Regulatory bodies across the world knew in January 2021 that toxic lipid nano-particles permeated blood plasma and from there into liver, spleen, ovum, thymus, uterus, testes, brain and bone marrow

The Australian regulator knew of this and you can be sure that every other health regulator had access to the same information.

Note the paper referenced below shows that the spread of the toxic lipid nano-particles in the injections goes to major organs and IS NOT DOSE DEPENDENT.

Note that tests were done for the lipid nano-particles BUT NOT A COMPARISON OF THE SPREAD OF THE SPIKE PROTEIN VIA THE BLOOD STREAM TO VITAL ORGANS

The complete logic fail of regulatory authorities that has damaged 5.6 billion out of 8 billion people on the planet stems from the fallacy that it is “healthy” to move:

from facts known in early 2021 (and from clinical trials) that

“the “natural  infection mucosal pathway” occurs in a minority (less than 10% per year) of people – most (99%) of whom recover after a few weeks at most”

to

“injection of instructions to manufacture spike protein in unknown amounts and durations to the majority of the population (vaxx mandates that have resulted in 90% of adults in the US receiving at least one dose).”

The entire delivery mechanism of the C19 mRNA injections is poisonous – from PEG coating to lipid nano-particle, to the mRNA instructions, to the spike protein that the instructions create.

From the 17 minute video from Dr John Campbell here:

Australian government biodistribution data - YouTube

Referencing this TGA document here that focuses on the Pfizer injection:

FOI 2389 document 6 (tga.gov.au)

Dr Campbell’s cliff notes:

“In vitro studies indicated minor metabolism of ALC-0159 and ALC-0315 in liver, with most of the lipids found unchanged at the end of the 2 or 4 h incubation period

This should have immediately halted the roll-out of C19 mRNA injections.

(Ed: REGULATORY BODIES GLOBALLY HAD ACCESS TO THE FACT THAT THE LIPID NANO-PARTICLES PERMEATED BLOOD PLASMA AND VITAL ORGANS AND ELECTED TO POISON THE PEOPLE WHOSE HEALTH THEY WERE RESPINSIBLE FOR – PRE-MEDITATED RANDOM MURDER AND INJURY).

Tissue distribution (lipid nanoparticles encapsulation RNA) (Page 44)

Rats after i.m. vaccine injection (Ed: “i.m. = intra muscular rather than intra venous – remember we were told that the injection would stay in the shoulder muscle? Not all people injecting doses aspirated the injections to make sure that only an injection into muscle was achieved, but the intention was (to aspirate the injection) to make sure that injections did NOT enter the blood stream).

The concentration of radioactive lipid marker reached the peak level in plasma (8.9 μg lipid eqv/mL), between 1 – 4 h post-dose, and distribution mainly into liver, adrenal glands, spleen and ovaries over 48 h Concentrations were higher in plasma than in blood, with mean blood: plasma ratios of 0.5 – 0.6.

DISTRIBUTION (page 40)

The distribution of LNP-BNT162b2 (V9) mRNA or expressed S protein was not studied.

Table 4-2.

Mean concentration of radioactivity (sexes combined) in tissue and blood following a single IM dose of 50 μg mRNA/rat (page 45)

Mean total radioactivity was greatest at the injection site followed by the liver, with much lower total recovery in spleen, adrenal glands and ovaries

The tissue distribution pattern was similar in 100 μg mRNA/animal dose group as noted above for 50 μg mRNA/animal dose, with highest distribution into liver, adrenal glands and spleen.

Conclusions

Slow but significant distribution of lipid nanoparticles from the site of injection with major uptake into liver. Minor distribution in spleen, adrenal glands and ovaries over 48 h.

Mean blood:plasma ratios of 0.5-0.6 indicating nanoparticles mainly present in plasma fraction of blood with peak concentrations in plasma at approx. 2 h post-dose. Liver concentrations over time.”

Dr Campbell released this video after another 47 minute video with Australian Senator Rennick who has been holding the Australian Government to account for its wilful and knowing infliction of harms onto Australians.

Senator Rennick, full interview - YouTube

Quick return access to the Australia report

Nonclinical Evaluation Report BNT162b2 [mRNA] COVID-19 vaccine (COMIRNATYTM)

FOI 2389 document 6 (tga.gov.au)

Onwards!

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