Electromagnetic Programmable Lipid Nanoparticles (LNPs) & Bio-Synthetic Life Forms (Spike Glycol-Proteins) - Karen Kingston & Dr. Ana Maria Mihalcea

It would appear that all roads lead to a Democidal, Disease-Causing, Transhumanism Agenda

To my knowledge, DARPA is a co-patent owner of the Lipid Nanoparticle (LNP) Hydrogel, which is used to transport the toxic “Wuhan”/UNC-Chapel Hill modified toxic, electromagnetic, shape-shifting Spike-Glycol Protein to all organs of the CVD jab recipient’s body.
Dr. Ardis pointed out a French study that showed that the body has hardly any ACE-2 receptors in the lungs. If the ACE-2 furin cleaver Sequence adaptation/addition was designed to have a negative health impact, it would be through it now having been added to the Spike Protein sequence and injected using an organ-bypassing Lipid Nanoparticle Hydrogel. This does not mean our Microbiome isn’t being exposed to novel AI-designed “gain-of-function” nanoparticle toxins (it could be), but this Jab of Pharmakeia seems designed to cause harm at the flick of a switch.
A deeper investigation gets one to realize that the PLANdemic was created for the Jabs, and mankind is under attack by Evil Principalities.

Dr. Ana Maria Mihalcea interviews Karen Kingston on her discoveries regarding the Self-Assembling Programmable Nano Bio/Tech “CVD” injections posing as “Greater-Good Immunizers”.

Must Watch -

• Truth Science & Spirit COVID 19 Nanotech & Synthetic Biology Bioweapons Ep 3: Convo w Karen Kingston (here)

Show Notes -

• Shot of a Lifetime: How Pfizer Developed its Own Raw Materials to Ensure a Steady Supply for the COVID-19 Vaccine (here)

• Inside the Delivery Vehicles Critical to the Success of mRNA (here)

• Moderna’s (Master patent) The modified polynucleotides are the 4 layers of the lipid nanoparticle covalent technology i.e, can go from positive to negative to neutral and vice versa. The LNP has a mean particle size of between 80nm and 160nm and contains a modified mRNA encoding a polypeptide. The lipid nanoparticles include a cationic lipid, a neutral lipid, a cholesterol, and a PEG (polyethylene glycol – plastic, not fat) lipid. The mRNA contains a 5’cap, 5 ’ UTR, N1-methyl-pseudouridine (synthetic), a 3 '-UTR, and a poly-A region with at least 100 nucleotides.
  Additionally, these microsponges may be able to exhibit an extraordinary degree of protection from degradation by ribonucleases. In another embodiment, the polymer-based self-assembled nanoparticles, such as, but not limited to, micro-sponges, may be fully programmable nanoparticles. The geometry, size, and stoichiometry of the nanoparticle may be precisely controlled to create the optimal nanoparticle for delivery of cargo such as, but not limited to, polynucleotides, primary constructs, and/or modified mRNA.
  The mod mRNA may be encapsulated into any hydrogel known in the art, which may form a gel when injected into a subject. These hydrogels are highly absorbent, containing 99% water.
  Dr. Ana Maria Mihalcea explains that these hydrogels can mimic organ systems and are artificial technological constructs, and according to MIT, hydrogels can operate as a brain-computer interface substance.
  Hydrogels are natural or synthetic polymers that can create biosynthetic structures that mimic many substances, such as silk, rubber, and plastic. Hence, the long fiber clots that were removed from people’s bodies during postmortem autopsies.
  Due to its significant water content, hydrogels possess a great degree of flexibility similar to natural tissue. Hydrogels allow for electroconductivity.
  US10703789B2 - Modified polynucleotides for the production of secreted proteins (here)

