Visit http://www.CancerCanBeBeaten.com to get the book!

.

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I was most excited to stumble across this page of information on the Sloan-Kettering website. An entire page about zeolite which validates the information I have been stating all along. Zeolite has been shown SCIENTIFICALLY to have anti-tumor effects in animals. Although it hasn’t been validated in humans because the company decided to take the ORIGINAL zeolite product to market as a nutritional supplement. This is because the cost of clinical trials in humans is HUGE.

There are a number of texts and studies listed on this page as resources as well.

However, we certainly now know that zeolite and cancer go hand in hand in testimonials. Please note that Sloan-Kettering does NOT mention zeolite enhanced with DHQ, humic acid, fulvic acid or any other additives. That’s because the originak zeolite is the ONLY one that has given reported results. Don’t be duped by Robert Sopias and his "11 natural therapies to conquer cancer". loan-Kettering mentions the Original Zeolite company for a reason.

If you want to know why, download The Liquid Zeolite Book for FREE!

Here is an excerpt from Sloan Kettering followed by the link to the page on Cancer and Zeolite.

Mechanism of Action

http://www.mskcc.org/mskcc/html/69424.cfm

References

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WHAT IS NATURAL Liquid Zeolite

Cancer Strategy: Use Zeolite To Kill Cancer Cells… Without Harming Your Body

(Says Robert Sopias in his report "11 Natural Remedies to Conquer Cancer") When chemotherapy and radiation therapy are used to kill the cancerous cells, they harm healthy cells in the process. In fact, they can kill people faster than the cancer would have done. This report focuses on natural supplements that do a good job of killing cancerous cells, but do not cause harm to your body. In this report you will learn only about completely safe cancer supplements that can be used with no supervision.
 

 

You may well ask, why a safe and natural product that is able to kill cancer cells is not recommend by your doctor. The answer is, he probably does not know about it, but even if he did, he is not likely to use it.
It’s the nature of the medical/drug industry, doctors only use and recommend drugs that are approved in a process that costs hundreds of millions of dollars. Because of this high cost, the drug companies will only make drugs that can be patented. That way they can sell them for huge mark-ups and have no competition. Unfortunately, because these drugs have been altered from nature, which they must be, to be patented, they become toxic in your body, with harmful side effects. Your body can handle natural foods and herbs, however, the altered ones have toxic side-effects because your body cannot handle them. This is the reason why the biggest cause of deaths in the US are from medical drugs.
 

Because of the high cost of getting approval for drugs, no company would ever take an unpatentable natural product through the drug approval process. Consequently natural supplements are not tested or approved by the FDA to be used for cancer or other health condition. As these natural supplements are not approved, doctors or most doctors, will not use them, and most probably do not even know about them.
 

If a doctor is not tied in and blinded by the medical/drug industry, finds a comprehensive approach to fighting cancer using powerful supplements that deal with the many different issues in cancers works much better than only using drugs and treatments that harm the body, they would turn to these other resources to find a safe cancer killer. One of the best cancer killer supplements proven, is zeolite.
 

Zeolite is a unique volcanic mineral that is highly effective at destroying cancer cells. In fact, results have been so impressive, anyone fighting cancer or wishing to prevent cancer should be using zeolite. It comes in two basic forms, a liquid zeolite, and a powdered micronized zeolite.
Zeolite work on a couple of the basic issues in cancer. It is a powerful detoxifier, and improves the alkalinity of your body. More importantly though, zeolite is a cancer killer as it can, when pulled into cancer cells, activate the P21 gene which tells a cancer cell to die, or literally destroy the nucleus of cancerous cells.
 

How zeolite works.

Zeolite fights cancer several other ways.
 

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Usually we treat that with nutritional support and traditional chelators. The introduction of liquid activated zeolite into my practice has radically transformed the outcome of many of these cases and also my whole level of enthusiasm and excitement in treating these children and being able to offer the parents a highly effective detoxifying agent that has such an incredible safety profile.

It has truly surpassed all my expectations. It is just a magnificent tool in this particular setting and in many other settings.

This is not about treating a particular condition.

In fact I think it’s very wrong to think of liquid zeolite as being applied to any particular disease. It is a spectacularly effective detoxification agent and has usefulness in virtually every chronic disease .

I believe toxicity plays a part in the pathology of practically every chronic disease and to that extent, liquid zeolite can be a marvelous tool in helping people recover. In conditions where toxicity is primarily the concerns like developmental issues, it is spectacularly effective .

There was a follow up that I saw this morning, a four year old boy who I began working with at the beginning of February, and at that time he was still in diapers, was totally non-communicative, was grinding his teeth and temper-tantruming on an extremely regular basis.

I started him on some nutrients and liquid zeolite and within three days of starting the liquid zeolite, he was potty trained. Which completely blew his parents away, and me as well.

Over the next six weeks his speech literally exploded, his spontaneous emotional expression exploded, he came into my office today asking a whole raft of different questions, including “why’s”. He wanted to know “why this, why that” all of which indicates normal cognitive function was really starting up in him.

His temperament was vastly improved, his teeth grinding had completely resolved. His appetite and digestion had improved, it was just a truly spectacular response. Not every child responds in that spectacular a way, but certainly there’s an across-the-board response to this product in that group of children that I haven’t ever seen with any other single product.

I have another lady that I followed up with this week who was diagnosed six weeks ago with metastatic pancreatic carcinoma and it was involved in her spine, in her lymph nodes and her liver.

When she came in six weeks ago she was feeling very run down, and had a tremendous amount of back pain which is a characteristic and ominous sign of pancreatic cancer .

One month later she walked into my office full of energy. Her complexion looked great, her energy and mood was great and she had no back pain. Now, her story is certainly not over, but nonetheless there’s pretty convincing clinical evidence that her condition has improved tremendously and the only thing that she has been doing in that month is taking liquid zeolite.

So there’s two follow-ups I had this week that were both pretty impressive and powerful testimonies to the incredible ability this product has to pull toxins out of the body , and allow the natural healing mechanisms to operate fully and freely and the results speak for themselves .

With typical chelators, you simply do not see the quality of the response that I’ve been seeing with liquid zeolite. These kids seem to respond much more quickly and much more fully than with traditional chelating agents. It’s really a pleasure to use and it’s almost a delight to have a new child come in because I know that I have something that’s truly going to help this child in all likelihood. Previously there were things I could do and things that would help the children, but nothing to this extent. I would say that it is the most powerful tool that I have in my clinical arsenal to help this group of children.

