In Vivo Anticancer Activities of Vanillin Thiosemicarbazone Complexes with Co ( II ) and Ni ( II )

S. Shahriar, S. M. M. Ali, M. Jesmin
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引用次数: 3

Abstract

Sha M. S. Shahriar Department of Applied Chemistry and Chemical Engineering, University of Rajshahi, Rajshahi-6205, Bangladesh. e-mail: shahan.acrubd@yahoo.com ABSTRACT The anticancer activities of vanillin thiosemicarbazone complexes with Co(II) and Ni(II) have been studied against Ehrlich ascites carcinoma (EAC) cells in Swiss albino mice. Both the complexes were administrated into the intraperitoneal cavity of the EAC-inoculated mice at two doses (5 and 7.5 mg/kg i.p.). The anticancer activities were studied by monitoring the parameters such as cell growth inhibition, tumor weight measurement, survival time of EAC-bearing mice, as well as the changes in depleted hematological parameters due to tumorigenesis. All data were compared with those of a known standard drug bleomycin at the dose of 0.3 mg/kg (i.p.). It has been found that these complexes significantly increased the life span of tumor-bearing mice and decreased the rate of growth and weight of tumor cells. They also restored modestly the depleted hematological parameters such as hemoglobin content, RBC count, and WBC count to normal. They enhanced the number of macrophages in normal mice with minor host toxicity. It is concluded that these compounds can be primarily considered as potent anticancer agents.
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香兰素硫代氨基脲配合物Co (II)和Ni (II)的体内抗癌活性
sham . S. Shahriar Rajshahi大学应用化学与化学工程系,孟加拉国Rajshahi-6205摘要本文研究了香兰素硫代氨基脲与Co(II)、Ni(II)配合物对瑞士白化小鼠Ehrlich腹水癌(EAC)细胞的抗癌作用。这两种复合物分别以5和7.5 mg/kg / p两种剂量给药于接种了eac的小鼠腹腔。通过监测eac小鼠的细胞生长抑制、肿瘤重量测定、存活时间以及肿瘤发生后血液学指标的变化来研究其抗癌活性。将所有数据与已知标准药物博来霉素0.3 mg/kg (i.p)的数据进行比较。研究发现,这些复合物显著延长了荷瘤小鼠的寿命,降低了肿瘤细胞的生长速度和重量。他们还适度地恢复了血液学参数,如血红蛋白含量、红细胞计数和白细胞计数正常。它们增加了正常小鼠巨噬细胞的数量,但具有轻微的宿主毒性。结论是,这些化合物可以主要被认为是有效的抗癌剂。
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