The FDA approved nano-virile protein bacteria eaters that work on deli meats and other ready-to-eat foods in August, 2006. Food manufacturers started spraying this new nantechnology viruses on meats and vegetables in August 2006.Intralytix Corporation
, based in Baltimore, first petitioned the FDA in 2002 to allow the viruses to be used as an additive. It has since licensed the product to a multinational company, which is marketing the virus spray worldwide.
The viruses are known as bacteriophages, viruses that kill bacteria, or phages for short. Phages have been around a long time, living as parasites inside many bacteria.
Intralytix uses biotechnology to grow viral phages in a culture with Listeria, in theory teaching the viruses to recognize the bacteria. The FDA-approved cocktail contains six different viruses intended to attack one strain of bacteria.http://www.dldewey.com/morgel.htm
----------------------------------FDA, EPA and Nanotechnology — .
Nanotechnlogy is the ability to control things at an atomic and molecular scale of between one and 100 nanometers and has been met with enthusiasm across a variety of industries. Critics highlight the murky area of how nanoparticles affect toxicity and they say nanoparticles should be treated as new, potentially harmful materials and tested for safety accordingly. (5)
Unlike pharmaceuticals, which must go through a series of pre-market approvals, finished dietary supplements need no pre-market approval. Under the Dietary Supplement Health and Education Act (DSHEA), which is part of the Food and Cosmetic Act, only ingredients not marketed in the US before October 1994 must be approved by FDA before use in consumer products. Thus, as it stands, pre-market regulation of nanotechnology in dietary supplements, biological pesticides, and other man made nanotechnology does not fall under FDA, EPA, OSHA, FIFRA and other regulatory agencies in the USA, just for the simple reason that the nanotechnology is so small that the conventional regulatory laboratory methods do not have equipment to measure at 9 decimals below the zero and are only addressing 3 and 4 decimals (ppm, ppb, and ppt). " (Staninger, Dr. Hildegarde, ibid.)
The following is from Dr. Staninger's paper that was presented at the
National Registry of Environmental Professionals Conference
in Nashville, TN, on Oct. 18th, 2006 Read Dr. Staninger's entire paper HERE: http://www.dldewey.com/stan.htm
So is this NANO technology Bacteriophage virus a cause of the bizarre symptoms of the little known, 'X-Files'
like disorder of Morgellons Disease?Morgellons
- A disease in which individuals have the growth of fibers from their skin that burn at 1,700 degrees F and do not melt.
A private study to determine the chemical and biological composition of these fibers has shown that the fibers' outer casing is made up of high density polyethylene fiber (HDPE).
The fiber material is used commonly in the manufacture of fiber optics. There is no history of the individual in that industry or coming into contact with this material. It was further determined that this material is used throughout the bio nanotechnology world as a compound to encapsulate a viral protein envelope, which is composed of a viron (1/150th times smaller than a virus) with DNA, RNA, RNAi (mutated RNA) or RNAsi linear or ring plasmids for specific functions. (21, 22) Toxicological pathology identification of tissue biopsies from an individual diagnosed with Morgellons revealed the presence of continual silica or glass tubules with the presence of silicone. (23) It must be noted that the core toxicological effects of silicone alone have been demonstrated throughout the breast implant industry and litigation cases. (24, 25) Furthermore, silicone cannot make silica, but silica or silica bicarbonate can make silicone through natural cellular interaction in a biological system. The subject did not have breast implants or any other implant or silicon glue injections.