Several procedures based on the shake-flask method and designed to require a minimum amount of drug for octanol-water partition coefficient determination have been established and developed. The procedures have been validated by a 28 substance set with a lipophilicity range from -2.0 to 4.5 (logD7.4). The experimental partition is carried out using aqueous phases buffered with phosphate (pH 7.4) and n-octanol saturated with buffered water and the analysis is performed by liquid chromatography. In order to have accurate results, four procedures and eight different ratios between phase volumes are proposed. Each procedure has been designed and optimized (for partition ratios) for a specific range of drug lipophilicity (low, regular and high lipophilicity) and solubility (high and low aqueous solubility). The procedures have been developed to minimize the measurement in the octanolic phase. Experimental logD7.4 values obtained from different procedures and partition ratios show a standard deviation lower than 0.3 and there is a nice agreement when these values are compared with the reference literature ones.
Keywords: Acetanilide (PubChem CID: 904); Atenolol (PubChem CID: 2249); Caffeine (PubChem CID: 2519); Haloperidol (PubChem CID: 3559); Hydrophobicity; Ketoconazole (PubChem CID: 456201); Lipophilicity; Metoprolol (PubChem CID: 4171); Octanol–water partition; Paracetamol (PubChem CID: 1983); Phenothiazine (PubChem CID: 7108); Salicylic acid (PubChem CID: 338); Shake-flask technique; Warfarin (PubChem CID: 54678486); logD; logP(o)(/w).
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