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Synergy of Hydeal-D(®) and Hyaluronic Acid for Protecting and Restoring Urothelium: In Vitro Characterization
Interstitial cystitis (IC) or painful bladder syndrome is a chronic dysfunction due to an inflammatory condition, characterized by bladder pain and urinary frequency. Currently, no gold standard therapy is available since IC does not respond to conventional ones. Given these premises, the aim of thi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465558/ https://www.ncbi.nlm.nih.gov/pubmed/34575526 http://dx.doi.org/10.3390/pharmaceutics13091450 |
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author | Ruggeri, Marco Pavan, Mauro Soato, Matteo Panfilo, Susi Barbera, Carlo Galesso, Devis Miele, Dalila Rossi, Silvia Di Lucia, Alba Ferrari, Franca Sandri, Giuseppina |
author_facet | Ruggeri, Marco Pavan, Mauro Soato, Matteo Panfilo, Susi Barbera, Carlo Galesso, Devis Miele, Dalila Rossi, Silvia Di Lucia, Alba Ferrari, Franca Sandri, Giuseppina |
author_sort | Ruggeri, Marco |
collection | PubMed |
description | Interstitial cystitis (IC) or painful bladder syndrome is a chronic dysfunction due to an inflammatory condition, characterized by bladder pain and urinary frequency. Currently, no gold standard therapy is available since IC does not respond to conventional ones. Given these premises, the aim of this work was the in vitro characterization of biological properties (mucoadhesion and anti-inflammatory activity) of a commercial product (HydealCyst–HydC) based on hyaluronic acid (HA) and the benzyl ester of HA (Hydeal-D(®)) intended for bladder instillation to restore and/or protect the urothelial layer of glycosamino glycans (GAGs). The in vitro characterization demonstrated that an interaction product is formed between HA and Hydeal-D(®) that has a role in the rheological behavior and mucoadhesive properties. HA was identified as a key component to form the mucoadhesive joint, while the interaction of HA with Hydeal-D(®) improved polysaccharide stability and prolonged the activity ex vivo. Moreover, HydC is cytocompatible with urothelial cells (HTB-4) and possesses an anti-inflammatory effect towards these cells by decreasing the secretion of IL-6 and IL-8, which were both increased in patients with IC, and by increasing the secretion of sulfated GAGs. These two findings, along with the resilience properties of the formulation due to mucoadhesion, suggest the active role of HydC in protecting and restoring urothelium homeostasis. |
format | Online Article Text |
id | pubmed-8465558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84655582021-09-27 Synergy of Hydeal-D(®) and Hyaluronic Acid for Protecting and Restoring Urothelium: In Vitro Characterization Ruggeri, Marco Pavan, Mauro Soato, Matteo Panfilo, Susi Barbera, Carlo Galesso, Devis Miele, Dalila Rossi, Silvia Di Lucia, Alba Ferrari, Franca Sandri, Giuseppina Pharmaceutics Article Interstitial cystitis (IC) or painful bladder syndrome is a chronic dysfunction due to an inflammatory condition, characterized by bladder pain and urinary frequency. Currently, no gold standard therapy is available since IC does not respond to conventional ones. Given these premises, the aim of this work was the in vitro characterization of biological properties (mucoadhesion and anti-inflammatory activity) of a commercial product (HydealCyst–HydC) based on hyaluronic acid (HA) and the benzyl ester of HA (Hydeal-D(®)) intended for bladder instillation to restore and/or protect the urothelial layer of glycosamino glycans (GAGs). The in vitro characterization demonstrated that an interaction product is formed between HA and Hydeal-D(®) that has a role in the rheological behavior and mucoadhesive properties. HA was identified as a key component to form the mucoadhesive joint, while the interaction of HA with Hydeal-D(®) improved polysaccharide stability and prolonged the activity ex vivo. Moreover, HydC is cytocompatible with urothelial cells (HTB-4) and possesses an anti-inflammatory effect towards these cells by decreasing the secretion of IL-6 and IL-8, which were both increased in patients with IC, and by increasing the secretion of sulfated GAGs. These two findings, along with the resilience properties of the formulation due to mucoadhesion, suggest the active role of HydC in protecting and restoring urothelium homeostasis. MDPI 2021-09-11 /pmc/articles/PMC8465558/ /pubmed/34575526 http://dx.doi.org/10.3390/pharmaceutics13091450 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ruggeri, Marco Pavan, Mauro Soato, Matteo Panfilo, Susi Barbera, Carlo Galesso, Devis Miele, Dalila Rossi, Silvia Di Lucia, Alba Ferrari, Franca Sandri, Giuseppina Synergy of Hydeal-D(®) and Hyaluronic Acid for Protecting and Restoring Urothelium: In Vitro Characterization |
title | Synergy of Hydeal-D(®) and Hyaluronic Acid for Protecting and Restoring Urothelium: In Vitro Characterization |
title_full | Synergy of Hydeal-D(®) and Hyaluronic Acid for Protecting and Restoring Urothelium: In Vitro Characterization |
title_fullStr | Synergy of Hydeal-D(®) and Hyaluronic Acid for Protecting and Restoring Urothelium: In Vitro Characterization |
title_full_unstemmed | Synergy of Hydeal-D(®) and Hyaluronic Acid for Protecting and Restoring Urothelium: In Vitro Characterization |
title_short | Synergy of Hydeal-D(®) and Hyaluronic Acid for Protecting and Restoring Urothelium: In Vitro Characterization |
title_sort | synergy of hydeal-d(®) and hyaluronic acid for protecting and restoring urothelium: in vitro characterization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465558/ https://www.ncbi.nlm.nih.gov/pubmed/34575526 http://dx.doi.org/10.3390/pharmaceutics13091450 |
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