谷胱甘肽
细胞毒性
荧光
体外
化学
反应性(心理学)
细胞培养
分子
生物物理学
生物
生物化学
医学
量子力学
物理
病理
有机化学
酶
遗传学
替代医学
作者
Defeng Shen,Shanshan Wu,Ruirui Wang,Qiang Zhang,Zhongjuan Ren,Hong Shi Liu,Huadong Guo,Guang‐Gang Gao
出处
期刊:Small
[Wiley]
日期:2016-09-26
卷期号:12 (44): 6153-6159
被引量:33
标识
DOI:10.1002/smll.201601936
摘要
A structure‐determined silver nanocluster of [Ag 10 (Eth) 4 (CF 3 COO) 6 (CH 3 OH) 3 ]·3CH 3 OH (Eth = ethisterone) ( 1 ), is firstly demonstrated by self‐assembly of silver salt and ethisterone. Due to the thiophilicity of silver(I) ions, complex 1 shows reactivity with glutathione (GSH) molecules in solution and induces the fluorescence quenching behavior. Thus, complex 1 can be used as a fluorescent sensor for GSH. In consideration of the higher level of GSH in cancerous cells, complex 1 presents significant tumor suppression reactivity toward the human hepatocellular carcinoma (HepG2) cells with IC 50 value of 165 × 10 −9 m . Especially, complex 1 displays 3.4‐fold higher in vitro cytotoxicity to HepG2 cells than that of the normal CCC‐HEL‐1 cells, which makes complex 1 a potential targeting suppression agent for cancerous cells. The molecular design of complex 1 not only generates a new medicine‐silver(I) cluster family, but also opens a new avenue to the targeting anticancer organosilver(I) materials.
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