Double domain polyethylenimine-based nanoparticles for integrin receptor mediated delivery of plasmid DNA

Abstract The objective of the present study is to conjugate L-thyroxine PEI derivative onto another PEI to compensate the amine content of the whole structure which has been utilized for the ligand conjugation. Since αvβ3 integrin receptors are over-expressed on cancer cells and there is binding sit...

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Autores principales: Hossein Sadeghpour, Bahman Khalvati, Elaheh Entezar-Almahdi, Narjes Savadi, Samira Hossaini Alhashemi, Mohammad Raoufi, Ali Dehshahri
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Publicado: Nature Portfolio 2018
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Acceso en línea:https://doaj.org/article/69be0bdf915a4505a56c2e70a2ebd46a
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spelling oai:doaj.org-article:69be0bdf915a4505a56c2e70a2ebd46a2021-12-02T16:08:03ZDouble domain polyethylenimine-based nanoparticles for integrin receptor mediated delivery of plasmid DNA10.1038/s41598-018-25277-z2045-2322https://doaj.org/article/69be0bdf915a4505a56c2e70a2ebd46a2018-05-01T00:00:00Zhttps://doi.org/10.1038/s41598-018-25277-zhttps://doaj.org/toc/2045-2322Abstract The objective of the present study is to conjugate L-thyroxine PEI derivative onto another PEI to compensate the amine content of the whole structure which has been utilized for the ligand conjugation. Since αvβ3 integrin receptors are over-expressed on cancer cells and there is binding site for L-thyroxine on these receptors, PEI conjugation by L-thyroxine along with restoring the PEI amine content might be an efficient strategy for targeted delivery using polymeric nanoparticles. The results demonstrated the ability of the PEI conjugate in the formation of nanoparticles with the size of around 210 nm with higher buffering capacity. The conjugated PEI derivative increased the transfection efficiency in the cell lines over-expressing integrin by up to two folds higher than unmodified PEI, whereas in the cell lines lacking the integrin receptors there was no ligand conjugation-associated difference in gene transfer ability. The specificity of transfection demonstrated the delivery of plasmid DNA through integrin receptors. Also, the results of in vivo imaging of the polyplexes revealed that 99mTc-labeled PEI/plasmid DNA complexes accumulated in kidney and bladder 4 h post injection. Therefore, this PEI derivative could be considered as an efficient targeted delivery system for plasmid DNA.Hossein SadeghpourBahman KhalvatiElaheh Entezar-AlmahdiNarjes SavadiSamira Hossaini AlhashemiMohammad RaoufiAli DehshahriNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-12 (2018)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Hossein Sadeghpour
Bahman Khalvati
Elaheh Entezar-Almahdi
Narjes Savadi
Samira Hossaini Alhashemi
Mohammad Raoufi
Ali Dehshahri
Double domain polyethylenimine-based nanoparticles for integrin receptor mediated delivery of plasmid DNA
description Abstract The objective of the present study is to conjugate L-thyroxine PEI derivative onto another PEI to compensate the amine content of the whole structure which has been utilized for the ligand conjugation. Since αvβ3 integrin receptors are over-expressed on cancer cells and there is binding site for L-thyroxine on these receptors, PEI conjugation by L-thyroxine along with restoring the PEI amine content might be an efficient strategy for targeted delivery using polymeric nanoparticles. The results demonstrated the ability of the PEI conjugate in the formation of nanoparticles with the size of around 210 nm with higher buffering capacity. The conjugated PEI derivative increased the transfection efficiency in the cell lines over-expressing integrin by up to two folds higher than unmodified PEI, whereas in the cell lines lacking the integrin receptors there was no ligand conjugation-associated difference in gene transfer ability. The specificity of transfection demonstrated the delivery of plasmid DNA through integrin receptors. Also, the results of in vivo imaging of the polyplexes revealed that 99mTc-labeled PEI/plasmid DNA complexes accumulated in kidney and bladder 4 h post injection. Therefore, this PEI derivative could be considered as an efficient targeted delivery system for plasmid DNA.
format article
author Hossein Sadeghpour
Bahman Khalvati
Elaheh Entezar-Almahdi
Narjes Savadi
Samira Hossaini Alhashemi
Mohammad Raoufi
Ali Dehshahri
author_facet Hossein Sadeghpour
Bahman Khalvati
Elaheh Entezar-Almahdi
Narjes Savadi
Samira Hossaini Alhashemi
Mohammad Raoufi
Ali Dehshahri
author_sort Hossein Sadeghpour
title Double domain polyethylenimine-based nanoparticles for integrin receptor mediated delivery of plasmid DNA
title_short Double domain polyethylenimine-based nanoparticles for integrin receptor mediated delivery of plasmid DNA
title_full Double domain polyethylenimine-based nanoparticles for integrin receptor mediated delivery of plasmid DNA
title_fullStr Double domain polyethylenimine-based nanoparticles for integrin receptor mediated delivery of plasmid DNA
title_full_unstemmed Double domain polyethylenimine-based nanoparticles for integrin receptor mediated delivery of plasmid DNA
title_sort double domain polyethylenimine-based nanoparticles for integrin receptor mediated delivery of plasmid dna
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/69be0bdf915a4505a56c2e70a2ebd46a
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