Cytotoxicity of Pd nanostructures supported on PEN: Influence of sterilization on Pd/PEN interface
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
27770919
DOI
10.1016/j.msec.2016.09.032
PII: S0928-4931(16)31292-9
Knihovny.cz E-resources
- Keywords
- Annealing, Cytotoxicity, Nanostructure, Palladium, Polyethylene naphthalate, Sputtering, Sterilization,
- MeSH
- Cell Death drug effects MeSH
- NIH 3T3 Cells MeSH
- Fibroblasts cytology drug effects MeSH
- Microscopy, Atomic Force MeSH
- Mice MeSH
- Naphthalenes chemistry MeSH
- Nanostructures chemistry MeSH
- Palladium pharmacology MeSH
- Polyethylene chemistry MeSH
- Polyethylenes chemistry MeSH
- Surface Properties MeSH
- RAW 264.7 Cells MeSH
- Static Electricity MeSH
- Sterilization * MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Naphthalenes MeSH
- Palladium MeSH
- poly(ethylene naphthalate) MeSH Browser
- Polyethylene MeSH
- Polyethylenes MeSH
Non-conventional antimicrobial agents, such as palladium nanostructures, have been increasingly used in the medicinal technology. However, experiences uncovering their harmful and damaging effects to human health have begun to appear. In this study, we have focused on in vitro cytotoxicity assessment of Pd nanostructures supported on a biocompatible polymer. Pd nanolayers of variable thicknesses (ranging from 1.1 to 22.4nm) were sputtered on polyethylene naphthalate (PEN). These nanolayers were transformed by low-temperature post-deposition annealing into discrete nanoislands. Samples were characterized by AFM, XPS, ICP-MS and electrokinetic analysis before and after annealing. Sterilization of samples prior to cytotoxicity testing was done by UV irradiation, autoclave and/or ethanol. Among the listed sterilization techniques, we have chosen the gentlest one which had minimal impact on sample morphology, Pd dissolution and overall Pd/PEN interface quality. Cytotoxic response of Pd nanostructures was determined by WST-1 cell viability assay in vitro using three model cell lines: mouse macrophages (RAW 264.7) and two types of mouse embryonic fibroblasts (L929 and NIH 3T3). Finally, cell morphology in response to Pd/PEN was evaluated by means of fluorescence microscopy.
Institute of Hydrobiology Biology Centre of the AS CR 370 05 Ceske Budejovice Czech Republic
Materials Centre of Usti n L J E Purkyne University 400 96 Usti nad Labem Czech Republic
References provided by Crossref.org
Nanostructured Materials for Artificial Tissue Replacements