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Chemical and Physical Characterisation of Human Serum Albumin Nanocolloids: Kinetics, Strength and Specificity of Bonds with (99m)Tc and (68)Ga

Nanoparticles of Human Serum Albumin (NC) labelled with (99m)Tc are widely used in Nuclear Medicine and represent the gold-standard for the intraoperative detection of the sentinel lymph node in many kinds of cancer, mainly breast cancer and melanoma. A significant amount of radionuclides can be inc...

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Autores principales: Marenco, Manuela, Canziani, Letizia, De Matteis, Gianluca, Cavenaghi, Giorgio, Aprile, Carlo, Lodola, Lorenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308145/
https://www.ncbi.nlm.nih.gov/pubmed/34361162
http://dx.doi.org/10.3390/nano11071776
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author Marenco, Manuela
Canziani, Letizia
De Matteis, Gianluca
Cavenaghi, Giorgio
Aprile, Carlo
Lodola, Lorenzo
author_facet Marenco, Manuela
Canziani, Letizia
De Matteis, Gianluca
Cavenaghi, Giorgio
Aprile, Carlo
Lodola, Lorenzo
author_sort Marenco, Manuela
collection PubMed
description Nanoparticles of Human Serum Albumin (NC) labelled with (99m)Tc are widely used in Nuclear Medicine and represent the gold-standard for the intraoperative detection of the sentinel lymph node in many kinds of cancer, mainly breast cancer and melanoma. A significant amount of radionuclides can be incorporated into the HSA particle, due to the multiple binding sites, and HSA-based nanocolloid catabolism is a fast and easy process that results in innocuous degradation products. NCs labelled with different isotopes represent an interesting radiopharmaceutical for extending diagnostic accuracy and surgical outcome, but the knowledge of the chemical bond between NCs and isotopes has not been fully elucidated, including information on its strength and specificity. The aim of this study is to investigate and compare the physicochemical characteristics of the bond between NCs and (99m)Tc and (68)Ga isotopes. Commercial kits of HSA-based nanocolloid particles (NanoAlbumon(®)) were used. For this purpose, we have primarily studied the kinetic orders of NC radiolabelling. Langmuir isotherms and pH effect on radiolabelling were tested and the stability of the radiometal complex was verified through competition reactions carried out in presence of different ligands. The future goal of our research is the development of inexpensive and instant kits, easily labelled with a wide spectrum of diagnostic and therapeutic isotopes, thus facilitating the availability of versatile and multipurpose radiopharmaceuticals.
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spelling pubmed-83081452021-07-25 Chemical and Physical Characterisation of Human Serum Albumin Nanocolloids: Kinetics, Strength and Specificity of Bonds with (99m)Tc and (68)Ga Marenco, Manuela Canziani, Letizia De Matteis, Gianluca Cavenaghi, Giorgio Aprile, Carlo Lodola, Lorenzo Nanomaterials (Basel) Article Nanoparticles of Human Serum Albumin (NC) labelled with (99m)Tc are widely used in Nuclear Medicine and represent the gold-standard for the intraoperative detection of the sentinel lymph node in many kinds of cancer, mainly breast cancer and melanoma. A significant amount of radionuclides can be incorporated into the HSA particle, due to the multiple binding sites, and HSA-based nanocolloid catabolism is a fast and easy process that results in innocuous degradation products. NCs labelled with different isotopes represent an interesting radiopharmaceutical for extending diagnostic accuracy and surgical outcome, but the knowledge of the chemical bond between NCs and isotopes has not been fully elucidated, including information on its strength and specificity. The aim of this study is to investigate and compare the physicochemical characteristics of the bond between NCs and (99m)Tc and (68)Ga isotopes. Commercial kits of HSA-based nanocolloid particles (NanoAlbumon(®)) were used. For this purpose, we have primarily studied the kinetic orders of NC radiolabelling. Langmuir isotherms and pH effect on radiolabelling were tested and the stability of the radiometal complex was verified through competition reactions carried out in presence of different ligands. The future goal of our research is the development of inexpensive and instant kits, easily labelled with a wide spectrum of diagnostic and therapeutic isotopes, thus facilitating the availability of versatile and multipurpose radiopharmaceuticals. MDPI 2021-07-08 /pmc/articles/PMC8308145/ /pubmed/34361162 http://dx.doi.org/10.3390/nano11071776 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Marenco, Manuela
Canziani, Letizia
De Matteis, Gianluca
Cavenaghi, Giorgio
Aprile, Carlo
Lodola, Lorenzo
Chemical and Physical Characterisation of Human Serum Albumin Nanocolloids: Kinetics, Strength and Specificity of Bonds with (99m)Tc and (68)Ga
title Chemical and Physical Characterisation of Human Serum Albumin Nanocolloids: Kinetics, Strength and Specificity of Bonds with (99m)Tc and (68)Ga
title_full Chemical and Physical Characterisation of Human Serum Albumin Nanocolloids: Kinetics, Strength and Specificity of Bonds with (99m)Tc and (68)Ga
title_fullStr Chemical and Physical Characterisation of Human Serum Albumin Nanocolloids: Kinetics, Strength and Specificity of Bonds with (99m)Tc and (68)Ga
title_full_unstemmed Chemical and Physical Characterisation of Human Serum Albumin Nanocolloids: Kinetics, Strength and Specificity of Bonds with (99m)Tc and (68)Ga
title_short Chemical and Physical Characterisation of Human Serum Albumin Nanocolloids: Kinetics, Strength and Specificity of Bonds with (99m)Tc and (68)Ga
title_sort chemical and physical characterisation of human serum albumin nanocolloids: kinetics, strength and specificity of bonds with (99m)tc and (68)ga
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308145/
https://www.ncbi.nlm.nih.gov/pubmed/34361162
http://dx.doi.org/10.3390/nano11071776
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