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新型亲脂性制剂中抗HIV药物N'-[2-(2-噻吩基)乙基]-N'-[2-(5-溴吡啶基)]-硫脲(HI-443)口服生物利用度的提高。

Improved oral bioavailability of anti-HIV agent N'-[2-(2-thiophene)ethyl]-N'-[2-(5-bromopyridyl)]-thiourea (HI-443) in a novel lipophilic formulation.

作者信息

Uckun Fatih M, Erbeck Douglas, Tibbles Heather, Qazi Sanjive, Venkatachalam Taracad K

机构信息

Paradigm Pharmaceuticals, 2139 Fourth Street, White Bear Lake, MN 55110, USA.

出版信息

Arzneimittelforschung. 2007;57(3):164-70. doi: 10.1055/s-0031-1296600.

Abstract

N'-[2-(2-Thiophene)ethyl]-N'-[2-(5-bromopyridyl)]-thiourea (CAS 258340-15-7, HI-443) is a rationally designed non-nucleoside reverse transcriptase inhibitor (NNRTI) with potent anti-HIV activity at nanomolar concentrations but poor oral bioavailability. Here the identification of a novel oleic acid containing lead formulation of HI-443 is described which resulted in a approximately 10-fold improvement of its oral bioavailability yielding 10-fold higher systemic exposure levels in mice. Formulated HI-443 exhibited a favorable pharmacokinetics and toxicity profile in mice.

摘要

N'-[2-(2-噻吩基)乙基]-N'-[2-(5-溴吡啶基)]-硫脲(CAS 258340-15-7,HI-443)是一种经过合理设计的非核苷类逆转录酶抑制剂(NNRTI),在纳摩尔浓度下具有强大的抗HIV活性,但口服生物利用度较差。本文描述了一种新型的含油酸的HI-443先导制剂的鉴定过程,该制剂使其口服生物利用度提高了约10倍,在小鼠体内产生了高10倍的全身暴露水平。制剂化的HI-443在小鼠体内表现出良好的药代动力学和毒性特征。

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