The effect of surface modification of TiMg composite on the in-vitro degradation response, cell survival, adhesion, and proliferation.

Corrosion Cytotoxicity Focal adhesion Surface roughness Titanium-magnesium xCELLigence

Journal

Materials science & engineering. C, Materials for biological applications
ISSN: 1873-0191
Titre abrégé: Mater Sci Eng C Mater Biol Appl
Pays: Netherlands
ID NLM: 101484109

Informations de publication

Date de publication:
Aug 2021
Historique:
received: 02 02 2021
revised: 21 05 2021
accepted: 07 06 2021
entrez: 6 7 2021
pubmed: 7 7 2021
medline: 8 7 2021
Statut: ppublish

Résumé

This study is aimed to evaluate the influence of mechanical surface treatment on the degradation response, cell survival, adhesion, and proliferation of a TiMg composite material. Two sets of the TiMg samples with different surface characteristics were studied: i) as-machined samples (TiMg-T) and ii) samples with a mechanically modified surface (TiMg-P). Surface roughness was determined using a confocal microscope. Degradation rates (DR) were evaluated in artificial Plasma, HBSS, and NaCl 0.9%. The cell viability was evaluated using an MTT assay. The initial cell adhesion and spreading were investigated using the direct contact assay. An xCELLigence system was employed to provide real-time cell proliferation. The focal adhesion and cell morphological changes were also examined. The DR of TiMg-P decreased by ⁓5 times compared with that of TiMg-T. Surface of the TiMg-P specimens after 72 h exposure to either HBSS or Plasma was passivated by a layer enriched with bioactive Ca/P species. The cell viability of L929 and Saos-2 after 72 h incubation for TiMg-P was 94.6% and 94.8% compared with 73.8% and 74.3% obtained for TiMg-T, respectively. The direct contact assay showed that the initial adhesion and spreading of the L929 cells incubated with TiMg-P was more pronounced compared with that of TiMg-T. The proliferation rate of Saos-2 cells incubated with TiMg-P was higher when compared with that of TiMg-T, and was almost comparable to that of the DMEM-blank between the 24 and 72 h interval. TiMg-P had a pronounced difference in the number and area of Focal Adhesions (FA) compared with that of TiMg-T. The morphology of cells incubated with TiMg-P was not altered. The results confirmed that the smooth and less strained surface of the TiMg-P samples effectively improved the in-vitro degradation response, cell survival, adhesion, and proliferation.

Identifiants

pubmed: 34225844
pii: S0928-4931(21)00398-2
doi: 10.1016/j.msec.2021.112259
pii:
doi:

Substances chimiques

Titanium D1JT611TNE

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

112259

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Ahmed Mohamed Hassan Ibrahim (AMH)

Institute of Materials and Machine Mechanics, The Slovak Academy of Sciences, Dubravska cesta 9, 84513 Bratislava, Slovakia; Centre of Excellence for Advanced Materials Application, The Slovak Academy of Sciences, Dubravska cesta 9, 84511 Bratislava, Slovakia; Institute of Materials Science, Faculty of Materials Science and Technology in Trnava, Slovak University of Technology in Bratislava, Paulinska 16, 91724 Trnava, Slovakia.

Martina Takacova (M)

Biomedical Research Center, Institute of Virology, Department of Cancer Biology, The Slovak Academy of Sciences, Dubravska cesta 9, 84505 Bratislava, Slovakia.

Lenka Jelenska (L)

Biomedical Research Center, Institute of Virology, Department of Cancer Biology, The Slovak Academy of Sciences, Dubravska cesta 9, 84505 Bratislava, Slovakia.

Lucia Csaderova (L)

Biomedical Research Center, Institute of Virology, Department of Cancer Biology, The Slovak Academy of Sciences, Dubravska cesta 9, 84505 Bratislava, Slovakia.

Martin Balog (M)

Institute of Materials and Machine Mechanics, The Slovak Academy of Sciences, Dubravska cesta 9, 84513 Bratislava, Slovakia; Centre of Excellence for Advanced Materials Application, The Slovak Academy of Sciences, Dubravska cesta 9, 84511 Bratislava, Slovakia. Electronic address: martin.balog@savba.sk.

Juraj Kopacek (J)

Centre of Excellence for Advanced Materials Application, The Slovak Academy of Sciences, Dubravska cesta 9, 84511 Bratislava, Slovakia; Biomedical Research Center, Institute of Virology, Department of Cancer Biology, The Slovak Academy of Sciences, Dubravska cesta 9, 84505 Bratislava, Slovakia.

Eliska Svastova (E)

Centre of Excellence for Advanced Materials Application, The Slovak Academy of Sciences, Dubravska cesta 9, 84511 Bratislava, Slovakia; Biomedical Research Center, Institute of Virology, Department of Cancer Biology, The Slovak Academy of Sciences, Dubravska cesta 9, 84505 Bratislava, Slovakia.

Peter Krizik (P)

Institute of Materials and Machine Mechanics, The Slovak Academy of Sciences, Dubravska cesta 9, 84513 Bratislava, Slovakia.

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Classifications MeSH