Free James Kimball

How Liquid Deprenyl Citrate (LDC) Was Developed

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 LDC the animal and human trials which transpired in the next nine years far surpassed all of Kimball's expectations.

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, located at the top of this page.

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 Lascorbic 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.

Once scientists learned how to "man-make" so to speak, ascorbic acid or Vitamin C, they now needed to separate the L side, which was the active side, from the D side which appeared to have no benefit at all.

Vitamin C was now man-made and no longer needed to be extracted from grapefruit and other food products. Now the challenge was, just how pure was the industry going to make the L-Ascorbic Acid for human consumption. The answer from the industry was purely money. It's more expensive to produce a pure product than a not so pure product. Most every chemical company that produced Vitamin C or L Ascorbic Acid produced it at a purity of between 87 - 95% pure. They then sold it to vitamin companies to add ingredients called pill fillers, to make pills and sell it to the public as Vitamin C.

Only one company that Kimball is aware of in the world produces L Ascorbic Acid at 99% purity, or above. The companies that tablet Vitamin C do not use the higher purity Vitamin C, because it costs a little more to purchase. However, in tests, the higher purity Vitamin C at 99% was 15 to 20 timesmore effective than all the other vitamin C products being produced. The cost however was only 4 times more for the higher priced Vitamin C product. It would actually be cheaper for the public to purchase the purer Vitamin C, simply because they would be taking 15-20 times less, while receiving better benefits from the purer product.

For your information the only company in the world that Kimball knows producing L-Ascorbic Acid or Vitamin C at 99% purity and above is B.A.S.F. in Germany.

There is only one company Kimball knows of that actually purchases B.A.S.F.'s L-Ascorbic Acid at +99% purity; re-crystallizes the L-Ascorbic Acid to gain even a higher purity level; places the extreme high purity L-Ascorbic Acid in a capsule without any fillers and sells the Vitamin C to the public and doctors.

Kimball cannot disclose the name of the company doing this; simply because, the US Government would construe the Vitamin C being sold currently as a drug. This due to the content on this website stating how effective properly made L-Ascorbic Acid or Vitamin C is, in treating and preventing heart disease and cancer. You may review the effectiveness in the use of high potency Vitamin C under Cancer - Is There A Cure? and also FDA - Death By Deprivation where it talks about the fact, high potency Vitamin C is extremely effective in treating and preventing heart disease.

Aforestated Liquid Deprenyl Citrate (LDC) is very similar to Vitamin C. Selegiline HCL which was developed in Budapest had a L side - minus, and a D side - plus. The Selegiline HCL that appeared to be effective in neurological disease was the L side while the D side appeared to do nothing at all.

Selegiline was made from an extract of a plant, which was eventually turned into a man-made product the same as Vitamin C.

At the time DEDI was attempting to develop a product similar to Selegiline HCL, the FDA had approved a prescription drug called Eldepryl. Eldepryl was FDA approved to be used "only" with another very dangerous prescription drug called Levodopa, which had very serious side effects. The combination of those two drugs were approved by the FDA only to be used together for patients that were afflicted with one terminal disease: Parkinson.

One of the very first things DEDI did was to take the drug "Eldepryl" apart in 1990. DEDI found Eldepryl was not a pure product and contained contaminants from 1 - 2 %. The FDA was informed of the contaminants but didn't care. Dr. Barltrop who was working with Dr. Owen for Discovery Experimental (DEDI), on the Selegiline HCL project, called the Eldepryl product rubbish.

Dr. Barltrop was a lecturer and faculty member at Oxford University in England. Dr. Barltrop was assisting Dr. Owen who was head of the organic chemistry department at the university of South Florida. Dr. Owen was in charge of the development of a Selegiline or similar product for DEDI.

When the product containing Selegiline HCL was developed in Budapest the scientist which developed the product called it "Deprenyl." DEDI had no idea exactly how pure, or exactly everything the Deprenyl product contained.

What DEDI did find out, is that the drug Eldepryl FDA approved to use only with another dangerous drug was manufactured in Budapest, Hungary, and was rubbish. It wasn't until 1994 that DEDI found out just how dangerous a product Selegiline HCL was when human trials in England were released revealing that the exact combination the FDA had approved for Parkinson patients to take (Selegiline HCL and Levodopa) killed patients at a much higher rate than patients using Levodopa by itself.

DEDI also found out that no one in the world was able to develop Selegiline in a liquid form and stabilize the product for human use. Nor did it appear that anyone had been able to produce Selegiline HCL at or above 99% purity.

The fact was Selegiline HCL could only be produced by adding Hydrochloric Acid and making the product in pill form.

After almost a year of working on the product Dr. Owen and Dr. Barltrop came up with Selegiline, without the use of Hydrochloric Acid in the form of a liquid and stabilized it, which again, had never been accomplished before. Not only had Dr. Owen come up with the perfect stabilizing agents; he had come up with every one of the stabilizing agents, being natural products. This in Kimball's mind made a world of difference. Now the product could be deemed a dietarysupplement because all the ingredients within DEDI's product were either direct food products or their origin came from a plant. Not only that, Selegiline HCL which was in the FDA approved pills in combination, was not the same chemical as Selegiline liquid. DEDI named the product Liquid Deprenyl Citrate (LDC).

DEDI's President Kimball, immediately petitioned the FDA to deem the LDC a food supplement; food additive, or vitamin in mid-1991. The FDA immediately violated Kimball's 1 stAmendment Rights of Petition, sent Kimball's petition back and refused to formally review the petition as required by law.

Kimball then formed a company in Tijuana, Mexico and began to sell the LDC to people all over the world. The LDC product was sold into the United States under a FDA exemption which stated in essence: any US citizen could import from a foreign country a 3 month supply of products without Government intervention.

DEDI had conferred with doctors and scientists all over the world prior to the sale of its LDC as to the amounts and side effects that may be forthcoming. Additionally, prior to LDC's introduction, doctors and scientists had been using LDC for nearly eight months. The benefits appeared outstanding while adverse side effects appeared to be non-existent as expected.

When LDC was finally offered for sale through Discovery in Mexico, in late 1991, a monitoring system was set up with doctors and individuals, to secure information as to how effective the product was, and if it had any adverse side effects that weren't taken into consideration.

Doctors reported the results, as did individual users, while forms were sent out to all purchasers to report whatever effects each one experienced using LDC.

DEDI knew, that they had developed and produced a product never developed before; which should be very effective with all kinds of neurological diseases. If the product worked the way it was designed to; it should have, at the least, dramatically improve the quality of life of the elderly.

LDC did far more that it was ever expected to do, as the reports came flooding in.

How LDC worked and the results of doctors' trials and individual reports review How LDC Worked And Trial Results

An in dept accounting of the development of this product and others and what the Pharmaceutical Companies, FDA, and Florida Department of health did to stop Kimball; review Kimball’s affidavit written in 1994

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