At this point, I cannot think of a single child (out of 40) that I have used the liquid zeolite with, who has not responded to some degree.

This latest generation of children is probably the sickest generation of children in American history . The number of allergies, the incidence of asthma, diabetes, juvenile rheumatoid arthritis, developmental issues and chronic conditions of every sort has literally mushroomed in this last generation. When you see this type of global, multi-faceted deterioration in the level of health in an entire generation – 30% of these children are on some kind of chronic medication – that is clearly an indication of tremendous environmental toxicity that’s impacted these children tremendously.

Liquid Zeolite is probably the single most effective agent that can favorably influence every single one of these conditions . This product is probably the single most valuable tool that a physician or a parent can use to help recover the health of their children .

I understand that that’s a very big statement to say, and I’m certainly not saying it glibly.

I truly believe that this product is a godsend and something that is vitally necessary for us to start recovering our health.

Systemic toxicity is probably responsible for 90% or more of all of the illnesses that doctors see in their offices every single day. There’s not a person on this planet who does not have some kind of ailment that is the result of some kind of toxicity.

Every single human being on this planet would benefit from taking liquid zeolite. I have not the slightest doubt about that and every condition that you could possibly mention in my opinion would benefit to some degree from reducing the toxic burden."

Dr. Prociuk, M.D.
 

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Zeolite Liquid Patent

Epithelial cell cancer drug

A method of treating epithelial cell cancer comprising administering to a mammalian patient diagnosed as having an epithelial cell cancer a therapeutically effective amount of 4,5 di-cyclo, disilico, dimagnesium, dialumino, oxyo, trihydrate, or its acetate, sulfate, hydrochlorate, or brominate salts. The composition is synthesized from a naturally occurring non-toxic zeolites, and has a 100% kill rate within 72 hours against buccal mucosa and ling squamous epithelial cell cancers. It is not cytoxic to healthy human cells.

Primary Examiner: O’Sullivan; Peter
Attorney, Agent or Firm: Moxon, II; George W. McDowell; Brouse
 

What I claim is:

1. 4,6 cyclo, trisilico, trimagnesium, trialumino, oxyo, trihydrate acetate.

2. 4,6 cyclo, trisilico, trimagnesium, trialumino, oxyo, trihydrate sulfate.

3. 4,6 cyclo, trisilico, trimagnesium, trialumino, oxyo, trihydrate hydrochlorate.

4. 4,6 cyclo, trisilico, trimagnesium, trialumino, oxyo, trihydrate brominate.

5. A composition consisting essentially of 4,5 di-cyclo, disilico, dimagnesium, dialumino, oxyo, trihydrate acetate, sulfate, chlorate, or brominate.

6. A pharmaceutical composition comprising a drug selected from the group consisting essentially of 4,5 cyclo, trisilico, trimagnesium, trialumino, oxyo, trihydrate acetate, 4,6 cyclo, trisilico, trimagnesium, trialumino, oxyo, trihydrate sulfate, 4,6 cyclo, trisilico, trimagnesium, trialumino, oxyo, trihydrate chlorate, and 4,6 cyclo, trisilico, trimagnesium, trialumino, oxyo, trihydrate brominate, and a pharmaceutically acceptable carrier.

7. The composition of claim 6 wherein said drug is present in an amount of between about 0.001 and about 1000 milligrams.

8. The composition of claim 6 wherein said drug is present in an amount of between about 20 and about 300 milligrams.

9. A cancer drug comprising the reaction product of a sodium magnesium aluminosilicate and an acid selected from the group consisting of glacial acetic, hydrochloric, sulfuric, hydro-bromic, and gluconic.

10. The composition of claim 9 wherein the reaction is conducted in the presence of a poloxy compound.

11. The composition of claim 10 wherein the poloxy compound is selected from the group consisting essentially of iron oxide, calcium oxide, and sodium oxide.

12. The composition of claim 9 wherein the reaction is conducted at a temperature of between about 200 and 250.degree. F.

13. The composition of claim 9 wherein the silicate is present in an amount of 20 to 40% by weight of the mixture and the acid is present in an amount of about 80 to about 60% by weight of the mixture of the silicate and the acid.

14. The composition of claim 10 wherein the poloxy compound is present in an amount of between about 0.0001 and 0.005% by weight.

15. A method of treating epithelial cell cancer comprising administering to a mamalian patient diagnosed as having an epithelial cell cancer a therapeutically effective amount of a drug selected from the group consisting of 4,5 di-cyclo, disilico, dimagnesium, dialumino, oxyo, trihydrate acetate, sulfate, chlorate, and brominate.

16. The method of claim 15 wherein the drug is dosed is about 0.001 to about 1000 milligrams.

17. The method of claim 15 wherein the drug is dosed is about 20 to about 300 milligrams.

18. The method of claim 15 wherein said compound is administered to a human.

19. The method of claim 15 wherein said compound is in combination with a pharmaceutically acceptable dilutent or carrier.

BACKGROUND OF THE INVENTION

The present invention is directed to a new and unique anticancer drug, which is identified generically as 4,5 di-cyclo, disilico, dimagnesium, dialumino, oxyo, trihydrate (3Mg++.3Al.sub.2 O.sub.3.3SiO.sub.2.3H.sub.2 O), which is a magnesium aluminosilicate (referred to hereinafter as "MAS"), and which are in the acetate, sulfate, chloride, or brominate form. These compositions come from a class of inorganic aluminosilicate chemicals known as zeolites. The compounds of the present invention are particularly useful in treating epithelial cell cancers in mammals.

The involvement of cancerous epithelial cells, which lead to the formation of solid tumors in humans, in such organs as the lungs, breast, skin, mouth, and colon are known as carcinomas. Most of the epithelial cell cancers are treated using chemotherapeutic agents and these tend to be toxic, and have immunosuppressive side effects. When treated this way, the cancer patient must then wait up to 3 weeks for his next treatment, until his immune system has restored itself.

Cancers involving human epithelial cells come from solid tumors of the breast, lung, stomach, liver, uterus, colon, skin, mouth and uterine cervix can form. Adenocarcinomas from secretory tissue and squamous carcinomas from protective linings are the two basic categories of carcinomas. Epithelial cell based cancers proliferate rapidly respecting no cellular boundaries. To fully understand how to treat epithelial cell based cancer, one must start at the cellular level, this involving use of cell culturing techniques. Present day drugs used for chemotherapy do not directly attack the cancer cell with any great accuracy. Drugs such as Methotrexate and Vincristine are toxic to normal healthy cells and diminish immune system functions. These usually offer the cancer patient extremely disquieting side effects such as diarrhea, hair loss, vomiting and weakness. The toxicity of these drugs often shorten their use or require a very intermittent use. The average chemotherapy cannot be used more than once a month.