• Nano-sized, Inorganic materials (plastics, metals, synthetic materials) are dispersed throughout the body. These are made into polymers, and with the use of quantum dot technology, they create the electric fields that allow dispersion to happen. The design enables this biotech to go undetected by the body’s protective defenses and be dispersed throughout the body, i.e, not stay at the deltoid.    A metal particle catalyst is needed to start the self-assembly process of the polymer.   
  Water-dispensed nanoparticles are prepared by coating the surface of a hydrophobic nanoparticle comprised of a semi-conductive or metallic material with a multiply amphipathic dispersant.
  Semiconductor nanocrystals (also known as quantum dot particles) are nanoparticles composed of an inorganic, crystalline semi-conductive material and have unique photo-physical, photochemical, and nonlinear optical properties arising from quantum size effects, they have the potential applicability in a variety of contexts, e.g., as detectable labels in biological applications, and as useful materials in the areas of photocatalysis, charge transfer devices, and analytical chemistry.  
  US 2012/0228565 A1 - Method for preparing surface-modified semi-conductive and metallic nanoparticles having enhanced dispersibility in aqueous media (here)

• US8691384B2 - Metallic nanoparticles having enhanced dispersibility in aqueous media comprising a polymer having alkyl acrylamide side chains (here)

• Therma Fisher is in contract with Moderna and the US Government. This delivery mechanism ensures the toxic “Wuhan” modified “Spike protein” (and other proteins) gets delivered to the heart, liver, spleen, lungs, throat, kidneys, and brain. I think Karen forgot to mention that it goes to the reproductive organs, too. Quantum dots are both toxic and highly inflammatory.
  Qdot Label Conjugates for Cell & Tissue Staining (here)

• Karen puts forward a version explaining an interesting description of the word “virus” - The NIH calls “viruses” dead DNA, dead genetic material. A “virus” is foreign genetic material to a species, and the body will have a robust response to get rid of it. She explains (based on current understandings) that these CVD Jabs LNP are designed to fly below the radar and bypass the body’s protective white blood cells. Then hijack the cells in the jab recipient’s body, which then begin producing foreign DNA, at which point the body begins to attack those cells producing the foreign DNA. (I stand to correction, but I believe this is all based on a “Germ Theory, Immunology, Perspective”), One, I believe, needs to be very much reevaluated. Needless to say, we are dealing with multiple toxic nanoparticles being delivered to all organs of the body; however, if you cut it, it’s bad. What gets me is the use of AI to create a BioTech that operates on frequency and electricity and is programmable, i.e, the Human Hack, and this is of extreme importance for mankind to expose this Long Con.
  Interestingly, nanoparticle-based vaccines can induce a higher protective immunity response, rather than conventional antigen-based vaccines. For this purpose, gold, Ag, silver sulfide, titanium oxide, zirconium, and graphene have been suggested.
  Dr. Ana Maria Mihalcea explains how synthetic nanoparticles are being made from computer sequences that have NOTHING to do with “Biological Viruses” (if Pharma “isolated viruses” exist at all - re: www.viroliegy.com).
  Karen points out that “viruses” have always been “micro” size, never “nano” size, and that it would appear that engineered self-assembling proteins and peptide-based nanoparticles are being manufactured to create “respiratory viruses” i.e, symptoms blamed on a “Fear Thy Neighbour’s virus”. Self-assembling nano-bio-technology has advanced dramatically, and one would only give informed consent to receiving these Pharmakeia’s injections if one were insane; otherwise, what’s being “informed” doesn’t scratch the surface of what’s going on.
  DARPA understands that EcoHealth wanted to create aerosolized nanoparticles created from a modified sequence and spray them into a Bat Cave.
  “The COVID-19 genome is 80% similar to SARS (another virus that caused a pandemic in 2002), so it is named SARS-CoV-2. COVID-19 is an enveloped, positive-sense, and single-stranded RNA virus [12]. It has a genome of 30 kb and a diameter of 60–140 nm [13]. Due to the virus’s small size, any mitigation method that can deal with it in a corresponding “nano” size would be more efficient.”
  In the patent, it says that this nanotechnology is both Therapeutic and Diagnostic. A diagnostic is always a device, i.e, the Quantum dot can target, track, trace, and collect data, which can emit electromagnetic fields that can communicate information.
  “Various nanomaterials, such as quantum dots, can be used as biosensors to diagnose COVID-19. Nanotechnology offers benefits from the use of nanosystems, such as liposomes, polymeric and lipid nanoparticles, metallic nanoparticles, and micelles, for drug encapsulation, and facilitates the improvement of pharmacological drug properties. Antiviral functions for nanoparticles can target the binding, entry, replication, and budding of COVID-19.” The toxicity-related inorganic nanoparticles are one of the limiting factors of its use that should be further investigated and modified
  Nanomedicine for COVID-19: the role of nanotechnology in the treatment and diagnosis of COVID-19 (here)

