癌变·畸变·突变 ›› 2010, Vol. 22 ›› Issue (6): 465-468.doi: 10.3969/j.issn.1004-616x.2010.06.014

• 检测研究 • 上一篇    下一篇

杂多化合物九钨三钛硅酸盐的毒性研究

梅树江1,刘 娅2,王宝贵2,张桂英2,章培标3,赵林伊2   

  1. 1.深圳市疾病预防控制中心,广东 深圳 518055; 2.吉林大学公共卫生学院,吉林 长春 130021; 3.中国科学院长春应用化学研究所,吉林 长春 130022
  • 收稿日期:2010-09-18 修回日期:2010-10-20 出版日期:2010-11-30 发布日期:2010-11-30
  • 通讯作者: 刘 娅

The toxicological effects of polyoxometalates α_Ti3

MEI Shu-jiang1, LIU Ya2,, WANG Bao-gui2, ZHANG Gui-ying2, ZHANG Pei-biao3,ZHAO Lin-yi2   

  1. 1. Shenzhen Center for Disease Control and Prevention,Shenzhen 518020, Guangdong; 2. Public Health College of Jilin University, Changchun 130021; 3. Changchun Institute of Applied Chemistry,Chinese Academy of Sciences,Changchun 130022,Jilin, China
  • Received:2010-09-18 Revised:2010-10-20 Online:2010-11-30 Published:2010-11-30
  • Contact: LIU Ya

摘要: 目的: 对杂多化合物九钨三钛硅酸盐(α_K8H2[SiW9Ti3O40]·15H2O,α_Ti3)的毒性进行研究,为其临床应用提供科学依据。 方法: 采用小鼠经口急性毒性试验、蓄积毒性试验、Ames试验、中国仓鼠卵巢细胞(CHO)染色体畸变试验和细胞毒性试验对α_Ti3毒性进行检测。 结果: 小鼠经口急性毒性试验的半数致死剂量(LD50)为2 055.36 mg/kg,属低毒物质;蓄积毒性试验提示α_Ti3在体内蓄积系数K>5,为轻度蓄积;Ames试验在每皿31.3~500 μg浓度范围内,无论加S9与否,每皿菌落回变数均未超过阴性对照组的两倍;中国仓鼠卵巢细胞染色体畸变试验在40~320 μg/ml范围内,无论加S9与否,CHO染色体畸变率与阴性对照组比较均无明显增加。对大鼠外周血细胞毒性和骨髓细胞毒性的半数抑制浓度(IC50)分别为0.135、0.223 mg/ml,高于S180腹水瘤细胞和小鼠肝癌细胞,说明该药对正常细胞的毒性作用较低。 结论: 在本实验条件下,杂多化合物九钨三钛硅酸盐属低毒物质,提示其具有良好的应用前景。

关键词: 杂多化合物, 急性毒性, 蓄积毒性, 致突变试验, 细胞毒性

Abstract: OBJECTIVE: To investigate the toxicity of polyoxometalates α_K8H2[SiW9Ti3O40]·15H2O(α_Ti3) for clinic application. METHODS: The studies were conducted with acute toxicity test, cumulative toxicity test, Ames test and chromosome aberration test on CHO cell in vitro and cytotoxicity test. RESULTS: LD50 in mice was 2 055.36 mg/kg, α_Ti3 was a low_grade toxicity compound. The cumulation coefficient was exceed 5, it showed α_Ti3 was low cumulation. The results of Ames test showed no mutagenic effects with the concentration ranged from 31.3 to 500 μg/utensil with or without S9 mixture added. The chromosome aberration ratio of α_Ti3 groups was no significant discrepancy compared with the control on CHO cells,with the concentration ranged from 40 to 320 μg/ml with or without S9 mixture added. IC50 of medulla cells and peripheral blood lymphocytes of rats in vitro treated with α_Ti3 were 0.223 and 0.135 mg/ml,respectively. However,IC50 of S180 ascites tumor cell and mice hepatoma carcinoma cell were low. It showed the toxicity of α_Ti3 was low on normal cell. CONCLUSION: The toxicity of α_Ti3 was low and no mutagenicity was observed in this experiment,the results suggested that α_Ti3 should be a better anti_tumor drug in clinic chemical theropy.

Key words: polyoxometalates, acute toxicity, cumulative toxicity, mutagenicity test, cytotoxicity