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Removal of Circulating Tumor Cells from Blood Samples of Cancer Patients Using Highly Magnetic Nanoparticles: A Translational Research Project
The count of circulating tumor cells (CTCs) has been associated with a worse prognosis in different types of cancer. Perioperatively, CTCs detach due to mechanical forces. Diagnostic tools exist to detect and isolate CTCs, but no therapeutic technique is currently available to remove CTCs in vivo fr...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315588/ https://www.ncbi.nlm.nih.gov/pubmed/35890293 http://dx.doi.org/10.3390/pharmaceutics14071397 |
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author | Doswald, Simon Herzog, Antoine F. Zeltner, Martin Zabel, Anja Pregernig, Andreas Schläpfer, Martin Siebenhüner, Alexander Stark, Wendelin J. Beck-Schimmer, Beatrice |
author_facet | Doswald, Simon Herzog, Antoine F. Zeltner, Martin Zabel, Anja Pregernig, Andreas Schläpfer, Martin Siebenhüner, Alexander Stark, Wendelin J. Beck-Schimmer, Beatrice |
author_sort | Doswald, Simon |
collection | PubMed |
description | The count of circulating tumor cells (CTCs) has been associated with a worse prognosis in different types of cancer. Perioperatively, CTCs detach due to mechanical forces. Diagnostic tools exist to detect and isolate CTCs, but no therapeutic technique is currently available to remove CTCs in vivo from unprocessed blood. The aim of this study was to design and test new magnetic nanoparticles to purify whole blood from CTCs. Novel magnetic carbon-coated cobalt (C/Co) nanoparticles conjugated with anti-epithelial cell adhesion molecule (EpCAM) antibodies were synthesized, and their antifouling and separation properties were determined. The newly developed C/Co nanoparticles showed excellent separation and antifouling properties. They efficiently removed tumor cells that were added to healthy subjects’ blood samples, through an anti-EpCAM antibody interaction. The nanoparticles did not interact with other blood components, such as lymphocytes or the coagulation system. In blood samples of carcinoma patients suffering from metastatic disease, on average, ≥68% of CTCs were removed. These nanoparticles could prompt the development of a blood purification technology, such as a dialysis-like device, to perioperatively remove CTCs from the blood of cancer patients in vivo and potentially improve their prognosis. |
format | Online Article Text |
id | pubmed-9315588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93155882022-07-27 Removal of Circulating Tumor Cells from Blood Samples of Cancer Patients Using Highly Magnetic Nanoparticles: A Translational Research Project Doswald, Simon Herzog, Antoine F. Zeltner, Martin Zabel, Anja Pregernig, Andreas Schläpfer, Martin Siebenhüner, Alexander Stark, Wendelin J. Beck-Schimmer, Beatrice Pharmaceutics Article The count of circulating tumor cells (CTCs) has been associated with a worse prognosis in different types of cancer. Perioperatively, CTCs detach due to mechanical forces. Diagnostic tools exist to detect and isolate CTCs, but no therapeutic technique is currently available to remove CTCs in vivo from unprocessed blood. The aim of this study was to design and test new magnetic nanoparticles to purify whole blood from CTCs. Novel magnetic carbon-coated cobalt (C/Co) nanoparticles conjugated with anti-epithelial cell adhesion molecule (EpCAM) antibodies were synthesized, and their antifouling and separation properties were determined. The newly developed C/Co nanoparticles showed excellent separation and antifouling properties. They efficiently removed tumor cells that were added to healthy subjects’ blood samples, through an anti-EpCAM antibody interaction. The nanoparticles did not interact with other blood components, such as lymphocytes or the coagulation system. In blood samples of carcinoma patients suffering from metastatic disease, on average, ≥68% of CTCs were removed. These nanoparticles could prompt the development of a blood purification technology, such as a dialysis-like device, to perioperatively remove CTCs from the blood of cancer patients in vivo and potentially improve their prognosis. MDPI 2022-07-01 /pmc/articles/PMC9315588/ /pubmed/35890293 http://dx.doi.org/10.3390/pharmaceutics14071397 Text en © 2022 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 Doswald, Simon Herzog, Antoine F. Zeltner, Martin Zabel, Anja Pregernig, Andreas Schläpfer, Martin Siebenhüner, Alexander Stark, Wendelin J. Beck-Schimmer, Beatrice Removal of Circulating Tumor Cells from Blood Samples of Cancer Patients Using Highly Magnetic Nanoparticles: A Translational Research Project |
title | Removal of Circulating Tumor Cells from Blood Samples of Cancer Patients Using Highly Magnetic Nanoparticles: A Translational Research Project |
title_full | Removal of Circulating Tumor Cells from Blood Samples of Cancer Patients Using Highly Magnetic Nanoparticles: A Translational Research Project |
title_fullStr | Removal of Circulating Tumor Cells from Blood Samples of Cancer Patients Using Highly Magnetic Nanoparticles: A Translational Research Project |
title_full_unstemmed | Removal of Circulating Tumor Cells from Blood Samples of Cancer Patients Using Highly Magnetic Nanoparticles: A Translational Research Project |
title_short | Removal of Circulating Tumor Cells from Blood Samples of Cancer Patients Using Highly Magnetic Nanoparticles: A Translational Research Project |
title_sort | removal of circulating tumor cells from blood samples of cancer patients using highly magnetic nanoparticles: a translational research project |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315588/ https://www.ncbi.nlm.nih.gov/pubmed/35890293 http://dx.doi.org/10.3390/pharmaceutics14071397 |
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