Cargando…

Nanostructured Dense Collagen‐Polyester Composite Hydrogels as Amphiphilic Platforms for Drug Delivery

Associating collagen with biodegradable hydrophobic polyesters constitutes a promising method for the design of medicated biomaterials. Current collagen‐polyester composite hydrogels consisting of pre‐formed polymeric particles encapsulated within a low concentrated collagen hydrogel suffer from poo...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Xiaolin, Ronsin, Olivier, Gravez, Basile, Farman, Nicolette, Baumberger, Tristan, Jaisser, Frédéric, Coradin, Thibaud, Hélary, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025010/
https://www.ncbi.nlm.nih.gov/pubmed/33854901
http://dx.doi.org/10.1002/advs.202004213
_version_ 1783675427829579776
author Wang, Xiaolin
Ronsin, Olivier
Gravez, Basile
Farman, Nicolette
Baumberger, Tristan
Jaisser, Frédéric
Coradin, Thibaud
Hélary, Christophe
author_facet Wang, Xiaolin
Ronsin, Olivier
Gravez, Basile
Farman, Nicolette
Baumberger, Tristan
Jaisser, Frédéric
Coradin, Thibaud
Hélary, Christophe
author_sort Wang, Xiaolin
collection PubMed
description Associating collagen with biodegradable hydrophobic polyesters constitutes a promising method for the design of medicated biomaterials. Current collagen‐polyester composite hydrogels consisting of pre‐formed polymeric particles encapsulated within a low concentrated collagen hydrogel suffer from poor physical properties and low drug loading. Herein, an amphiphilic composite platform associating dense collagen hydrogels and up to 50 wt% polyesters with different hydrophobicity and chain length is developed. An original method of fabrication is disclosed based on in situ nanoprecipitation of polyesters impregnated in a pre‐formed 3D dense collagen network. Composites made of poly(lactic‐co‐glycolic acid) (PLGA) and poly(lactic acid) (PLA) but not polycaprolactone (PCL) exhibit improved mechanical properties compared to those of pure collagen dense hydrogels while keeping a high degree of hydration. Release kinetics of spironolactone, a lipophilic steroid used as a drug model, can be tuned over one month. No cytotoxicity of the composites is observed on fibroblasts and keratinocytes. Unlike the incorporation of pre‐formed particles, the new process allows for both improved physical properties of collagen hydrogels and controlled drug delivery. The ease of fabrication, wide range of accessible compositions, and positive preliminary safety evaluations of these collagen‐polyesters will favor their translation into clinics in wide areas such as drug delivery and tissue engineering.
format Online
Article
Text
id pubmed-8025010
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-80250102021-04-13 Nanostructured Dense Collagen‐Polyester Composite Hydrogels as Amphiphilic Platforms for Drug Delivery Wang, Xiaolin Ronsin, Olivier Gravez, Basile Farman, Nicolette Baumberger, Tristan Jaisser, Frédéric Coradin, Thibaud Hélary, Christophe Adv Sci (Weinh) Full Papers Associating collagen with biodegradable hydrophobic polyesters constitutes a promising method for the design of medicated biomaterials. Current collagen‐polyester composite hydrogels consisting of pre‐formed polymeric particles encapsulated within a low concentrated collagen hydrogel suffer from poor physical properties and low drug loading. Herein, an amphiphilic composite platform associating dense collagen hydrogels and up to 50 wt% polyesters with different hydrophobicity and chain length is developed. An original method of fabrication is disclosed based on in situ nanoprecipitation of polyesters impregnated in a pre‐formed 3D dense collagen network. Composites made of poly(lactic‐co‐glycolic acid) (PLGA) and poly(lactic acid) (PLA) but not polycaprolactone (PCL) exhibit improved mechanical properties compared to those of pure collagen dense hydrogels while keeping a high degree of hydration. Release kinetics of spironolactone, a lipophilic steroid used as a drug model, can be tuned over one month. No cytotoxicity of the composites is observed on fibroblasts and keratinocytes. Unlike the incorporation of pre‐formed particles, the new process allows for both improved physical properties of collagen hydrogels and controlled drug delivery. The ease of fabrication, wide range of accessible compositions, and positive preliminary safety evaluations of these collagen‐polyesters will favor their translation into clinics in wide areas such as drug delivery and tissue engineering. John Wiley and Sons Inc. 2021-02-18 /pmc/articles/PMC8025010/ /pubmed/33854901 http://dx.doi.org/10.1002/advs.202004213 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Wang, Xiaolin
Ronsin, Olivier
Gravez, Basile
Farman, Nicolette
Baumberger, Tristan
Jaisser, Frédéric
Coradin, Thibaud
Hélary, Christophe
Nanostructured Dense Collagen‐Polyester Composite Hydrogels as Amphiphilic Platforms for Drug Delivery
title Nanostructured Dense Collagen‐Polyester Composite Hydrogels as Amphiphilic Platforms for Drug Delivery
title_full Nanostructured Dense Collagen‐Polyester Composite Hydrogels as Amphiphilic Platforms for Drug Delivery
title_fullStr Nanostructured Dense Collagen‐Polyester Composite Hydrogels as Amphiphilic Platforms for Drug Delivery
title_full_unstemmed Nanostructured Dense Collagen‐Polyester Composite Hydrogels as Amphiphilic Platforms for Drug Delivery
title_short Nanostructured Dense Collagen‐Polyester Composite Hydrogels as Amphiphilic Platforms for Drug Delivery
title_sort nanostructured dense collagen‐polyester composite hydrogels as amphiphilic platforms for drug delivery
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8025010/
https://www.ncbi.nlm.nih.gov/pubmed/33854901
http://dx.doi.org/10.1002/advs.202004213
work_keys_str_mv AT wangxiaolin nanostructureddensecollagenpolyestercompositehydrogelsasamphiphilicplatformsfordrugdelivery
AT ronsinolivier nanostructureddensecollagenpolyestercompositehydrogelsasamphiphilicplatformsfordrugdelivery
AT gravezbasile nanostructureddensecollagenpolyestercompositehydrogelsasamphiphilicplatformsfordrugdelivery
AT farmannicolette nanostructureddensecollagenpolyestercompositehydrogelsasamphiphilicplatformsfordrugdelivery
AT baumbergertristan nanostructureddensecollagenpolyestercompositehydrogelsasamphiphilicplatformsfordrugdelivery
AT jaisserfrederic nanostructureddensecollagenpolyestercompositehydrogelsasamphiphilicplatformsfordrugdelivery
AT coradinthibaud nanostructureddensecollagenpolyestercompositehydrogelsasamphiphilicplatformsfordrugdelivery
AT helarychristophe nanostructureddensecollagenpolyestercompositehydrogelsasamphiphilicplatformsfordrugdelivery