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Effective gene delivery using size dependant nano core-shell in human cervical cancer cell lines by magnetofection
Biocompatible magnetic nanoparticles are effective for gene delivery in vitro and in vivo transfection. These mediators are mainly used to deliver drugs and genes. It can also be used as probes to diagnose and treat various diseases. Magnetic nanoparticles, primarily iron oxide nanoparticles, are us...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484435/ https://www.ncbi.nlm.nih.gov/pubmed/37676882 http://dx.doi.org/10.1371/journal.pone.0289731 |
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author | Sundara Rajan R., Srinivasa Thomas, Jobin Francis, Dileep Daniel, Elcey C. |
author_facet | Sundara Rajan R., Srinivasa Thomas, Jobin Francis, Dileep Daniel, Elcey C. |
author_sort | Sundara Rajan R., Srinivasa |
collection | PubMed |
description | Biocompatible magnetic nanoparticles are effective for gene delivery in vitro and in vivo transfection. These mediators are mainly used to deliver drugs and genes. It can also be used as probes to diagnose and treat various diseases. Magnetic nanoparticles, primarily iron oxide nanoparticles, are used in various biological applications. However, preparing stable and small-size biocompatible core-shell is crucial in site direct gene delivery. In the present study, superparamagnetic iron oxide nanoparticles were synthesized using the chemical co-precipitation method and were functionalized with starch to attain stable particles. These SPIONs were coated with polyethylenimine to give a net positive charge. The fluorescent plasmid DNA bound to the SPIONs were used as a core shell for gene delivery into the HeLa cells via magnetofection. UV-Visible Spectrophotometry analysis showed a peak at 200 nm, which confirms the presence of FeO nanoparticles. The Scanning Electron Microscopy images revealed the formation of spherical-shaped nanoparticles with an average size of 10 nm. X-ray Diffraction also confirmed FeO as a significant constituent element. Vibrating Sample Magnetometry ensures that the nanoparticles are superparamagnetic. Atomic Force Microscopy images show the DNA bound on the surface of the nanoparticles. The gene delivery and transfection efficiency were analyzed by flow cytometry. These nanoparticles could effectively compact the pDNA, allowing efficient gene transfer into the HeLa cell lines. |
format | Online Article Text |
id | pubmed-10484435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-104844352023-09-08 Effective gene delivery using size dependant nano core-shell in human cervical cancer cell lines by magnetofection Sundara Rajan R., Srinivasa Thomas, Jobin Francis, Dileep Daniel, Elcey C. PLoS One Research Article Biocompatible magnetic nanoparticles are effective for gene delivery in vitro and in vivo transfection. These mediators are mainly used to deliver drugs and genes. It can also be used as probes to diagnose and treat various diseases. Magnetic nanoparticles, primarily iron oxide nanoparticles, are used in various biological applications. However, preparing stable and small-size biocompatible core-shell is crucial in site direct gene delivery. In the present study, superparamagnetic iron oxide nanoparticles were synthesized using the chemical co-precipitation method and were functionalized with starch to attain stable particles. These SPIONs were coated with polyethylenimine to give a net positive charge. The fluorescent plasmid DNA bound to the SPIONs were used as a core shell for gene delivery into the HeLa cells via magnetofection. UV-Visible Spectrophotometry analysis showed a peak at 200 nm, which confirms the presence of FeO nanoparticles. The Scanning Electron Microscopy images revealed the formation of spherical-shaped nanoparticles with an average size of 10 nm. X-ray Diffraction also confirmed FeO as a significant constituent element. Vibrating Sample Magnetometry ensures that the nanoparticles are superparamagnetic. Atomic Force Microscopy images show the DNA bound on the surface of the nanoparticles. The gene delivery and transfection efficiency were analyzed by flow cytometry. These nanoparticles could effectively compact the pDNA, allowing efficient gene transfer into the HeLa cell lines. Public Library of Science 2023-09-07 /pmc/articles/PMC10484435/ /pubmed/37676882 http://dx.doi.org/10.1371/journal.pone.0289731 Text en © 2023 Sundara Rajan R. et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Sundara Rajan R., Srinivasa Thomas, Jobin Francis, Dileep Daniel, Elcey C. Effective gene delivery using size dependant nano core-shell in human cervical cancer cell lines by magnetofection |
title | Effective gene delivery using size dependant nano core-shell in human cervical cancer cell lines by magnetofection |
title_full | Effective gene delivery using size dependant nano core-shell in human cervical cancer cell lines by magnetofection |
title_fullStr | Effective gene delivery using size dependant nano core-shell in human cervical cancer cell lines by magnetofection |
title_full_unstemmed | Effective gene delivery using size dependant nano core-shell in human cervical cancer cell lines by magnetofection |
title_short | Effective gene delivery using size dependant nano core-shell in human cervical cancer cell lines by magnetofection |
title_sort | effective gene delivery using size dependant nano core-shell in human cervical cancer cell lines by magnetofection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484435/ https://www.ncbi.nlm.nih.gov/pubmed/37676882 http://dx.doi.org/10.1371/journal.pone.0289731 |
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