A large effort has been put forth by the medical research community to find new drugs for the treatment of epithelial cell based cancers. Carcinoma of the lung, breast, prostate, and colon all together account for more than half of the deaths from cancer in North America. Anticancer drugs have for the most part been categorized into alkylating agents such as cytoxan, antitumor antibiotics such as dactinomycin and antimetablite drugs such as methotrexate. Most, if not all, of these chemotherapies have major side effects and are toxic.

It is well known that chemicals cause 95% of all cancers contracted by humans. Some of the most potent carcinogens are aldehydes, ketones, pyrenes, benzpyrenes, benzene, and nitrosamines. Nitrosamines were looked at early on because they are carcinogenic agents found in cigarette smoke and in the causative agents of rubber polymers.

Zeolites are natural hydrated silicates of aluminum and, usually, either sodium or calcium or both. Zeolites such as sodium aluminosilicate have a unique multi-dimensional structure of cavities into which small to medium size molecules and cells can be trapped. They exist in natural and artificial forms and are used extensively for water softening, as detergent builders, and cracking catalysts. Natural zeolites include analcite, chabuzite, heulandite, natrolite, stilbite, and thomosonite.

Zeolites have been used in animal feed. For example, as reported in "World Food & Drink Report", Apr. 19, 1990, hydrated sodium calcium aluminosilicate, an anti-caking agent used in animal feed, may reduce levels of aflatoxin in the milk of animals eating contaminated grain. Further, German patent DE19755921 teaches the use of zeolites or klinopitolites, that are used as food additives for human consumption as an aid to health, after they are treated with tribomechanical action to increase their surface area and destabilize their structure to release their chemical potential. These materials are thought to be a useful defense against cancers such as lung cancer, cancer of the colon, and skin cancer, and they are recommended for improving blood circulation.

SUMMARY OF THE INVENTION

The present invention has resulted from the discovery that epithelial cell cancer can be treated by administering to a mammalian patient having an epithelial cell cancer a therapeutically effective amount of 4,5 di-cyclo, disilico, dimagnesium, dialumino, oxyo, trihydrate acetate, sulfate, hydrochlorate, or bromate. The composition of the present invention is synthesized from a naturally occurring non-toxic zeolites, and has a 100% kill rate within 72 hours against buccal mucosa and ling squamous epithelial cell cancers. It is not cytoxic to healthy human cells.

BRIEF DESCRIPTION OF THE DRAWINGS

The file of this patent contains at least one drawing executed in color. Copies of this patent with color drawing(s) will be provided by the Patent and Trademark Office upon request and payment of the necessary fee.

FIG. 1 is a photomicrograph of stained cells showing vacuoles containing the composition of the present invention prior to being brought into the cancer cells.

FIG. 2 is a photomicrograph showing the transition of vacuoles containing the new drug composition into the cancer cells.

FIGS. 3-6 are photomicrographs showing the transition of the new drug composition into the cancer cells.

FIG. 7 is a photomicrograph showing the destruction of the cancer cells.

FIGS. 8 and 9 show illustrations of non-cancerous crown gall pin oak leaf cells.

FIGS. 10 and 11 are illustrations showing cancerous gall pin oak leaf cells.

FIG. 12 is an illustration of crown gall pin oak leaf cells after treatment.

FIGS. 13-17 are photomicrographs of stained cells showing the progressive killing of the epithelial cancer by the drug composition of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

The composition of the present invention is 4,5 di-cyclo, disilico, dimagnesium, dialumino, oxyo, trihydrate ("MAS") salt synthesized from zeolites. It is used in its acetate, sulfate, hydrochlorate, or bromate salt forms. Zeolites are generally recognized as safe for humans. When these zeolites are converted and reacted with acetates, chlorides, sulfates, bromides, or gluconates the resultant product is a 4, 5, and 6-sided network of cavities holding anions and cations. The composition of the present invention has a molecular weight (weight average) of 1500 putting it into the polymer family.

The starting zeolite is sodium magnesium aluminosilicate. Preferably Hydrex R which is available from J. M. Huber Corporation. Alternatively it could be a zeolite such as Thomsonite, where magnesium is substituted for the calcium. It is processed by reacting the zeolite starting material with an acid, such as a 5 molar glacial acetic, hydrochloric, sulfuric, hydro-bromic or gluconic acid, preferably at 1 milliliter per 250 milliliters of hypotonic saline solution, in the presence of a poloxy compound, such as iron oxide Fe.sub.2 O.sub.3 being preferred), calcium oxide, or sodium oxide, with iron oxide being preferred, at an amount of between about 0.0001 and 0.005% by weight with 0.003% by weight being preferred. The ratio of the mixture of the zeolite and the acid will preferably be about 30% by weight of a zeolite with 70% by weight of the acid, at 5% concentration, although it could be in a range of about 20 to 40% by weight of zeolite and 80 to 60% of acid. The reaction takes about two hours at a temperature of about 200 to 250.degree. F.

Synthesis of the MAS

The synthesis of the new drug was carried out in a 500-milliliter three neck reaction flask, fitted with a stirrer, thermometer and cold water condenser apparatus. The zeolite starting material was Hydrex R, a sodium magnesium alumino silicate in an amount of 150 grams, available from the J. M. Huber Corporation. The amount of a 5 molar acid was 350 grams, and the iron oxide compound was 1.5 grams. The starting ingredients were combined and were reacted at 250 C for 2 hours followed by cooling. The acid was sulfuric acid at 1 milliliter per 250 milliliters of hypotonic saline solution. The final product was then diluted by adding twice as much sterile water and filtered via sterile millipore filtration apparatus. Quality control, and characterization of the compound was done using derivatization techniques, ASTM 3526, paper chromatographic analysis, molecular weight studies, and various wet bench analytical techniques. The average concentration of the drug of the present invention was 98 MG per milliliter of water.

In order to see if the composition of the present invention had any biological activity or "kill power" against the harshest microorganisms known, including streptococcus, staphylococcus, bacillus, fungus, and mildews, the microorganisms were cultured in RPMI 1640 cell culture media and in a starch-based, solid matrix culture media. All of these microorganisms were destroyed and also prevented from growing when first initiated with the patent substance. Thus the new composition of the present invention has been found to be bacteriostatic and bacteriocidal, fungistatic, and fungicidal, and a mildewicide.

