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James Kimball

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How Liquid Deprenyl Citrate Was Developed

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How Liquid Deprenyl Citrate Was Developed

How LDC Worked And Trial Results

How FDA Approved Eldepryl Appeared To Kill People

Selegiline Hydrochloride

As soon as Discovery Experimental and Development, Inc. (DEDI) was formed, the first product to be researched was Selegiline Hydrochloride (HCL). Selegiline HCL was developed over 50 years ago in Budapest, Hungary.

Kimball, the President of DEDI had done a good deal of research regarding the chemical Selegiline HCL prior to forming DEDI. Kimball believed at the time that Selegiline HCL, or a similar type product could be developed, which could dramatically improve most everyone's quality of life; to include dramatic life extension. Once DEDI developed Liquid Deprenyl Citrate (LDC) the animal and human trials which transpired in the next nine years far surpassed all of Kimball's expectations.

One Company's Vitamin C Is Different From Another's

For any lay person to fully understand how dietary supplements and drugs are developed and come into being, they first must understand that a dietary supplement, or a vitamin such as Vitamin C, is not the same Vitamin C produced by different companies.

The same chemical product produced by 2 different companies are almost never the same chemical, unless one company gave their exact manufacturing method (trade secrets to their competition) which almost never happens. Six different companies producing the same chemical will in essence, produce six different chemicals. The United States Government allows each product to have the same chemical name when they are closely related. The US Government never fully explained the differences in chemical products with the same name to the public.

This subject is fully explained under FDA - Death By Deprivation. In brief, all scientists, chemists and the FDA knows, that each chemical product made by a different company is not the same chemical. That's exactly why the FDA uses the term Generic when it speaks about pharmaceutical drugs. Generic really means (forgetting any dictionary meaning) a close similarity to something else. That's why some pharmaceutical drugs with the same chemical names work, while some do not. Some have few adverse side effects, while others may have serious side effects, up to death.

The FDA invented the word Generic to use instead of telling the public that there is a similar chemical product which may be as effective as the original one, or may not be. That choice is up to the public who essentially is not properly informed.

What the FDA doesn't tell the public is many of the Generic drugs are far superior to the original drugs developed. What the FDA in concert with the patent office and the pharmaceutical cartel has done, is to allow pharmaceutical companies to obtain a 17 or more year patent, or exclusive right to manufacture and sell a certain chemical product which, it gained FDA approval for. The pharmaceutical company, which now has the protection of the FDA and patent office; price gouges the public for at least 17 years making billions, if not trillions of dollars on a few FDA approved products. While the FDA and the US Government Patent Office knows perfectly well that if five or six small pharmaceutical companies were to produce the same named chemical product the chemical products or drugs would be different. The patent office and the FDA also know, the chemical structure of each product would be different. So each product could be patented and each product is in fact different. The FDA knows that if small companies were allowed to produce their different/similar (Generic) products, the price to the public would be about 90% less, while some of the Generic products would work better than the original product produced and approved by the FDA.

The FDA and the pharmaceutical industry screams we spend all these millions developing a product and we need the patent rights so we can get our money back. That is the biggest lie of all. Again, this subject is well covered under FDA - Death By Deprivation.

Explaining How LDC Was Developed

To fully explain how LDC was developed; it is much easier to understand by explaining the make up in Vitamin C, as LDC's development was a duplicate of Vitamin C.

Vitamin C is in grapefruit and many other fruits. When it was discovered that Vitamin C had the potential to be a wonder drug or vitamin, researchers set out to find and separate the Vitamin C out of food. Once scientists found what the active chemical was that made up this substance called Vitamin C, the researchers wanted to make this wonder-drug using other chemicals instead of the very costly process of extracting Vitamin C from food. In other words have a man-made synthetic version of Vitamin C.

Scientists found the active ingredient within Vitamin C was Ascorbic Acid. They also found that the chemical ascorbic acid has 2 different sides. Something like a battery. A battery has a plus and a minus side. Ascorbic acid has a Levo (L) side, which would be the minus side of a battery and a Dextro (D) side, which would be a plus side of a battery. In other words (L) in chemistry means Levo or minus and (D) in chemistry means Dextro or plus.

Once scientists found that ascorbic acid or Vitamin C had a plus and minus side; they needed to find out what side of ascorbic acid would benefit people's health.

Scientists discovered that it was the L or minus side of ascorbic acid that would benefit mankind, health-wise and that the D side or + side was a totally different product and didn't appear to benefit anyone. However, each side of ascorbic acid or combination of both sides of ascorbic acid is allowed to be called ascorbic acid or Vitamin C, even though the L Ascorbic acid and D ascorbic acid are opposite and different and would have a totally different effects upon a person. Also the purity of ascorbic acid makes a big difference in how effective ascorbic acid is; or any other medicinal product. Also, the purity of any medicinal product, in actuality, changes the structure of the chemical and makes the product a different product, even though the FDA allows the chemicals to have the same name, though they are totally different; having different effects upon people.