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PLGA–PEI nanoparticles for gene delivery to pulmonary epithelium
Pulmonary gene delivery is thought to play an important role in treating genetically related diseases and may induce immunity towards pathogens entering the body via the airways. In this study we prepared poly (d,l-lactide-co-glycolide) (PLGA) nanoparticles bearing polyethyleneimine (PEI) on their s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127346/ https://www.ncbi.nlm.nih.gov/pubmed/15207531 http://dx.doi.org/10.1016/j.ejpb.2004.03.008 |
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author | Bivas-Benita, Maytal Romeijn, Stefan Junginger, Hans E. Borchard, Gerrit |
author_facet | Bivas-Benita, Maytal Romeijn, Stefan Junginger, Hans E. Borchard, Gerrit |
author_sort | Bivas-Benita, Maytal |
collection | PubMed |
description | Pulmonary gene delivery is thought to play an important role in treating genetically related diseases and may induce immunity towards pathogens entering the body via the airways. In this study we prepared poly (d,l-lactide-co-glycolide) (PLGA) nanoparticles bearing polyethyleneimine (PEI) on their surface and characterized them for their potential in serving as non-viral gene carriers to the pulmonary epithelium. Particles that were synthesized at different PLGA–PEI ratios and loaded with DNA in several PEI–DNA ratios, exhibited narrow size distribution in all formulations, with mean particle sizes ranging between 207 and 231 nm. Zeta potential was strongly positive (above 30 mV) for all the PEI–DNA ratios examined and the loading efficiency exceeded 99% for all formulations. Internalization of the DNA-loaded PLGA–PEI nanoparticles was studied in the human airway submucosal epithelial cell line, Calu-3, and DNA was detected in the endo-lysosomal compartment 6 h after particles were applied. Cytotoxicity of these nanoparticles was dependent on the PEI–DNA ratio and best cell viability was achieved by PEI–DNA ratios 1:1 and 0.5:1. These findings demonstrate that PLGA–PEI nanoparticles are a potential new delivery system to carry genes to the lung epithelium. |
format | Online Article Text |
id | pubmed-7127346 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71273462020-04-08 PLGA–PEI nanoparticles for gene delivery to pulmonary epithelium Bivas-Benita, Maytal Romeijn, Stefan Junginger, Hans E. Borchard, Gerrit Eur J Pharm Biopharm Article Pulmonary gene delivery is thought to play an important role in treating genetically related diseases and may induce immunity towards pathogens entering the body via the airways. In this study we prepared poly (d,l-lactide-co-glycolide) (PLGA) nanoparticles bearing polyethyleneimine (PEI) on their surface and characterized them for their potential in serving as non-viral gene carriers to the pulmonary epithelium. Particles that were synthesized at different PLGA–PEI ratios and loaded with DNA in several PEI–DNA ratios, exhibited narrow size distribution in all formulations, with mean particle sizes ranging between 207 and 231 nm. Zeta potential was strongly positive (above 30 mV) for all the PEI–DNA ratios examined and the loading efficiency exceeded 99% for all formulations. Internalization of the DNA-loaded PLGA–PEI nanoparticles was studied in the human airway submucosal epithelial cell line, Calu-3, and DNA was detected in the endo-lysosomal compartment 6 h after particles were applied. Cytotoxicity of these nanoparticles was dependent on the PEI–DNA ratio and best cell viability was achieved by PEI–DNA ratios 1:1 and 0.5:1. These findings demonstrate that PLGA–PEI nanoparticles are a potential new delivery system to carry genes to the lung epithelium. Elsevier B.V. 2004-07 2004-04-30 /pmc/articles/PMC7127346/ /pubmed/15207531 http://dx.doi.org/10.1016/j.ejpb.2004.03.008 Text en Copyright © 2004 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Bivas-Benita, Maytal Romeijn, Stefan Junginger, Hans E. Borchard, Gerrit PLGA–PEI nanoparticles for gene delivery to pulmonary epithelium |
title | PLGA–PEI nanoparticles for gene delivery to pulmonary epithelium |
title_full | PLGA–PEI nanoparticles for gene delivery to pulmonary epithelium |
title_fullStr | PLGA–PEI nanoparticles for gene delivery to pulmonary epithelium |
title_full_unstemmed | PLGA–PEI nanoparticles for gene delivery to pulmonary epithelium |
title_short | PLGA–PEI nanoparticles for gene delivery to pulmonary epithelium |
title_sort | plga–pei nanoparticles for gene delivery to pulmonary epithelium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127346/ https://www.ncbi.nlm.nih.gov/pubmed/15207531 http://dx.doi.org/10.1016/j.ejpb.2004.03.008 |
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