If a new drug is highly lipophilic and small, what absorption modification would most increase its rate of passive uptake across enterocytes?

Administering it with a competitive polar nutrient that uses the same channel, since channel competition enhances passive uptake across bilayers.

Adding a large charged moiety to the molecule to increase its water solubility so it will dissolve in the lumen and be absorbed faster by passive diffusion.

Co-administering it with a fatty meal to enhance its solubilization and partitioning into the lipid bilayer, increasing passive absorption.

Blocking all lacteals so lipophilic molecules cannot enter lymph and therefore will be forced to diffuse directly into portal capillaries.