Multiparametric cytotoxicity assessment: the effect of gold nanoparticle ligand functionalization on SKOV3 ovarian carcinoma cell death.
AuNP
Gold nanoparticles
cell death
cytotoxicity
nanoparticle chemistry
nanotoxicology
ovarian cancer
Journal
Nanotoxicology
ISSN: 1743-5404
Titre abrégé: Nanotoxicology
Pays: England
ID NLM: 101233132
Informations de publication
Date de publication:
04 2022
04 2022
Historique:
pubmed:
6
7
2022
medline:
3
8
2022
entrez:
5
7
2022
Statut:
ppublish
Résumé
Gold nanoparticles (AuNP) are promising anti-cancer agents because of their modifiable properties and high biocompatibility. This study used multiple parallel analyses to investigate the cytotoxic properties of 5 nm AuNP conjugated to four different ligands with distinct surface chemistry: polyethylene glycol (PEG), trimethylammonium bromide (TMAB), 4-dimethylaminopyridine (DMAP), and carboxyl (COOH). We used a range of biochemical and high-content microscopy methods to evaluate the metabolic function, oxidative stress, cell health, cell viability, and cell morphology in SKOV3 ovarian cancer cells. Each AuNP displayed a distinct cytotoxicity profile. All AuNP species assessed exhibited signs of dose-dependent cytotoxicity when morphology, clonogenic survival, lysosomal uptake, or cell number were measured as the marker of toxicity. All particles except for AuNP-COOH increased SKOV3 apoptosis. In contrast, AuNP-TMAB was the only particle that did not alter the metabolic function or induce significant signs of oxidative stress. These results demonstrate that AuNP surface chemistry impacts the magnitude and mechanism of SKOV3 cell death. Together, these findings reinforce the important role for multiparametric cytotoxicity characterization when considering the utility of novel particles and surface chemistries.
Identifiants
pubmed: 35787735
doi: 10.1080/17435390.2022.2095312
doi:
Substances chimiques
Ligands
0
Polyethylene Glycols
3WJQ0SDW1A
Gold
7440-57-5
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM