|
|
MJ-12:
At 10^15, think less "swimming pool" and more "the Pacific." Consider further that typically homeopathic solutions are dripped onto dextrose or some other sugar.
general:
anyway, going back to the original post, barring the movement over to more modern homeopathic theory of water imprint....
let's say the efficacy--biological activity--of the molecules is the product of clustering due to dilution.
in homeopathy, that entire vat of water with one drop of "active agent" is parcelled out as medicine...constituting hundreds of doses.
given only the statement of the original article, aren't you shit out of luck if you don't have the drop with the clusters in it?
Ethical question start here...
This is part of why the "afterimage" theory was invented...someone did the math of dilutions versus quantity of medicine versus Avagadro's number. Mathematically, yours odds of getting one molecule of medicine was tiny....
Furthermore--the first post mentions they used fullerenes--molecules made entirely of carbon lattices (with the occasional hydrogen), which have incredibly unusual electrostatic (and pretty much everything else) properties.
Most of the agents used in homeopathic dilutions are organic molecules--composed primarily of carbon, nitrogen, hydrogen, oxygen--and, in terms of ionic attraction and electrostatics, are an entirely different kettle of fish than a fullerene. That both have carbon doesn't say a lot.
So the original article could be a legit discovery about fullerenes, but doesn't necessarily carry over to homeopathy, unless the prescription happens to be for buckministerfullerene.
Furthermore, if I remember my biochem correctly, lipids (carbon-hydrogen chain-based molecules) nonpolar, thus are hydrophobic (due the sum configuration of the electron shells, bonding, etc.)
Dropped in water, lipids form miceles (sp? basically a hollow sphere) to minimize contact between the nonpolar carbon-chain and the covalent-but-polar water (h2o)
This is the basis for the cell wall of pretty much all eukaryotes...a phospholipid--a really polar molecule (po4) glued to the end of a nonpolar chain of carbon, forms a double-side micelle.
fullerenes are also carbon aggregates with a wee bit o' hydrogen , and should thus be nonpolar, barring alteration through chemical rxn (addition of a oxygen, phosphor group, etc.). Hence their "clustering" may be a product of a similar function to micelle-formation in chain-lipids.
Will try and find/make molecular diagrams for some of what I'm talking about.
[ 30-01-2002: Message edited by: [infinite monkeys] ] |
|
|