The composition has a structure as follows: ##STR1##

wherein M.sub.1 is silicon, M.sub.2 is magnesium, and M.sub.3 is aluminum.

The drug must be administered directly into the cancer tumor by injection or a 24-hour intravenous slow drip. The patent substance must be in close proximity to or infused into the cancer cells and/or in the blood stream supplying the tumor. The precise amount dosed will vary and does not appear to be critical as long as it is pharmaceutically effective. Usually, this will be in the range of from about 0.001 to 1000 milligrams, with between about 20 and 300 being preferred.

The method of the invention can be practiced on any mammal having a susceptible cancer, i.e., a malignant cell population or tumor. Compounds of the invention are effective on human tumors in vivo as well as on human cell lines in vitro. The present compounds may be particularly useful for the treatment of solid tumors for which relatively few treatments are available. Such tumors include epidermoid and myeloid tumors, acute or chronic. Such tumors also include, nonsmall cell, squamous, liver, cervical, renal, adrenal, stomach, esophageal, oral and mucosal tumors, as well as lung, ovarian, breast and colon carcinoma, and melanomas (including amelanotic subtypes). The present compounds can also be used against endometrial tumors, bladder cancer, pancreatic cancer, lymphoma, Hodgkin’s disease, prostate cancer, sarcomas and testicular cancer as well as against tumors of the central nervous system, such as brain tumors, neuroblastomas and hematopoietic cell cancers such as B-cell leukemia/lymphomas, myelomas, T-cell leukemia/lymphomas, small cell leukemia/lymphomas, as well as null cell, sezary, monocytic, myelomonocytic and Hairy cell leukemia. These leukemia/lymphomas can be either acute or chronic.

While not wishing to be bound by a particular theory, the composition of the present invention can react, or chelate into a complex, with carcinogenic agents. The basic chelation, or complexing ability of the Mg.sup.++, (magnesium ions), O, (oxygen atoms) and aluminum ions which are inside the six (6) sided cavity of the zeolite composition of the present invention. This complexation now ties up the nitrogen to nitrogen to oxygen portion of the nitrosamine (–N–N–O) and prevents it from being metabolically activated by human liver enzymes inside cells to become the nitrous free radicals which then enter the healthy human cells nucleus, damaging the DNA of the chromosome and producing a rogue cell or cancer cell. The complexing of these carcinogenic nitrosamines was proven by using ASTM 3526 pager chromatography.

The compounds of the present invention target the cancerous epithelial cells, only, due to the different surface chemistry of the cancer cell itself Photomicrographs FIGS. 1 and 2, under X1000 oil immersion, show the formation of vacuoles containing MAS, which are prior to being brought into the cancer cell by endocytosis. Once inside, lysosomes attach and chemical breakdown of the MAS. The trimetallic portion of the MAS molecule crosses the nucleus of the cancer cell intercalates with the cell mutated DNA and destroys the cancer cell from within.

The formulations disclosed within the terms of the present invention may also comprise any additives, carriers, or fillers commonly in usage with drugs to facilitate their delivery.

The following examples are illustrative of the present invention, and should not limit the scope of the invention.

EXAMPLE 1

The following experiment was for the purpose of demonstrating the functionality of the compounds of the present invention with respect to carcinogenic compounds.

Ten (10) grams of a cured natural rubber compound were cut up to act as a control. This natural rubber compound contained 2 rubber additives which are known to generate nitrosamines; N-t-Butyl-2-benzothiazyl sulfonamide and zinc dimethyldithiocarbonate. Another 10 grams of this natural rubber compound, the same compound, contained 0.25 parts per hundred of the composition of the present invention. Both of the samples were extracted with warm acetone for 20 minutes, then cooled and the acetone carefully evaporated off. The remaining solids were dissolved in 0.5 ml of acetone and spotted in a paper chromatogram according to ASTM 3526. A 95% acetone, 5% ethyl acetate solvent system was employed. As can be seen in Table 1, the control generated nitrosamine at Rf (retention time) of 0.037. The composition of the present invention, at 0.25 pHR gave no nitrosamine fraction at 0.037, but the large, (high molecular weight) complex was at the origin or Rf=0, retention time 0. The nitrosamine was complexed by the patent substance and thus was made non-mutagenic, and non-carcinogenic.

TABLE 1 Sample Rf Fraction Cured Natural Rubber Compound 0.037 Nitrosamine " .0448 Trace Santocure NS " 0.761 Trace Methasan " 0.970 Process Oil " Cured Natural Rubber Compound 0 Nitrosamine plus 0.25 phr of MAS Cured Natural Rubber Compound 0.492 Trace Santocure NS plus 0.25 phr of MAS Cured Natural Rubber Compound 0.716 Trace Methasan plus 0.25 phr of MAS Cured Natural Rubber Compound 0.940 Process Oil plus 0.25 phr of MAS

EXAMPLE 2

Over a three (3) year period of study, oral cavity epithelial cells were obtained from buccal mucosa harvests from a single source. The cells were immediately placed in RPMI 1640 medium, which is a standard medium developed at the Roswell Park Memorial Institute. The medium was supplemented with L-glutamine, penicillin and streptomycin in all cultures, and then incubated at 98.6 F. The study cultures were supplemented with a carcinogen and strong promoter, sodium or magnesium saccharin. The sodium form being preferred. The cultures were incubated for 120 hours with one medium change for the extended time cultures. The sterile solutions of sodium or magnesium saccharin were made to a strength of 250 milligrams per milliliter of hypotonic saline solution, the combination penicillin-streptomycin antibiotic system were used at 100 units per milliliter of hypotonic saline solution.

The carcinogen-promoter supplemented cell cultures, also incubated at 98.6 C, once producing cancerous epithelial cells were given 300 microliter additions of the 4,5 sided ring MAS sulfate having concentrations of 60 milligrams per milliliter of hypotonic saline solution. Slides were prepared at room temperature using giemsa stain and observed and analyzed using bright field microscopy up to X1000 magnification with photomicrographs taken by the Polaroid Microcam System.

Phase contract microscopy at X100, and X200 power was also used, with photographs taken by the Polaroid Microcam System. All solutions used were sterilized via filtration. All cell counts were done on grided 2 chamber, cell culture slide chambers.

The epithelial cells used were obtained from sterile "Buccal Smears" of human cheek cells and were placed in sterile RPMI 1640 cell cultures with and without the composition of the present invention. The concentration of sodium saccharin used to promote the epithelial cell human cancer was 300 microliters of a 5 gram per milliliter working solution. All in-vitro, cell cultures were analyzed over a 3 day period (72 hours). Cancerous-like changes were seen in these cell cultures within 8-16 hours, and all the cancer cells were killed before 72 hours had lapsed.

