REQUIMTE, Departamento de Química, Faculdade de Farmácia, Universidade do Porto, Rua Aníbal Cunha, Porto, Portugal.
Nat Protoc. 2010 Nov;5(11):1823-30. doi: 10.1038/nprot.2010.137. Epub 2010 Oct 21.
Partition coefficients (K(p)) of drugs between the phospholipid bilayer and the aqueous phase provide useful information in quantitative structure-activity relationship studies. Hexadecylphosphocholine (HePC) micelles, composed of a zwitterionic hydrophilic surface and a hydrophobic core, mimic the biomembranes and have several advantages over other lipid structures to assess K(p) values. Their preparation is easy, fast and avoids the use of toxic organic solvents, and the output has fewer spectroscopic interferences. Here, we describe a high-throughput microplate protocol for assessing the K(p) of drugs using HePC micelles as membrane models and derivative spectrophotometry as the detection technique. Moreover, the time-consuming data treatment to assess K(p) values is easily performed by a dedicated Excel routine developed here and described in detail. The K(p) values of nonsteroidal anti-inflammatory drugs (acemetacin, clonixin, diclofenac and indomethacin) were determined to show the simplicity of the method and to validate this protocol, which provides K(p) values (n = 3) of two drugs in ∼ 2 h.
药物在磷脂双层和水相之间的分配系数(K(p))为定量构效关系研究提供了有用的信息。十六烷基磷酸胆碱(HePC)胶束由两性离子亲水表面和疏水核心组成,模拟生物膜,并具有优于其他脂质结构的几个优点,可用于评估 K(p) 值。它们的制备简单、快速,且避免了使用有毒有机溶剂,并且输出结果具有较少的光谱干扰。在这里,我们描述了一种使用 HePC 胶束作为膜模型并采用导数分光光度法作为检测技术来评估药物 K(p) 的高通量微板方案。此外,通过此处开发的专用 Excel 例程可轻松处理耗时的数据处理来评估 K(p) 值,并且详细描述了该例程。测定了非甾体抗炎药(醋氨酚、氯诺昔康、双氯芬酸和吲哚美辛)的 K(p) 值,以显示该方法的简单性并验证该方案,该方案在约 2 小时内提供了两种药物的 K(p) 值(n = 3)。