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Surface modification of gold nanoparticles with neuron-targeted exosome for enhanced blood–brain barrier penetration

Gold nanoparticles (AuNPs) have been extensively used as nanomaterials for theranostic applications due to their multifunctional characteristics in therapeutics, imaging, and surface modification. In this study, the unique functionalities of exosome-derived membranes were combined with synthetic AuN...

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Autores principales: Khongkow, Mattaka, Yata, Teerapong, Boonrungsiman, Suwimon, Ruktanonchai, Uracha Rungsardthong, Graham, Duncan, Namdee, Katawut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547645/
https://www.ncbi.nlm.nih.gov/pubmed/31164665
http://dx.doi.org/10.1038/s41598-019-44569-6
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author Khongkow, Mattaka
Yata, Teerapong
Boonrungsiman, Suwimon
Ruktanonchai, Uracha Rungsardthong
Graham, Duncan
Namdee, Katawut
author_facet Khongkow, Mattaka
Yata, Teerapong
Boonrungsiman, Suwimon
Ruktanonchai, Uracha Rungsardthong
Graham, Duncan
Namdee, Katawut
author_sort Khongkow, Mattaka
collection PubMed
description Gold nanoparticles (AuNPs) have been extensively used as nanomaterials for theranostic applications due to their multifunctional characteristics in therapeutics, imaging, and surface modification. In this study, the unique functionalities of exosome-derived membranes were combined with synthetic AuNPs for targeted delivery to brain cells. Here, we report the surface modification of AuNPs with brain-targeted exosomes derived from genetically engineered mammalian cells by using the mechanical method or extrusion to create these novel nanomaterials. The unique targeting properties of the AuNPs after fabrication with the brain-targeted exosomes was demonstrated by their binding to brain cells under laminar flow conditions as well as their enhanced transport across the blood brain barrier. In a further demonstration of their ability to target brain cells, in vivo bioluminescence imaging revealed that targeted-exosome coated AuNPs accumulated in the mouse brain after intravenous injection. The surface modification of synthetic AuNPs with the brain-targeted exosome demonstrated in this work represents a highly novel and effective strategy to provide efficient brain targeting and shows promise for the future in using modified AuNPs to penetrate the brain.
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spelling pubmed-65476452019-06-10 Surface modification of gold nanoparticles with neuron-targeted exosome for enhanced blood–brain barrier penetration Khongkow, Mattaka Yata, Teerapong Boonrungsiman, Suwimon Ruktanonchai, Uracha Rungsardthong Graham, Duncan Namdee, Katawut Sci Rep Article Gold nanoparticles (AuNPs) have been extensively used as nanomaterials for theranostic applications due to their multifunctional characteristics in therapeutics, imaging, and surface modification. In this study, the unique functionalities of exosome-derived membranes were combined with synthetic AuNPs for targeted delivery to brain cells. Here, we report the surface modification of AuNPs with brain-targeted exosomes derived from genetically engineered mammalian cells by using the mechanical method or extrusion to create these novel nanomaterials. The unique targeting properties of the AuNPs after fabrication with the brain-targeted exosomes was demonstrated by their binding to brain cells under laminar flow conditions as well as their enhanced transport across the blood brain barrier. In a further demonstration of their ability to target brain cells, in vivo bioluminescence imaging revealed that targeted-exosome coated AuNPs accumulated in the mouse brain after intravenous injection. The surface modification of synthetic AuNPs with the brain-targeted exosome demonstrated in this work represents a highly novel and effective strategy to provide efficient brain targeting and shows promise for the future in using modified AuNPs to penetrate the brain. Nature Publishing Group UK 2019-06-04 /pmc/articles/PMC6547645/ /pubmed/31164665 http://dx.doi.org/10.1038/s41598-019-44569-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Khongkow, Mattaka
Yata, Teerapong
Boonrungsiman, Suwimon
Ruktanonchai, Uracha Rungsardthong
Graham, Duncan
Namdee, Katawut
Surface modification of gold nanoparticles with neuron-targeted exosome for enhanced blood–brain barrier penetration
title Surface modification of gold nanoparticles with neuron-targeted exosome for enhanced blood–brain barrier penetration
title_full Surface modification of gold nanoparticles with neuron-targeted exosome for enhanced blood–brain barrier penetration
title_fullStr Surface modification of gold nanoparticles with neuron-targeted exosome for enhanced blood–brain barrier penetration
title_full_unstemmed Surface modification of gold nanoparticles with neuron-targeted exosome for enhanced blood–brain barrier penetration
title_short Surface modification of gold nanoparticles with neuron-targeted exosome for enhanced blood–brain barrier penetration
title_sort surface modification of gold nanoparticles with neuron-targeted exosome for enhanced blood–brain barrier penetration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547645/
https://www.ncbi.nlm.nih.gov/pubmed/31164665
http://dx.doi.org/10.1038/s41598-019-44569-6
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