Katchen B, Dancik S, Millington G
J Invest Dermatol. 1976 Jun;66(6):379-82. doi: 10.1111/1523-1747.ep12483004.
This study was designed to determine the fate of the nonsteroid antiandrogen flutamide in men following a single 6-hr topical application of 5 mg 14C-labeled drug dissolved in 50% ethanol/50% propylene glycol. Analysis of 0-120 hr urine shows at least 16% of the applied flutamide is absorbed. Fifty-six percent of the dose is recovered from the site of application with cotton swabs moistened with 50% ethanol/50% propylene glycol. Flutamide plasma levels peak in 4 to 6 hr at about 1.3 ng/ml and then decline rapidly to about 0.08 ng/ml 24 hr after application. Only 13% of plasma 14C is associated with flutamide 6 hr after drug application. There are at least 10 plasma metabolites, of which 6 have been tentatively identified. These are alpha, alpha, alpha-trifluoro-4'-amino-m-acetotoluidide (A); alpha, alpha, alpha-trifluoro-4'-amino-2-methyl-m-lactotoluidide (B); alpha, alpha, alpha-trifluoro-4'-nitro-m-acetotoluidide (C); alpha, alpha, alpha-trifluoro-2-methyl-4'-nitro-m-lactotoluidide (D); alpha, alpha, alpha-trifluoro-4'-amino-2-methyl-m-propionotoluidide (E); and alpha, alpha, alpha-trifluoro-6-nitro-m-toluidine (F). (D) is the major plasma metabolite, and its concentration exceeds flutamide's between 8 and 24 hr after drug. All the plasma metabolites are found in 0-24 hr urine in minor amounts. An additional metabolite, alpha, alpha, alpha-trifluoro-amino-5-nitro-p-cresol (G), accounts for 27% of urine 14C.
本研究旨在确定单次6小时局部应用溶解于50%乙醇/50%丙二醇中的5毫克14C标记药物后,非甾体抗雄激素氟他胺在男性体内的转归。对0至120小时尿液的分析显示,至少16%的外用氟他胺被吸收。用50%乙醇/50%丙二醇浸湿的棉签从用药部位回收了56%的剂量。氟他胺血浆水平在4至6小时达到峰值,约为1.3纳克/毫升,然后在用药后24小时迅速降至约0.08纳克/毫升。用药6小时后,血浆中只有13%的14C与氟他胺相关。血浆中至少有10种代谢产物,其中6种已初步鉴定。它们是α,α,α-三氟-4'-氨基间乙酰甲苯胺(A);α,α,α-三氟-4'-氨基-2-甲基间乳酰甲苯胺(B);α,α,α-三氟-4'-硝基间乙酰甲苯胺(C);α,α,α-三氟-2-甲基-4'-硝基间乳酰甲苯胺(D);α,α,α-三氟-4'-氨基-2-甲基间丙酰甲苯胺(E);以及α,α,α-三氟-6-硝基间甲苯胺(F)。(D)是主要的血浆代谢产物,其浓度在用药后8至24小时超过氟他胺。所有血浆代谢产物在0至24小时尿液中的含量都很少。另一种代谢产物α,α,α-三氟氨基-5-硝基对甲酚(G)占尿液中14C的27%。