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Chondroitin sulfate-AuNRs electroactive scaffolds for on-demand release of biofactors

Controlled release systems are often integrated into polymeric scaffolds to supply essential biofactors to trigger physiological processes in engineered tissues. Here, we report the modification of chondroitin sulfate (CS) electroactive polymer with gold nanorods (AuNRs) to create hybrid macroporous...

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Autores principales: Malki, Maayan, Shapira, Assaf, Dvir, Tal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8805416/
https://www.ncbi.nlm.nih.gov/pubmed/35101034
http://dx.doi.org/10.1186/s12951-022-01261-8
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author Malki, Maayan
Shapira, Assaf
Dvir, Tal
author_facet Malki, Maayan
Shapira, Assaf
Dvir, Tal
author_sort Malki, Maayan
collection PubMed
description Controlled release systems are often integrated into polymeric scaffolds to supply essential biofactors to trigger physiological processes in engineered tissues. Here, we report the modification of chondroitin sulfate (CS) electroactive polymer with gold nanorods (AuNRs) to create hybrid macroporous scaffolds for enhanced on-demand release of growth factors and cytokines. The mechanical properties, porosity and degradation of the hybrid scaffolds were evaluated, and the viability and functionality of seeded cardiac cells were assessed. Following, the ability to control the release of the enzyme lysozyme, and the cytokine, stromal cell-derived factor 1 (SDF-1) by applying electrical stimulation, was demonstrated. The AuNRs were able to increase the current through the scaffolds, providing an efficient on–off release profile of SDF-1, which resulted in higher migration of cells expressing CXCR4 receptor. Finally, the engineered scaffolds were transplanted in rats and SDF-1 was released daily by electrical stimulation, promoting blood vessel-forming cell infiltration and vascularization. We envision that gold nanoparticles and other conducting nanomaterials can be incorporated into different electroactive materials to improve their capabilities not only for tissue engineering applications, but for a variety of biomedical applications, where enhanced electrical stimulation is needed. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-88054162022-02-03 Chondroitin sulfate-AuNRs electroactive scaffolds for on-demand release of biofactors Malki, Maayan Shapira, Assaf Dvir, Tal J Nanobiotechnology Research Controlled release systems are often integrated into polymeric scaffolds to supply essential biofactors to trigger physiological processes in engineered tissues. Here, we report the modification of chondroitin sulfate (CS) electroactive polymer with gold nanorods (AuNRs) to create hybrid macroporous scaffolds for enhanced on-demand release of growth factors and cytokines. The mechanical properties, porosity and degradation of the hybrid scaffolds were evaluated, and the viability and functionality of seeded cardiac cells were assessed. Following, the ability to control the release of the enzyme lysozyme, and the cytokine, stromal cell-derived factor 1 (SDF-1) by applying electrical stimulation, was demonstrated. The AuNRs were able to increase the current through the scaffolds, providing an efficient on–off release profile of SDF-1, which resulted in higher migration of cells expressing CXCR4 receptor. Finally, the engineered scaffolds were transplanted in rats and SDF-1 was released daily by electrical stimulation, promoting blood vessel-forming cell infiltration and vascularization. We envision that gold nanoparticles and other conducting nanomaterials can be incorporated into different electroactive materials to improve their capabilities not only for tissue engineering applications, but for a variety of biomedical applications, where enhanced electrical stimulation is needed. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2022-01-31 /pmc/articles/PMC8805416/ /pubmed/35101034 http://dx.doi.org/10.1186/s12951-022-01261-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Malki, Maayan
Shapira, Assaf
Dvir, Tal
Chondroitin sulfate-AuNRs electroactive scaffolds for on-demand release of biofactors
title Chondroitin sulfate-AuNRs electroactive scaffolds for on-demand release of biofactors
title_full Chondroitin sulfate-AuNRs electroactive scaffolds for on-demand release of biofactors
title_fullStr Chondroitin sulfate-AuNRs electroactive scaffolds for on-demand release of biofactors
title_full_unstemmed Chondroitin sulfate-AuNRs electroactive scaffolds for on-demand release of biofactors
title_short Chondroitin sulfate-AuNRs electroactive scaffolds for on-demand release of biofactors
title_sort chondroitin sulfate-aunrs electroactive scaffolds for on-demand release of biofactors
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8805416/
https://www.ncbi.nlm.nih.gov/pubmed/35101034
http://dx.doi.org/10.1186/s12951-022-01261-8
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