This study was performed to characterize the protonation equilibrium at the molecular level and pH-dependent lipophilicity of olamufloxacin.The deprotonation fraction of the carboxyl group as a function of pH was specifically calculated at the critical wavelength 294 nm,where UV pH-dependent absorbance of olamufloxacin was independent of the ionized state of the aminopyrrolidinyl amino group but heavily depended on that of the carboxyl moiety.Accordingly,micro-protonation equilibrium could be described using a nonlinear leastsquares regression program MULTI.In contrast,macro-protonation equilibrium was depicted at most wavelengths where olamufloxacin absorbance was influenced by ionized states of both proton-binding groups,results coinciding with the former.Furthermore,distribution features of four microspecies in aqueous phase were assessed. The apparent partition coefficient versus pH profile of olamufloxacin showed a parabolic curve in n-octanol/buffer system which reached peak near pH8,agreeing with the above determined isoelectric point(pI).Ion-pair effect was observed for olamufloxacin under an acidic condition, eliciting experimental values higher than those theoretically calculated,which was similar to ciprofloxacin but not levofloxacin due to amino group type.Moreover,olamufloxacin was moderately lipophilic in comparison with other quinolones,with an apparent partition coefficient of 1.95 at pH7.4.