A microscopic view shows normal check cell morphology, nuclear size, cell wall and membrane capacity and growth clustering; no ghosting or other abnormal changes were seen. The results are dramatic cell changes due to the sodium saccharin introduction to the cell culture. Observation of these cell cultures at X400, and X100 showed very enlarged cell morphology, formation of enlarged, crescent shaped nuclei, cell wall membrane swelling, multi-nucleated cell areas, formation of elongated or hook type epithelial cells in large sheaths were observed, plus the very telling formation of abnormal protein growth "Blebs" seen on the outer cell wall of these cells. These are illustrated in photomicrographs, FIGS. 3 through 6.

When the composition of the present invention is used as a non-toxic, anti-cancer agent in the cancerous epithelial cell cultures, at both 300 and 400 microliter dosages in these cell cultures, 100% epithelial cells induced to cancerous state were destroyed within 24 hours. This is shown in photomicrograph FIG. 7 by the "ghosting" or destruction of these cancer cells by the destruction of the cancer cell nucleus and cytoplasmic organelles. In some cases the cancer cells were destroyed in an outward burst of the cytoplasm by increased osmotic pressure. The composition of the present invention is totally amenable to the different receptor sites, cell wall membrane proteins, and surface chemistry of the cancer cell only. It does not effect ordinary, healthy cells as already shown and claimed above.

EXAMPLE 3

In this example, the plant cancer of study was the Pin Oak Tree Leaf Crown Gall plant cancer. The agrobacterium Tuma Faciens and its metabolites cause this well studied plant cancer. Normal leaf plant cells, and crown gall cancer cells were cultured in RPMI 1640 cell culture media, containing an antibiotic, and concentrations of the patent substance in its sulfate form. The average dosage of the patent substance was 300 microliters of a 98 milligram per milliliter concentration. Within 24-48 hours all cancer cells in the crown gall cell culture were dead as analyzed by Giensa stained microscope slides at X400, and X1000, power. The control cell culture of healthy pin oak leave section showed no cytotoxicity at all. The crown gall cells (cancer cells) were "ghosted" by the composition of the present invention.

The composition of the present invention crossed the cancer cell membrane, due to its different receptor site configuration and surface chemistry, destroyed the elongated nucleus and the cytoplasm bulged to one side of the cancer cell and the entire cellular contents dissipated into the surrounding environment. The membrane of most cells remained intact, but no cellular structures were left. Some cells were totally destroyed by cell wall and membrane collapse.

The healthy pin and cell cultures showed no ghosting, no elongated nuclear structure, or cell wall and membrane swelling. No extracellular growth or "Bleb" protein on the healthy cell wall, and membrane outer surface was noted. Usual cell counts were in the 300-500 cell range. FIGS. 8 and 9 show normal, non-cancerous (crown gall, non-cancerous) pin oak leaf cells. In FIG. 8, leaf section 1 is depicted with stoma 2. FIG. 9 shows normal non-cancerous crown gall pin oak leaf cells. FIGS. 10 and 11 show the pin oak crown gall cells, which are cancerous. FIG. 10 shows a cancerous cell in which has gel like, "eye" cells, 3, "hook" cells, 4, which are elongated, "nucleii" gels, and "ghosted" filiments, 5. FIG. 11 shows the enlarged cell membrane 6 as well as the filaments 5. FIG. 12 depicts crown gall pin oak leaf cells after treatment with 400 microliters of the composition of the present invention at 98 MG per milliliter. The xylem cells, 7, had some brownish color but no cellular damage. The lower cells were green, 8, below the boundary layer 9.

All cell culture preparations were done in sterile petri dishes with 25 milliters of RPMI 1640 cell culture media, and 100 microliters of antibiotic, cell counts ranged in member from 300-500, GIEMSA stained microscopic slides were prepared and observed at X400, and X1000. The concentration of composition of the present invention used was 300 and 400 microliters of a 98 MG per milliliter preparation.

EXAMPLE 4

Squamous cell human lung cancer cell cultures, which are commercially available as the A549 cell line from Bio-Whitaker Company, were cultured in RPMI 1640 Medium supplemented with L-glutamine, penicillin, and streptomycin. This culture was also incubated at 98.6.degree. F., with cell culture times up to 96 hours, with at least one medium change. These cultures were also supplemented with doses of the drug of the present invention at 300 microliters of a concentration of 60 milligrams per milliliter of hypotonic saline solution. Fresh venous blood samples of 2 ml each were taken and placed in heparinized sterile test tubes for % hemolysis studies.

It has been shown that sodium saccharine or its magnesium counter is a weak carcinogen, but a strong promoter which increases the proliferation of epithelial cancer cells during cell cycling, over a three year period cell cultures of RPMI 1640 cells culture medium supplemented with L-glutamine and 100-200 microliters of penicillin and streptomycin each at 100 units per milliliter hypotonic saline solution, and dosed with 200-400 microliters of a concentrated solution of sodium saccharine (250 milligrams per milliliter of hyptotonic saline solution), incubated at 98.6.degree. F., produced cancerous cells within 24-48 hours. Using phase contrast microscopy at X100, and X200 magnification and employing temporary slides for examination at X100,X400, and X1000 oil immersion magnification transitions from normal epithelial cells to well formed cancer cells could be cultured. In photomicrograph FIGS. 1, 7 and 13-14, giemsa stained cells and photographed at X1000 oil immersion magnification (using Polaroid microcam) we can easily see the transition of the healthy epithelial cells in photomicrograph FIGS. 1-3 to the transition of pre-cancerous cells of photomicrographs FIGS. 4-6 where we observe a darkening of the cell cytoplasm, development of multinucleation, and a consistent swelling noted in the plasma membranes and large changes in cell morphology. Strikingly in photomicrographs FIGS. 7 and 13 we see the formation of oral cavity epithelial cells which have become cancerous in nature. We observe the proliferation of distorted cellular morphology to swollen, misshapen elongated, hook like cells, with thick fibrous cytoplasm and the growth of fibrous, abnormal proteins on the cells outer wall (`BLEBS`), multinucleation and nuclei that seem to elongate and become abnormal in shape, similar to the morphology changes of the cancer cell itself, are seen along a medial axis. A typical cell count of these cell cultures shows that the number of epithelial cells declines at the same rate as does the growth of the cancer cells, which result is shown by the data in Table 2. Normal control cultures lacking, the supplement of sodium saccharine, also incubated at 98.6.degree. F. gave normal, healthy cell cultures of oral cavity epithelial cells. See photomicrograph FIGS. 1-3.

