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. Author manuscript; available in PMC: 2017 Feb 10.
Published in final edited form as: Int J Pharm. 2015 Nov 28;498(0):12–22. doi: 10.1016/j.ijpharm.2015.11.045

Figure 6.

Figure 6

(A) Plasma Concentration vs. Time profile of PL after intravenous administration at a dose of 10 mg/kg in C57-BL/6 mice. (B) Values of the pharmacokinetic parameters along with standard error and %CV of PL evaluated by two-compartment model using WinNonlin. (C) Concentration vs. Time profile of free PL and PL loaded nanoemulsion administered orally at a dose of 10 mg/kg. (D) Values of the pharmacokinetic parameters calculated based on Concentration vs. Time profile obtained upon oral administration of free PL or PL loaded nanoemulsions.