PHOSPHOLIPID BILAYER PERMEABILITY OF beta;-LACTAM ANTIBIOTICS

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Liposomes containing penicillinase or cephalosporinase were prepared from the phospholipids of Escherichia coli. After free β-lactamase was inactivated by clavulanic acid or penicillanic acid sulfone followed by separation of inactivated enzyme and inhibitor from liposomes by gel filtration, the permeability of these liposomes to ampicillin, cefazolin and cephaloridine was estimated by measuring the hydrolysis of these antibiotics by the entrapped enzymes. The permeability parameter C (minute^-1 μM lipid^-1) of ampicillin, cefazolin and cephaloridine was calculated to be 2.35×10^-4, 0.33×10^-4 and 0.52×10^-4, respectively. The lipid bilayer permeability of these antibiotics was also measured by using the liposomes containing these antibiotics. About half of the initially entrapped ampicillin was released from the liposomes within 80 minutes, while no significant release of cefazolin and cephaloridine could be detected during the same period. These results clearly indicates that the lipid bilayer membrane is more permeable to ampicillin than cefazolin and cephaloridine, and they are consistent with the observations of SAWAI et al.¹⁾, who showed that ampicillin was a more effective antibacterial drug than cefazolin and cephaloridine against the porin-deficient mutants.