• GQDs are able to respond to physical stimuli, such as magnetic fields, ultrasound, and light. These unique responding features allow the accurate control of drug release. GQDs are able to selectively interact with DNA or RNA. The GQD gene editing (electrical charges) can wipe out codons and nucleotides, not “nano-scissors”. Studies show that QDs grow under electromagnetic fields.
  Structurally, mRNA is a single-stranded polynucleotide that in cells is transcribed from a DNA template prior to translation into protein. mRNA molecules are, however, large, carrying a net charge, and are unstable in most biological fluids. Composite particles made from mRNA and GQDs would ameliorate many of these problems due to the surface properties and colloidal stability of GQDs, i.e, managing the body’s reaction to toxicity through making a solid form into a liquid.
  Naked, unformulated mRNA is, however, unable to cross the cell membrane and is susceptible to degradation. Here we use graphene quantum dots (GQDs) functionalized with polyethyleneimine (PEI) as a novel mRNA delivery system i.e. to ensure cell penetration. These modified GQDs can be used to deliver intact and functional mRNA to Huh-7 hepatocarcinoma cells at low doses, as the GQDs are not toxic, although “cellular toxicity” is a problem for these first-generation modified particles.

• A Novel Graphene Quantum Dot-Based mRNA Delivery Platform (here)
  Video (43min in) Karen explains the manufacturing of the Spike glycoprotein.
  Pfizer’s Structural Biological Drug Design document shows how the Spike protein is manufactured.

To ensure the “Spike glycol-protein” (SGP) would more easily enter the cells it had to be a Trimeric shape. This was genetically modified with the use of AI modeling software. This image was posted on the NIH’s website in 2017. Historically, Cryo-microscopy has been used in Artificial Intelligence bio-technology development. The SGP is an artificially created protein developed from human embryonic cells to create new “biological life forms” that then absorb (liquid) graphene and gold.

• We conclude that the spike protein of “SARS-CoV-2” (and especially its RBD) is unusually vulnerable to external electric fields. Results of Fig. 2 show that the ensuing states under EF application clearly represent distinct atomic rearrangements depending on field strength, i.e, the SGP can change shape depending on the electric-magnetic field. It seems to me that specific frequencies may be necessary to exist before injecting people with the CVD bioweapon, i.e, 5G was rolled out a good year before mass jabbing occurred. Jab recipients whose bodies were exposed to excessive EMFs could result in blood clots. No one was informed that being injected with nano-materials that host electric fields can change the electric charge of their blood, and that no human DNA was merged with this biotechnology.

  The SARS-CoV-2 spike protein is vulnerable to moderate electric fields (here)

• Quantum dot is used to create Inorganic-Organic Nanoparticles. The SGP is a bio-synthetic nanoparticle. They’ve succeeded in taking technology and creating a bio-synthetic life form.
  Fluorescent Inorganic-Organic Hybrid Nanoparticles (here)

• This article came out in April 2021, but this in no way means this biotech knowledge was not used in the development of the mRNA biotech weapons.
  “Among the numerous ways to synthesize these hydrogel materials, directly assembling genetically engineered proteins into higher-order structures turned out to be a powerful strategy for hydrogel design, i.e, creating new life forms.
  In recent years, the resulting genetically engineered (GE) hydrogels, noted for their modularity, versatility, and genetic programmability, are gaining traction with materials scientists and synthetic biologists who are eyeing the prospect of mass producing these materials via biosynthesis.” 
  “Biosynthesis” uses cells in a species to proliferate biosynthetic material.
  “Self-propagating ‘living” materials through the combined use of self-assembly and synthetic biology will continue to arouse great excitement from across disciplines in the years to come.”
  Dr. Ana Maria Mihalcea says that it’s not a bacteria, it’s a misnomer, an advanced living nano-biotech material.
  Self-Assembly and Genetically Engineered Hydrogels (here)

• In some embodiments, the small molecule is a toxin. In some embodiments, the toxin is from a Chemical weapon, an agent of biowarfare, or a hazardous environmental agent.
  Current “Vaccines” have the potential to create immunogenicity, i.e, the body kills itself.
  “mRNA technology is a good fit for gene editing. We want to make these editing proteins (SGP) for just a short period of time to modify the genome. And producing the editing enzymes transiently helps to reduce the potential for off-target effects.” – Pfizer. It appears that the purpose is not “Immunity” and that “short period” of time has morphed out of control.

