Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Bivas-Benita, Maytal, Romeijn, Stefan, Junginger, Hans E., Borchard, Gerrit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2004
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
_version_ 1783516340316798976
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
work_keys_str_mv AT bivasbenitamaytal plgapeinanoparticlesforgenedeliverytopulmonaryepithelium
AT romeijnstefan plgapeinanoparticlesforgenedeliverytopulmonaryepithelium
AT jungingerhanse plgapeinanoparticlesforgenedeliverytopulmonaryepithelium
AT borchardgerrit plgapeinanoparticlesforgenedeliverytopulmonaryepithelium