Gunnarsson P O, Forshell G P, Fritjofsson A, Norlén B J
Scand J Urol Nephrol. 1981;15(3):201-5. doi: 10.3109/00365598109179603.
Plasma concentrations of estramustine phosphate and its major metabolites were measured in patients with prostatic carcinoma treated with increasing oral doses, 70-650 mg/day, of estramustine phosphate (Estracyt). Parent drug and estradiol were measured by radioimmunoassay, and estramustine and its estrone analogue (Leo 271) utilizing gas chromatography. The concentrations of estramustine phosphate and estramustine were below or close to the limits of the methods. A linear correlation was found between the daily dose of estramustine phosphate, and plasma concentrations of Leo 271-the main metabolite-and estradiol, which suggests that no capacity limiting processes are involved in the pharmacokinetics of estramustine phosphate in man. Plasma was also analyzed during prolonged treatment with 560 mg/day. The metabolite pattern was not changed by two to three years of estramustine phosphate treatment.
对接受递增口服剂量(70 - 650毫克/天)磷酸雌莫司汀(癌腺治)治疗的前列腺癌患者,测定其血浆中磷酸雌莫司汀及其主要代谢产物的浓度。母体药物和雌二醇通过放射免疫测定法测量,雌莫司汀及其雌酮类似物(Leo 271)利用气相色谱法测量。磷酸雌莫司汀和雌莫司汀的浓度低于或接近方法的检测限。发现磷酸雌莫司汀的日剂量与主要代谢产物Leo 271和雌二醇的血浆浓度之间存在线性相关性,这表明在人体中,磷酸雌莫司汀的药代动力学不涉及容量限制过程。在以560毫克/天进行长期治疗期间也对血浆进行了分析。磷酸雌莫司汀治疗两到三年后,代谢产物模式未发生改变。