ElogPoct: a tool for lipophilicity determination in drug discovery.

We present an RP-HPLC method, for the determination of logPoct values for neutral drugs, which combines ease of operation with high accuracy and which has been shown to work for a set of 36 molecules comprised largely of drugs. The general features of the method are as follows: (i) compound sparing (< or = 1 mL of a 30-50 microg/mL solution needed), (ii) rapid determinations (20 min on average), (iii) low sensitivity to impurities, (iv) wide lipophilicity range (6 logPoct units), (v) good accuracy, (vi) excellent reproducibility. A linear free energy relationship (LFER) analysis, based on solvation parameters, shows that the method encodes the same information obtained from a shake-flask logPoct determination. To the best of our knowledge a similar performance, on a set of noncongeneric drugs, has not been previously reported. We refer to the value generated via this method as ElogPoct.

[1]  P. Carrupt,et al.  Structural Properties Governing Retention Mechanisms on RP-HPLC Stationary Phases Used for Lipophilicity Measurements , 1995 .

[2]  A. Avdeef,et al.  pH-metric log P. 4. Comparison of partition coefficients determined by HPLC and potentiometric methods to literature values. , 1994, Journal of pharmaceutical sciences.

[3]  J. Sangster Octanol-Water Partition Coefficients: Fundamentals and Physical Chemistry , 1997 .

[4]  F. Lombardo,et al.  Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings , 1997 .

[5]  S. Jezequel Fluconazole: Interspecies Scaling and Allometric Relationships of Pharmacokinetic Properties , 1994, The Journal of pharmacy and pharmacology.

[6]  E. Falch,et al.  Allopurinol prodrugs. II. Synthesis, hydrolysis kinetics and physicochemical properties of various N-acyloxymethyl allopurinol derivatives , 1985 .

[7]  C. Horváth,et al.  Stationary phase effects in reversed-phase chromatography , 1980 .

[8]  D. Weaver,et al.  Determination of Octanol‐water Partition Coefficients by an HPLC Method for Anticonvulsant Structure‐activity Studies , 1995, The Journal of pharmacy and pharmacology.

[9]  D A Smith,et al.  Design of drugs involving the concepts and theories of drug metabolism and pharmacokinetics , 1996, Medicinal research reviews.

[10]  C. Bevan,et al.  Chromatographic Hydrophobicity Index by Fast-Gradient RP-HPLC:  A High-Throughput Alternative to log P/log D. , 1997, Analytical chemistry.

[11]  S. Yalkowsky,et al.  Solubility and partitioning I: Solubility of nonelectrolytes in water. , 1980, Journal of pharmaceutical sciences.

[12]  C. Hansch,et al.  Structure-activity relationship of chloramphenicols. , 1973, Journal of medicinal chemistry.

[13]  M. A. Patrick,et al.  A comprehensive method for determining hydrophobicity constants by reversed-phase high-performance liquid chromatography. , 1988, Journal of medicinal chemistry.

[14]  T. Yotsuyanagi,et al.  Solubilization of steroid hormones by polyoxyethylene lauryl ether. , 1978 .

[15]  K. Patel,et al.  Effect of lipophilicity of nitroimidazoles on radiosensitization of hypoxic bacterial cells in vitro. , 1979, British Journal of Cancer.

[16]  J. Frenz,et al.  Modeling octanol—water partition coefficients by reversed-phase liquid chromatography , 1989 .

[17]  M M Morelock,et al.  Estimation and correlation of drug water solubility with pharmacological parameters required for biological activity. , 1994, Journal of pharmaceutical sciences.

[18]  M. I. Rotonda,et al.  Relationships between Octanol-Water Partition Data, Chromatographic Indices and Their Dependence on pH in a Set of Nonsteroidal Anti-Inflammatory Drugs , 1983 .

[19]  C. Hansch,et al.  SUBSTITUENT CONSTANTS FOR ALIPHATIC FUNCTIONS OBTAINED FROM PARTITION COEFFICIENTS. , 1965, Journal of medicinal chemistry.

[20]  Michael H. Abraham,et al.  Scales of solute hydrogen-bonding: their construction and application to physicochemical and biochemical processes , 2010 .