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屈洛昔芬及其代谢产物在乳腺癌患者中的药代动力学。

Pharmacokinetics of droloxifene and its metabolites in breast cancer patients.

作者信息

Grill H J, Pollow K

机构信息

Abteilung für Experimentelle Endokrinologie, Klinikum der Johannes Gutenberg Universität, Mainz, Germany.

出版信息

Am J Clin Oncol. 1991;14 Suppl 2:S21-9. doi: 10.1097/00000421-199112002-00006.

Abstract

Pharmacokinetics and metabolism of droloxifene, a new antiestrogenic drug, have been investigated by single- and multiple-dose studies in postmenopausal patients with advanced breast cancer. Short terminal elimination half-life, low accumulation, and improved drug tolerability are the most striking features of this safe and effective new antiestrogen. Bioequivalence of film-coated tablet, tablet, and standard solution of droloxifene has been shown. The concentrations of droloxifene and its metabolites have been determined by a highly selective HPLC method.

摘要

已通过对晚期乳腺癌绝经后患者进行单剂量和多剂量研究,对新型抗雌激素药物屈洛昔芬的药代动力学和代谢情况展开了调查。短的末端消除半衰期、低蓄积性以及改善的药物耐受性是这种安全有效的新型抗雌激素最为显著的特征。已证实屈洛昔芬薄膜包衣片、普通片和标准溶液具有生物等效性。屈洛昔芬及其代谢物的浓度已通过一种高选择性高效液相色谱法测定。

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