Modification of PCL Scaffolds by Reactive Magnetron Sputtering: A Possibility for Modulating Macrophage Responses

dc.contributor.authorStankevich, Ksenia S.
dc.contributor.authorKudryavtseva, Valeriya L.
dc.contributor.authorBolbasov, Evgeny N.
dc.contributor.authorShesterikov, Evgeny V.
dc.contributor.authorLarionova, Irina V.
dc.contributor.authorShapovalova, Yelena G.
dc.contributor.authorDomracheva, Liubov V.
dc.contributor.authorVolokhova, Apollinariya A.
dc.contributor.authorKurzina, Irina A.
dc.contributor.authorZhukov, Yuri M.
dc.contributor.authorMalashicheva, Anna B.
dc.contributor.authorKzhyshkowska, Julia G.
dc.contributor.authorTverdokhlebov, Sergei I.
dc.date.accessioned2022-03-04T17:46:03Z
dc.date.available2022-03-04T17:46:03Z
dc.date.issued2020
dc.description.abstractDirect current (DC) reactive magnetron sputtering is as an efficient method for enhancing the biocompatibility of poly(ε-caprolactone) (PCL) scaffolds. However, the PCL chemical bonding state, the composition of the deposited coating, and their interaction with immune cells remain unknown. Herein, we demonstrated that the DC reactive magnetron sputtering of the titanium target in a nitrogen atmosphere leads to the formation of nitrogen-containing moieties and the titanium dioxide coating on the scaffold surface. We have provided the possible mechanism of PCL fragmentation and coating formation supported by XPS results and DFT calculations. Our preliminary biological studies suggest that DC reactive magnetron sputtering of the titanium target could be an effective tool to control macrophage functional responses toward PCL scaffolds as it allows to inhibit respiratory burst while retaining cell viability and scavenging activity.en_US
dc.identifier.citationKsenia S. Stankevich, Valeriya L. Kudryavtseva, Evgeny N. Bolbasov, Evgeny V. Shesterikov, Irina V. Larionova, Yelena G. Shapovalova, Liubov V. Domracheva, Apollinariya A. Volokhova, Irina A. Kurzina, Yuri M. Zhukov, Anna B. Malashicheva, Julia G. Kzhyshkowska, and Sergei I. Tverdokhlebov, ACS Biomaterials Science & Engineering 2020 6 (7), 3967-3974 DOI: 10.1021/acsbiomaterials.0c00440en_US
dc.identifier.issn2373-9878
dc.identifier.urihttps://scholarworks.montana.edu/handle/1/16682
dc.language.isoen_USen_US
dc.rightsThis document is the unedited Author’s version of a Submitted Work that was subsequently accepted for publication in ACS Biomaterials Science & Engineering, copyright © American Chemical Society after peer review. To access the final edited and published work see https://doi.org/10.1021/acsbiomaterials.0c00440en_US
dc.titleModification of PCL Scaffolds by Reactive Magnetron Sputtering: A Possibility for Modulating Macrophage Responsesen_US
dc.typeArticleen_US
mus.citation.extentfirstpage3967en_US
mus.citation.extentlastpage3974en_US
mus.citation.issue7en_US
mus.citation.journaltitleACS Biomaterials Science & Engineeringen_US
mus.citation.volume6en_US
mus.data.thumbpage9en_US
mus.identifier.doi10.1021/acsbiomaterials.0c00440en_US
mus.relation.collegeCollege of Letters & Scienceen_US
mus.relation.departmentChemistry & Biochemistry.en_US
mus.relation.universityMontana State University - Bozemanen_US

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