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Assessment of a Coated Mitomycin-Releasing Biodegradable Ureteral Stent as an Adjuvant Therapy in Upper Urothelial Carcinoma: A Comparative In Vitro Study

A major limitation of the treatment of low-grade upper tract urothelial carcinoma is the difficulty of intracavitary instillation of adjuvant therapy. Therefore, the aim of this in vitro study was to develop and to assess a new design of biodegradable ureteral stent coated with a silk fibroin matrix...

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Autores principales: Soria, Federico, Aznar-Cervantes, Salvador David, de la Cruz, Julia E., Budia, Alberto, Aranda, Javier, Caballero, Juan Pablo, Serrano, Álvaro, Sánchez Margallo, Francisco Miguel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9370495/
https://www.ncbi.nlm.nih.gov/pubmed/35956574
http://dx.doi.org/10.3390/polym14153059
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author Soria, Federico
Aznar-Cervantes, Salvador David
de la Cruz, Julia E.
Budia, Alberto
Aranda, Javier
Caballero, Juan Pablo
Serrano, Álvaro
Sánchez Margallo, Francisco Miguel
author_facet Soria, Federico
Aznar-Cervantes, Salvador David
de la Cruz, Julia E.
Budia, Alberto
Aranda, Javier
Caballero, Juan Pablo
Serrano, Álvaro
Sánchez Margallo, Francisco Miguel
author_sort Soria, Federico
collection PubMed
description A major limitation of the treatment of low-grade upper tract urothelial carcinoma is the difficulty of intracavitary instillation of adjuvant therapy. Therefore, the aim of this in vitro study was to develop and to assess a new design of biodegradable ureteral stent coated with a silk fibroin matrix for the controlled release of mitomycin C as a chemotherapeutic drug. For this purpose, we assessed the coating of a biodegradable ureteral stent, BraidStent(®), with silk fibroin and subsequently loaded the polymeric matrix with two formulations of mitomycin to evaluate its degradation rate, the concentration of mitomycin released, and changes in the pH and the weight of the stent. Our results confirm that the silk fibroin matrix is able to coat the biodegradable stent and release mitomycin for between 6 and 12 h in the urinary environment. There was a significant delay in the degradation rate of silk fibroin and mitomycin-coated stents compared to bare biodegradable stents, from 6–7 weeks to 13–14 weeks. The present study has shown the feasibility of using mitomycin C-loaded silk fibroin for the coating of biodegradable urinary stents. The addition of mitomycin C to the coating of silk fibroin biodegradable stents could be an attractive approach for intracavitary instillation in the upper urinary tract.
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spelling pubmed-93704952022-08-12 Assessment of a Coated Mitomycin-Releasing Biodegradable Ureteral Stent as an Adjuvant Therapy in Upper Urothelial Carcinoma: A Comparative In Vitro Study Soria, Federico Aznar-Cervantes, Salvador David de la Cruz, Julia E. Budia, Alberto Aranda, Javier Caballero, Juan Pablo Serrano, Álvaro Sánchez Margallo, Francisco Miguel Polymers (Basel) Article A major limitation of the treatment of low-grade upper tract urothelial carcinoma is the difficulty of intracavitary instillation of adjuvant therapy. Therefore, the aim of this in vitro study was to develop and to assess a new design of biodegradable ureteral stent coated with a silk fibroin matrix for the controlled release of mitomycin C as a chemotherapeutic drug. For this purpose, we assessed the coating of a biodegradable ureteral stent, BraidStent(®), with silk fibroin and subsequently loaded the polymeric matrix with two formulations of mitomycin to evaluate its degradation rate, the concentration of mitomycin released, and changes in the pH and the weight of the stent. Our results confirm that the silk fibroin matrix is able to coat the biodegradable stent and release mitomycin for between 6 and 12 h in the urinary environment. There was a significant delay in the degradation rate of silk fibroin and mitomycin-coated stents compared to bare biodegradable stents, from 6–7 weeks to 13–14 weeks. The present study has shown the feasibility of using mitomycin C-loaded silk fibroin for the coating of biodegradable urinary stents. The addition of mitomycin C to the coating of silk fibroin biodegradable stents could be an attractive approach for intracavitary instillation in the upper urinary tract. MDPI 2022-07-28 /pmc/articles/PMC9370495/ /pubmed/35956574 http://dx.doi.org/10.3390/polym14153059 Text en © 2022 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
Soria, Federico
Aznar-Cervantes, Salvador David
de la Cruz, Julia E.
Budia, Alberto
Aranda, Javier
Caballero, Juan Pablo
Serrano, Álvaro
Sánchez Margallo, Francisco Miguel
Assessment of a Coated Mitomycin-Releasing Biodegradable Ureteral Stent as an Adjuvant Therapy in Upper Urothelial Carcinoma: A Comparative In Vitro Study
title Assessment of a Coated Mitomycin-Releasing Biodegradable Ureteral Stent as an Adjuvant Therapy in Upper Urothelial Carcinoma: A Comparative In Vitro Study
title_full Assessment of a Coated Mitomycin-Releasing Biodegradable Ureteral Stent as an Adjuvant Therapy in Upper Urothelial Carcinoma: A Comparative In Vitro Study
title_fullStr Assessment of a Coated Mitomycin-Releasing Biodegradable Ureteral Stent as an Adjuvant Therapy in Upper Urothelial Carcinoma: A Comparative In Vitro Study
title_full_unstemmed Assessment of a Coated Mitomycin-Releasing Biodegradable Ureteral Stent as an Adjuvant Therapy in Upper Urothelial Carcinoma: A Comparative In Vitro Study
title_short Assessment of a Coated Mitomycin-Releasing Biodegradable Ureteral Stent as an Adjuvant Therapy in Upper Urothelial Carcinoma: A Comparative In Vitro Study
title_sort assessment of a coated mitomycin-releasing biodegradable ureteral stent as an adjuvant therapy in upper urothelial carcinoma: a comparative in vitro study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9370495/
https://www.ncbi.nlm.nih.gov/pubmed/35956574
http://dx.doi.org/10.3390/polym14153059
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