Tsopelas Fotios, Vallianatou Theodosia, Tsantili-Kakoulidou Anna
Laboratory of Pharmaceutical Chemistry, School of Pharmacy, University of Athens, Panepistimiopolis, Zografou 157 71, Athens, Greece; Laboratory of Inorganic and Analytical Chemistry, School of Chemical Engineering, National Technical University of Athens, Iroon Polytechniou 9, 157 80 Athens, Greece.
Laboratory of Pharmaceutical Chemistry, School of Pharmacy, University of Athens, Panepistimiopolis, Zografou 157 71, Athens, Greece.
Eur J Pharm Sci. 2016 Jan 1;81:82-93. doi: 10.1016/j.ejps.2015.09.020. Epub 2015 Oct 19.
The potential of immobilized artificial membrane (IAM) chromatography to estimate human oral absorption (%HOA) was investigated. For this purpose, retention indices on IAM stationary phases reported previously by our group or measured by other authors under similar conditions were used to model %HOA data, compiled from literature sources. Considering the pH gradient in gastrointestinal tract, the highest logkw(IAM) values were considered, obtained either at pH7.4 or 5.5, defined as logkw(IAM)(best). Non linear models were established upon introduction of additional parameters and after exclusion of drugs which are substrates either to efflux or uptake transporters. The best model included Abraham's hydrogen-bond acidity parameter, molecular weight as well as the positively and negatively charged molecular fractions. For reasons of comparison between IAM chromatography and traditional lipophilicity, corresponding models were derived by replacing IAM retention factors with octanol-water distribution coefficients (logD). An overexpression of electrostatic interactions with phosphate anions was observed in the case of IAM retention as expressed by the negative contribution of the positively charged fraction F(+). The same parameter is statistically significant also in the logD model, but with a positive sign, indicating the attraction of basic drugs in the negatively charged inner membrane. To validate the obtained models a blind test set of 22 structurally diverse drugs was used, whose logkw(IAM)(best) values were determined and analyzed in the present study under similar conditions. IAM retention factors were further compared with MDCK cell lines permeability data taken from literature for a set of validation drugs. The overexpression of electrostatic interactions with phosphate anions on IAM surface was also evident in respect to MDCK permeability. In contrast to the clear classification between drugs with high and poor (or intermediate) absorption provided by MDCK permeability, %HOA plotted versus both IAM and logD data result in a saturation curve with a smoother ascending line.
研究了固定化人工膜(IAM)色谱法估算人体口服吸收率(%HOA)的潜力。为此,使用了我们小组先前报道的或其他作者在类似条件下测得的IAM固定相上的保留指数,对从文献来源汇编的%HOA数据进行建模。考虑到胃肠道中的pH梯度,采用在pH7.4或5.5时获得的最高logkw(IAM)值,定义为logkw(IAM)(最佳)。在引入额外参数并排除作为外排或摄取转运体底物的药物后,建立了非线性模型。最佳模型包括亚伯拉罕氢键酸度参数、分子量以及带正电和带负电的分子分数。出于IAM色谱法与传统亲脂性比较的原因,通过用正辛醇-水分配系数(logD)替代IAM保留因子来推导相应模型。在IAM保留的情况下,观察到与磷酸根阴离子的静电相互作用过度表达,如带正电部分F(+)的负贡献所表示。相同参数在logD模型中也具有统计学意义,但为正号,表明碱性药物在带负电的内膜中的吸引力。为了验证所得模型,使用了一组22种结构多样的药物的盲测集,在本研究中在类似条件下测定并分析了它们的logkw(IAM)(最佳)值。将IAM保留因子与从文献中获取的一组验证药物的MDCK细胞系通透性数据进行了进一步比较。就MDCK通透性而言,IAM表面与磷酸根阴离子的静电相互作用过度表达也很明显。与MDCK通透性提供的高吸收和低吸收(或中等吸收)药物之间的明确分类不同,%HOA与IAM和logD数据绘制的结果是一条上升线较平滑的饱和曲线。