  US9539210B2 - Vaccine nanotechnology (here)

• This is all based on the “Virus Hypothesis” on how the body works, i.e, trying to create “immunity” to a false cause based on pseudo-science, “virus isolation”.
  Harnessing the immune system’s full potential to fight human disease. (here)
  They claim it’s a computer-aided drug delivery system, but they are in fact storing the genomes of patients on Amgen.

• NVIDIA BioNeMo, which is fueling the computer-aided drug discovery ecosystem, now features more than a dozen generative AI models and cloud services.
  NVIDIA Generative AI Is Opening the Next Era of Drug Discovery and Design (here)

• Transfection & Gene Editing (here)

• Biotechnology company plans to advance drug discovery using NVIDIA DGX SuperPOD-powered insights from world-leading human datasets. NVIDIA is the next generation in Cloud Gaming.
  Amgen to Build Generative AI Models for Novel Human Data Insights and Drug Discovery (here)

• There are 54 LNP Trials Initiated in 2023
  Advancing LNPs to Deliver Novel Payloads with Specificity, Stability & Scalability
  3rd Annual Summit - LNP Formulation & Process Development Summit
  https://lnp-formulation-process-development-pharma.com

These LNP are electro-magnetic devices, biotechnology, that are changing the electromagnetic field inside the body which is part of what is causing disease, and these mRNA jabs are not “vaccines” (neither are conventional vaccines, vaccines) i.e. they are designed to change a recipient’s Gnome which results in diseases.

Additional Supportive Research

1. PREPARE FOR MARBURG, 5G INDUCED ZOMBIE APOCALYPSE BY WAY OF 1P36 DELETION SYNDROME - TODD CALLENDAR (here)

2. These ticks are capable of transmitting Crimean-Congo Hemorrhagic Fever (CCHF), a virus with up to a 30% human fatality rate and no approved treatment in the United States.
   The “Deep State Pharmakeia-Protection Racket” has the legal structure to take advantage of a Hemorrhagic Fever PLANdemic
   EXPOSED: US Labs Breeding Deadly Foreign Ticks in Bid for mRNA Vaccines (here)

3. Let's cause more disease and endlessly profit (here)

4. VACCINE CHEMTRAILS EXPOSED! - Are They Spraying Us With Aerosolized mRNA Poison? (here)

5. Can "Contrails & GeoEngineering" create "Certificate Of Vaccination I.D. (AI)" flu-like detox symptoms? (here).

6. VAX CARPET BOMBS: Aerosolized “vaccines” being developed that can be sprayed on human cities for automatic depopulation (here)

7. Researchers Create Aerosolized mRNA COVID Vaccine｜Facts Matter (here)

8. HUMANITY IN THE MIDST OF WW3: BIG PHARMA’S BIOWEAPON IS DESIGNED TO DESTROY THE HUMAN GENOME (here)

9. April 19, 2023: COVID-19 mRNA vaccines are not vaccines at all, but quite literally bioengineering nanotechnologies that are categorized as electromagnetic devices by the FDA and US Department of Defense (DoD).
   Pfizer's mRNA nanoparticles are electromagnetic devices per their DoD contract and the FDA. No one agreed to be injected with devices that would kill surrounding cells and tissue when activated by EMF
   Pfizer's mRNA Vaccines Contain Electromagnetic Devices (here)

10. Dismantling the COVID-19 Deceptions: COVID-19 was caused by mRNA lipid nanoparticles and 'vaccines' that contain mRNA lipid nanoparticles which are electromagnetic biosynthetic pathogens.
    Part 8: The Unvaccinated are Safe (here)

