18 F‐FDG MicroPET and MRI Targeting Breast Cancer Mouse Model with Designed Synthesis Nanoparticles

The first aim of this study was the development of real‐time, quantitative, and noninvasive visual observation that necessitates different noninvasive multimodal imaging methods. Second, the design of a high‐sensitivity imaging free‐ligand green chemistry nanoprobe is a critical diagnosis of breast...

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Veröffentlicht in:Journal of nanomaterials 2022-01, Vol.2022 (1)
Hauptverfasser: Rezaei Aghdam, Hakimeh, Bitarafan Rajabi, Ahmad, Sadat Ebrahimi, Seyed Esmaeil, Beiki, Davood, Abdi, Khosrou, Mousavi Motlagh, Seyed Shahaboddin, Kiani Dehkordi, Banafsheh, Darbandi Azar, Amir, Shafiee Ardestani, Mehdi
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container_title Journal of nanomaterials
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creator Rezaei Aghdam, Hakimeh
Bitarafan Rajabi, Ahmad
Sadat Ebrahimi, Seyed Esmaeil
Beiki, Davood
Abdi, Khosrou
Mousavi Motlagh, Seyed Shahaboddin
Kiani Dehkordi, Banafsheh
Darbandi Azar, Amir
Shafiee Ardestani, Mehdi
description The first aim of this study was the development of real‐time, quantitative, and noninvasive visual observation that necessitates different noninvasive multimodal imaging methods. Second, the design of a high‐sensitivity imaging free‐ligand green chemistry nanoprobe is a critical diagnosis of breast cancer mouse models. The gadolinium‐based nanoparticles as box‐Behnken design (BBD) experiment are synthesized. A small biomolecule L‐glutamine is attached to its surface nanoparticles as a template. Large surface‐area‐to‐volume ratios of nanoparticles enhance the capacity for interactions with biomolecules and present more sites for conjugation. G. 2‐Deoxy‐2[ 18 F]fluoro‐D‐glucose ([ 18 F]F‐FDG) is a quantitative and sensitive tracking instrument in Positron Emission Tomography (PET), also applicable for the in vivo and in vitro characterization of L‐glutamine SiGdNPs. Optical imaging was done for 4T1 breast cancer tumor‐induced mice. 18 F‐NP uptake values were significantly higher in primary breast cancer and brain tumors than [ 18 F]F‐FDG in PET at 30 min, injected (20 μ l/g) via the tail vein with about 300 μ Ci of 18 F‐FDG loading. After 15 min of the administration of injection (26 μ l/g), the first passed the lung intravenously without any injury to the lung showing promising T1‐T2 MRI contrast properties. We receive these by application of a variety of imaging modalities, especially microPET and MRI.
doi_str_mv 10.1155/2022/5737835
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title 18 F‐FDG MicroPET and MRI Targeting Breast Cancer Mouse Model with Designed Synthesis Nanoparticles
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