TABLE 2 Typical Cell Count Statistics After Introduction of Sodium Saccharine Time # of Normal # of Transition # of Cancer Hours Epithelial Cells Cells Cells T = 0 462 0 0 T = 24 200 60 260 T = 48 5 10 500

Over a three year period the cell cultures produced were treated with MAS Sulfate within 24-48 hours of the formation of epithelial cancer cells. Dosages of 100-400 microliters of MAS Sulfate at 60 milligrams per milliliter of drug were, and within 72 hours of addition, 100% of all epithelial cancer cells were destroyed, showing cell casts and/or entirely "ghosted" cells. In Table 3 we can see cell counts on a typical cell culture where MAS Sulfate was added. The photomicrographs were taken from giemsa stained slides at X100magnification, using oil immersion. Photomicrograph FIGS. 7 and 14-16 show the progressive killing of the epithelial cancer by MAS Sulfate. It will also be shown MAS Sulfate non-cytoxic to date.

TABLE 3 Data Obtained from a Hemolytic Titer of MAS Sulfate on Human Red Blood Cells Dilution of MAS Sulfate in % Hemolysis of Human 1000 Microliters Hypotonic Saline Red Cells 7.40 Microliters 0 8.00 Microliters 0 10.00 Microliters 0 50.00 Microliters 0 100.00 Microliters 0 200.00 Microliters 0 500.00 Microliters 0 700.00 Microliters 0 1000.00 Microliters 1.99 2000.00 Microliters 2.35

MAS Sulfate is not cytotoxic to these cells and preferentially target epithelial cancer cells only. A hemolytic titer study was done on the new drug to show non-cytotoxicity. Typical data obtained using human red cells shows the lack of cytotoxicity to cells. The concentration of MAS Sulfate used was 60 milligrams per milliliter of hypotonic saline solution. No hemolysis appears until 1 full milliliter of MAS Sulfate and then only 2.00% hemolysis. The next data point shows that at a concentration of 2.00 milliliters of MAS Sulfate only 2.50% hemolysis of red blood cells occurs. A concentration of 0.35 microliters of human red blood cells was used for each sample titer. Table 2 shows the titer data in graphic form exhibiting a flat line effect until the 1.00 milliliter sample of MAS Sulfate.

A close look at the cell count in Table 3 clearly shows the rapidity of MAS to selectively cross the epithelial cell (cancerous) plasma membrane, in cell culture experiments and provide 100% kill rates within relatively short time period (48 to 72 hours), in this case 1,090 cells counted at 48 hours after addition of a total of 300 microliters of MAS Sulfate at a concentration of 60 milligrams per milliliter hypotonic saline solution. Also MAS Sulfate shows a strong inhibitory action in reducing cell culture proliferation of the cancer cells to 0.82%. MAS Sulfate and its family of conjugate drugs are totally water-soluble such that by % hemolysis studies concentrations up to 120 milligrams, where red blood cell hemolysis is barely perceptible, can be tolerated.

By repeating these same experiments with a cell line of squamous cell lung cancers (BIO-WHITTAKER A549), similar results are achieved as seen in Table 4.

TABLE 4 Quantitative Cell Culture of Human Buccal Mucosa Epithelial Cells Time Time # % (AGG) of Vol. Vol. # Transi- # # Dead Increase of DME Sodium DME Total Normal tion Cancer Cancer # Cell Cell Culture Add Saccharin ML Cells Cells Cells Cells cells Growth Growth 0 — 200 ML — 463 463 0 0 0 0 0 24 — – — 661 561 68 32 0 198 42.76 48 — 100 ML — 749 230 200 319 0 88 13.31 72 — – — 805 60 45 700 0 56 7.48 96 — – — 873 3 10 860 0 68 8.45 120 0 — 100 1020 0 0 1020 0 147 16.84 144 24 — 200 1081 0 0 250 831 61 5.98 168 48 — – 1090 0 0 0 1090 9 0.82

It has been seen that pre-cancerous and cancerous cells have extremely different cellular characteristics and surface cell chemistry than normal cells. Predominantly amongst these characteristics are the gross morphological changes of the cancerous epithelial, lack of yet totally unknown plasma membrane protein growths familiarly known as `BLEBS,` changes in numbers of and mutations in receptor sites such as the EFG, and VEG F receptor sites controlling cell cycle functions. Proteolytic enzymes and increased lysosomal activity are also important changes in the cytoplasm of these cells. It has been seen during our research studies that the MAS molecule itself is transported, selectively across the cancerous epithelial cell membrane and once in the environs, crosses the nuclear membrane and deactivates cancer cell replication by action on the mutated DNA. Then, with the collapse of the nucleus osmotic pressure within the cancer cell ruptures the plasma membrane outwardly. Photomicrograph FIGS. 1-7 and 13-16 show these cancer cell "casts" and "ghosted" cytoplasms of our treated epithelial cancer cells within the time of 48 to 72 hours as seen in Table 4. Referring to Table 4, the number of cancer cells here represent cells in G2 or late S phase at the time of introduction of the sodium saccharin, (all additions of sodium saccharin and MAS Sulfate were added after cell counts were taken). They were affected by the sodium saccharin to cause cancer as early as 24 hours after inoculation. The transition cell’s morphology may represent affects of the sodium saccharin to cells in the early S phase of the cell cycle from the time of inoculation to the time of cell count at 24 hours. As seen in this data the number of normal cells seen after 24 hours of exposure to sodium saccharin represents cells safely in G2 phase of the cell cycle prior to the addition of the sodium saccharin. Referring to Table 4, normal cells seen after 48 hours in cell culture may represent cells that have survived in the culture unaffected by the sodium saccharin treatment the difference of the cell count 561-230 could possibly be cells experiencing normal cell death. In referring to Table 4, our cell cycle model, the transition cells increased in numbers after 48 hours, due to cells that were in the G1 cycle at the time of addition of the second dosage of sodium saccharin and only partially affected by the first dosage. As seen in Table 4, cancer cell counts reflect the total affect of the cells being exposed to the X2 dose of the sodium saccharin. The cells have transformed into transition (pre-cancer cells) and cancer cells within 24 to 48 hours after inoculation. The first sign of cancer cells after 24 hours is probably representative of cells in synthetic period of the cell cycle at the time of addition of the sodium saccharin. The rapid progression of cells to the transition state and consequently to the cancer cell state shows an aggressive division process that took place in the first 3-4 days in the cell culture. By the addition of the MAS Sulfate to the culture, there is a rapid demise of the cancer cell population after 24 hours and total cell death after 48 hours. The MAS Sulfate molecule, represented in Formula I selectively enters the cancer cell’s plasma membrane.

