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Bioresorbable Drug-Eluting Magnesium-Alloy Scaffold for Treatment of Coronary Artery Disease
The introduction of metallic drug-eluting stents has reduced the risk of restenosis and widened the indications of percutaneous coronary intervention in treatment of coronary artery disease. However, this medical device can induce hypersensitive reaction that interferes with the endothelialization a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876123/ https://www.ncbi.nlm.nih.gov/pubmed/24351829 http://dx.doi.org/10.3390/ijms141224492 |
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author | Campos, Carlos M. Muramatsu, Takashi Iqbal, Javaid Zhang, Ya-Jun Onuma, Yoshinobu Garcia-Garcia, Hector M. Haude, Michael Lemos, Pedro A. Warnack, Boris Serruys, Patrick W. |
author_facet | Campos, Carlos M. Muramatsu, Takashi Iqbal, Javaid Zhang, Ya-Jun Onuma, Yoshinobu Garcia-Garcia, Hector M. Haude, Michael Lemos, Pedro A. Warnack, Boris Serruys, Patrick W. |
author_sort | Campos, Carlos M. |
collection | PubMed |
description | The introduction of metallic drug-eluting stents has reduced the risk of restenosis and widened the indications of percutaneous coronary intervention in treatment of coronary artery disease. However, this medical device can induce hypersensitive reaction that interferes with the endothelialization and healing process resulting in late persistent or acquired malapposition of the permanent metallic implant. Delayed endotheliaization and malapposition may lead to late and very late stent thrombosis. Bioresorbable scaffolds (BRS) have been introduced to potentially overcome these limitations, as they provide temporary scaffolding and then disappear, liberating the treated vessel from its cage. Magnesium is an essential mineral needed for a variety of physiological functions in the human body and its bioresorbable alloy has the strength-to-weight ratio comparable with that of strong aluminum alloys and alloy steels. The aim of this review is to present the new developments in Magnesium BRS technology, to describe its clinical application and to discuss the future prospects of this innovative therapy. |
format | Online Article Text |
id | pubmed-3876123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-38761232013-12-31 Bioresorbable Drug-Eluting Magnesium-Alloy Scaffold for Treatment of Coronary Artery Disease Campos, Carlos M. Muramatsu, Takashi Iqbal, Javaid Zhang, Ya-Jun Onuma, Yoshinobu Garcia-Garcia, Hector M. Haude, Michael Lemos, Pedro A. Warnack, Boris Serruys, Patrick W. Int J Mol Sci Review The introduction of metallic drug-eluting stents has reduced the risk of restenosis and widened the indications of percutaneous coronary intervention in treatment of coronary artery disease. However, this medical device can induce hypersensitive reaction that interferes with the endothelialization and healing process resulting in late persistent or acquired malapposition of the permanent metallic implant. Delayed endotheliaization and malapposition may lead to late and very late stent thrombosis. Bioresorbable scaffolds (BRS) have been introduced to potentially overcome these limitations, as they provide temporary scaffolding and then disappear, liberating the treated vessel from its cage. Magnesium is an essential mineral needed for a variety of physiological functions in the human body and its bioresorbable alloy has the strength-to-weight ratio comparable with that of strong aluminum alloys and alloy steels. The aim of this review is to present the new developments in Magnesium BRS technology, to describe its clinical application and to discuss the future prospects of this innovative therapy. Molecular Diversity Preservation International (MDPI) 2013-12-16 /pmc/articles/PMC3876123/ /pubmed/24351829 http://dx.doi.org/10.3390/ijms141224492 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Campos, Carlos M. Muramatsu, Takashi Iqbal, Javaid Zhang, Ya-Jun Onuma, Yoshinobu Garcia-Garcia, Hector M. Haude, Michael Lemos, Pedro A. Warnack, Boris Serruys, Patrick W. Bioresorbable Drug-Eluting Magnesium-Alloy Scaffold for Treatment of Coronary Artery Disease |
title | Bioresorbable Drug-Eluting Magnesium-Alloy Scaffold for Treatment of Coronary Artery Disease |
title_full | Bioresorbable Drug-Eluting Magnesium-Alloy Scaffold for Treatment of Coronary Artery Disease |
title_fullStr | Bioresorbable Drug-Eluting Magnesium-Alloy Scaffold for Treatment of Coronary Artery Disease |
title_full_unstemmed | Bioresorbable Drug-Eluting Magnesium-Alloy Scaffold for Treatment of Coronary Artery Disease |
title_short | Bioresorbable Drug-Eluting Magnesium-Alloy Scaffold for Treatment of Coronary Artery Disease |
title_sort | bioresorbable drug-eluting magnesium-alloy scaffold for treatment of coronary artery disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876123/ https://www.ncbi.nlm.nih.gov/pubmed/24351829 http://dx.doi.org/10.3390/ijms141224492 |
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