Catinella S, Pelizzi N, Puccini P, Marchetti S, Zanol M, Acerbi D, Ventura P
Chiesi Farmaceutici SpA, R&D, Analytical Chemistry and Pharmacokinetics Departments, Via Palermo 26/A, I-43100 Parma, Italy.
J Mass Spectrom. 2001 Dec;36(12):1287-93. doi: 10.1002/jms.228.
Ganstigmine, a new acetylcholinesterase inhibitor, was incubated with rat liver microsomes and the resulting metabolites were identified by high-performance liquid chromatographic/mass spectrometric (HPLC/MS) and HPLC/MS/MS analyses. The results showed the formation of eight main metabolites, among which geneseroline and molecules corresponding to mono-hydroxylated, demethylated and reduced ganstigmine. The metabolic profile drawn for humans, dog and monkey showed a pattern very similar to that of rat: only in the case of liver dog microsomes higher amounts of geneseroline and of a metabolite identified as demethylated and reduced drug were detected.
加兰他敏,一种新型乙酰胆碱酯酶抑制剂,与大鼠肝微粒体一起孵育,通过高效液相色谱/质谱(HPLC/MS)和HPLC/MS/MS分析鉴定所得代谢产物。结果显示形成了8种主要代谢产物,其中包括加兰他灵和与单羟基化、去甲基化和还原型加兰他敏相对应的分子。绘制的人、狗和猴的代谢图谱显示出与大鼠非常相似的模式:仅在狗的肝微粒体中检测到了更高含量的加兰他灵以及一种被鉴定为去甲基化和还原型药物的代谢产物。