Volná Tereza, Motyka Kamil, Hlaváč Jan
Department of Organic Chemistry, Faculty of Science, Palacký University in Olomouc, 17. listopadu 12, 771 46 Olomouc, Czech Republic.
Department of Organic Chemistry, Faculty of Science, Palacký University in Olomouc, 17. listopadu 12, 771 46 Olomouc, Czech Republic.
J Pharm Biomed Anal. 2017 Feb 5;134:143-148. doi: 10.1016/j.jpba.2016.11.038. Epub 2016 Nov 27.
The proposed HPLC method using solely or nearly 100% aqueous mobile buffer as mobile phase offers fast determination of dissociation constant for compounds in relatively wide range of lipophilicity (log P from -2.26 to 2.26). The dissociation constant value for simpler chemical compounds can be determined via only 8 chromatographic runs. The number of needed chromatographic separations depends on the structural complexity of the tested compound. Moreover, the proposed method does not require a measurement of Yasuda-Shedlovsky extrapolation that includes several pK determinations in solutions with different methanol content which speeds up considerably the procedure. The methodology is suitable for evaluation of large series of drug candidates, which can be present as complex mixtures and in small amounts.
所提出的高效液相色谱法使用纯或近100%的水性流动缓冲液作为流动相,能够快速测定亲脂性范围相对较宽(log P从-2.26至2.26)的化合物的解离常数。对于较简单的化合物,仅通过8次色谱运行即可确定其解离常数。所需的色谱分离次数取决于被测化合物的结构复杂性。此外,所提出的方法不需要进行Yasuda-Shedlovsky外推法测量,该方法包括在不同甲醇含量的溶液中进行多次pK测定,从而大大加快了测定过程。该方法适用于评估大量候选药物,这些候选药物可能以复杂混合物形式存在且含量较少。