TY - JOUR
T1 - Correlation between Ionic Liquid Cytotoxicity and Liposome–Ionic Liquid Interactions
AU - Ruokonen, Suvi Katriina
AU - Sanwald, Corinna
AU - Robciuc, Alexandra
AU - Hietala, Sami
AU - Rantamäki, Antti H.
AU - Witos, Joanna
AU - King, Alistair W.T.
AU - Lämmerhofer, Michael
AU - Wiedmer, Susanne K.
N1 - Funding Information:
Financial support from the Academy of Finland (project number 266342 SKW) and Magnus Ehrnrooth foundation (project number 4703943 SKW) are greatly acknowledged. Harry Ahlgren, Ganesh Poudel, Jesper Långbacka, and Jean-Paul Heeb are acknowledged for their assistance with the DSC, DLS, and NMR measurements.
Publisher Copyright:
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2018/2/21
Y1 - 2018/2/21
N2 - This study aims at extending the understanding of the toxicity mechanism of ionic liquids (ILs) using various analytical methods and cytotoxicity assays. The cytotoxicity of eight ILs and one zwitterionic compound was determined using mammalian and bacterial cells. The time dependency of the IL toxicity was assessed using human corneal epithelial cells. Hemolysis was performed using human red blood cells and the results were compared with destabilization data of synthetic liposomes upon addition of ILs. The effect of the ILs on the size and zeta potential of liposomes revealed information on changes in the lipid bilayer. Differential scanning calorimetry was used to study the penetration of the ILs into the lipid bilayer. Pulsed field gradient nuclear magnetic resonance spectroscopy was used to determine whether the ILs occurred as unimers, micelles, or if they were bound to liposomes. The results show that the investigated ILs can be divided into three groups based on the cytotoxicity mechanism: cell wall disrupting ILs, ILs exerting toxicity through both cell wall penetration and metabolic alteration, and ILs affecting solely on cell metabolism.
AB - This study aims at extending the understanding of the toxicity mechanism of ionic liquids (ILs) using various analytical methods and cytotoxicity assays. The cytotoxicity of eight ILs and one zwitterionic compound was determined using mammalian and bacterial cells. The time dependency of the IL toxicity was assessed using human corneal epithelial cells. Hemolysis was performed using human red blood cells and the results were compared with destabilization data of synthetic liposomes upon addition of ILs. The effect of the ILs on the size and zeta potential of liposomes revealed information on changes in the lipid bilayer. Differential scanning calorimetry was used to study the penetration of the ILs into the lipid bilayer. Pulsed field gradient nuclear magnetic resonance spectroscopy was used to determine whether the ILs occurred as unimers, micelles, or if they were bound to liposomes. The results show that the investigated ILs can be divided into three groups based on the cytotoxicity mechanism: cell wall disrupting ILs, ILs exerting toxicity through both cell wall penetration and metabolic alteration, and ILs affecting solely on cell metabolism.
KW - analytical methods
KW - cytotoxicity
KW - ionic liquids
KW - liposomes
KW - toxicology
KW - Cell Line
KW - Magnetic Resonance Spectroscopy
KW - Humans
KW - Liposomes/chemistry
KW - Aliivibrio fischeri/drug effects
KW - Erythrocytes/cytology
KW - Hemolysis/drug effects
KW - Calorimetry, Differential Scanning
KW - Epithelium, Corneal/cytology
KW - Ionic Liquids/chemistry
KW - Dynamic Light Scattering
UR - http://www.scopus.com/inward/record.url?scp=85041013346&partnerID=8YFLogxK
U2 - 10.1002/chem.201704924
DO - 10.1002/chem.201704924
M3 - Article
C2 - 29265502
AN - SCOPUS:85041013346
SN - 0947-6539
VL - 24
SP - 2669
EP - 2680
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 11
ER -