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. 1998 Jan;42(1):45–52. doi: 10.1128/aac.42.1.45

FIG. 5.

FIG. 5

Comparison of ciprofloxacin pharmacokinetics after i.v. and i.p. administration. (A) Levels of free (•,▪) or liposomal (▴,⧫) ciprofloxacin in plasma after i.v. (•,▴) or i.p. (▪,⧫) administration. Liposomes were composed of SM/chol, and the dose of ciprofloxacin injected for all groups was 15 mg/kg. (B) Ciprofloxacin/lipid ratios in plasma after i.v. (▴) or i.p. (⧫) administration of ciprofloxacin encapsulated in SM/chol liposomes. Data represent means ± standard errors from three mice.