Robboe
Posts: 908
Joined: 6/9/2003
From: Newcastle, UK
Status: offline
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Twin Peak will ellaborate a lot more than me, but here' s the gist: 1. A lot of compounds have poor bioavailability - that is, you eat them, the liver ****s them and renders them mostly useless, and then you piss them out. 2. By going topically/transdermally, you can get the compound through the skin straight into the bloodstream, avoiding the liver almost completely. Thus, you get more of the compound doing the job. This is idea for some prohormones like 4diol (ace transdermal, not so ace oral). However, compounds like 1,4 andro actually has good oral bioavailability, so you can take it either way and get good blood concentrations.
(in reply to Marc David)
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