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J Pharm Biomed Anal ; 37(2): 389-93, 2005 Feb 23.
Article in English | MEDLINE | ID: mdl-15708683

ABSTRACT

This study was performed to characterise the protonation equilibrium at the molecular level and pH-dependent lipophilicity of moxifloxacin. After determining macro- and micro-constants, distribution features of four microspecies in aqueous phase were assessed. The apparent partition coefficient versus pH profile of moxifloxacin showed a parabolic curve in n-octanol/buffer system which reached near pI. The true partition coefficient was calculated from the log P(app) and microconstants values.


Subject(s)
Aza Compounds/chemistry , Lipids/chemistry , Protons , Quinolines/chemistry , 1-Octanol , Buffers , Fluoroquinolones , Hydrogen-Ion Concentration , Models, Chemical , Moxifloxacin , Solutions , Spectrophotometry, Ultraviolet
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