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Microinjecting C60oo in blood cells?

c60 microinjection

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#1 youngandold

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Posted 30 January 2016 - 08:23 PM


First drawing out blood (either human or mice) and then using Microinjection techniques to insert C60oo directly inside blood cells to see if they live any longer (under culture), if they look any different under the microscope, or if they behave differently under cellular tests and chemicals.

Then such microinjected blood can be injected back in the body to see if they trigger a (hopefully positive) chain reaction.

So far it ain't clear if oral C60oo stays inside cells so microinjections can bypass or hasten up cell transport/diffusion issues.
It makes it also possible to directly deliver C60 to specific parts of the cell like the nucleus and mitochondria.

Equipment is expensive for DIYers so its better left for those with access to existing labs.

#2 Turnbuckle

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Posted 30 January 2016 - 10:35 PM

Red blood cells don't have mitochondria and will likely not be effected by C60. White blood cells (leukocytes) and platelets do have them, however the various types of white blood cells probably live too long or not long enough, and the death of platelets is not understood. But you shouldn't have to inject them, as cells with mitochondria should absorb them like any cell that burns oxygen and needs fuel.

 

Since platelets in CVD patients show high levels of epigenetic methylation, it would be interesting to treat isolated platelets with C60/OO and measure the methylation before and after. A relevant paper--

 

It is now becoming clear that a broad range of pathologies which present clinically with symptoms predominantly in one organ, such as the brain or kidney, also modulate mitochondrial energetics in platelets and leukocytes allowing these cells to serve as “the canary in the coal mine” for bioenergetic dysfunction. This opens up the possibility that circulating platelets and leukocytes can sense metabolic stress in patients and serve as biomarkers of mitochondrial dysfunction in human pathologies such as diabetes, neurodegeneration and cardiovascular disease...

 

http://www.sciencedi...213231714000093

 

 


Edited by Turnbuckle, 30 January 2016 - 10:39 PM.

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#3 treonsverdery

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Posted 30 June 2016 - 09:50 PM

I think placng C60 (with or without the oo) at erythrocytes is nifty research, one of the ways other scientists have measured the beneficial effects of antioxidants it to place them with erythrocytes at culture then see if they function longer, so there is already literature about coculturing chemicals with erythrocytes to find out if there are longevity benefits.  nifty idea, youngandold

 

the nifty things is that being absent mitochondria, if c60 causes longer functionality then researchers will know it is a different, or at least cofunctional mechanism


Edited by treonsverdery, 30 June 2016 - 09:51 PM.






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