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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2013
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.
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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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