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Development of a Bioactive Polymeric Drug Eluting Coronary Stent Coating Using Electrospraying

Drug-eluting stents are now routinely used in the treatment of acute coronary syndromes caused by coronary artery disease. Whilst the sustained release of anti-proliferative drugs from these devices has greatly reduced the need for repeat revascularisation procedures, this approach is not suitable f...

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Autores principales: McKittrick, C. M., Cardona, M. J., Black, R. A., McCormick, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6928095/
https://www.ncbi.nlm.nih.gov/pubmed/31441008
http://dx.doi.org/10.1007/s10439-019-02346-6
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author McKittrick, C. M.
Cardona, M. J.
Black, R. A.
McCormick, C.
author_facet McKittrick, C. M.
Cardona, M. J.
Black, R. A.
McCormick, C.
author_sort McKittrick, C. M.
collection PubMed
description Drug-eluting stents are now routinely used in the treatment of acute coronary syndromes caused by coronary artery disease. Whilst the sustained release of anti-proliferative drugs from these devices has greatly reduced the need for repeat revascularisation procedures, this approach is not suitable for all patients and appears to delay regrowth of the endothelium, necessitating the use of prolonged dual anti-platelet therapy. Although the development of more advanced stent platforms and drug coatings has produced modest improvements in performance, these devices have not fully addressed the limitations experienced with their first-generation counterparts. In the present study, we developed a novel stent coating that provides controlled sirolimus release from a bioactive polymer (accelerate™ AT) that has previously been shown to support endothelial cell growth in vitro. A bespoke electrospray deposition process provided control over the coating thickness, surface roughness, drug load, and release kinetics. The resultant optimised coating combines rapid release of an anti-proliferative agent from a bioactive polymer coating that promotes re-endothelialisation, thereby offering potential protection against in-stent restenosis and thrombosis. This novel, dual-action coating therefore has significant therapeutic potential, with the enhanced control of drug load and release kinetics offered by electrospray deposition also opening up opportunities for more personalised treatment approaches. Further development and evaluation of these technologies in vitro and in vivo is therefore warranted. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10439-019-02346-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-69280952020-01-07 Development of a Bioactive Polymeric Drug Eluting Coronary Stent Coating Using Electrospraying McKittrick, C. M. Cardona, M. J. Black, R. A. McCormick, C. Ann Biomed Eng Original Article Drug-eluting stents are now routinely used in the treatment of acute coronary syndromes caused by coronary artery disease. Whilst the sustained release of anti-proliferative drugs from these devices has greatly reduced the need for repeat revascularisation procedures, this approach is not suitable for all patients and appears to delay regrowth of the endothelium, necessitating the use of prolonged dual anti-platelet therapy. Although the development of more advanced stent platforms and drug coatings has produced modest improvements in performance, these devices have not fully addressed the limitations experienced with their first-generation counterparts. In the present study, we developed a novel stent coating that provides controlled sirolimus release from a bioactive polymer (accelerate™ AT) that has previously been shown to support endothelial cell growth in vitro. A bespoke electrospray deposition process provided control over the coating thickness, surface roughness, drug load, and release kinetics. The resultant optimised coating combines rapid release of an anti-proliferative agent from a bioactive polymer coating that promotes re-endothelialisation, thereby offering potential protection against in-stent restenosis and thrombosis. This novel, dual-action coating therefore has significant therapeutic potential, with the enhanced control of drug load and release kinetics offered by electrospray deposition also opening up opportunities for more personalised treatment approaches. Further development and evaluation of these technologies in vitro and in vivo is therefore warranted. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10439-019-02346-6) contains supplementary material, which is available to authorized users. Springer US 2019-08-22 2020 /pmc/articles/PMC6928095/ /pubmed/31441008 http://dx.doi.org/10.1007/s10439-019-02346-6 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
McKittrick, C. M.
Cardona, M. J.
Black, R. A.
McCormick, C.
Development of a Bioactive Polymeric Drug Eluting Coronary Stent Coating Using Electrospraying
title Development of a Bioactive Polymeric Drug Eluting Coronary Stent Coating Using Electrospraying
title_full Development of a Bioactive Polymeric Drug Eluting Coronary Stent Coating Using Electrospraying
title_fullStr Development of a Bioactive Polymeric Drug Eluting Coronary Stent Coating Using Electrospraying
title_full_unstemmed Development of a Bioactive Polymeric Drug Eluting Coronary Stent Coating Using Electrospraying
title_short Development of a Bioactive Polymeric Drug Eluting Coronary Stent Coating Using Electrospraying
title_sort development of a bioactive polymeric drug eluting coronary stent coating using electrospraying
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6928095/
https://www.ncbi.nlm.nih.gov/pubmed/31441008
http://dx.doi.org/10.1007/s10439-019-02346-6
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