Počet záznamů: 1  

Quaternized chitosan/heparin polyelectrolyte multilayer films for protein delivery

  1. 1.
    0563944 - ÚMCH 2023 RIV US eng J - Článek v odborném periodiku
    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.
    Biomacromolecules. Roč. 23, č. 11 (2022), s. 4734-4748. ISSN 1525-7797. E-ISSN 1526-4602
    Grant CEP: GA ČR(CZ) GA20-08679S; GA MŠk LX22NPO5102
    Institucionální podpora: RVO:61389013
    Klíčová slova: quaternized chitosan * layer-by-layer film * protein release
    Obor OECD: Polymer science
    Impakt faktor: 6.2, rok: 2022
    Způsob publikování: Open access
    https://pubs.acs.org/doi/10.1021/acs.biomac.2c00926

    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.
    Trvalý link: https://hdl.handle.net/11104/0335736


    Vědecká data: Supporting Information
     
    Název souboruStaženoVelikostKomentářVerzePřístup
    0563944.pdf17.1 MB Creative Commons CC-BYVydavatelský postprintpovolen
     
Počet záznamů: 1  

  Tyto stránky využívají soubory cookies, které usnadňují jejich prohlížení. Další informace o tom jak používáme cookies.