It is the belief that this new pharmacological approach of selectively targeting cancer cells is a significant step in providing a new therapy, which is also non-cytoxic, for the treatment of carcinomas. The use of this drug will shorten the gap betweeen the number of patients getting cancer and a chemotherapeutic approach to saving lives. The ramifications of a substance which will target epithelial cancer cells selectively without harming normal tissue is overwhelming with regards to cancer treatment. Of ever greater significance, may be its ability to destroy transitional cells serving as a preventive agent in numerous clinical opportunities.

The drug of the present invention, in cell culture, effectively kills epithelial cell based cancers, at 100% "kill power" from the work presented. A patient could receive the new anticancer drug more than once every three weeks, perhaps several times a week.

The formation of cell wall membrane irregular proteins (Blebs) in these, nuclei as large as the cytoplasm, very differential cell morphology, some in shapes of hooks, others in large sheaths, and, formation of cell membrane swelling. It was also observed that the widespread deformation of these cancer cell nuclei are enlarged, crescent shaped, peanut shaped, and appear to be multi-nucleated in this study. The drug of the present invention was added to the known human cancer cell cultures and within 24-48 hours as 100% lower cancer cell kill was established. The cancer cells have been "ghosted", their nuclei and organelles destroyed from within. This allows for stopping-cancer cell division, decreasing tumor size, stopping cancer metastasis, and not effecting healthy cells, like t-cells in the human immune system. The composition of the present invention can be used as a cancer chemotherapy systemically via IV or directly infused into the tumor and made available to the cancer patient several times weekly.

EXAMPLE 5

A study was conducted using standard immunodeficient (SCID) mice. Some of the mice were injected with the standard A549 squamous cancer cell line, with the C.B-17/IcrCrl-scidBR strain being selected, while some of the mice were injected with the A549 cell line and MAS sulfate drug prepared in accordance with the present invention. The mice were divided into three groups:

Group I: Two mice were a control and were not treated with either the A549 cell line nor the MAS sulfate drug.

Group II: Four mice were treated with the A549 cell line, but not the MAS sulfate drug.

Group III: Four mice were treated with the A549 cell line and the MAS sulfate drug.

The A549 cell line dose was at 2.5.times.10.sup.6 cells per milliliter. The MAS sulfate was dosed at 30 miligrams per injection, three times per week. The injections were in dorsal thorax area.

The animals were about six to seven weeks of age at the start of the test and their weight variation did not exceed .+-.20 percent of mean weight. The animals underwent a quarantine/acclimation period of five days prior to implantation with the A549 cells. The animals were handled in accordance with the "Guide for the Care and Use of Laboratory Animals", published by the Institute of Laboratory Animal Resources, Commission on Life Sciences, National Research Counsel, including environmental conditions, handling, storage and feeding.

The observations of the changes in the body weights are shown in Table 5, which shows expected weight gains.

TABLE 5 Body Weights in Grams Pretest Week 1 Week 2 Week 3 Week 4 Weight in Weight in Weight in Weight in Weight in Animals Grams Grams Grams Grams Grams Group I A 21.4 22.8 23.7 25.1 25.8 B 21.5 22.8 23.8 25.4 26.2 Mean Wt. 21.5 22.8 23.8 25.3 26.0 Group II A 20.0 21.6 21.6 22.6 22.8 B 19.9 20.5 20.9 22.3 23.5 C 20.9 22.5 22.7 24.3 25.0 D 22.3 23.8 24.6 26.0 26.8 Mean Wt. 20.8 22.1 22.5 23.8 24.5 Group III A 20.7 22.4 22.1 23.3 24.5 B 21.9 23.4 23.5 24.5 25.6 C 21.8 23.3 23.2 24.7 25.2 D 21.0 22.5 22.5 24.0 24.3 Mean Wt. 21.4 22.9 22.8 24.1 24.9

At the end of the observation period of the study, which was approximately five weeks, the mice were humanely terminated using a standard procedure of carbon dioxide asphyxiation and opening the thoracic cavity or exsanguination. Necropsies were performed and tissues, namely liver, kidney, spleen, lung, and any other abnormal appearing tissue, were examined via histopathology. The results are shown as follows in Tables 6 and 7.

TABLE 6 Tumor Mass Measurements Week 2 Week 3 Week 4 Week 5 Animal L .times. W .times. H Vol. L .times. W .times. H Vol. L .times. W .times. H Vol. L .times. W .times. H Vol. Group I A No Mass No Mass No Mass No Mass B No Mass No Mass No Mass No Mass Group II A 9 .times. 6 .times. 3 162 8 .times. 8 .times. 3 192 10 .times. 6 .times. 6 360 12 .times. 11 .times. 8 1056 B 9 .times. 7 .times. 3 189 10 .times. 5 .times. 3 150 14 .times. 8 .times. 4 448 15 .times. 10 .times. 9 1350 C 5 .times. 5 .times. 3 75 12 .times. 3 .times. 10 360 15 .times. 12 .times. 8 1440 20 .times. 14 .times. 5 1400 D 2 .times. 2 .times. 1 4 10 .times. 7 .times. 3 210 12 .times. 9 .times. 4 432 16 .times. 10 .times. 8 1280 Mean 107.5 228.0 670.0 1271.5 Std Dev 84.4 91.5 514.8 151.9 Group III A 1 .times. 3 .times. 2 6 10 .times. 7 .times. 3 210 13 .times. 7 .times. 4 364 18 .times. 9 .times. 6 972 B 1 .times. 3 .times. 2 6 10 .times. 4 .times. 3 120 14 .times. 7 .times. 4 392 17 .times. 8 .times. 6 816 C 5 .times. 3 .times. 2 30 10 .times. 7 .times. 3 210 11 .times. 8 .times. 5 440 13 .times. 10 .times. 6 780 D 3 .times. 4 .times. 2 24 10 .times. 5 .times. 3 150 11 .times. 6 .times. 4 264 14 .times. 9 .times. 5 630 Mean 16.5 172.5 365.0 799.5 Std Dev 12.4 45.0 74.3 140.4

