Faller Bernard, Grimm Hans Peter, Loeuillet-Ritzler Frédérique, Arnold Sabine, Briand Xavier
Novartis Institutes for BioMedical Research, WSJ-350.3.04, CH-4002 Basel, and GiMS mbH, Maulbeerstrasse 44, CH-4058 Basel.
J Med Chem. 2005 Apr 7;48(7):2571-6. doi: 10.1021/jm049377w.
We report on a new, high-throughput assay designed to measure octanol/water partition coefficients in early drug discovery. The assay is carried out in 96-well microtiterplates and measures the diffusion of compounds between two aqueous compartments separated by a thin octanol liquid layer. Octanol/water partition coefficients are derived from the apparent permeability (P(a)) values using a calibration curve. The assay can measure partition coefficients within the range -2 to + 8; thus, a dynamic range of 10 log units can be covered in one single run. Unlike chromatographic methods, the technology is not restricted to neutral and weakly basic compounds, and, as no stationary phase is involved, the data can be strictly compared with values obtained from traditional methods such as shake-flask/HPLC or dual-phase potentiometric titration.
我们报告了一种新的高通量测定方法,旨在测量早期药物发现中的正辛醇/水分配系数。该测定在96孔微量滴定板中进行,测量化合物在由薄正辛醇液层分隔的两个水相之间的扩散。正辛醇/水分配系数通过使用校准曲线从表观渗透率(P(a))值推导得出。该测定可以测量-2至+8范围内的分配系数;因此,单次运行即可覆盖10个对数单位的动态范围。与色谱方法不同,该技术不限于中性和弱碱性化合物,并且由于不涉及固定相,数据可以与通过传统方法(如摇瓶/HPLC或双相电位滴定法)获得的值进行严格比较。