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Benefits of polidocanol endovenous microfoam (Varithena®) compared with physician-compounded foams

OBJECTIVE: To compare foam bubble size and bubble size distribution, stability, and degradation rate of commercially available polidocanol endovenous microfoam (Varithena®) and physician-compounded foams using a number of laboratory tests. METHODS: Foam properties of polidocanol endovenous microfoam...

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Autores principales: Carugo, Dario, Ankrett, Dyan N, Zhao, Xuefeng, Zhang, Xunli, Hill, Martyn, O’Byrne, Vincent, Hoad, James, Arif, Mehreen, Wright, David DI, Lewis, Andrew L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838175/
https://www.ncbi.nlm.nih.gov/pubmed/26036246
http://dx.doi.org/10.1177/0268355515589063
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author Carugo, Dario
Ankrett, Dyan N
Zhao, Xuefeng
Zhang, Xunli
Hill, Martyn
O’Byrne, Vincent
Hoad, James
Arif, Mehreen
Wright, David DI
Lewis, Andrew L
author_facet Carugo, Dario
Ankrett, Dyan N
Zhao, Xuefeng
Zhang, Xunli
Hill, Martyn
O’Byrne, Vincent
Hoad, James
Arif, Mehreen
Wright, David DI
Lewis, Andrew L
author_sort Carugo, Dario
collection PubMed
description OBJECTIVE: To compare foam bubble size and bubble size distribution, stability, and degradation rate of commercially available polidocanol endovenous microfoam (Varithena®) and physician-compounded foams using a number of laboratory tests. METHODS: Foam properties of polidocanol endovenous microfoam and physician-compounded foams were measured and compared using a glass-plate method and a Sympatec QICPIC image analysis method to measure bubble size and bubble size distribution, Turbiscan™ LAB for foam half time and drainage and a novel biomimetic vein model to measure foam stability. Physician-compounded foams composed of polidocanol and room air, CO(2), or mixtures of oxygen and carbon dioxide (O(2):CO(2)) were generated by different methods. RESULTS: Polidocanol endovenous microfoam was found to have a narrow bubble size distribution with no large (>500 µm) bubbles. Physician-compounded foams made with the Tessari method had broader bubble size distribution and large bubbles, which have an impact on foam stability. Polidocanol endovenous microfoam had a lower degradation rate than any physician-compounded foams, including foams made using room air (p < 0.035). The same result was obtained at different liquid to gas ratios (1:4 and 1:7) for physician-compounded foams. In all tests performed, CO(2) foams were the least stable and different O(2):CO(2) mixtures had intermediate performance. In the biomimetic vein model, polidocanol endovenous microfoam had the slowest degradation rate and longest calculated dwell time, which represents the length of time the foam is in contact with the vein, almost twice that of physician-compounded foams using room air and eight times better than physician-compounded foams prepared using equivalent gas mixes. CONCLUSION: Bubble size, bubble size distribution and stability of various sclerosing foam formulations show that polidocanol endovenous microfoam results in better overall performance compared with physician-compounded foams. Polidocanol endovenous microfoam offers better stability and cohesive properties in a biomimetic vein model compared to physician-compounded foams. Polidocanol endovenous microfoam, which is indicated in the United States for treatment of great saphenous vein system incompetence, provides clinicians with a consistent product with enhanced handling properties.
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spelling pubmed-48381752016-04-22 Benefits of polidocanol endovenous microfoam (Varithena®) compared with physician-compounded foams Carugo, Dario Ankrett, Dyan N Zhao, Xuefeng Zhang, Xunli Hill, Martyn O’Byrne, Vincent Hoad, James Arif, Mehreen Wright, David DI Lewis, Andrew L Phlebology Original Articles OBJECTIVE: To compare foam bubble size and bubble size distribution, stability, and degradation rate of commercially available polidocanol endovenous microfoam (Varithena®) and physician-compounded foams using a number of laboratory tests. METHODS: Foam properties of polidocanol endovenous microfoam and physician-compounded foams were measured and compared using a glass-plate method and a Sympatec QICPIC image analysis method to measure bubble size and bubble size distribution, Turbiscan™ LAB for foam half time and drainage and a novel biomimetic vein model to measure foam stability. Physician-compounded foams composed of polidocanol and room air, CO(2), or mixtures of oxygen and carbon dioxide (O(2):CO(2)) were generated by different methods. RESULTS: Polidocanol endovenous microfoam was found to have a narrow bubble size distribution with no large (>500 µm) bubbles. Physician-compounded foams made with the Tessari method had broader bubble size distribution and large bubbles, which have an impact on foam stability. Polidocanol endovenous microfoam had a lower degradation rate than any physician-compounded foams, including foams made using room air (p < 0.035). The same result was obtained at different liquid to gas ratios (1:4 and 1:7) for physician-compounded foams. In all tests performed, CO(2) foams were the least stable and different O(2):CO(2) mixtures had intermediate performance. In the biomimetic vein model, polidocanol endovenous microfoam had the slowest degradation rate and longest calculated dwell time, which represents the length of time the foam is in contact with the vein, almost twice that of physician-compounded foams using room air and eight times better than physician-compounded foams prepared using equivalent gas mixes. CONCLUSION: Bubble size, bubble size distribution and stability of various sclerosing foam formulations show that polidocanol endovenous microfoam results in better overall performance compared with physician-compounded foams. Polidocanol endovenous microfoam offers better stability and cohesive properties in a biomimetic vein model compared to physician-compounded foams. Polidocanol endovenous microfoam, which is indicated in the United States for treatment of great saphenous vein system incompetence, provides clinicians with a consistent product with enhanced handling properties. SAGE Publications 2015-06-01 2016-05 /pmc/articles/PMC4838175/ /pubmed/26036246 http://dx.doi.org/10.1177/0268355515589063 Text en © The Author(s) 2015 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) 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 page(https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Carugo, Dario
Ankrett, Dyan N
Zhao, Xuefeng
Zhang, Xunli
Hill, Martyn
O’Byrne, Vincent
Hoad, James
Arif, Mehreen
Wright, David DI
Lewis, Andrew L
Benefits of polidocanol endovenous microfoam (Varithena®) compared with physician-compounded foams
title Benefits of polidocanol endovenous microfoam (Varithena®) compared with physician-compounded foams
title_full Benefits of polidocanol endovenous microfoam (Varithena®) compared with physician-compounded foams
title_fullStr Benefits of polidocanol endovenous microfoam (Varithena®) compared with physician-compounded foams
title_full_unstemmed Benefits of polidocanol endovenous microfoam (Varithena®) compared with physician-compounded foams
title_short Benefits of polidocanol endovenous microfoam (Varithena®) compared with physician-compounded foams
title_sort benefits of polidocanol endovenous microfoam (varithena®) compared with physician-compounded foams
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838175/
https://www.ncbi.nlm.nih.gov/pubmed/26036246
http://dx.doi.org/10.1177/0268355515589063
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