPs) and MRI. A mouse model of GBM was developed. In vivo MRI acquisitions were performed before and after intravenous or orotracheal administration of the nanoparticles to identify and segment the tumor. The accumulation of the nanoparticles in neoplastic lesions was assessed ex vivo through fluorescence microscopy. Before the administration of contrast agents, MR images allowed the identification of the presence of abnormal brain tissue in 73% of animals. After orotracheal or intravenous administration of USRPs, in all the mice an excellent co-localization of the position of the tumor with MRI and histology was observed. The elimination time of the USRPs from the tumor after the orotracheal administration was approximately 70% longer compared with intravenous injection. MRI and USRPs were shown to be powerful imaging tools able to detect, quantify and longitudinally monitor the development of GBMs. The absence of ionizing radiation and high resolution of MRI, along with the complete non-invasiveness and good reproducibility of the proposed protocol, make this technique potentially translatable to humans. To our knowledge, this is the first time that the advantages of a needle-free orotracheal administration route have been demonstrated for the investigation of the pathomorphological changes due to GBMs.Entities:
Keywords: MRI; contrast agents; fluorescence imaging; glioblastoma; lungs; orotracheal administration
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Year: 2015 PMID: 25921808 DOI: 10.1002/nbm.3295
Source DB: PubMed Journal: NMR Biomed ISSN: 0952-3480 Impact factor: 4.044