J 2021

Modifications of Parylene by Microstructures and Selenium Nanoparticles: Evaluation of Bacterial and Mesenchymal Stem Cell Viability

PEKARKOVA, Jana, Imrich GABLECH, Tatiana FIALOVA, Ondrej BILEK, Zdenka FOHLEROVÁ et. al.

Basic information

Original name

Modifications of Parylene by Microstructures and Selenium Nanoparticles: Evaluation of Bacterial and Mesenchymal Stem Cell Viability

Authors

PEKARKOVA, Jana, Imrich GABLECH (203 Czech Republic), Tatiana FIALOVA (203 Czech Republic), Ondrej BILEK (203 Czech Republic) and Zdenka FOHLEROVÁ (203 Czech Republic, guarantor, belonging to the institution)

Edition

Frontiers in bioengineering and biotechnology, Laussane, Frontiers Media S.A. 2021, 2296-4185

Other information

Language

English

Type of outcome

Článek v odborném periodiku

Field of Study

10608 Biochemistry and molecular biology

Country of publisher

Switzerland

Confidentiality degree

není předmětem státního či obchodního tajemství

References:

Impact factor

Impact factor: 6.064

RIV identification code

RIV/00216224:14110/21:00123976

Organization unit

Faculty of Medicine

UT WoS

000731445100001

Keywords in English

parylene-C; micropillars; selenium nanoparticles; biocompatibility; antimicrobial

Tags

Tags

International impact, Reviewed
Změněno: 27/1/2022 13:52, Mgr. Tereza Miškechová

Abstract

V originále

Parylene-based implants or coatings introduce surfaces suffering from bacteria colonization. Here, we synthesized polyvinylpyrrolidone-stabilized selenium nanoparticles (SeNPs) as the antibacterial agent, and various approaches are studied for their reproducible adsorption, and thus the modification of parylene-C-coated glass substrate. The nanoparticle deposition process is optimized in the nanoparticle concentration to obtain evenly distributed NPs on the flat parylene-C surface. Moreover, the array of parylene-C micropillars is fabricated by the plasma etching of parylene-C on a silicon wafer, and the surface is modified with SeNPs. All designed surfaces are tested against two bacterial pathogens, Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive). The results show no antibacterial effect toward S. aureus, while some bacteriostatic effect is observed for E. coli on the flat and microstructured parylene. However, SeNPs did not enhance the antibacterial effect against both bacteria. Additionally, all designed surfaces show cytotoxic effects toward mesenchymal stem cells at high SeNP deposition. These results provide valuable information about the potential antibacterial treatment of widely used parylene-C in biomedicine.