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.

Základní údaje

Originální název

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

Autoři

PEKARKOVA, Jana, Imrich GABLECH (203 Česká republika), Tatiana FIALOVA (203 Česká republika), Ondrej BILEK (203 Česká republika) a Zdenka FOHLEROVÁ (203 Česká republika, garant, domácí)

Vydání

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

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

10608 Biochemistry and molecular biology

Stát vydavatele

Švýcarsko

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 6.064

Kód RIV

RIV/00216224:14110/21:00123976

Organizační jednotka

Lékařská fakulta

UT WoS

000731445100001

Klíčová slova anglicky

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

Štítky

Příznaky

Mezinárodní význam, Recenzováno
Změněno: 27. 1. 2022 13:52, Mgr. Tereza Miškechová

Anotace

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.