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Lipid peptide nanocomplexes for gene delivery and magnetic resonance imaging in the brain

Gadolinium-labelled nanocomplexes offer prospects for the development of real-time, non-invasive imaging strategies to visualise the location of gene delivery by MRI. In this study, targeted nanoparticle formulations were prepared comprising a cationic liposome (L) containing a Gd-chelated lipid at...

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Autores principales: Writer, Michele J., Kyrtatos, Panagiotis G., Bienemann, Alison S., Pugh, John A., Lowe, Andrew S., Villegas-Llerena, Claudio, Kenny, Gavin D., White, Edward A., Gill, Steven S., McLeod, Cameron W., Lythgoe, Mark F., Hart, Stephen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Publishers 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657147/
https://www.ncbi.nlm.nih.gov/pubmed/22800579
http://dx.doi.org/10.1016/j.jconrel.2012.07.002
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author Writer, Michele J.
Kyrtatos, Panagiotis G.
Bienemann, Alison S.
Pugh, John A.
Lowe, Andrew S.
Villegas-Llerena, Claudio
Kenny, Gavin D.
White, Edward A.
Gill, Steven S.
McLeod, Cameron W.
Lythgoe, Mark F.
Hart, Stephen L.
author_facet Writer, Michele J.
Kyrtatos, Panagiotis G.
Bienemann, Alison S.
Pugh, John A.
Lowe, Andrew S.
Villegas-Llerena, Claudio
Kenny, Gavin D.
White, Edward A.
Gill, Steven S.
McLeod, Cameron W.
Lythgoe, Mark F.
Hart, Stephen L.
author_sort Writer, Michele J.
collection PubMed
description Gadolinium-labelled nanocomplexes offer prospects for the development of real-time, non-invasive imaging strategies to visualise the location of gene delivery by MRI. In this study, targeted nanoparticle formulations were prepared comprising a cationic liposome (L) containing a Gd-chelated lipid at 10, 15 and 20% by weight of total lipid, a receptor-targeted, DNA-binding peptide (P) and plasmid DNA (D), which electrostatically self-assembled into LPD nanocomplexes. The LPD formulation containing the liposome with 15% Gd-chelated lipid displayed optimal peptide-targeted, transfection efficiency. MRI conspicuity peaked at 4 h after incubation of the nanocomplexes with cells, suggesting enhancement by cellular uptake and trafficking. This was supported by time course confocal microscopy analysis of transfections with fluorescently-labelled LPD nanocomplexes. Gd-LPD nanocomplexes delivered to rat brains by convection-enhanced delivery were visible by MRI at 6 h, 24 h and 48 h after administration. Histological brain sections analysed by laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) confirmed that the MRI signal was associated with the distribution of Gd(3 +) moieties and differentiated MRI signals due to haemorrhage. The transfected brain cells near the injection site appeared to be mostly microglial. This study shows the potential of Gd-LPD nanocomplexes for simultaneous delivery of contrast agents and genes for real-time monitoring of gene therapy in the brain.
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spelling pubmed-36571472013-05-18 Lipid peptide nanocomplexes for gene delivery and magnetic resonance imaging in the brain Writer, Michele J. Kyrtatos, Panagiotis G. Bienemann, Alison S. Pugh, John A. Lowe, Andrew S. Villegas-Llerena, Claudio Kenny, Gavin D. White, Edward A. Gill, Steven S. McLeod, Cameron W. Lythgoe, Mark F. Hart, Stephen L. J Control Release Article Gadolinium-labelled nanocomplexes offer prospects for the development of real-time, non-invasive imaging strategies to visualise the location of gene delivery by MRI. In this study, targeted nanoparticle formulations were prepared comprising a cationic liposome (L) containing a Gd-chelated lipid at 10, 15 and 20% by weight of total lipid, a receptor-targeted, DNA-binding peptide (P) and plasmid DNA (D), which electrostatically self-assembled into LPD nanocomplexes. The LPD formulation containing the liposome with 15% Gd-chelated lipid displayed optimal peptide-targeted, transfection efficiency. MRI conspicuity peaked at 4 h after incubation of the nanocomplexes with cells, suggesting enhancement by cellular uptake and trafficking. This was supported by time course confocal microscopy analysis of transfections with fluorescently-labelled LPD nanocomplexes. Gd-LPD nanocomplexes delivered to rat brains by convection-enhanced delivery were visible by MRI at 6 h, 24 h and 48 h after administration. Histological brain sections analysed by laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) confirmed that the MRI signal was associated with the distribution of Gd(3 +) moieties and differentiated MRI signals due to haemorrhage. The transfected brain cells near the injection site appeared to be mostly microglial. This study shows the potential of Gd-LPD nanocomplexes for simultaneous delivery of contrast agents and genes for real-time monitoring of gene therapy in the brain. Elsevier Science Publishers 2012-09-10 /pmc/articles/PMC3657147/ /pubmed/22800579 http://dx.doi.org/10.1016/j.jconrel.2012.07.002 Text en © 2012 Elsevier B.V. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Writer, Michele J.
Kyrtatos, Panagiotis G.
Bienemann, Alison S.
Pugh, John A.
Lowe, Andrew S.
Villegas-Llerena, Claudio
Kenny, Gavin D.
White, Edward A.
Gill, Steven S.
McLeod, Cameron W.
Lythgoe, Mark F.
Hart, Stephen L.
Lipid peptide nanocomplexes for gene delivery and magnetic resonance imaging in the brain
title Lipid peptide nanocomplexes for gene delivery and magnetic resonance imaging in the brain
title_full Lipid peptide nanocomplexes for gene delivery and magnetic resonance imaging in the brain
title_fullStr Lipid peptide nanocomplexes for gene delivery and magnetic resonance imaging in the brain
title_full_unstemmed Lipid peptide nanocomplexes for gene delivery and magnetic resonance imaging in the brain
title_short Lipid peptide nanocomplexes for gene delivery and magnetic resonance imaging in the brain
title_sort lipid peptide nanocomplexes for gene delivery and magnetic resonance imaging in the brain
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657147/
https://www.ncbi.nlm.nih.gov/pubmed/22800579
http://dx.doi.org/10.1016/j.jconrel.2012.07.002
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