Determination of n-Octanol/Water Partition Coefficients of Naphthalenes and Anthraquinones Using Quantitative Structure. Retention Relationship Models by Reversed Phase. High Performance Liquid Chromatography

被引:2
作者
Yu Hui-Min [1 ]
Han Shu-Ying [1 ]
Deng Hai-Shan [1 ]
Chi Yu-Mei [1 ]
机构
[1] Nanjing Univ Chinese Med, Coll Pharm, Nanjing 210023, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
n-Octanol/water partition coefficients; Apparent n-octanol/water partition coefficients; Reversed-phase high performance liquid chromatography; Quantitative structure-retention relationship model; Shake-flask method; Naphthalenes and anthraquinones; RP-HPLC; MASS-SPECTROMETRY; MOBILE-PHASE; LIPOPHILICITY; IDENTIFICATION; PREDICTION; MECHANISM; QSRRS;
D O I
10.11895/j.issn.0253.3820.150997
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
n-Octanol/water partition coefficients (K-ow) is an important parameter commonly used to explain toxicity, activity and transmembrane of drugs. However, it is difficult to be detected by direct experimental determination. In this work, a set of 29 neutral and acidic analogues of naphthalene and anthraquinone with reliable experimental K-ow data was chosen as model compounds for establishing linear relationship between the logarithm of apparent n-Octanol/water partition coefficient (lgK(ow)"), and the logarithm of reversed phase. high performance liquid chromatography (RP-HPLC) retention factor of the solutes corresponding to neat aqueous fraction of mobile phase (lgk(w)) as the quantitative structure. retention relationship (QSRR) model. Methanol. water mixture was used as mobile phase at various pH, and retention time (t(R)) was rectified by a dual. point retention time correction (DP. RTC) in this method. The experiment results indicated that the proposed QSRR model had good correlation coefficient R-2 = 0. 974 -0. 976 with satisfactory results of internal and external validation (the cross. validated correlation coefficient R-cv(2) of 0. 970-0. 973, and 1. 4% <= relative error (RE) <= 7. 9% for all the 6 verification compounds). In addition, this QSRR model was compared with linear solvation energy relationship (LSER) involved in different descriptors of molecular structure, showing no differences. The QSRR model was applied to measure K-ow of 11 naphthalenes and anthraquinones, and the predicted data were compared with Shake. flask method (SFM) experimental ones, as well as calculated ones obtained by software. The results suggested that the proposed method for K-ow determination in this work was more accurate, simple and fast. To the best of our knowledge, this is the first report on measuring K-ow data for these compounds. The proposed strategy provides the possibility in determining K-ow of lipophilic components in complex mixture more quickly and accurately by RP-HPLC.
引用
收藏
页码:958 / 964
页数:7
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