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机构地区:[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
出 处:《公共卫生与临床医学》2009年第2期94-96,共3页Public health and dinical medicine
基 金:国家自然科学基金资助项目(30873101)
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刚0806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。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 of curcumine.
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