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Effect of Hyaluronic Acid and Pluronic-F68 on the Surface Properties of Foam as a Delivery System for Polidocanol in Sclerotherapy
The use of foams to deliver bioactive agents and drugs is increasing in pharmaceutics. One example is the use of foam as a delivery system for polidocanol (POL) in sclerotherapy, with the addition of bioactive compounds to improve the delivery system being a current subject of study. This work shows...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693533/ https://www.ncbi.nlm.nih.gov/pubmed/33143001 http://dx.doi.org/10.3390/pharmaceutics12111039 |
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author | del Castillo-Santaella, Teresa Yang, Yan Martínez-González, Inmaculada Gálvez-Ruiz, María José Cabrerizo-Vílchez, Miguel Ángel Holgado-Terriza, Juan Antonio Selles-Galiana, Fernando Maldonado-Valderrama, Julia |
author_facet | del Castillo-Santaella, Teresa Yang, Yan Martínez-González, Inmaculada Gálvez-Ruiz, María José Cabrerizo-Vílchez, Miguel Ángel Holgado-Terriza, Juan Antonio Selles-Galiana, Fernando Maldonado-Valderrama, Julia |
author_sort | del Castillo-Santaella, Teresa |
collection | PubMed |
description | The use of foams to deliver bioactive agents and drugs is increasing in pharmaceutics. One example is the use of foam as a delivery system for polidocanol (POL) in sclerotherapy, with the addition of bioactive compounds to improve the delivery system being a current subject of study. This work shows the influence of two bioactive additives on the structure and stability of POL foam: hyaluronic acid (HA) and Pluronic-F68 (F68). HA is a natural non-surface-active biopolymer present in the extracellular matrix while F68 is a surface-active poloxamer that is biocompatible with plasma-derived fluids. Both additives increase the bulk viscosity of the sample, improving foam stability. However, HA doubled and F68 quadruplicated the foam half lifetime of POL. HA reduced the size and polydispersity of the bubble size distribution and increased the surface elasticity with respect to POL. Both facts have a positive impact in terms of foam stability. F68 also altered bubble structure and increased surface elasticity, again contributing to the enhancement of foam stability. The surface characterization of these systems is important, as in foam sclerotherapy it is crucial to assure the presence of POL at the surface of the bubbles in order to deliver the sclerosant agent in the target vein. |
format | Online Article Text |
id | pubmed-7693533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76935332020-11-28 Effect of Hyaluronic Acid and Pluronic-F68 on the Surface Properties of Foam as a Delivery System for Polidocanol in Sclerotherapy del Castillo-Santaella, Teresa Yang, Yan Martínez-González, Inmaculada Gálvez-Ruiz, María José Cabrerizo-Vílchez, Miguel Ángel Holgado-Terriza, Juan Antonio Selles-Galiana, Fernando Maldonado-Valderrama, Julia Pharmaceutics Article The use of foams to deliver bioactive agents and drugs is increasing in pharmaceutics. One example is the use of foam as a delivery system for polidocanol (POL) in sclerotherapy, with the addition of bioactive compounds to improve the delivery system being a current subject of study. This work shows the influence of two bioactive additives on the structure and stability of POL foam: hyaluronic acid (HA) and Pluronic-F68 (F68). HA is a natural non-surface-active biopolymer present in the extracellular matrix while F68 is a surface-active poloxamer that is biocompatible with plasma-derived fluids. Both additives increase the bulk viscosity of the sample, improving foam stability. However, HA doubled and F68 quadruplicated the foam half lifetime of POL. HA reduced the size and polydispersity of the bubble size distribution and increased the surface elasticity with respect to POL. Both facts have a positive impact in terms of foam stability. F68 also altered bubble structure and increased surface elasticity, again contributing to the enhancement of foam stability. The surface characterization of these systems is important, as in foam sclerotherapy it is crucial to assure the presence of POL at the surface of the bubbles in order to deliver the sclerosant agent in the target vein. MDPI 2020-10-30 /pmc/articles/PMC7693533/ /pubmed/33143001 http://dx.doi.org/10.3390/pharmaceutics12111039 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article del Castillo-Santaella, Teresa Yang, Yan Martínez-González, Inmaculada Gálvez-Ruiz, María José Cabrerizo-Vílchez, Miguel Ángel Holgado-Terriza, Juan Antonio Selles-Galiana, Fernando Maldonado-Valderrama, Julia Effect of Hyaluronic Acid and Pluronic-F68 on the Surface Properties of Foam as a Delivery System for Polidocanol in Sclerotherapy |
title | Effect of Hyaluronic Acid and Pluronic-F68 on the Surface Properties of Foam as a Delivery System for Polidocanol in Sclerotherapy |
title_full | Effect of Hyaluronic Acid and Pluronic-F68 on the Surface Properties of Foam as a Delivery System for Polidocanol in Sclerotherapy |
title_fullStr | Effect of Hyaluronic Acid and Pluronic-F68 on the Surface Properties of Foam as a Delivery System for Polidocanol in Sclerotherapy |
title_full_unstemmed | Effect of Hyaluronic Acid and Pluronic-F68 on the Surface Properties of Foam as a Delivery System for Polidocanol in Sclerotherapy |
title_short | Effect of Hyaluronic Acid and Pluronic-F68 on the Surface Properties of Foam as a Delivery System for Polidocanol in Sclerotherapy |
title_sort | effect of hyaluronic acid and pluronic-f68 on the surface properties of foam as a delivery system for polidocanol in sclerotherapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693533/ https://www.ncbi.nlm.nih.gov/pubmed/33143001 http://dx.doi.org/10.3390/pharmaceutics12111039 |
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