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姜黄素衍生物FM17对K562细胞增殖影响及其与P210^bcr/ab1激活的信号途径关系
  • 期刊名称:《公共卫生与临床医学》
  • 时间:0
  • 分类:R73-34[医药卫生—肿瘤;医药卫生—临床医学]
  • 作者机构:[1]福建医科大学药学院福建医科大学临床药理所,福建福州350004
  • 相关基金:国家自然科学基金资助项目(30873101)
中文摘要:

目的研究姜黄素前体药物的稳定性及其水解动力学。方法利用HPLC法测定FM0806在不同pH值的缓冲溶液、血浆及肝匀浆中药物水解动力学。结果姜黄素前体药物FM0806在pH为2~10时水解速率常数不受pH影响,而在血浆及肝均浆中FM0806可迅速水解。结论FM0806是一个具有良好前景的姜黄素前体药物。

英文摘要:

Objective To investigate the stability and the kinetic of curcumine prodrug FM0806. Methods Prodrug hydrolysis was studied in aqueous buffer solutions with pH 2-10 as well as 80% rat plasma solution and homogenized liver by the reversed-phase high performance liquid chromatography (RP-HPLC) Method. Results The velocity of hydrolysis of FM0806 kept the same level under pH 2-10,and it could be hydrolyzed fast by enzymes in blood plasma, homogenized liver. Conclusions FM0806 was a promising prodrug ofcurcumine.

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