Technetium-99m chelator-free radiolabeling of specific glutamine tumor imaging nanoprobe: in vitro and in vivo evaluations

Nowadays, molecular imaging radiopharmaceuticals', nanoparticles', and/or small-molecule biomarkers' applications are increasing rapidly worldwide. Thus, researchers focus on providing the novel, safe, and cost-effective ones. In the present experiment, technetium-99m ( Tc)-labeled PE...

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Published in:International journal of nanomedicine Vol. 13; pp. 4671 - 4683
Main Authors: Ghoreishi, Seyedeh Masoumeh, Khalaj, Ali, Sabzevari, Omid, Badrzadeh, Leila, Mohammadzadeh, Pardis, Mousavi Motlagh, Seyed Shahaboddin, Bitarafan-Rajabi, Ahmad, Shafiee Ardestani, Mehdi
Format: Journal Article
Language:English
Published: New Zealand Dove Medical Press Limited 01-01-2018
Taylor & Francis Ltd
Dove Medical Press
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Summary:Nowadays, molecular imaging radiopharmaceuticals', nanoparticles', and/or small-molecule biomarkers' applications are increasing rapidly worldwide. Thus, researchers focus on providing the novel, safe, and cost-effective ones. In the present experiment, technetium-99m ( Tc)-labeled PEG-citrate dendrimer-G conjugated with glutamine (nanoconjugate) was designed and assessed as a novel tumor imaging probe both in vitro and in vivo. Nanoconjugate was synthesized and the synthesis was confirmed by Fourier transform infrared, proton nuclear magnetic resonance, liquid chromatography-mass spectrometry, dynamic light scattering, and static light scattering techniques. The toxicity was assessed by XTT and apoptosis and necrosis methods. Radiochemical purity indicates that the anionic dendrimer has a very high potential to complex formation with Tc and is also very stable in the human serum in different times. Results from the imaging procedures showed potential ability of nanoconjugates to detect tumor site. Suitable features of the anionic dendrimer show that it is a promising agent to improve nanoradiopharmaceuticals.
ISSN:1178-2013
1176-9114
1178-2013
DOI:10.2147/IJN.S157426