Escuder-Gilabert L, Molero-Monfort M, Villanueva-Camañas R M, Sagrado S, Medina-Hernández M J
Departamento de Química Analítica, Universidad de Valencia, C/Vicente Andrés Estellés s/n, 46100 Burjassot, Valencia, Spain.
J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Aug 5;807(2):193-201. doi: 10.1016/j.jchromb.2004.04.004.
The blood-brain barrier (BBB) is considered to be the main barrier to drug transport into the central nervous system (CNS). The BBB restricts the passive diffusion of many drugs from blood to brain. The ease with which any particular drug diffuses across the BBB is determined largely by the molecular features of drugs, and it is therefore possible to predict the BBB permeability of a drug from its molecular structure. Biopartitioning micellar chromatography (BMC), a mode of micellar liquid chromatography that uses micellar mobile phases of Brij35 in adequate experimental conditions, can be useful in mimicking the drug partitioning process into biological systems. Retention in BMC depends on the hydrophobicity, electronic and steric properties of drugs. In this paper, the usefulness of BMC for predicting the BBB penetration ability of drugs expressed as the brain/blood distribution coefficient (BB) is demonstrated. A multiple linear regression (MLR) model that relates the BB distribution coefficients data with BMC retention data and total molar charge is proposed. The model is obtained using 44 heterogeneous drugs including, neutral, anionic, and cationic compounds. A comparison with other reported methodologies to predict the BBB permeability is also presented.
血脑屏障(BBB)被认为是药物进入中枢神经系统(CNS)的主要屏障。血脑屏障限制了许多药物从血液到脑的被动扩散。任何特定药物跨血脑屏障扩散的难易程度在很大程度上取决于药物的分子特征,因此可以从药物的分子结构预测其血脑屏障通透性。生物分配胶束色谱法(BMC)是一种胶束液相色谱模式,在适当的实验条件下使用Brij35的胶束流动相,可用于模拟药物在生物系统中的分配过程。BMC中的保留取决于药物的疏水性、电子和空间性质。本文证明了BMC用于预测以脑/血分配系数(BB)表示的药物血脑屏障穿透能力的有效性。提出了一个将BB分配系数数据与BMC保留数据和总摩尔电荷相关联的多元线性回归(MLR)模型。该模型是使用44种异类药物获得的,包括中性、阴离子和阳离子化合物。还与其他报道的预测血脑屏障通透性的方法进行了比较。