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November 17th, 2021 
Awake Goy
Biological weapons are microorganisms like virus, bacteria, fungi, or other toxins that are produced and released deliberately to cause disease and death in humans. Pfizer-BioNtech COVID-19 mRNA vaccines contain a number of toxins that poses serious health risks.
Toxins can be small molecules, peptides, or proteins that are capable of causing disease on contact with or absorption by body tissues interacting with biological macromolecules such as enzymes or cellular receptors.
The encapsulation technique used by Pfizer/BioNTech is a lipid nanoparticle (LNP) composed of four lipids: ALC-0315 (Formal name: 4-hydroxybutyl) azanediyl)bis (hexane-6,1-diyl)bis(2-hexyldecanoate), ALC-0159 = 2-[(polyethylene glycol)-2000]-N,N-ditetradecylacetamide, 1,2-Distearoyl-sn-glycero-3-phosphocholine (DSPC), and cholesterol.
2 of Pfizer-BioNtech COVID-19 mRNA vaccine’s ingredients are already known to be harmful. Safety Data Sheets record that they are suspected of causing cancer and damage to the unborn child.
1,2-Distearoyl-sn-glycero-3-phosphocholine may be irritating to the mucous membranes and upper respiratory tract.
Carcinogenicity (Category 2), H351 = Suspected of causing cancer
Reproductive toxicity (Category 2), H361d = Suspected of damaging the unborn child
Specific target organ toxicity – single exposure (Category 3), Central nervous system, H336 = May cause drowsiness or dizziness
Specific target organ toxicity – repeated exposure (Category 1), Liver, Kidney, H372 = Causes damage to organs (Liver, Kidney) through prolonged or repeated exposure
N,N-ditetradecylacetamide may cause harm to the unborn child.
Reproductive Toxicity Category 1B = PRESUMED to produce an adverse effect on reproductive ability or capacity or on development in humans.
The cationic lipid ALC-0315 harbours very serious risks.
Most of our investigational medicines are formulated and administered in an LNP which may lead to systemic side effects related to the components of the LNP which may not have ever been tested in humans. While we have continued to optimize our LNPs, there can be no assurance that our LNPs will not have undesired effects. Our LNPs could contribute, in whole or in part, to one or more of the following: immune reactions, infusion reactions, complement reactions, opsonation reactions, antibody reactions including IgA, IgM, IgE or IgG or some combination thereof, or reactions to the PEG from some lipids or PEG otherwise associated with the LNP.
The raw materials used to produce polyethylene glycol (PEG) in both Pfizer-BioNTech and Moderna COVID-19 mRNA vaccine are by-products from petroleum refining and can also be derived from natural gas or coal.
Polyethylene glycol (PEG) is made from ethylene glycol (ethane-1,2-diol). Ethylene glycol is a synthetic liquid substance that absorbs water. It is odorless, but has a sweet taste. Ethylene glycol is used to make antifreeze and de-icing solutions for cars, airplanes, and boats. It is also used in hydraulic brake fluids and inks used in stamp pads, ballpoint pens, and print shops.
Experts are of the unanimous opinion that the adverse effects of nanoparticles cannot be predicted (or derived) from the known toxicity of material of macroscopic size, which obey the laws of classical physics. This has led the UK Royal Society and the Royal Academy of Engineering to recommend “that chemicals in the form of nanoparticles or nanotubes be treated as new substances under the existing Notification of New Substances (NONS) regulations and in the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH)” (Chapter 8 “Regulatory issues”, Point 18, p. 71).
nanoparticles may be able to translocate from the lung into the blood resulting in systemic exposure of internal organs, although the extent of this may vary.
European Commission SCIENTIFIC COMMITTEE ON EMERGING
AND NEWLY IDENTIFIED HEALTH RISKS
Unlike larger particles, nanoparticles may be taken up by the cell’s mitochondria and nucleus. Nanoparticles can interact with proteins and enzymes and alter gene expression, affecting biological behavior at the organ, tissue, cellular, subcellular and protein levels. Because of this, nanoparticle toxicity may result in increased oxidative stress; inflammation; damage to proteins, membranes and DNA; and cellular death.
The Italian researchers (Antonietta M. Gatti and Stefano Montanari) hypothesized that vaccine micro- and nanocontaminants could explain both immediate and delayed adverse events following vaccination, particularly because the contaminants’ “final destination” is likely to vary from person to person. If nanocontaminants reach the brain rapidly, individuals may experience damage within a few hours of vaccination. On the other hand, it is also plausible that contaminants could travel to the microbiota and there interfere with the production of enzymes necessary to carry out critical neurological functions, prompting symptoms weeks later.
In order to hide the mRNA from our immune system, which would ordinarily kill the foreign material once injected into our bodies, the LNPs in the two Covid vaccines are coated with a potentially dangerous substance called polyethylene glycol (PEG) using a process called “PEGylation.” PEGylated LNPs and PEG are not new to the drug market, but this is the first time they have been used in vaccines. The inclusion of PEG in both the Moderna and Pfizer injections is troubling in light of PEG’s well-documented immunogenicity. A large and growing body of scientific literature shows that PEGylated compounds often trigger the formation of anti-PEG antibodies, which in some people leads to “hypersensitivity reactions. . . entailing severe allergic symptoms with occasionally fatal anaphylaxis.” A study published in 2016 by University of North Carolina researchers found that up to 72 percent of people may harbor anti-PEG antibodies—at levels, in about 7 percent of people, high enough to predispose them to anaphylactic reactions.
Weston A. Price Foundation, Washington DC
The results showed that the toxicity of the cationic lipid had a close relationship with its headgroup structures, and the cytotoxic mechanism was mainly via the caspase activation dependent signaling pathway and mitochondrial dysfunction.
cationic lipids still have the problem of toxicity, as they can activate several cellular pathways like pro-apoptotic and pro-inflammatory cascades, which has become one of the main bottlenecks for their applications.
2018 Oxford Academic Toxicology Research paper –Correlation of the cytotoxic effects of cationic lipids with their headgroups
This is the first occasion in which polyethylene glycol (PEG), a polymer made from petroleum, has been injected into human subjects. As the EMA explains: “ALC-0159 is comprised of a polyethylene glycol (PEG) headgroup (~2000 M.Wt.) attached to hydrophobic carbon chains (ie, the lipid anchor)” and “is present BNT162 at a low mol% (<2 mol%), and therefore dose, relative to the other lipids.
It amounts to only “2%-6% [of the NLP] in the case of BioNTech” but is the substance likely to cause anaphylactic shocks.
The most important and dangerous of the four NLPs is ALC-0139. Because “ALC-0315 has no known biology”, Pfizer could only guess at how long it would take to be removed from the human body, that guess being “4-5 months for 95% elimination”, a particularly long period for such a toxic ingredient.
New Zealand Christchurch High Court legal proceeding
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