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. Author manuscript; available in PMC: 2011 Mar 19.
Published in final edited form as: J Control Release. 2009 Nov 14;142(3):361–367. doi: 10.1016/j.jconrel.2009.10.036

Fig. 2.

Fig. 2

Amount of doxepin transported (A) and retained (B) in the epidermis in case of passive and electroporation mediated delivery. The amount of drug transported and retained in epidermis in case of PDS-control was 0.16±0.03μg/cm2 and 1.32±0.48μg/cm2 respectively. The amount of drug transported across epidermis in case of CDS-control was below detectable levels and the amount of drug retained in the epidermis was 0.40±0.11μg/cm2. The data points represent an average of n=5±S.D.