it appears that the mucous membranes of the mouth is an excellent method to deliver epiandrosterone into the blood stream. i have tried both FRL's 5-alpha test and LG's liquid MMv3 and i can certainly feel both of them within a few minutes after administering them... DAM! feeling it right now actually.. hits you hard about 5 minutes after talking it.
anyways, i only feel the initial rush these sublingual doses for a little while so my question is when epiandrosterone is administered sublingually/linings of the mouth, is it metabolized more quickly than those absorbed through the GI track or even those absorbed through the lymphatic system such as how PP's products claimed to be? i remember reading somewhere that this was the case but i dont remember where. so, would this method cause the compound to have a shorter half life compared to the other currently available stano products or even androhard?
on a side note, i dont get any sort of rush from ingested stano/androhard products, even when dosed very high.
thoughts, opinions, broscience, and research welcome. thanks in advance.
jbry, this seems like something you would have some knowledge about.