11. BREAKING! THE WORLDWIDE HOLOCAUST OF BILLIONS CAUSED BY GRAPHENE OXIDE & 5G POISONING! (here)

12. Dr.Giordano is a researcher and task leader of the EU Human Brain Project and has served as an appointed member of the Neuroethics Legal and Social Issues Advisory Panel of the Defense Advanced Research Projects Agency (DARPA) and Senior Advisory Fellow of the Strategic Multi-layer Assessment Branch of the Joint Staff of the Pentagon.
    In this video from 2019 he gives a lecture to West Point cadets about how advancements in neuroscience and neurotechnology will impact the future of war.
    In light of what we have lived through in the last four years, it is shocking how he describes Nanoparticulate Matter - Aerosolized & Weaponized (chemtrails?) and Nano-scale Robotic Units (self-assembling graphene oxide in the jabs?)
    NANOPARTICLES AS A WEAPON (here)

13. Noninvasive Remote-Controlled Release of Drug Molecules in Vitro Using Magnetic Actuation of Mechanized Nanoparticles (here)

14. Graphitic Carbon Coated Magnetite Nanoparticles for Dual Mode Imaging and Hyperthermia (here)

15. Principles of Magnetic Hyperthermia: A Focus on Using Multifunctional Hybrid Magnetic Nanoparticles (here)

16. Study on the electromagnetism of vaccinated persons in Luxembourg (here)

17. Celeste Solum says these kill shots were ready to go in the 2009 Swine flu pandemic.
    Celeste Solum: Why Graphene and Hydrogel is in Almost Everything. The Weaponization of Everything. Netherlands Food War. War Over Time and Space (here)

18. PLANDEMIC 2 VACCINE PUSH 2024 INCOMING! 5G RADIATION CAUSING FLU-LIKE SYMPTOMS! DON’T FALL FOR IT! (here)

19. Mark Steele explains his research on the traffic lights in London and his findings on Directed Energy Laser Weapons. He explains that Thales, a defense contractor that develops directed energy weapons, partnered with the Chinese company Huawei and Gemalto. This technology is now deployed in smart cities for compartmentalized covert nano and electromagnetic neuro-strike weapons. The more metals people have in their bodies, the greater the capacity for tracking individuals, and the greater the ability to target the individual and even kill them.
    Directed Energy Weapons In Smart Cities, Science and Spirit Ep 51 – Conversation with Weapons Expert Mark Steele (here)

20. A new study finds spike protein in blood vessels of female stroke patients 17 months after mRNA 'vaccination'.
    A groundbreaking study has uncovered something startling: SARS-CoV-2 spike protein was detected in the cerebral arteries of female (not male) hemorrhagic stroke patients up to 17 months after mRNA ‘vaccination’.
    Published in the Journal of Clinical Neuroscience1, this study’s finding raises urgent questions:

    Does the spike protein linger in blood vessels longer than previously thought?

    Could this contribute to rare but serious vascular complications?

    Why were only female patients affected in this study?
    Spike Protein: Long-Term Presence in Cerebral Arteries After mRNA Vaccination (here)

21. A groundbreaking study reveals that the extent to which nanoparticles accumulate in the female reproductive system varies through the menstrual cycle.
    Attention Women! What Nanoparticles Do To You Depends On When You Get Them (here)

22. Will Zionist Vaxpass Killers use EMFs to compromise Jab-Recipients’ DNA? (here)

23. According to Prof. Cahill, a covert cocktail of metallic nanoparticles, injected via COVID-19 vaccines, and “radiation micro-bursts” in urban areas could trigger symptoms like brain hemorrhages and mini-strokes.
    “They Can Fake Ebola”: Dr. Dolores Cahill’s Explosive Claim About Nanotech, Radiation & Bio-Psyops (here)

    Prof. Delorus Cahill warning regarding EMF micro bursting (here)

24. The FDA has made an alarming admission, revealing that the mRNA-injected are at risk of suffering a sudden and unexpected death for up to 15 years after they were last “vaccinated.”

    The study suggested this means fatal pulmonary hemorrhage should be considered a potential “consequence of the novel product, even months to years after the last injection.”

    FDA: Covid-Vaxxed Face Sudden Death Ticking Time Bomb for Several Years After Injection (here)

    Delayed Fatal Pulmonary Hemorrhage Following Covid-19 Vaccination: Case Report, Batch Analysis, and Proposed Autopsy Checklist (here)

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