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N-乙酰-1,6-二氨基己烷的固定化及其诱导肿瘤细胞分化机理的研究
引用本文:颉东旭,任礼勤,李树本. N-乙酰-1,6-二氨基己烷的固定化及其诱导肿瘤细胞分化机理的研究[J]. 色谱, 1998, 16(4): 327-330
作者姓名:颉东旭  任礼勤  李树本
作者单位:兰州军区总医院医务部,中国科学院兰州化学物理研究所羰基合成与选择氧化国家重点实验室
基金项目:甘肃省科委青年科学基金,中国科学院兰州化学物理研究所羰基合成与选择氧化国家重点实验室资助
摘    要:合成了N-乙酰-1,6-二氨基己烷(N-acetyl-1,6-diaminohexane,NADAH)并偶联到甘油氧丙基硅胶上用以制备高效液相色谱柱,用液相色谱法研究了NADAH及六亚甲基二乙酰胺(hexamethylenebisacetamied,HMBA)诱导肿瘤细胞分化的机理。结果表明NADAH对肿瘤细胞的成分无离子交换及亲和效应,而对一些膜蛋白提取物和DNA有强的疏水作用。因此,NADAH和HMBA对肿瘤细胞的诱导分化与它们对蛋白质和DNA的疏水作用有关。

关 键 词:6-二氨基己烷  N-乙酰-1  分化机理  高效液相色谱法  六亚甲基二乙酰胺  

Immobilization of N Acetyl 1,6 Diaminohexane(NADAH) on Diol Silica and Study of Mechanism of NADAH and Hexamethylene Bisacetamide(HMBA)Inducing Tumor Cells Differentiation
Xie Dongxu and Ren Liqin. Immobilization of N Acetyl 1,6 Diaminohexane(NADAH) on Diol Silica and Study of Mechanism of NADAH and Hexamethylene Bisacetamide(HMBA)Inducing Tumor Cells Differentiation[J]. Chinese journal of chromatography, 1998, 16(4): 327-330
Authors:Xie Dongxu and Ren Liqin
Affiliation:Administration Department, General Hospital of Lanzhou Command PLA, Lanzhou, 730050.
Abstract:A method for separating NADAH and its immobilization onto diol-silica have been developed. HMBA and its meabolite NADAH were used as the inducers for many types of tumor cells' differentiation. The inducing mechanism of HMBA is not clear yet. Experiments show that HMBA and NADAH have a relatively strong hydrophobic reaction and hardly ion-exchange with some DNA and some proteins of the cytosolic fraction of HL-60 human acute progranulocytic leukemia cells, BIU-87 human bladder carcinoma cells and the human erythrocyte membrane, when utilizing immobilization of NADAH. The retention time of the proteins and DNA was longer than that of the phosphatides. These results show that the adsorption of HMBA and NADAH with some proteins and DNA is higher than that with the phosphatides. The expected receptor binding biospecifically with HMBA has not been found.
Keywords:high performance liquid chromatography   N acetyl 1  6 diaminohexane   hexamethylene bisaceta mide  differentiation mechanism  
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