摘要
目的本文介绍了一种新的铂类抗癌药物的合成方法,以及此药物对肝癌的体外抑制作用。方法本药物以胆酸作为载体,通过与铂配合,形成有机铂化合物。结果体外试验表明本药物对肝癌细胞株BEL-7402及Hep G2的生长均具有明显的抑制作用。结论胆酸铂的抗癌作用明显高于顺铂。
Objective In this paper,a new synthesis methods of platinum anticancer drugs was introduced,as well as the drug in vitro inhibitor^^effect on liver cancer.Methods The drugs used cholic acid as the carrier,and chelated to platinum,for^ned organic compounds of platinum.Results In vitro experiments show-ed that bile acid platinum can inhibit the growth of liver cancer cell line BEL-7402 and HepG2.Conclusion The anticancer effect of cholate platinum was significantly higher than that of cisplatin.
作者
肖毅
XIAO Yi(Wuhan Bio-Raid Biotechnology Co.,Ltd.,Wuhan 430075,China)
出处
《药学研究》
CAS
2018年第2期122-124,共3页
Journal of Pharmaceutical Research
关键词
铂类抗癌药物
胆酸
二氨基丙酸
抗癌药物
Platinum anti-cancer drug
Cholic acid
Diaminopropionic acid
Anticancer drug