Divisions of Molecular Pharmaceutics, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Drug Metab Dispos. 2013 Feb;41(2):518-28. doi: 10.1124/dmd.112.048231. Epub 2012 Dec 6.
DB868 [2,5-bis [5-(N-methoxyamidino)-2-pyridyl] furan], a prodrug of the diamidine DB829 [2,5-bis(5-amidino-2-pyridyl) furan], has demonstrated efficacy in murine models of human African trypanosomiasis. A cross-species evaluation of prodrug bioconversion to the active drug is required to predict the disposition of prodrug, metabolites, and active drug in humans. The phase I biotransformation of DB868 was elucidated using liver microsomes and sandwich-cultured hepatocytes from humans and rats. All systems produced four NADPH-dependent metabolites via O-demethylation (M1, M2) and N-dehydroxylation (M3, M4). Compartmental kinetic modeling of the DB868 metabolic pathway suggested an unusual N-demethoxylation reaction that was supported experimentally. A unienzyme Michaelis-Menten model described the kinetics of M1 formation by human liver microsomes (HLMs) (K(m), 11 μM; V(max), 340 pmol/min/mg), whereas a two-enzyme model described the kinetics of M1 formation by rat liver microsomes (RLMs) (K(m1), 0.5 μM; V(max1), 12 pmol/min/mg; K(m2), 27 μM; V(max2), 70 pmol/min/mg). Human recombinant CYP1A2, CYP3A4, and CYP4F2, rat recombinant Cyp1a2 and Cyp2d2, and rat purified Cyp4f1 catalyzed M1 formation. M2 formation by HLMs exhibited allosteric kinetics (S(50), 18 μM; V(max), 180 pmol/mg), whereas M2 formation by RLMs was negligible. Recombinant CYP1A2/Cyp1a2 catalyzed M2 formation. DB829 was detected in trace amounts in HLMs at the end of the 180-min incubation and was detected readily in sandwich-cultured hepatocytes from both species throughout the 24-h incubation. These studies demonstrated that DB868 biotransformation to DB829 is conserved between humans and rats. An improved understanding of species differences in the kinetics of DB829 formation would facilitate preclinical development of a promising antitrypanosomal prodrug.
DB868 [2,5-双[5-(N-甲氧基酰胺基)-2-吡啶基]呋喃],二脒 DB829 [2,5-双(5-酰胺基-2-吡啶基)呋喃]的前药,在人类非洲锥虫病的小鼠模型中显示出疗效。需要对前药生物转化为活性药物进行种间评估,以预测前药、代谢物和活性药物在人体内的处置。使用来自人和大鼠的肝微粒体和三明治培养肝细胞阐明了 DB868 的 I 相生物转化。所有系统均通过 O-去甲基化(M1、M2)和 N-去羟化(M3、M4)产生四种 NADPH 依赖性代谢物。DB868 代谢途径的房室动力学模型表明存在一种不寻常的 N-去甲氧基化反应,该反应得到了实验支持。单酶米氏-门坦模型描述了人肝微粒体(HLMs)中 M1 形成的动力学(K(m),11 μM;V(max),340 pmol/min/mg),而双酶模型描述了大鼠肝微粒体(RLMs)中 M1 形成的动力学(K(m1),0.5 μM;V(max1),12 pmol/min/mg;K(m2),27 μM;V(max2),70 pmol/min/mg)。人重组 CYP1A2、CYP3A4 和 CYP4F2、大鼠重组 Cyp1a2 和 Cyp2d2 以及大鼠纯化 Cyp4f1 均催化 M1 形成。HLMs 中 M2 的形成表现出变构动力学(S(50),18 μM;V(max),180 pmol/mg),而 RLMs 中 M2 的形成可以忽略不计。重组 CYP1A2/Cyp1a2 催化 M2 形成。DB829 在 180 分钟孵育结束时在 HLMs 中以痕量存在,并在两种物种的三明治培养肝细胞中在 24 小时孵育过程中均容易检测到。这些研究表明,DB868 向 DB829 的生物转化在人和大鼠之间是保守的。对 DB829 形成动力学种间差异的更好理解将有助于有前途的抗锥虫前药的临床前开发。