| Literature DB >> 26886076 |
Menachem Motiei1, Tamar Dreifuss1, Oshra Betzer1, Hana Panet1, Aron Popovtzer2, Jordan Santana1, Galith Abourbeh3, Eyal Mishani3, Rachela Popovtzer1.
Abstract
One of the main limitations of the highly used cancer imaging technique, PET-CT, is its inability to distinguish between cancerous lesions and post treatment inflammatory conditions. The reason for this lack of specificity is that [(18)F]FDG-PET is based on increased glucose metabolic activity, which characterizes both cancerous tissues and inflammatory cells. To overcome this limitation, we developed a nanoparticle-based approach, utilizing glucose-functionalized gold nanoparticles (GF-GNPs) as a metabolically targeted CT contrast agent. Our approach demonstrates specific tumor targeting and has successfully distinguished between cancer and inflammatory processes in a combined tumor-inflammation mouse model, due to dissimilarities in angiogenesis occurring under different pathologic conditions. This study provides a set of capabilities in cancer detection, staging and follow-up, and can be applicable to a wide range of cancers that exhibit high metabolic activity.Entities:
Keywords: CT; FDG-PET; cancer; gold nanoparticles; metabolic-based imaging
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Year: 2016 PMID: 26886076 DOI: 10.1021/acsnano.5b07576
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881