Wins for what? I don't think plastination is an option for human preservation today. When it becomes an option, it probably wins.
The problem with plastination is scaling up the volume that can be done at once. This is a matter of pumping fluids around. Tiny chunks of mouse brain that were plastinated 50 years ago have readable synapses today. The experiment is whether new methods of applying chemicals to whole mouse brains work as well as first cutting up the brain; and whether cutting after plastination preserves enough information.
After scaling up plastination, it has the remaining downside that it displaces lots of chemicals. RH asks to preserve "two dozen chemical densities," which it probably fails at. Also, lots of sub-synapse detail (eg, type and placement of ion channels) is probably lost.
(This comment is largely repeating something from my blog)
I would suggest storing, along with the brain, a representative "snapshot" of the working brain, possibly an EEG under standardized conditions.
In the cryonics model, storing your EEG's didn't make much sense. When (if) resuscitation "restarted your motor", your brainwaves would come back on their own. Why keep a reference for them?
But plastination assumes from the start that revival consists of scanning your brain in and emulating it. Reconstructing you would surely be done co...
Comments? If superior brain preservation can be demonstrated under a 5nm-resolution 3D scan, plastination wins over vitrification hands-down. Is Robin missing anything here, or is this indeed as important as he says?