mRNA Vaccines are a Sham. People are Being Injected with Nanotech

Written by Karen Kingston on March 31, 2023. Posted in Current News

mRNA cationic liposome ‘vaccines’ are nanotechnologies used to introduce non-human DNA into the bodies of adults and children, turning cells into disease-causing, spike-protein bioweapon factories

When the new ‘mRNA vaccines’ first became available in December of 2020, the American people were told that the ‘mRNA vaccines’ contained lipids that served as a protective bubble around the SARS-CoV-2 mRNA that would make our bodies produce the spike protein.

After being injected, our bodies would produce the spike protein and our immune system would produce antibodies so that we would NOT be able to get infected and NOT be able to infect other people with SARS-CoV-2.

In 2020/2021, everyone thought the ‘mRNA vaccine’ pitch sounded reasonable, safe and pretty much in alignment with other biological vaccines from the past.

The only problem is that everything we were told about what the mRNA ‘vaccines’ ARE is a misnomer and a lie, down to the very term mRNA vaccine. The COVID-19 injections are not mRNA vaccines. The COVID-19 mRNA shots are nanotechnology injections.

For example, the lipids and phospholipids in the mRNA injections are not lipids. Lipids are are naturally occurring molecules that make up fatty compounds such as fats and cholesterol. Lipids are part of our cells’ membranes to help control what goes in and out of cells.

The ‘lipids’ in the mRNA injections are electronically charged synthetic molecules (not natural) and can host electromagnetic fields. They are electronic devices.

Pfizer’s website states that without the cationic lipid (electronic nanotechnology) there, “could be no Pfizer-BioNTech mRNA vaccine.”

So who invented the nanotechnology that Pfizer and Moderna deceptively refer to as a a cationic lipid? And what purpose does this nanotechnology serve?

The Inventor of mRNA Nanotechnology

On June 10, 2021, Brent Weinstein hosted an interview on the Dark Horse podcast with Dr. Robert Malone and Steve Kirsch. The three men discussed both the unknown and some of the known risks of the COVID-19 ‘mRNA vaccines’.

Dr. Robert Malone was introduced as the inventor of ‘mRNA vaccine technology’ and has owned this title in dozens, if not hundreds of subsequent interviews with other media hosts.

Dr. Malone rightfully earned the title of Inventor of mRNA Vaccine Technology per Dr. Malone’s website where he lists his major publications and patents contributing to the invention of mRNA Vaccine Technology (which is nanotechnology) including Dr. Malone’s 1989 publication, “Cationic Liposome – Mediated RNA Transfection.”

Per the paper’s abstract, Dr. Malone and two of his colleagues, “developed an efficient and reproducible method for RNA transfection, using a synthetic cationic lipid, incorporated into a liposome (lipofectin).”

Electronic Nanoparticles are Not Lipids, They’re Nanotechnology

BTW- a synthetic substance that carries an electronic charge is NOT a lipid. It’s a nanotechnology/electronic device. Being injected with lipids just sounds a heck of a lot better than being injected with electronic nanotechnologies. We were told electronic nanotechnologies are lipid encapsulated mRNA vaccines because no one in their right mind would agree to be injected with an electronic nanotechnology device.

Have Cationic Liposomes Ever Been Considered a Nanotechnology?

According to the December 2020 paper, Nanomedicine for COVID-19: The Role of Nanotechnology and Diagnosis of COVID-19, liposomes were considered nanotechnologies/(nano-medicine delivery devices) per the FDA’s 2007 Nanotechnology Task Force Report.

What is the Purpose of Cationic Nanotechnology?

Cationic means that the nanotechnology independently hosts a positive electronic charge (because after all technology that doesn’t host electricity on its own is just…a piece of metal-like material? Anyway…)

Per the 1996 patent Delivery of Exogenous DNA Sequences in a Mammal, the purpose of the mRNA cationic nanotechnology was to produce non-mammal DNA (or non-human DNA) in a mammal (or a human). Non-mammal DNA could include DNA from reptiles, insects, or other non-vertebrae species.

Per ThermoFisher’s website, cationic lipids are gene-editing nanotechnologies used to deliver DNA and silencing RNA (siRNA) into cells.

ThermoFisher’s website further explains how the cationic liposome gene-editing nanotechnologies release encoded foreign genetic material into a cell’s nucleus so the cell then can produce or express foreign genetic material.

How has Human Research with Nanotechnologies Been Allowed under the FDA and NIH Regulations?

Nanotechnologies have been researched and developed under the guise of cancer research and for the ‘treatment’ of rare autoimmune diseases.

Because research subjects were often only given days or weeks left to live, the fact that mRNA nanotechnologies genetically alter the cells of the human body to ‘attack self’ and to adsorb inorganic genetic material (i.e. metals or reptilian toxins) into the cytoplasm or nucleus of human cells often resulting in new autoimmune diseases (some of which have near-term disabling or lethal consequences) went unnoticed as human subjects were often already disabled and at a high-risk for near-term death.

Per Dr. Malone’s 1989 clinical publication, he used Lipofectin to penetrate mammalian cells in order to have the cells of mice express the DNA from from the traditional Northeastern firefly, African clawed frog, and fruit fly.

Per ThermoFisher’s website, Lipofectin is the reagent of choice to integrate foreign DNA and RNA into endothelial cells. Endothelial cells are the cells that line our blood vessels, lymph nodes, and heart.

Lipofectin is Used to Integrate the Genetic Sequences of Aggressive Cancer into Humanized Cells

Lipofectin is also very effective at successfully integrating HeLa (the mRNA codes for the most aggressive form of cancer known to man) into human cells to produce cancer inside a mammal (human).

Per the 1996 patent that Dr. Malone is listed as an inventor of, Delivery of Exogenous DNA Sequences in a Mammal, the cationic liposome nanotechnologies can deliver payloads of non-mammal toxic peptides to human cells, such as the bioweapon ricin or cobra snake venom.

When doctors at the University of Pittsburgh tested the respiratory fluid from eight (8) patients who died from severe COVID-19 in 2020 in Lombardy, Italy, they found that the SARS-CoV-2 spike protein contained synthetically recreated cobra venom, Krait venom, rabies virus, and HIV glycoprotein-120.

This is taken from a long document, with a lot more images. Read the rest here substack.com

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