Tamvakopoulos Constantin, Sofianos Zacharias D, Garbis Spiros D, Pantazis Panayotis
Department of Pharmacology-Pharmacotechnology, Foundation for Biomedical Research of the Academy of Athens, Athens, Greece.
Eur J Drug Metab Pharmacokinet. 2007 Jan-Mar;32(1):51-7. doi: 10.1007/BF03190990.
In this study, we have described a novel approach for determining the metabolic scheme of diferuloylmethane (curcumin) in mouse and human liver microsomal preparations using a hybrid quadrupole linear ion trap mass spectrometer coupled with liquid chromatography for the detection of new metabolites. Application of various acquisition modes allowed targeted searches for metabolites with high sensitivity and selectivity using information of the mass spectral fragmentation properties of curcumin. Structural assignments for metabolites previously reported in the literature were made with confidence using the described approach. In addition, we identified curcumin metabolites that had not previously been reported, such as curcumin bisglucuronide and O-demethylated derivatives. The major pathways of curcumin metabolism in vitro have been summarized. Finally, very similar metabolic pathways of curcumin were observed in human and mouse microsomes.
在本研究中,我们描述了一种新方法,该方法使用混合四极杆线性离子阱质谱仪与液相色谱联用,用于检测新代谢物,以此来确定小鼠和人肝微粒体制剂中双阿魏酰甲烷(姜黄素)的代谢方案。通过应用各种采集模式,利用姜黄素的质谱裂解特性信息,能够高灵敏度和高选择性地靶向搜索代谢物。使用所描述的方法,可以可靠地对文献中先前报道的代谢物进行结构鉴定。此外,我们还鉴定出了以前未报道过的姜黄素代谢物,如姜黄素双葡萄糖醛酸苷和O-去甲基化衍生物。总结了姜黄素体外代谢的主要途径。最后,在人和小鼠微粒体中观察到了非常相似的姜黄素代谢途径。