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Graphene-incorporated hyaluronic acid-based hydrogel as a controlled Senexin A delivery system
Perivascular delivery of therapeutic agents against established aetiologies for occlusive vascular remodelling has great therapeutic potential for vein graft failure. However, none of the perivascular drug delivery systems tested experimentally have been translated into clinical practice. In this st...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Chinese Medical Multimedia Press Co., Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9465987/ https://www.ncbi.nlm.nih.gov/pubmed/36105568 http://dx.doi.org/10.12336/biomatertransl.2022.02.007 |
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author | Maturavongsadit, Panita Wu, Weiwei Fan, Jingyu Roninson, Igor B. Cui, Taixing Wang, Qian |
author_facet | Maturavongsadit, Panita Wu, Weiwei Fan, Jingyu Roninson, Igor B. Cui, Taixing Wang, Qian |
author_sort | Maturavongsadit, Panita |
collection | PubMed |
description | Perivascular delivery of therapeutic agents against established aetiologies for occlusive vascular remodelling has great therapeutic potential for vein graft failure. However, none of the perivascular drug delivery systems tested experimentally have been translated into clinical practice. In this study, we established a novel strategy to locally and sustainably deliver the cyclin-dependent kinase 8/19 inhibitor Senexin A (SenA), an emerging drug candidate to treat occlusive vascular disease, using graphene oxide-hybridised hyaluronic acid-based hydrogels. We demonstrated an approach to accommodate SenA in hyaluronic acid-based hydrogels through utilising graphene oxide nanosheets allowing for non-covalent interaction with SenA. The resulting hydrogels produced sustained delivery of SenA over 21 days with tunable release kinetics. In vitro assays also demonstrated that the hydrogels were biocompatible. This novel graphene oxide-incorporated hyaluronic acid hydrogel offers an optimistic outlook as a perivascular drug delivery system for treating occlusive vascular diseases, such as vein graft failure. |
format | Online Article Text |
id | pubmed-9465987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Chinese Medical Multimedia Press Co., Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-94659872022-09-13 Graphene-incorporated hyaluronic acid-based hydrogel as a controlled Senexin A delivery system Maturavongsadit, Panita Wu, Weiwei Fan, Jingyu Roninson, Igor B. Cui, Taixing Wang, Qian Biomater Transl Research Article Perivascular delivery of therapeutic agents against established aetiologies for occlusive vascular remodelling has great therapeutic potential for vein graft failure. However, none of the perivascular drug delivery systems tested experimentally have been translated into clinical practice. In this study, we established a novel strategy to locally and sustainably deliver the cyclin-dependent kinase 8/19 inhibitor Senexin A (SenA), an emerging drug candidate to treat occlusive vascular disease, using graphene oxide-hybridised hyaluronic acid-based hydrogels. We demonstrated an approach to accommodate SenA in hyaluronic acid-based hydrogels through utilising graphene oxide nanosheets allowing for non-covalent interaction with SenA. The resulting hydrogels produced sustained delivery of SenA over 21 days with tunable release kinetics. In vitro assays also demonstrated that the hydrogels were biocompatible. This novel graphene oxide-incorporated hyaluronic acid hydrogel offers an optimistic outlook as a perivascular drug delivery system for treating occlusive vascular diseases, such as vein graft failure. Chinese Medical Multimedia Press Co., Ltd 2022-06-28 /pmc/articles/PMC9465987/ /pubmed/36105568 http://dx.doi.org/10.12336/biomatertransl.2022.02.007 Text en https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work noncommercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Research Article Maturavongsadit, Panita Wu, Weiwei Fan, Jingyu Roninson, Igor B. Cui, Taixing Wang, Qian Graphene-incorporated hyaluronic acid-based hydrogel as a controlled Senexin A delivery system |
title | Graphene-incorporated hyaluronic acid-based hydrogel as a controlled Senexin A delivery system |
title_full | Graphene-incorporated hyaluronic acid-based hydrogel as a controlled Senexin A delivery system |
title_fullStr | Graphene-incorporated hyaluronic acid-based hydrogel as a controlled Senexin A delivery system |
title_full_unstemmed | Graphene-incorporated hyaluronic acid-based hydrogel as a controlled Senexin A delivery system |
title_short | Graphene-incorporated hyaluronic acid-based hydrogel as a controlled Senexin A delivery system |
title_sort | graphene-incorporated hyaluronic acid-based hydrogel as a controlled senexin a delivery system |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9465987/ https://www.ncbi.nlm.nih.gov/pubmed/36105568 http://dx.doi.org/10.12336/biomatertransl.2022.02.007 |
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