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作 者:潘阳霖[1] 颜江华[2] 于贤勇[3] 杨叔禹[4] 李学军[4] 蔡淑惠[3] 陈忠[1]
机构地区:[1]厦门大学生物医学工程研究中心,福建厦门361005 [2]厦门大学抗癌研究中心,福建厦门361005 [3]厦门大学物理系,福建厦门361005 [4]厦门市第一医院,福建厦门361003
出 处:《湖南科技大学学报(自然科学版)》2008年第1期101-105,共5页Journal of Hunan University of Science And Technology:Natural Science Edition
基 金:厦门市重大疾病攻关研究基金(3502Z20051027);卫生部福建省卫生教育联合攻关计划(Wkj2005-2-019);湖南省自然科学基金(06JJ30004)
摘 要:在细胞和动物实验水平上,研究了双过氧钒化合物NH4[OV(O2)2(C8H7N3)]×4H2O(简写bpV(Imi-Py))对癌细胞的增殖作用,碱性磷酸酶的活性抑制和体内抗肿瘤作用.研究结果显示bpV(Imi-Py)对胃癌细胞株MGC-803、肺癌细胞株95D和L342的IC50值分别为8.27、26.37和9.54μmol/L,而对人正常肾胚胎细胞HEK293的IC50值达6 642μmol/L,表明该化合物对肿瘤细胞具有特异杀伤作用.研究还表明bpV(Imi-Py)对MGC-803细胞提取液的碱性磷酸酶(ALP)也有明显抑制作用,呈现量效关系.动物体内抗肿瘤实验发现bpV(Imi-Py)能抑制肝癌细胞生长,肿瘤体积实验组较对照组下降35.6%,表明bpV(Imi-Py)有较好的抗肿瘤活性.另外,小鼠急性毒性实验的LD50为147.2mg.kg-1,说明bpV(Imi-Py)是一种中等毒性的抗肿瘤化合物.图4,表1,参15.A diperoxovanadate complex NH4[OV (O2) 2{2-( 2'-pyridyl )-imidazole}]×4H20, bpV ( Imi-Py ) for short, was investigated at the level of cell and animal based on its proliferation on cancer cells, inhibition on alkaline phosphatase and anti-tumor in animal experiments. The results showed that the IC50 values of bpV (Imi-Py) for gastric cancer cell line MGC-803, lung cancer cell line 95D and L342 were 8.27, 26.37, and 9.54 μmol/L, respectively. However, its IC50 value for normal human embryonic kidney cell cultures HEK293 is 6642 μ mol/L, indicating that cancer cells can be selectively inhibited by bpV (Imi-Py). The inhibition of bpV (Imi-Py) on alkaline phosphatase is also obvious, and showed the dose-response relationship. At the same time, animal tumor trail showed that bpV (Imi-Py) inhibited hepatocarcinoma cells. The volume of tumor was reduced by about 35.6% relative to control. It suggests that bpV (Imi-py) has good anti-tumor activity. In addition, the LD50 of bpV (Imi-Py) is 147.2 mg· kg^-1 intravenously in mice, indicating its moderate toxicity. In conclusion, bpV (Imi-Py) is one kind of anti-tumor complex with :moderate toxicity.
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