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A versatile method for the preparation of particle-loaded microbubbles for multimodality imaging and targeted drug delivery

Microbubbles are currently in clinical use as ultrasound contrast agents and under active investigation as mediators of ultrasound therapy. To improve the theranostic potential of microbubbles, nanoparticles can be attached to the bubble shell for imaging, targeting and/or enhancement of acoustic re...

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Autores principales: Owen, Joshua, Crake, Calum, Lee, Jeong Yu, Carugo, Dario, Beguin, Estelle, Khrapitchev, Alexandre A, Browning, Richard J, Sibson, Nicola, Stride, Eleanor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830459/
https://www.ncbi.nlm.nih.gov/pubmed/28299722
http://dx.doi.org/10.1007/s13346-017-0366-7
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author Owen, Joshua
Crake, Calum
Lee, Jeong Yu
Carugo, Dario
Beguin, Estelle
Khrapitchev, Alexandre A
Browning, Richard J
Sibson, Nicola
Stride, Eleanor
author_facet Owen, Joshua
Crake, Calum
Lee, Jeong Yu
Carugo, Dario
Beguin, Estelle
Khrapitchev, Alexandre A
Browning, Richard J
Sibson, Nicola
Stride, Eleanor
author_sort Owen, Joshua
collection PubMed
description Microbubbles are currently in clinical use as ultrasound contrast agents and under active investigation as mediators of ultrasound therapy. To improve the theranostic potential of microbubbles, nanoparticles can be attached to the bubble shell for imaging, targeting and/or enhancement of acoustic response. Existing methods for fabricating particle-loaded bubbles, however, require the use of polymers, oil layers or chemical reactions for particle incorporation; embed/attach the particles that can reduce echogenicity; impair biocompatibility; and/or involve multiple processing steps. Here, we describe a simple method to embed nanoparticles in a phospholipid-coated microbubble formulation that overcomes these limitations. Magnetic nanoparticles are used to demonstrate the method with a range of different microbubble formulations. The size distribution and yield of microbubbles are shown to be unaffected by the addition of the particles. We further show that the microbubbles can be retained against flow using a permanent magnet, can be visualised by both ultrasound and magnetic resonance imaging (MRI) and can be used to transfect SH-SY5Y cells with fluorescent small interfering RNA under the application of a magnetic field and ultrasound field. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13346-017-0366-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-58304592018-03-05 A versatile method for the preparation of particle-loaded microbubbles for multimodality imaging and targeted drug delivery Owen, Joshua Crake, Calum Lee, Jeong Yu Carugo, Dario Beguin, Estelle Khrapitchev, Alexandre A Browning, Richard J Sibson, Nicola Stride, Eleanor Drug Deliv Transl Res Methods Article Microbubbles are currently in clinical use as ultrasound contrast agents and under active investigation as mediators of ultrasound therapy. To improve the theranostic potential of microbubbles, nanoparticles can be attached to the bubble shell for imaging, targeting and/or enhancement of acoustic response. Existing methods for fabricating particle-loaded bubbles, however, require the use of polymers, oil layers or chemical reactions for particle incorporation; embed/attach the particles that can reduce echogenicity; impair biocompatibility; and/or involve multiple processing steps. Here, we describe a simple method to embed nanoparticles in a phospholipid-coated microbubble formulation that overcomes these limitations. Magnetic nanoparticles are used to demonstrate the method with a range of different microbubble formulations. The size distribution and yield of microbubbles are shown to be unaffected by the addition of the particles. We further show that the microbubbles can be retained against flow using a permanent magnet, can be visualised by both ultrasound and magnetic resonance imaging (MRI) and can be used to transfect SH-SY5Y cells with fluorescent small interfering RNA under the application of a magnetic field and ultrasound field. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s13346-017-0366-7) contains supplementary material, which is available to authorized users. Springer US 2017-03-15 2018 /pmc/articles/PMC5830459/ /pubmed/28299722 http://dx.doi.org/10.1007/s13346-017-0366-7 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Methods Article
Owen, Joshua
Crake, Calum
Lee, Jeong Yu
Carugo, Dario
Beguin, Estelle
Khrapitchev, Alexandre A
Browning, Richard J
Sibson, Nicola
Stride, Eleanor
A versatile method for the preparation of particle-loaded microbubbles for multimodality imaging and targeted drug delivery
title A versatile method for the preparation of particle-loaded microbubbles for multimodality imaging and targeted drug delivery
title_full A versatile method for the preparation of particle-loaded microbubbles for multimodality imaging and targeted drug delivery
title_fullStr A versatile method for the preparation of particle-loaded microbubbles for multimodality imaging and targeted drug delivery
title_full_unstemmed A versatile method for the preparation of particle-loaded microbubbles for multimodality imaging and targeted drug delivery
title_short A versatile method for the preparation of particle-loaded microbubbles for multimodality imaging and targeted drug delivery
title_sort versatile method for the preparation of particle-loaded microbubbles for multimodality imaging and targeted drug delivery
topic Methods Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830459/
https://www.ncbi.nlm.nih.gov/pubmed/28299722
http://dx.doi.org/10.1007/s13346-017-0366-7
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