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Plasma-Activated Polydimethylsiloxane Microstructured Pattern with Collagen for Improved Myoblast Cell Guidance

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F24%3A43929636" target="_blank" >RIV/60461373:22310/24:43929636 - isvavai.cz</a>

  • Alternative codes found

    RIV/60461373:22330/24:43929636

  • Result on the web

    <a href="https://www.mdpi.com/1422-0067/25/5/2779" target="_blank" >https://www.mdpi.com/1422-0067/25/5/2779</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3390/ijms25052779" target="_blank" >10.3390/ijms25052779</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Plasma-Activated Polydimethylsiloxane Microstructured Pattern with Collagen for Improved Myoblast Cell Guidance

  • Original language description

    We focused on polydimethylsiloxane (PDMS) as a substrate for replication, micropatterning, and construction of biologically active surfaces. The novelty of this study is based on the combination of the argon plasma exposure of a micropatterned PDMS scaffold, where the plasma served as a strong tool for subsequent grafting of collagen coatings and their application as cell growth scaffolds, where the standard was significantly exceeded. As part of the scaffold design, templates with a patterned microstructure of different dimensions (50 x 50, 50 x 20, and 30 x 30 mu m2) were created by photolithography followed by pattern replication on a PDMS polymer substrate. Subsequently, the prepared microstructured PDMS replicas were coated with a type I collagen layer. The sample preparation was followed by the characterization of material surface properties using various analytical techniques, including scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS). To evaluate the biocompatibility of the produced samples, we conducted studies on the interactions between selected polymer replicas and micro- and nanostructures and mammalian cells. Specifically, we utilized mouse myoblasts (C2C12), and our results demonstrate that we achieved excellent cell alignment in conjunction with the development of a cytocompatible surface. Consequently, the outcomes of this research contribute to an enhanced comprehension of surface properties and interactions between structured polymers and mammalian cells. The use of periodic microstructures has the potential to advance the creation of novel materials and scaffolds in tissue engineering. These materials exhibit exceptional biocompatibility and possess the capacity to promote cell adhesion and growth.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    20501 - Materials engineering

Result continuities

  • Project

    <a href="/en/project/GA22-04006S" target="_blank" >GA22-04006S: Organized biopolymer nanopatterns constructed by replication</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2024

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

  • ISSN

    1661-6596

  • e-ISSN

    1422-0067

  • Volume of the periodical

    25

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    LT - LITHUANIA

  • Number of pages

    17

  • Pages from-to

    "2779/1"-17

  • UT code for WoS article

    001182725700001

  • EID of the result in the Scopus database

    2-s2.0-85187797728