vlad665
Rising Star
as we all know, lsa-aldehyde adducts are relatively easy to make given the right conditions(acidic ph ~4, darkness, and cold temperatures), the issue with them is keeping them in that form long enough to hit the receptors.
so i've been toying around with lecithin liposomal formations in my polypores extracts(alkaline, acidic, etoh, and fatty acid pulls) due to the need to mix those pulls in a single bottle for convenience. bought me an ultrasonic pot, mcgyvered some jars, pfte tubings/fittings, a vacuum pump and built myself a functional rotovap simulacrum, so i've been thinking i could try and apply the same reasoning to those adducts, trap them into the lecithin liposomes, under vacuum, low/nolight, acidic ~ph 4 solvent, cold environment), combined with the hand syringe extrusion to force liposomal formation.
the ideea is to encapsulate the adducts into liposomal form so they can pass the stomach then go through the lymphatic system directly due to lecithin. some sort of trojan horse. what do you guys think? would it work?
so i've been toying around with lecithin liposomal formations in my polypores extracts(alkaline, acidic, etoh, and fatty acid pulls) due to the need to mix those pulls in a single bottle for convenience. bought me an ultrasonic pot, mcgyvered some jars, pfte tubings/fittings, a vacuum pump and built myself a functional rotovap simulacrum, so i've been thinking i could try and apply the same reasoning to those adducts, trap them into the lecithin liposomes, under vacuum, low/nolight, acidic ~ph 4 solvent, cold environment), combined with the hand syringe extrusion to force liposomal formation.
the ideea is to encapsulate the adducts into liposomal form so they can pass the stomach then go through the lymphatic system directly due to lecithin. some sort of trojan horse. what do you guys think? would it work?
