Cargando…
Quaternized Chitosan/Heparin Polyelectrolyte Multilayer Films for Protein Delivery
[Image: see text] Layer-by-layer (LbL) polyelectrolyte coatings are intensively studied as reservoirs of bioactive proteins for modulating interactions between biomaterial surfaces and cells. Mild conditions for the incorporation of growth factors into delivery systems are required to maintain prote...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667497/ https://www.ncbi.nlm.nih.gov/pubmed/36289568 http://dx.doi.org/10.1021/acs.biomac.2c00926 |
_version_ | 1784831737256214528 |
---|---|
author | Urbaniak, Tomasz García-Briones, Gabriela S. Zhigunov, Alexander Hladysh, Sviatoslav Adrian, Edyta Lobaz, Volodymyr Krunclová, Tereza Janoušková, Olga Pop-Georgievski, Ognen Kubies, Dana |
author_facet | Urbaniak, Tomasz García-Briones, Gabriela S. Zhigunov, Alexander Hladysh, Sviatoslav Adrian, Edyta Lobaz, Volodymyr Krunclová, Tereza Janoušková, Olga Pop-Georgievski, Ognen Kubies, Dana |
author_sort | Urbaniak, Tomasz |
collection | PubMed |
description | [Image: see text] Layer-by-layer (LbL) polyelectrolyte coatings are intensively studied as reservoirs of bioactive proteins for modulating interactions between biomaterial surfaces and cells. Mild conditions for the incorporation of growth factors into delivery systems are required to maintain protein bioactivity. Here, we present LbL films composed of water-soluble N-[(2-hydroxy-3-trimethylammonium)propyl] chitosan chloride (HTCC), heparin (Hep), and tannic acid (TA) fabricated under physiological conditions with the ability to release heparin-binding proteins. Surface plasmon resonance analysis showed that the films formed on an anchoring HTCC/TA bilayer, with TA serving as a physical crosslinker, were more stable during their assembly, leading to increased film thickness and increased protein release. X-ray reflectivity measurements confirmed intermixing of the deposited layers. Protein release also increased when the proteins were present as an integral part of the Hep layers rather than as individual protein layers. The 4-week release pattern depended on the protein type; VEGF, CXCL12, and TGF-β1 exhibited a typical high initial release, whereas FGF-2 was sustainably released over 4 weeks. Notably, the films were nontoxic, and the released proteins retained their bioactivity, as demonstrated by the intensive chemotaxis of T-lymphocytes in response to the released CXCL12. Therefore, the proposed LbL films are promising biomaterial coating candidates for stimulating cellular responses. |
format | Online Article Text |
id | pubmed-9667497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96674972022-11-17 Quaternized Chitosan/Heparin Polyelectrolyte Multilayer Films for Protein Delivery Urbaniak, Tomasz García-Briones, Gabriela S. Zhigunov, Alexander Hladysh, Sviatoslav Adrian, Edyta Lobaz, Volodymyr Krunclová, Tereza Janoušková, Olga Pop-Georgievski, Ognen Kubies, Dana Biomacromolecules [Image: see text] Layer-by-layer (LbL) polyelectrolyte coatings are intensively studied as reservoirs of bioactive proteins for modulating interactions between biomaterial surfaces and cells. Mild conditions for the incorporation of growth factors into delivery systems are required to maintain protein bioactivity. Here, we present LbL films composed of water-soluble N-[(2-hydroxy-3-trimethylammonium)propyl] chitosan chloride (HTCC), heparin (Hep), and tannic acid (TA) fabricated under physiological conditions with the ability to release heparin-binding proteins. Surface plasmon resonance analysis showed that the films formed on an anchoring HTCC/TA bilayer, with TA serving as a physical crosslinker, were more stable during their assembly, leading to increased film thickness and increased protein release. X-ray reflectivity measurements confirmed intermixing of the deposited layers. Protein release also increased when the proteins were present as an integral part of the Hep layers rather than as individual protein layers. The 4-week release pattern depended on the protein type; VEGF, CXCL12, and TGF-β1 exhibited a typical high initial release, whereas FGF-2 was sustainably released over 4 weeks. Notably, the films were nontoxic, and the released proteins retained their bioactivity, as demonstrated by the intensive chemotaxis of T-lymphocytes in response to the released CXCL12. Therefore, the proposed LbL films are promising biomaterial coating candidates for stimulating cellular responses. American Chemical Society 2022-10-27 2022-11-14 /pmc/articles/PMC9667497/ /pubmed/36289568 http://dx.doi.org/10.1021/acs.biomac.2c00926 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Urbaniak, Tomasz García-Briones, Gabriela S. Zhigunov, Alexander Hladysh, Sviatoslav Adrian, Edyta Lobaz, Volodymyr Krunclová, Tereza Janoušková, Olga Pop-Georgievski, Ognen Kubies, Dana Quaternized Chitosan/Heparin Polyelectrolyte Multilayer Films for Protein Delivery |
title | Quaternized Chitosan/Heparin Polyelectrolyte Multilayer
Films for Protein Delivery |
title_full | Quaternized Chitosan/Heparin Polyelectrolyte Multilayer
Films for Protein Delivery |
title_fullStr | Quaternized Chitosan/Heparin Polyelectrolyte Multilayer
Films for Protein Delivery |
title_full_unstemmed | Quaternized Chitosan/Heparin Polyelectrolyte Multilayer
Films for Protein Delivery |
title_short | Quaternized Chitosan/Heparin Polyelectrolyte Multilayer
Films for Protein Delivery |
title_sort | quaternized chitosan/heparin polyelectrolyte multilayer
films for protein delivery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9667497/ https://www.ncbi.nlm.nih.gov/pubmed/36289568 http://dx.doi.org/10.1021/acs.biomac.2c00926 |
work_keys_str_mv | AT urbaniaktomasz quaternizedchitosanheparinpolyelectrolytemultilayerfilmsforproteindelivery AT garciabrionesgabrielas quaternizedchitosanheparinpolyelectrolytemultilayerfilmsforproteindelivery AT zhigunovalexander quaternizedchitosanheparinpolyelectrolytemultilayerfilmsforproteindelivery AT hladyshsviatoslav quaternizedchitosanheparinpolyelectrolytemultilayerfilmsforproteindelivery AT adrianedyta quaternizedchitosanheparinpolyelectrolytemultilayerfilmsforproteindelivery AT lobazvolodymyr quaternizedchitosanheparinpolyelectrolytemultilayerfilmsforproteindelivery AT krunclovatereza quaternizedchitosanheparinpolyelectrolytemultilayerfilmsforproteindelivery AT janouskovaolga quaternizedchitosanheparinpolyelectrolytemultilayerfilmsforproteindelivery AT popgeorgievskiognen quaternizedchitosanheparinpolyelectrolytemultilayerfilmsforproteindelivery AT kubiesdana quaternizedchitosanheparinpolyelectrolytemultilayerfilmsforproteindelivery |