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Lipid Nanoparticles Containing siRNA Synthesized by Microfluidic Mixing Exhibit an Electron-Dense Nanostructured Core

[Image: see text] Lipid nanoparticles (LNP) containing ionizable cationic lipids are the leading systems for enabling therapeutic applications of siRNA; however, the structure of these systems has not been defined. Here we examine the structure of LNP siRNA systems containing DLinKC2-DMA(an ionizabl...

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Autores principales: Leung, Alex K. K., Hafez, Ismail M., Baoukina, Svetlana, Belliveau, Nathan M., Zhigaltsev, Igor V., Afshinmanesh, Elham, Tieleman, D. Peter, Hansen, Carl L., Hope, Michael J., Cullis, Pieter R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2012
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434764/
https://www.ncbi.nlm.nih.gov/pubmed/22962627
http://dx.doi.org/10.1021/jp303267y
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author Leung, Alex K. K.
Hafez, Ismail M.
Baoukina, Svetlana
Belliveau, Nathan M.
Zhigaltsev, Igor V.
Afshinmanesh, Elham
Tieleman, D. Peter
Hansen, Carl L.
Hope, Michael J.
Cullis, Pieter R.
author_facet Leung, Alex K. K.
Hafez, Ismail M.
Baoukina, Svetlana
Belliveau, Nathan M.
Zhigaltsev, Igor V.
Afshinmanesh, Elham
Tieleman, D. Peter
Hansen, Carl L.
Hope, Michael J.
Cullis, Pieter R.
author_sort Leung, Alex K. K.
collection PubMed
description [Image: see text] Lipid nanoparticles (LNP) containing ionizable cationic lipids are the leading systems for enabling therapeutic applications of siRNA; however, the structure of these systems has not been defined. Here we examine the structure of LNP siRNA systems containing DLinKC2-DMA(an ionizable cationic lipid), phospholipid, cholesterol and a polyethylene glycol (PEG) lipid formed using a rapid microfluidic mixing process. Techniques employed include cryo-transmission electron microscopy, (31)P NMR, membrane fusion assays, density measurements, and molecular modeling. The experimental results indicate that these LNP siRNA systems have an interior lipid core containing siRNA duplexes complexed to cationic lipid and that the interior core also contains phospholipid and cholesterol. Consistent with experimental observations, molecular modeling calculations indicate that the interior of LNP siRNA systems exhibits a periodic structure of aqueous compartments, where some compartments contain siRNA. It is concluded that LNP siRNA systems formulated by rapid mixing of an ethanol solution of lipid with an aqueous medium containing siRNA exhibit a nanostructured core. The results give insight into the mechanism whereby LNP siRNA systems are formed, providing an understanding of the high encapsulation efficiencies that can be achieved and information on methods of constructing more sophisticated LNP systems.
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spelling pubmed-34347642012-09-06 Lipid Nanoparticles Containing siRNA Synthesized by Microfluidic Mixing Exhibit an Electron-Dense Nanostructured Core Leung, Alex K. K. Hafez, Ismail M. Baoukina, Svetlana Belliveau, Nathan M. Zhigaltsev, Igor V. Afshinmanesh, Elham Tieleman, D. Peter Hansen, Carl L. Hope, Michael J. Cullis, Pieter R. J Phys Chem C Nanomater Interfaces [Image: see text] Lipid nanoparticles (LNP) containing ionizable cationic lipids are the leading systems for enabling therapeutic applications of siRNA; however, the structure of these systems has not been defined. Here we examine the structure of LNP siRNA systems containing DLinKC2-DMA(an ionizable cationic lipid), phospholipid, cholesterol and a polyethylene glycol (PEG) lipid formed using a rapid microfluidic mixing process. Techniques employed include cryo-transmission electron microscopy, (31)P NMR, membrane fusion assays, density measurements, and molecular modeling. The experimental results indicate that these LNP siRNA systems have an interior lipid core containing siRNA duplexes complexed to cationic lipid and that the interior core also contains phospholipid and cholesterol. Consistent with experimental observations, molecular modeling calculations indicate that the interior of LNP siRNA systems exhibits a periodic structure of aqueous compartments, where some compartments contain siRNA. It is concluded that LNP siRNA systems formulated by rapid mixing of an ethanol solution of lipid with an aqueous medium containing siRNA exhibit a nanostructured core. The results give insight into the mechanism whereby LNP siRNA systems are formed, providing an understanding of the high encapsulation efficiencies that can be achieved and information on methods of constructing more sophisticated LNP systems. American Chemical Society 2012-07-18 2012-08-30 /pmc/articles/PMC3434764/ /pubmed/22962627 http://dx.doi.org/10.1021/jp303267y Text en Copyright © 2012 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org.
spellingShingle Leung, Alex K. K.
Hafez, Ismail M.
Baoukina, Svetlana
Belliveau, Nathan M.
Zhigaltsev, Igor V.
Afshinmanesh, Elham
Tieleman, D. Peter
Hansen, Carl L.
Hope, Michael J.
Cullis, Pieter R.
Lipid Nanoparticles Containing siRNA Synthesized by Microfluidic Mixing Exhibit an Electron-Dense Nanostructured Core
title Lipid Nanoparticles Containing siRNA Synthesized by Microfluidic Mixing Exhibit an Electron-Dense Nanostructured Core
title_full Lipid Nanoparticles Containing siRNA Synthesized by Microfluidic Mixing Exhibit an Electron-Dense Nanostructured Core
title_fullStr Lipid Nanoparticles Containing siRNA Synthesized by Microfluidic Mixing Exhibit an Electron-Dense Nanostructured Core
title_full_unstemmed Lipid Nanoparticles Containing siRNA Synthesized by Microfluidic Mixing Exhibit an Electron-Dense Nanostructured Core
title_short Lipid Nanoparticles Containing siRNA Synthesized by Microfluidic Mixing Exhibit an Electron-Dense Nanostructured Core
title_sort lipid nanoparticles containing sirna synthesized by microfluidic mixing exhibit an electron-dense nanostructured core
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3434764/
https://www.ncbi.nlm.nih.gov/pubmed/22962627
http://dx.doi.org/10.1021/jp303267y
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