New ionic derivatives of betulinic acid as highly potent anti-cancer agents

被引:64
作者
Suresh, Challa [1 ,2 ]
Zhao, Hua [1 ]
Gumbs, Angelique [1 ]
Chetty, Chellu S. [1 ]
Bose, Himangshu S. [3 ,4 ]
机构
[1] Savannah State Univ, Dept Nat Sci, Savannah, GA 31404 USA
[2] Natl Inst Nutr, Dept Biochem, Hyderabad 500007, Andhra Pradesh, India
[3] Mercer Univ, Sch Med, Savannah, GA 31404 USA
[4] Mem Hlth Univ Med Ctr, Anderson Canc Res Inst, Savannah, GA 31404 USA
基金
美国国家卫生研究院;
关键词
Betulinic acid; Anti-cancer agent; Melanoma cancer cell; Ionic derivative; Ionic liquid; HUMAN-MELANOMA; INDUCED APOPTOSIS; CELL-LINES; CANCER; ACTIVATION; LIQUIDS; CYTOTOXICITY; MITOCHONDRIA; TRITERPENES; COMBINATION;
D O I
10.1016/j.bmcl.2011.12.102
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Betulinic acid is a natural compound with high in vitro cytotoxicity toward many cancer cells. However, the poor water solubility of this compound hampers an effective in vivo cancer study. We prepared new ionic derivatives of betulinic acid with higher water solubilities, without losing the structural integrity and functionality of this compound. As a result, these new ionic derivatives have shown much higher inhibitory effects against different cancer cell lines such as melanoma A375, neuroblastoma SH-SY5Y and breast adenocarcinoma MCF7. For A375 cell lines, the derivative 5 exhibited a low IC50 value of 36 mu M (vs 154 mu M for betulinic acid); for MCF7 cell lines, the derivative 5 also exhibited a low IC50 value of 25 mu M (vs 112 mu M for betulinic acid). The high cytotoxicity of these new derivatives can be linked to their greatly improved water solubility. Our assay method used little DMSO in aiding the dissolution of these derivatives to demonstrate the advantage of improved water solubility and to mimic the in vivo study conditions. The cell viability studies based on both MTT and LDH assay methods have confirmed the high inhibitory effect of our ionic derivatives of betulinic acid (particularly 4 and 5) against different cancer cells. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1734 / 1738
页数:5
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