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A Novel Hybrid Drug Delivery System for Treatment of Aortic Aneurysms
Ongoing aortic wall degeneration and subsequent aneurysm exclusion failure are major concerns after an endovascular aneurysm repair with a stent-graft. An ideal solution would be a drug therapy that targets the aortic wall and inhibits wall degeneration. Here, we described a novel drug delivery syst...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432022/ https://www.ncbi.nlm.nih.gov/pubmed/32748844 http://dx.doi.org/10.3390/ijms21155538 |
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author | Yoshimura, Koichi Aoki, Hiroki Teruyama, Chie Iijima, Masumi Tsutsumi, Hiromori Kuroda, Shun’ichi Hamano, Kimikazu |
author_facet | Yoshimura, Koichi Aoki, Hiroki Teruyama, Chie Iijima, Masumi Tsutsumi, Hiromori Kuroda, Shun’ichi Hamano, Kimikazu |
author_sort | Yoshimura, Koichi |
collection | PubMed |
description | Ongoing aortic wall degeneration and subsequent aneurysm exclusion failure are major concerns after an endovascular aneurysm repair with a stent-graft. An ideal solution would be a drug therapy that targets the aortic wall and inhibits wall degeneration. Here, we described a novel drug delivery system, which allowed repetitively charging a graft with therapeutic drugs and releasing them to the aortic wall in vivo. The system was composed of a targeted graft, which was labeled with a small target molecule, and the target-recognizing nanocarrier, which contained suitable drugs. We developed the targeted graft by decorating a biotinylated polyester graft with neutravidin. We created the target-recognizing nanocarrier by conjugating drug-containing liposomes with biotinylated bio-nanocapsules. We successfully demonstrated that the target-recognizing nanocarriers could bind to the targeted graft, both in vitro and in blood vessels of live mice. Moreover, the drug released from our drug delivery system reduced the expression of matrix metalloproteinase-9 in mouse aortas. Thus, this hybrid system represents a first step toward an adjuvant therapy that might improve the long-term outcome of endovascular aneurysm repair. |
format | Online Article Text |
id | pubmed-7432022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74320222020-08-24 A Novel Hybrid Drug Delivery System for Treatment of Aortic Aneurysms Yoshimura, Koichi Aoki, Hiroki Teruyama, Chie Iijima, Masumi Tsutsumi, Hiromori Kuroda, Shun’ichi Hamano, Kimikazu Int J Mol Sci Article Ongoing aortic wall degeneration and subsequent aneurysm exclusion failure are major concerns after an endovascular aneurysm repair with a stent-graft. An ideal solution would be a drug therapy that targets the aortic wall and inhibits wall degeneration. Here, we described a novel drug delivery system, which allowed repetitively charging a graft with therapeutic drugs and releasing them to the aortic wall in vivo. The system was composed of a targeted graft, which was labeled with a small target molecule, and the target-recognizing nanocarrier, which contained suitable drugs. We developed the targeted graft by decorating a biotinylated polyester graft with neutravidin. We created the target-recognizing nanocarrier by conjugating drug-containing liposomes with biotinylated bio-nanocapsules. We successfully demonstrated that the target-recognizing nanocarriers could bind to the targeted graft, both in vitro and in blood vessels of live mice. Moreover, the drug released from our drug delivery system reduced the expression of matrix metalloproteinase-9 in mouse aortas. Thus, this hybrid system represents a first step toward an adjuvant therapy that might improve the long-term outcome of endovascular aneurysm repair. MDPI 2020-08-02 /pmc/articles/PMC7432022/ /pubmed/32748844 http://dx.doi.org/10.3390/ijms21155538 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Yoshimura, Koichi Aoki, Hiroki Teruyama, Chie Iijima, Masumi Tsutsumi, Hiromori Kuroda, Shun’ichi Hamano, Kimikazu A Novel Hybrid Drug Delivery System for Treatment of Aortic Aneurysms |
title | A Novel Hybrid Drug Delivery System for Treatment of Aortic Aneurysms |
title_full | A Novel Hybrid Drug Delivery System for Treatment of Aortic Aneurysms |
title_fullStr | A Novel Hybrid Drug Delivery System for Treatment of Aortic Aneurysms |
title_full_unstemmed | A Novel Hybrid Drug Delivery System for Treatment of Aortic Aneurysms |
title_short | A Novel Hybrid Drug Delivery System for Treatment of Aortic Aneurysms |
title_sort | novel hybrid drug delivery system for treatment of aortic aneurysms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432022/ https://www.ncbi.nlm.nih.gov/pubmed/32748844 http://dx.doi.org/10.3390/ijms21155538 |
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