Andersson S B, Gunnarsson P O, Nilsson T, Forshell G P
Eur J Drug Metab Pharmacokinet. 1981;6(2):149-54. doi: 10.1007/BF03189482.
Plasma samples from patients with prostatic cancer under oral treatment with estramustine phosphate (Estracyt) were quantitatively analyzed for the presence of the parent drug and some of its possible metabolites. Specific methods based on radioimmunoassay and gas chromatography-mass fragmentography were used. Dephosphorylation and oxidation at the 17-position of estradiol were shown to be the major metabolic routes. The estrone analogue of estramustine was found to be the main metabolite in plasma. Elevated levels of estradiol and estrone showed that hydrolysis of the carbamic ester also occurred in these patients. Their estrogen levels were compared with those of another group of prostatic cancer patients receiving conventional hormonal therapy, polyestradiol phosphate (Estradurin). Similar concentrations of estradiol were found in the two groups but the concentrations of estrone were higher in patients given estramustine phosphate.
对接受磷酸雌莫司汀(艾去适)口服治疗的前列腺癌患者的血浆样本进行了定量分析,以检测母体药物及其一些可能代谢物的存在情况。采用了基于放射免疫分析和气相色谱 - 质谱碎片分析的特定方法。结果表明,雌二醇17位的去磷酸化和氧化是主要代谢途径。磷酸雌莫司汀的雌酮类似物被发现是血浆中的主要代谢物。雌二醇和雌酮水平升高表明这些患者中也发生了氨基甲酸酯的水解。将他们的雌激素水平与另一组接受传统激素治疗——聚磷酸雌二醇(益维雌醇)的前列腺癌患者的雌激素水平进行了比较。两组中发现的雌二醇浓度相似,但接受磷酸雌莫司汀治疗的患者中雌酮浓度更高。