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Human Dose Assessment of (68)Ga-NODAGA-RGD-BBN Heterodimer Peptide based on Animal Data
AIMS: Calculation of the absorbed dose in human organs is one of the first steps for developing new radiopharmaceuticals. The aim of this study is to estimate the human absorbed dose of a newly developed (68)Ga-NODAGA-RGD-BBN radiolabeled compound. MATERIALS AND METHODS: (68)Ga-NODAGA-RGD-BBN was pr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847008/ https://www.ncbi.nlm.nih.gov/pubmed/36684706 http://dx.doi.org/10.4103/jmp.jmp_34_22 |
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author | Amraee, Naeimeh Alirezapour, Behrouz Hosntalab, Mohammad Yousefnia, Hassan |
author_facet | Amraee, Naeimeh Alirezapour, Behrouz Hosntalab, Mohammad Yousefnia, Hassan |
author_sort | Amraee, Naeimeh |
collection | PubMed |
description | AIMS: Calculation of the absorbed dose in human organs is one of the first steps for developing new radiopharmaceuticals. The aim of this study is to estimate the human absorbed dose of a newly developed (68)Ga-NODAGA-RGD-BBN radiolabeled compound. MATERIALS AND METHODS: (68)Ga-NODAGA-RGD-BBN was prepared by varying different parameters at optimized conditions. The stability of the radiolabeled peptide in phosphate-buffered saline (PBS) and in human serum was evaluated for 120 min. Afterward, the biodistribution of the complex was assessed in normal and tumor-bearing mice, at least for 120 min postinjection. Finally, the human absorbed dose of (68)Ga-NODAGA-RGD-BBN was estimated based on mice data using Radiation Dose Assessment Resource and Spark method. RESULTS: (68)Ga-NODAGA-RGD-BBN was produced with radiochemical purity of more than 98% (high-performance liquid chromatography/ radio thin layer chromatography (RTLC)) with high stability in PBS buffer and in human serum at least for 2 h. The complex demonstrated high uptake in gastrin-releasing peptide receptor-expressing tumors compared to other nontarget organs. Furthermore, the dose assessment for the complex showed that the kidneys receive the highest absorbed dose in comparison with other organs. CONCLUSION: The result of this study showed that 68Ga-NODAGA-RGD-BBN is an effective and radiolabeled ligand for tumor detection, however more studies are still needed. |
format | Online Article Text |
id | pubmed-9847008 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-98470082023-01-19 Human Dose Assessment of (68)Ga-NODAGA-RGD-BBN Heterodimer Peptide based on Animal Data Amraee, Naeimeh Alirezapour, Behrouz Hosntalab, Mohammad Yousefnia, Hassan J Med Phys Original Article AIMS: Calculation of the absorbed dose in human organs is one of the first steps for developing new radiopharmaceuticals. The aim of this study is to estimate the human absorbed dose of a newly developed (68)Ga-NODAGA-RGD-BBN radiolabeled compound. MATERIALS AND METHODS: (68)Ga-NODAGA-RGD-BBN was prepared by varying different parameters at optimized conditions. The stability of the radiolabeled peptide in phosphate-buffered saline (PBS) and in human serum was evaluated for 120 min. Afterward, the biodistribution of the complex was assessed in normal and tumor-bearing mice, at least for 120 min postinjection. Finally, the human absorbed dose of (68)Ga-NODAGA-RGD-BBN was estimated based on mice data using Radiation Dose Assessment Resource and Spark method. RESULTS: (68)Ga-NODAGA-RGD-BBN was produced with radiochemical purity of more than 98% (high-performance liquid chromatography/ radio thin layer chromatography (RTLC)) with high stability in PBS buffer and in human serum at least for 2 h. The complex demonstrated high uptake in gastrin-releasing peptide receptor-expressing tumors compared to other nontarget organs. Furthermore, the dose assessment for the complex showed that the kidneys receive the highest absorbed dose in comparison with other organs. CONCLUSION: The result of this study showed that 68Ga-NODAGA-RGD-BBN is an effective and radiolabeled ligand for tumor detection, however more studies are still needed. Wolters Kluwer - Medknow 2022 2022-11-08 /pmc/articles/PMC9847008/ /pubmed/36684706 http://dx.doi.org/10.4103/jmp.jmp_34_22 Text en Copyright: © 2022 Journal of Medical Physics https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Amraee, Naeimeh Alirezapour, Behrouz Hosntalab, Mohammad Yousefnia, Hassan Human Dose Assessment of (68)Ga-NODAGA-RGD-BBN Heterodimer Peptide based on Animal Data |
title | Human Dose Assessment of (68)Ga-NODAGA-RGD-BBN Heterodimer Peptide based on Animal Data |
title_full | Human Dose Assessment of (68)Ga-NODAGA-RGD-BBN Heterodimer Peptide based on Animal Data |
title_fullStr | Human Dose Assessment of (68)Ga-NODAGA-RGD-BBN Heterodimer Peptide based on Animal Data |
title_full_unstemmed | Human Dose Assessment of (68)Ga-NODAGA-RGD-BBN Heterodimer Peptide based on Animal Data |
title_short | Human Dose Assessment of (68)Ga-NODAGA-RGD-BBN Heterodimer Peptide based on Animal Data |
title_sort | human dose assessment of (68)ga-nodaga-rgd-bbn heterodimer peptide based on animal data |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9847008/ https://www.ncbi.nlm.nih.gov/pubmed/36684706 http://dx.doi.org/10.4103/jmp.jmp_34_22 |
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