UV can't get very far into the skin. Sunlight won't reach much into the nose and throat tract. Or lungs, unless you can push a UV light fiber in there.
Suppose the vacc has such nanoparticles and UV in sunlight activates it. But the vacc is supposed to stay in the arm and not zip around in the bloodstream, which is why in Europe they adjusted the procedure to check for blood -- they didn't want to jab into a vein.
So it stays around the arm and say it gets UV. Then your UV or heat therapy would only be good near the injection area. But the worst-hit (or most susceptible, due to ACE2 receptors) organ is often the lungs.
Zapping nanoparticles to kill cancer cells is common research. But virus replicates inside normal cells. How to target them? Ferretin cannot magically seek virus-infected cells. It's not a smart nanobot. Targeting is an issue here.
Well, about the induction current thing, you should try to find people who can zap nanoparticles with a coil and get them hot. Coupling a coil and nanoparticles? Can you induce viable current loops in a single Fe ion? (Because when complexed with Ferretin, it's all separate single Fe ions complexed with the protein.)
If magnetoferritin is in the vaccine, then with certainty - due to the amount of inflammation in the tissue in the injection site, it would in turn bind to that area, at least temporarily. Ordinary iron does so - even sweat can cause partial magnetism, so surely a concentration of magnetoferritin.
UV can't get very far into the skin. Sunlight won't reach much into the nose and throat tract. Or lungs, unless you can push a UV light fiber in there.
Suppose the vacc has such nanoparticles and UV in sunlight activates it. But the vacc is supposed to stay in the arm and not zip around in the bloodstream, which is why in Europe they adjusted the procedure to check for blood -- they didn't want to jab into a vein.
So it stays around the arm and say it gets UV. Then your UV or heat therapy would only be good near the injection area. But the worst-hit (or most susceptible, due to ACE2 receptors) organ is often the lungs.
Zapping nanoparticles to kill cancer cells is common research. But virus replicates inside normal cells. How to target them? Ferretin cannot magically seek virus-infected cells. It's not a smart nanobot. Targeting is an issue here.
Well, about the induction current thing, you should try to find people who can zap nanoparticles with a coil and get them hot. Coupling a coil and nanoparticles? Can you induce viable current loops in a single Fe ion? (Because when complexed with Ferretin, it's all separate single Fe ions complexed with the protein.)
It's late, I'll have to get back to you after I get some sleep, work, and have time again for research, but I'm not just gonna leave you hanging:
https://www.youtube.com/watch?v=8i2OVqWo9s0
"Heat." Maybe that's the idea? I don't know - opens a door though, have to look when I can.
Morning Edit:
Apparently, Trump beat me to it.
https://www.npr.org/sections/health-shots/2020/09/04/909348915/president-trumps-new-covid-19-advisor-is-making-public-health-experts-nervous
Back in September 2020, he selected a magnetic resonance imaging specialist as a leading Covid-19 advisor.
Magnetic Resonance Imaging deals directly with magnetoferritin as a nanoprobe to detect ‘infection’ in individuals - https://www.futuremedicine.com/doi/abs/10.2217/nnm-2016-0369?journalCode=nnm - deal
If magnetoferritin is in the vaccine, then with certainty - due to the amount of inflammation in the tissue in the injection site, it would in turn bind to that area, at least temporarily. Ordinary iron does so - even sweat can cause partial magnetism, so surely a concentration of magnetoferritin.
Further to be continued -
Need more research.