Research Article

Cytotoxicity of 1-dodecyl-3-methylimidazolium bromide on HepG2 cells

Published: October 27, 2015
Genet. Mol. Res. 14 (4) : 13342-13348 DOI: https://doi.org/10.4238/2015.October.26.31
Cite this Article:
T.H. Li, C.Q. Jing, K.L. Gao, W.Y. Yue, S.F. Li (2015). Cytotoxicity of 1-dodecyl-3-methylimidazolium bromide on HepG2 cells. Genet. Mol. Res. 14(4): 13342-13348. https://doi.org/10.4238/2015.October.26.31
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Abstract

We evaluated the cytotoxicity of 1-dodecyl-3-methylimidazo­lium bromide ([C12mim][Br]) on HepG2 cells and its influence on plasma membrane permeability. The results showed that [C12mim][Br] inhibited HepG2 cell growth and decreased cell viability in a concentration-depen­dent manner. The results also revealed that [C12mim][Br] exposure induced apoptosis in [C12mim][Br]-treated HepG2 cells. In addition, the results showed that [C12mim][Br] increased membrane permeability in HepG2 cells. These results suggest that plasma membrane permeability may be responsible for apoptosis induced by [C12mim][Br] in HepG2 cells.

We evaluated the cytotoxicity of 1-dodecyl-3-methylimidazo­lium bromide ([C12mim][Br]) on HepG2 cells and its influence on plasma membrane permeability. The results showed that [C12mim][Br] inhibited HepG2 cell growth and decreased cell viability in a concentration-depen­dent manner. The results also revealed that [C12mim][Br] exposure induced apoptosis in [C12mim][Br]-treated HepG2 cells. In addition, the results showed that [C12mim][Br] increased membrane permeability in HepG2 cells. These results suggest that plasma membrane permeability may be responsible for apoptosis induced by [C12mim][Br] in HepG2 cells.