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The Potential of Helianthin Loaded Into Magnetic Nanoparticles to Induce Cytotoxicity in Glioblastoma Cells
The central nervous system tumors are the most common solid tumors in adults.. Unlike other types of cancers, brain cancer is much difficult to treat because of the blood-brain barrier (BBB) that prevents drug substances from crossing it and accessing the brain. Different types of methods to overcom...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medical University Publishing House Craiova
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8679159/ https://www.ncbi.nlm.nih.gov/pubmed/35003774 http://dx.doi.org/10.12865/CHSJ.47.03.12 |
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author | COSTACHI, ALEXANDRA CIOC, CĂTĂLINA ELENA BUTEICĂ, SANDRA ALICE TACHE, DANIELA ELISE ARTENE, ŞTEFAN-ALEXANDRU SEVASTRE, ANI-SIMONA ALEXANDRU, OANA TĂTĂRANU, LIGIA GABRIELA POPESCU, ŞTEFANA OANA DRICU, ANICA |
author_facet | COSTACHI, ALEXANDRA CIOC, CĂTĂLINA ELENA BUTEICĂ, SANDRA ALICE TACHE, DANIELA ELISE ARTENE, ŞTEFAN-ALEXANDRU SEVASTRE, ANI-SIMONA ALEXANDRU, OANA TĂTĂRANU, LIGIA GABRIELA POPESCU, ŞTEFANA OANA DRICU, ANICA |
author_sort | COSTACHI, ALEXANDRA |
collection | PubMed |
description | The central nervous system tumors are the most common solid tumors in adults.. Unlike other types of cancers, brain cancer is much difficult to treat because of the blood-brain barrier (BBB) that prevents drug substances from crossing it and accessing the brain. Different types of methods to overcome BBB have been used in vivo and in vitro, of which the use of nanoparticle-mediated delivery of therapeutic drugs is particularly promising. In the present study, we used iron oxide magnetic nanoparticles (NPs) as carrier system for helianthin (He/NPs) to treat cancer cells derived from glioblastoma. An early passage cell cultures (GB1B), established in our laboratory from tissue obtained from a patient diagnosed with glioblastoma, was used. The cells were treated with different concentrations of NPs or HeNPs and then cell proliferation was measured at 24, 48 and 72 hours. Our results showed that the treatment with NPs was well tolerated by glioblastoma cells, the viability of the cells increased very slightly after the treatment. Furthermore, we demonstrated that helianthin loaded Fe3O4 magnetic nanoparticles induced cytotoxicity in human glioblastoma cells. The treatment with HeNPs induced dose and time dependent. |
format | Online Article Text |
id | pubmed-8679159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Medical University Publishing House Craiova |
record_format | MEDLINE/PubMed |
spelling | pubmed-86791592022-01-06 The Potential of Helianthin Loaded Into Magnetic Nanoparticles to Induce Cytotoxicity in Glioblastoma Cells COSTACHI, ALEXANDRA CIOC, CĂTĂLINA ELENA BUTEICĂ, SANDRA ALICE TACHE, DANIELA ELISE ARTENE, ŞTEFAN-ALEXANDRU SEVASTRE, ANI-SIMONA ALEXANDRU, OANA TĂTĂRANU, LIGIA GABRIELA POPESCU, ŞTEFANA OANA DRICU, ANICA Curr Health Sci J Original Paper The central nervous system tumors are the most common solid tumors in adults.. Unlike other types of cancers, brain cancer is much difficult to treat because of the blood-brain barrier (BBB) that prevents drug substances from crossing it and accessing the brain. Different types of methods to overcome BBB have been used in vivo and in vitro, of which the use of nanoparticle-mediated delivery of therapeutic drugs is particularly promising. In the present study, we used iron oxide magnetic nanoparticles (NPs) as carrier system for helianthin (He/NPs) to treat cancer cells derived from glioblastoma. An early passage cell cultures (GB1B), established in our laboratory from tissue obtained from a patient diagnosed with glioblastoma, was used. The cells were treated with different concentrations of NPs or HeNPs and then cell proliferation was measured at 24, 48 and 72 hours. Our results showed that the treatment with NPs was well tolerated by glioblastoma cells, the viability of the cells increased very slightly after the treatment. Furthermore, we demonstrated that helianthin loaded Fe3O4 magnetic nanoparticles induced cytotoxicity in human glioblastoma cells. The treatment with HeNPs induced dose and time dependent. Medical University Publishing House Craiova 2021 2021-09-30 /pmc/articles/PMC8679159/ /pubmed/35003774 http://dx.doi.org/10.12865/CHSJ.47.03.12 Text en Copyright © 2014, Medical University Publishing House Craiova https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Public License, which permits unrestricted use, adaptation, distribution and reproduction in any medium, non-commercially, provided the new creations are licensed under identical terms as the original work and the original work is properly cited. |
spellingShingle | Original Paper COSTACHI, ALEXANDRA CIOC, CĂTĂLINA ELENA BUTEICĂ, SANDRA ALICE TACHE, DANIELA ELISE ARTENE, ŞTEFAN-ALEXANDRU SEVASTRE, ANI-SIMONA ALEXANDRU, OANA TĂTĂRANU, LIGIA GABRIELA POPESCU, ŞTEFANA OANA DRICU, ANICA The Potential of Helianthin Loaded Into Magnetic Nanoparticles to Induce Cytotoxicity in Glioblastoma Cells |
title | The Potential of Helianthin Loaded Into Magnetic Nanoparticles to Induce Cytotoxicity in Glioblastoma Cells |
title_full | The Potential of Helianthin Loaded Into Magnetic Nanoparticles to Induce Cytotoxicity in Glioblastoma Cells |
title_fullStr | The Potential of Helianthin Loaded Into Magnetic Nanoparticles to Induce Cytotoxicity in Glioblastoma Cells |
title_full_unstemmed | The Potential of Helianthin Loaded Into Magnetic Nanoparticles to Induce Cytotoxicity in Glioblastoma Cells |
title_short | The Potential of Helianthin Loaded Into Magnetic Nanoparticles to Induce Cytotoxicity in Glioblastoma Cells |
title_sort | potential of helianthin loaded into magnetic nanoparticles to induce cytotoxicity in glioblastoma cells |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8679159/ https://www.ncbi.nlm.nih.gov/pubmed/35003774 http://dx.doi.org/10.12865/CHSJ.47.03.12 |
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