Author:
Wang Mao-Ze,Gao Jin,Chu Yang,Niu Jie,Chen Ming,Shang Qiang,Peng Li-Hua,Jiang Zhi-Hong
Abstract
Abstract
Background
Crocetin is a major active component of saffron, which has a wide range of pharmacological effects. However, due to its low solubility, the pharmacological effects of crocetin cannot be better utilized.
Methods
In this study, we modified the chemical structure of crocetin by conjugating with ethylamine and 4-Fluorbenzylamine to enhance its solubility and biological activities. The solubility and the influence of synthesized derivatives on the proliferation of tumor cells and the inflammatory effect of macrophage were investigated.
Results
It was shown that, compared with the crocetin, the synthesized derivatives have much higher solubility. Moreover, the inhibitory effect of the derivatives on varieties of tumor cells, including human ovarian carcinoma cell line, human lung cancer cell line, rat melanoma cell line was enhanced after the modification. Besides that, the derivatives were improved for the anti-inflammatory efficacy with the cytotoxicity decreased.
Conclusions
The synthesized derivatives were shown for their good solubility and the great potential in tumor and inflammation treatment.
Publisher
Springer Science and Business Media LLC
Subject
Complementary and alternative medicine
Cited by
7 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献