The chromatographic behavior of cephalexine, cefaclore, ceftriaxone, cefiui
me, and cefotaxime has been investigated on silica gel layers with binary m
obile phases containing different amounts of organic modifier. The influenc
e of type, chemical character, and position of substitution of functional g
roups (steric and structural effects) on the retention of analyzed compound
s was of particular interest.
Systematic investigation of the cephalosporins furnished much information a
bout their hydrophobicity (R-M(0)), the mechanism of adsorption, and the po
ssibilities of separation. Correlation of the hydrophobicity parameters R-M
(0), m, and C-0 with the lipophilicity parameter log P was established by u
se of linear equations.
The parameter C-0 was considered as directly applicable in quantitative str
ucture-activity relationships of the cephalosporins.