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Sustained Delivery System for Stem Cell-Derived Exosomes
Recent literature has ascribed that the paracrine action of stem cells is mediated by exosomes. Exosomes are nano-sized extracellular vesicles (30 to 100 nm) of endocytic origin that play important roles in intercellular communication. They have the ability to deliver various therapeutic effects, e....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868085/ https://www.ncbi.nlm.nih.gov/pubmed/31798457 http://dx.doi.org/10.3389/fphar.2019.01368 |
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author | Riau, Andri K. Ong, Hon Shing Yam, Gary H. F. Mehta, Jodhbir S. |
author_facet | Riau, Andri K. Ong, Hon Shing Yam, Gary H. F. Mehta, Jodhbir S. |
author_sort | Riau, Andri K. |
collection | PubMed |
description | Recent literature has ascribed that the paracrine action of stem cells is mediated by exosomes. Exosomes are nano-sized extracellular vesicles (30 to 100 nm) of endocytic origin that play important roles in intercellular communication. They have the ability to deliver various therapeutic effects, e.g., skin regeneration or cardiac function recovery, when applied topically or injected systemically. However, injection of exosomes has been shown to result in rapid clearance from blood circulation and accumulation of the exosomes in the liver, spleen, lung, and gastrointestinal tract can be found as early as 2 h after injection. Topical administration of exosomes on the skin or ocular surface would suffer the same fate due to rapid fluid turnover (sweat or tears). Biodegradable or highly porous hydrogels have been utilized to load exosomes and to deliver a sustained therapeutic effect. They can also prevent the exosomes from being cleared prematurely and allow the delivery of a more localized and concentrated exosome dosage by placing the hydrogel directly at or in the proximity of the target site. In this mini-review, we elaborate on the challenges of conventional exosome administration and highlight the solution to the shortcomings in the form of exosome-incorporated hydrogels. Different techniques to encapsulate exosomes and examples of hydrogels that have been used to create sustained delivery systems of exosomes are also discussed. |
format | Online Article Text |
id | pubmed-6868085 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68680852019-12-03 Sustained Delivery System for Stem Cell-Derived Exosomes Riau, Andri K. Ong, Hon Shing Yam, Gary H. F. Mehta, Jodhbir S. Front Pharmacol Pharmacology Recent literature has ascribed that the paracrine action of stem cells is mediated by exosomes. Exosomes are nano-sized extracellular vesicles (30 to 100 nm) of endocytic origin that play important roles in intercellular communication. They have the ability to deliver various therapeutic effects, e.g., skin regeneration or cardiac function recovery, when applied topically or injected systemically. However, injection of exosomes has been shown to result in rapid clearance from blood circulation and accumulation of the exosomes in the liver, spleen, lung, and gastrointestinal tract can be found as early as 2 h after injection. Topical administration of exosomes on the skin or ocular surface would suffer the same fate due to rapid fluid turnover (sweat or tears). Biodegradable or highly porous hydrogels have been utilized to load exosomes and to deliver a sustained therapeutic effect. They can also prevent the exosomes from being cleared prematurely and allow the delivery of a more localized and concentrated exosome dosage by placing the hydrogel directly at or in the proximity of the target site. In this mini-review, we elaborate on the challenges of conventional exosome administration and highlight the solution to the shortcomings in the form of exosome-incorporated hydrogels. Different techniques to encapsulate exosomes and examples of hydrogels that have been used to create sustained delivery systems of exosomes are also discussed. Frontiers Media S.A. 2019-11-14 /pmc/articles/PMC6868085/ /pubmed/31798457 http://dx.doi.org/10.3389/fphar.2019.01368 Text en Copyright © 2019 Riau, Ong, Yam and Mehta http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Riau, Andri K. Ong, Hon Shing Yam, Gary H. F. Mehta, Jodhbir S. Sustained Delivery System for Stem Cell-Derived Exosomes |
title | Sustained Delivery System for Stem Cell-Derived Exosomes |
title_full | Sustained Delivery System for Stem Cell-Derived Exosomes |
title_fullStr | Sustained Delivery System for Stem Cell-Derived Exosomes |
title_full_unstemmed | Sustained Delivery System for Stem Cell-Derived Exosomes |
title_short | Sustained Delivery System for Stem Cell-Derived Exosomes |
title_sort | sustained delivery system for stem cell-derived exosomes |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6868085/ https://www.ncbi.nlm.nih.gov/pubmed/31798457 http://dx.doi.org/10.3389/fphar.2019.01368 |
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