A rapid, reliable and simple microscale method for the determination of octanol-water partition coefficients has been developed and evaluated. Rapid solute partitioning and facile octanol-water phase separation is accomplished in a commercially available mixer-separator device. The relative concentration of solute in each phase is then measured directly by computer-based reverse phase HPLC. The procedure requires only 10 μg of sample, which need not be pure, and uses 1 ml or less of both n-octanol and pH 7.0 phosphate buffer. Log P values of 26 compounds, mainly nucleoside analogues with anti-HIV and antitumor activity, have been determined in the range 0.7 to -2.4 with a precision better than ±0.04 log units. For compounds with literature data available, measured log P values are in good agreement (better than ±0.2 log units) with those values obtained by traditional “shake-flask” methodology. The described method is applicable to both single compound analysis and simultaneous multiple compound determinations through use of isocratic or gradient HPLC techniques.
No takes yet. Share an insight, caveat, or question.
Ford et al. (1991) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: