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Dissipation and Release by Esters

nandroloner

New member
In looking at the "sust or enath" poll responses, I thought of something that I have never considered before. I'm sure someone here knows the answer, so, here it goes:

Say you have injected sustanon, which has 4 tests, each with different esters that allow the test to bind to your androgen receptors ONLY after the attached ester has released them. Now, these different esters are all shot into the same location in the muscle. Over time, the muscle will evenly dissipate the liquid into the bloodstream. So, the question is, what happens when a molecule of test that is still attached to an extended release ester gets into the bloodstream? It can't attach to a receptor because the ester is still attached to it. Does it get flushed out as waste or does it sit somewhere, in the liver for example, until it is released by the ester and then bind to a receptor? Or, does the ester prevent it from being dissipated into the bloodstream until it releases it?
 
Only a very, very small amount of an esterified testosterone is excreted via the kidneys and such. Why? They are fat soluble. The molecules are dissipated through the boy in the fatty acids until the ester is cleaved by an enzymatic process. As I'm sure you're well aware, fatty deposits are one of the very last things for the body to excrete.
 
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