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PLCL/PCL dressings with platelet lysate and growth factors embedded in fibrin for chronic wound regeneration

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    SYSNO ASEP0568881
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitlePLCL/PCL dressings with platelet lysate and growth factors embedded in fibrin for chronic wound regeneration
    Author(s) Táborská, Johanka (UMCH-V)
    Blanquer, Andreu (FGU-C) RID, ORCID
    Brynda, Eduard (UMCH-V) RID
    Filová, Elena (FGU-C) RID, ORCID
    Stiborová, Lenka (UMCH-V)
    Jenčová, V. (CZ)
    Havlíčková, K. (CZ)
    Riedelová, Zuzana (UMCH-V) ORCID
    Riedel, Tomáš (UMCH-V) RID, ORCID
    Source TitleInternational Journal of Nanomedicine. - : Dove Medical Press
    Roč. 18, 3 February (2023), s. 595-610
    Number of pages16 s.
    Languageeng - English
    CountryNZ - New Zealand
    Keywordshuman platelet lysate ; diabetic ulcer ; fibrin coating
    Subject RIVFB - Endocrinology, Diabetology, Metabolism, Nutrition
    OECD categoryEndocrinology and metabolism (including diabetes, hormones)
    R&D ProjectsNV18-01-00332 GA MZd - Ministry of Health (MZ)
    LX22NPO5104 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Method of publishingOpen access
    Institutional supportUMCH-V - RVO:61389013 ; FGU-C - RVO:67985823
    UT WOS000928064400001
    EID SCOPUS85147762343
    DOI10.2147/IJN.S393890
    AnnotationThe formation of diabetic ulcers (DU) is a common complication for diabetic patients resulting in serious chronic wounds. There is therefore, an urgent need for complex treatment of this problem. This study examines a bioactive wound dressing of a biodegradable electrospun nanofibrous blend of poly(L-lactide-co-ϵ-caprolactone) and poly(ϵ-caprolactone) (PLCL/PCL) covered by a thin fibrin layer for sustained delivery of bioactive molecules. Electrospun PLCL/PCL nanofibers were coated with fibrin-based coating prepared by a controlled technique and enriched with human platelet lysate (hPL), fibroblast growth factor 2 (FGF), and vascular endothelial growth factor (VEGF). The coating was characterized by scanning electron microscopy and fluorescent microscopy. Protein content and its release rate and the effect on human saphenous vein endothelial cells (HSVEC) were evaluated. The highest protein amount is achieved by the coating of PLCL/PCL with a fibrin mesh containing 20% v/v hPL (NF20). The fibrin coating serves as an excellent scaffold to accumulate bioactive molecules from hPL such as PDGF-BB, fibronectin (Fn), and α-2 antiplasmin. The NF20 coating shows both fast and a sustained release of the attached bioactive molecules (Fn, VEGF, FGF). The dressing significantly increases the viability of human saphenous vein endothelial cells (HSVECs) cultivated on a collagen-based wound model. The exogenous addition of FGF and VEGF during the coating procedure further increases the HSVECs viability. In addition, the presence of α-2 antiplasmin significantly stabilizes the fibrin mesh and prevents its cleavage by plasmin. The NF20 coating supplemented with FGF and VEGF provides a promising wound dressing for the complex treatment of DU. The incorporation of various bioactive molecules from hPL and growth factors has great potential to support the healing processes by providing appropriate stimuli in the chronic wound.
    WorkplaceInstitute of Macromolecular Chemistry
    ContactEva Čechová, cechova@imc.cas.cz ; Tel.: 296 809 358
    Year of Publishing2024
    Electronic addresshttps://www.dovepress.com/plclpcl-dressings-with-platelet-lysate-and-growth-factors-embedded-in--peer-reviewed-fulltext-article-IJN
Number of the records: 1  

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