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. Author manuscript; available in PMC: 2011 Aug 30.
Published in final edited form as: Int J Pharm. 2010 Jul 1;396(1-2):111–118. doi: 10.1016/j.ijpharm.2010.06.039

Fig. 6.

Fig. 6

Hydrolysis of potential prodrug CDCA-lysine-ketoprofen in rat liver homogenate. In panel A, data points indicate the time course of the disappearance of 1 μM (▲) and 5 μM (△) of CDCA-lysine-ketoprofen and the appearance ketoprofen from 1 μM (●) and 5 μM (○) CDCA-lysine-ketoprofen. In panel B, ketoprofen appearance from of 1 μM (●) and 5 μM (○) prodrug is re-plotted on a smaller scale.