5G Signals Are Being Used To Activate Graphene Oxide To Release Payloads Inside the Human Body
Dr. Robert Young Shares a Disturbing Video of the Cabals Plan to Use 5G to Destroy Humanity!
4G, 4G+, 5G Basic and 5G signals can be used to activate Graphene Oxide to release payloads inside the human body!
Connecting the dots on all this, 4G, 4G+, 5G Basic and 5G signals can be used to generate low voltage inside the human body, causing Graphene Oxide molecules to release predetermined payloads inside the body. The published paper, "Remotely controlled electro-responsive on-demand nano therapy based on amine-modified graphene oxide for synergistic dual drug delivery" can be found at the following link:
https://www.sciencedirect.com/science/article/abs/pii/S2468519422002166
Upon application of external stimuli, many materials are able to release drugs. However, most of them need sophisticated instruments except electrical stimulation. Electro-stimulated drug delivery has attracted attention due to the low expense, painless, and portability of the control equipment, making it manageable for customized applications. In this study, we used NGO as an electro-sensitive material to deliver drugs in a controllable manner.
"This is the first time we have used ASP and DOX as a model drug which can be delivered simultaneously by external voltage," the paper states. The conclusion of the paper adds: (emphasis added)
In conclusion, we have shown here that NGO can be used as a dual drug delivery agent, and the release of drugs can be controlled by an external voltage. To exploit the synergistic effect of ASP and DOX, we modified NGO and attached two drugs to it. Our lab made remote-controlled device efficiently released the anticancer drug. The releasing process can easily be switched on and off with a mobile phone by changing the bias voltage.
In the scientific paper quoted above, the payload was aspirin plus a common cancer drug. However, payloads can be almost anything of sufficiently small size, including both hydrophilic and hydrophobic molecules. From the study, "We have also demonstrated how hydrophilic (ASP) and hydrophobic drugs (DOX) can be delivered by using a single delivery platform."
This means that potent chemical weapons -- theoretically including nerve agents that are fatal at nanograms of exposure -- could be loaded into graphene oxide molecules which are surreptitiously delivered into the body via aggressively propagandized medical interventions such as fake vaccines or covid swabs.
Theoretically, such weapons can be delivered to the population via food, water and air vectors as well. Once in the body, a small amount of payload leakage may generate some level of nerve damage among inoculated victims, but the real payload delivery won't happen until a proper 4G, 4G+, 5G Basic or 5G signal is broadcast across the inoculated population, using the "release frequency" that generates the required voltage to unleash the payload.
In other words, a radio and/or microwave broadcast signal at the appropriate frequency could instantly cause graphene oxide molecules to release the payloads into the bodies of those who were previously inoculated or transfected through water, food or air with those payloads. This would happen simultaneously, across the entire population that is within range of the broadcast frequencies which generate the necessary voltage in the body.
If the payload were a nerve agent, the real world effect would be the sudden dropping dead of large portions of populations across cities where radio and microwave broadcast are able to saturate them. If payloads were nanoparticles, payload delivery could cause a large portion of the population to suddenly appear to be "infected" with a phantom plandemic virus that is spreading at unimaginable speed.
This technology, in other words, can be used as a "kill switch" to terminate whatever portion of the population was previously inoculated or transfected with payload-carrying graphene oxide.
To learn more about the graphene oxide and the work, research and findings of Dr. Robert O. Young go to:
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