In article <
4613361d-69f4-4e18-826e-b2906203e63bn@googlegroups.com>,
Treon Verdery <
treon3verdery@gmail.com> wrote:
the difference between the electrophoresisized proteins between the two co=
uld be noted and the physiochemicals more prevalent at the long lived tardi= >grades could be tested on yeast and c elegans for longevity effects, then t= >ested on mice and primates, similarly the shorter lived tardigrades could h= >ave a surplus of deleterious chemicals and if those modulate yeast and c el= >egans longevity then they could be tested at mice, with some amount of the = >mice being given antibodies to those chemicals to find out if they live lon= >ger, that could then become a human longevity technology
NaPCA, which as dry powder pulls water out of the air to make a puddle coul= >d be made a part of transdermal patches, it is possible this hyperhydrates = >the skin causing greater drug absorption, it is however also possible that = >this causes the drug to travel to the NaPCA
Alginate gel transdermal patches, it is possible a puffy transdermal drug p= >atch with a blob of alginate gel could have enzymes at it that disintegrate=
the gel causing s blob of water or water and solvent or harmless surfactan=
t on the dermis causing greater transport of the drug, enzymatically degrad= >able NaPCA could start out as a flat dry decal, puff up with water from the=
dermis, the NaPCA enzymatically disintegrates causing a bubble of water, s=
olvents, and surfactants on the skin under the decal
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