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作 者:赵玉玺[1] 魏莹[1] 陈珍[1] 张世鹏[1] 刘福 Zhao Yuxi, Wei Ying, Chen Zhen, Zhang Shipeng, Liu Fu(School of Pharmacy, Institute of medicine ,North Sichuan Medical University, Nanchong 637000, Chin)
机构地区:[1]川北医学院药学院药物研究所,四川南充637000
出 处:《广东化工》2018年第13期30-31,共2页Guangdong Chemical Industry
摘 要:目的:合成透明质酸-阿魏酸靶向药物并对其进行Lewis肺癌荷瘤小鼠的抑制作用研究。方法:使用丝氨酸甲酯作为中间连接物合成HA-FA靶向药物,采用紫外扫描图及1HNMR图谱进行结构确证;Bal b/c小鼠右腋皮下接种Lewis肺癌瘤株,连续腹腔注射给药20 d后,处死动物,摘取瘤体称重,并计算肿瘤生长抑制。结果:通过紫外扫描图可以初步证明HA-FA成功合成;1HNMR图谱进行结构确证。HA-FA对Lewis肺癌荷瘤小鼠的抑瘤率为57.97%(与模型组比较,P<0.05)。结论:HA-FA对Lewis肺癌荷瘤小鼠肿瘤生长具有明显抑制作用。Objects: To prepare hyaluronic acid targeted drug with ferulic acid and hyaluronic acid and to study the anti-tumor effect of HA-FA on Lewis lung cancer mice. Methods: Serine methyl ester was used as a linker to synthesis HA-FA targeted drugs. UV spectra and 1HNMR was used to identify its structure, Lewis lung cancer cells were inoculated subcutaneously into right axillary ofBal b/c mice, aiter continuous treatment of 20 d, we sacrificed the mice, removed tumor and weighed, and calculated the rate of tumor growth inhibition. Results: FA was successfully coupled with HA confirmed by UV spectra and IHNMR.HA-FA team inhibitory rates were 64.72 % (compared with the model group, P〈0.05).Conclusions: HA-HA can inhibit significantly Lewis lung cancer tumor growth of the tumor-bearing mice.
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