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Understanding the Mechanism of Drug Transfer and Retention of Drug-Coated Balloons

OBJECTIVE: The purpose of this study was to determine the impact of varying inflation parameters on paclitaxel delivery and retention using a commercially available DCB. BACKGROUND: Drug-coated balloons (DCB) have become the standard treatment for peripheral artery disease. Clinical data suggest tha...

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Autores principales: Villar-Matamoros, Estefanny, Stokes, Lauren, Lloret, Alyssa, Todd, Meagan, Tillman, Bryan W., Yazdani, Saami K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549471/
https://www.ncbi.nlm.nih.gov/pubmed/35972237
http://dx.doi.org/10.1177/10742484221119559
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author Villar-Matamoros, Estefanny
Stokes, Lauren
Lloret, Alyssa
Todd, Meagan
Tillman, Bryan W.
Yazdani, Saami K.
author_facet Villar-Matamoros, Estefanny
Stokes, Lauren
Lloret, Alyssa
Todd, Meagan
Tillman, Bryan W.
Yazdani, Saami K.
author_sort Villar-Matamoros, Estefanny
collection PubMed
description OBJECTIVE: The purpose of this study was to determine the impact of varying inflation parameters on paclitaxel delivery and retention using a commercially available DCB. BACKGROUND: Drug-coated balloons (DCB) have become the standard treatment for peripheral artery disease. Clinical data suggest that varying DCB delivery parameters directly impact patient outcome. Differences in delivery parameters can potentially alter the retention of the drug coating on DCBs. METHODS: Harvested porcine carotid arteries were utilized in an ex vivo pulsatile flow bioreactor system. The DCBs were then deployed at a DCB-to-artery ratio of 1:1 or 1.25:1, an inflation time of 30 seconds or 1 minute and transit time of 30 seconds or 3 minutes. The amount of drug retention in arterial tissue was evaluated by pharmacokinetic analysis at 1 hour and 1 day post DCB deployment. RESULTS: Arterial paclitaxel levels were found to be less at an inflation ratio of 1:1 with 3-minute transit time as compared to 30 seconds of transit time at 1 hour (12.3 ± 1.6 ng/mg vs. 391 ± 139 ng/mg, P = .036). At 1-day, DCBs deployed at a ratio of 1:1 resulted in less drug retention as compared to 1.25:1 (61.3 ± 23.1 ng/mg vs. 404 ± 195 ng/mg, P = .013). CONCLUSION: Arterial paclitaxel retention is reduced with extended transit times and sub-optimal expansion of the balloon. Optimization of delivery parameters can serve as an effective strategy to enhance clinical DCB outcomes.
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spelling pubmed-95494712022-10-10 Understanding the Mechanism of Drug Transfer and Retention of Drug-Coated Balloons Villar-Matamoros, Estefanny Stokes, Lauren Lloret, Alyssa Todd, Meagan Tillman, Bryan W. Yazdani, Saami K. J Cardiovasc Pharmacol Ther Article OBJECTIVE: The purpose of this study was to determine the impact of varying inflation parameters on paclitaxel delivery and retention using a commercially available DCB. BACKGROUND: Drug-coated balloons (DCB) have become the standard treatment for peripheral artery disease. Clinical data suggest that varying DCB delivery parameters directly impact patient outcome. Differences in delivery parameters can potentially alter the retention of the drug coating on DCBs. METHODS: Harvested porcine carotid arteries were utilized in an ex vivo pulsatile flow bioreactor system. The DCBs were then deployed at a DCB-to-artery ratio of 1:1 or 1.25:1, an inflation time of 30 seconds or 1 minute and transit time of 30 seconds or 3 minutes. The amount of drug retention in arterial tissue was evaluated by pharmacokinetic analysis at 1 hour and 1 day post DCB deployment. RESULTS: Arterial paclitaxel levels were found to be less at an inflation ratio of 1:1 with 3-minute transit time as compared to 30 seconds of transit time at 1 hour (12.3 ± 1.6 ng/mg vs. 391 ± 139 ng/mg, P = .036). At 1-day, DCBs deployed at a ratio of 1:1 resulted in less drug retention as compared to 1.25:1 (61.3 ± 23.1 ng/mg vs. 404 ± 195 ng/mg, P = .013). CONCLUSION: Arterial paclitaxel retention is reduced with extended transit times and sub-optimal expansion of the balloon. Optimization of delivery parameters can serve as an effective strategy to enhance clinical DCB outcomes. 2022 /pmc/articles/PMC9549471/ /pubmed/35972237 http://dx.doi.org/10.1177/10742484221119559 Text en https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Article
Villar-Matamoros, Estefanny
Stokes, Lauren
Lloret, Alyssa
Todd, Meagan
Tillman, Bryan W.
Yazdani, Saami K.
Understanding the Mechanism of Drug Transfer and Retention of Drug-Coated Balloons
title Understanding the Mechanism of Drug Transfer and Retention of Drug-Coated Balloons
title_full Understanding the Mechanism of Drug Transfer and Retention of Drug-Coated Balloons
title_fullStr Understanding the Mechanism of Drug Transfer and Retention of Drug-Coated Balloons
title_full_unstemmed Understanding the Mechanism of Drug Transfer and Retention of Drug-Coated Balloons
title_short Understanding the Mechanism of Drug Transfer and Retention of Drug-Coated Balloons
title_sort understanding the mechanism of drug transfer and retention of drug-coated balloons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549471/
https://www.ncbi.nlm.nih.gov/pubmed/35972237
http://dx.doi.org/10.1177/10742484221119559
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