Research division, Chugai Pharmaceutical Co. Ltd.
Laboratory of Biopharmacy, School of Pharmaceutical Sciences, University of Shizuoka.
Biol Pharm Bull. 2019;42(9):1600-1604. doi: 10.1248/bpb.b19-00221.
The purpose of this study was to establish a modified method of three-compartment model analysis that minimized the sampling frequency. A Caco-2 permeability assay was performed on ten structurally diverse compounds with passive diffusion. A three-compartment model was analyzed by a conventional method and a method with fewer sampling points, called the simplified method, using concentration-time profiles in the donor, intracellular, and receiver compartments. The concentration-time profiles in all compartments were well described by the conventional method. The calculated unbound fraction of intracellular (fu) and apparent permeability coefficient (P) were 0.0107-1.22 and 0.886-146 × 10 cm/s, respectively. The simplified method also described the concentration profiles in the compartments of all ten compounds except one, ibuprofen. The difference in values calculated by the simplified method compared to the conventional method was between -7 and 7% for fu and between -6 and 42% for P. These results suggested that the parameter values from the simplified method were comparable with those from the conventional method. The simplified method may be a promising approach to improve the throughput of three-compartment model analyses of Caco-2 permeability assays in the early stages of drug discovery.
本研究旨在建立一种改良的三房室模型分析方法,以最小化采样频率。对十种具有被动扩散性质的结构多样的化合物进行了 Caco-2 渗透性测定。通过常规方法和称为简化方法的较少采样点方法,使用供体、细胞内和受体腔室中的浓度-时间曲线对三房室模型进行了分析。所有腔室中的浓度-时间曲线均通过常规方法得到了很好的描述。计算得出的细胞内未结合分数(fu)和表观渗透系数(P)分别为 0.0107-1.22 和 0.886-146×10 cm/s。简化方法也描述了除布洛芬外的所有十种化合物的各个腔室的浓度曲线。简化方法计算出的参数值与常规方法相比,fu 的差异在-7%到 7%之间,P 的差异在-6%到 42%之间。这些结果表明,简化方法的参数值与常规方法相当。简化方法可能是在药物发现的早期阶段提高 Caco-2 渗透性测定的三房室模型分析通量的一种有前途的方法。