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. Author manuscript; available in PMC: 2021 Feb 1.
Published in final edited form as: Prostaglandins Other Lipid Mediat. 2019 Dec 10;146:106401. doi: 10.1016/j.prostaglandins.2019.106401

Figure 1. Pharmacokinetics of oral 17S-RvD1 in rats.

Figure 1.

After a single oral dose of 17S-RvD1 in 500μl of corn oil, rats were subjected to multiple blood draws at different time points. Plasma samples underwent SPE and 17S-RvD1 quantified by EIA. 17S-RvD1 plasma concentration increased gradually, peaked at 3 hours reaching a max concentration of 446pg/ml (1.18nM), and went back to baseline within 24 hours (n=3).