TABLE 7 Histopathology Incidence Table Group I Group II Group III Animal Animal Animal A B A B C D A B C D HEART Epicardium, Mineralization 2 3 3 KIDNEY X X X X X X C Cortex, Tubules, Regeneration 1 1 1 LACRIMAL GLAND X LIVER X X X X X X X X Hematopoiesis 1 1 LUNG Alveolus, Hemorrhage 1 2 1 1 1 2 1 Alveolus, Histiocytosis 2 Peribronchial Lymphoid Depletion 5 5 5 5 5 5 5 5 5 5 LYMPH NODE, NOS N SKIN/SUBCUTIS Carcinoma, NOS P P P P P P P P Adnexal Atrophy 1 1 1 2 Dermis, Fibrosis 1 1 2 1 Dermis, Inflammation, Chronic 1 1 2 Active Epidermis, Erosion/Ulceration 1 1 3 1 2 1 Epidermis, Hyperplasia 2 2 2 2 2 2 1 Epidermis, Inflammation, 2 2 1 Suppurative SPLEEN Hematopoiesis 4 4 4 4 5 4 4 4 4 4 Lymphoid Depletion 5 5 4 4 5 4 5 5 5 5 TESTIS N X = Not Remarkable N = No Section P = Present Scale: 1 = Minimal 2 = Slight/Mild 3 = Moderate 4 = Moderately Severe 5 = Severe/High

As seen in Table 6, the tumor mass in the mice that were not treated with the drug of the present invention was significantly higher than those that were treated. Further, the results in Table 7 show that for the spleen, the liver and the kidneys, no significant change occurred from the use of the drug of the present invention. Further, since mice are immunodeficient, the results were consistent with not dosing the mice with the cancer or the drug of the present invention.

The foregoing embodiments of the present invention have been presented for the purposes of illustration and description. These descriptions and embodiments are not intended to be exhaustive or to limit the invention to the precise form disclosed, and obviously many modifications and variations are possible in light of the above disclosure. The embodiments were chosen and described in order to best explain the principle of the invention and its practical applications to thereby enable others skilled in the art to best utilize the invention in its various embodiments and with various modifications as are suited to the particular use contemplated. It is intended that the invention be defined by the following claims.

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Nations sweep this problem under the carpet because they are committed to the industrialisation which produces almost all these toxins. And it is an easy problem for most to try to psychologically deny because these toxins are invisible, and their effects in our bodies are accumulative over time. Medical researchers have only relatively recently started to study long-term low-dose exposure, and they are coming up with some very worrying data. Just because toxin levels in our bodies are not usually high enough to kill us outright or induce obvious organ damage, does not mean that the body can cope with them. In fact, recent research is finding that chronic low-level toxic exposure — the kind we are all exposed to everyday of our lives — damages the immune system and interferes with enzyme activity, our hormone balance, cell growth and brain function. And over time, these have very serious repercussions such as cancer (75% or more of which has been attributed to environmental toxins) , vascular diseases, liver poisoning, mental-health diseases such as Alzheimer’s disease and dementia, and general ill health and low vitality.

Is it any wonder that cancer, for example, has become endemic in our civilization, with one in two men and one in three women developing this dreaded disease at some point in their lives? And the escalating number of cancer cases shows no sign of abating, despite our government’s "war on cancer" which has focused on throwing even more toxins (chemotherapy) at the body in an effort to poison the cancer, cancer which was likely to have been caused by poisons in the first place!

While conventional medicine has generally ignored this issue and continues to largely back pharmaceutical drug-solutions to health problems — which unfortunately exposes our bodies to even more toxins and their potential side-effects — alternative and complementary practitioners and doctors have always known that detoxification has to form the backbone of any healthcare treatment program for chronic diseases because toxification is the number one disease trigger. In fact, nobody in today’s polluted world can experience optimum health without minimising exposure to harmful chemicals and undergoing regularly detoxification. The first can largely be achieved by eating organic and unprocessed food whenever possible, using natural toiletries and cosmetics, avoiding tap water, and only taking drug medicines that are essential. The second — detoxification — can be best achieved by drinking 8 to 10 glasses of pure water a day whilst using a new health product called "liquid zeolite".

* * *

Imagine countless trillions of minuscule molecular cages circulating around in your body with the ability to selectively capture molecular toxins such as heavy metals, radioactive ions, viral particles and other damaging molecules before safely carting them out of your system, so that your toxic load is substantially reduced. Imagine if these tiny cages could also, by trapping excess protons, help alkalise our bodies, raising immunity and disease-resistance in the process. Imagine what a breakthrough in natural healthcare and disease prevention this would be.

A vision of some futuristic nanotechnology in a science fiction novel? No. These tiny molecular cages are very real and are derived from a natural mineral source. And they are used everyday by tens of thousands of people around the world to reach unimagined levels of health and vitality, because they offer a way for us to detoxify safely, efficiently and rapidly. In fact, no other detoxifier can come close to the efficiency of this new product. Suspended in a clear and tasteless solution that is simply added to water, these tiny mineral cages are sold in small plastic bottles labelled "Liquid Zeolite".

* * *

Zeolites are naturally occurring crystalline aluminosilicate minerals that can be found in rock deposits throughout the world. They are formed by a process known as devitrification or crystallization of volcanic ash, a process that takes place over millions of years when lava remains in contact with fresh or salt water. The word ‘zeolite’ itself is an amalgam of the two Greek words for ‘boiling stones’ because of the steam that is given off when these rock crystals are heated, due to their high water content. Zeolites have a molecular stacked-cage or honeycomb structure formed of silicon and aluminium oxides. As a result of the electronic configurations of the aluminium, silicon and oxygen that make up these tiny zeolite cages, each has an overall negative charge which means that they attract positively charged particles, in much the same way that a magnet attracts iron filings.

Generally, the molecular-size zeolite cages or holes come ready-packed with positively charged metal ions such as calcium, sodium, magnesium, potassium and iron, which balance out their negative charge, making them more electronically stable. However, the door of the box or cage is always open, so if another charged metal ion, free radical, viral particle or excess proton comes along with a greater attraction or affinity to the zeolite box then it will exchange with the metal ion already in the box. It is this exchange property of zeolite which gives it its remarkable detoxification properties.

Records show that zeolites have been used for nearly a thousand years and probably more in traditional remedies throughout Asia, and a zeolite powder was given to those affected by nuclear fallout from Chernobyl to remove radioactivity from their bodies (20 tons of it was also dropped on the reactor itself to mop up the radioactivity). These minerals have also been used for decades in water and air purifiers (NASA uses them in its shuttle life-support system) and in animal feeds because they increase gut nutrient absorption, and have, in the last 15 years, undergone extensive pharmaceutical research on their health-giving properties for humans. As a result, highly purified forms are increasingly turning up as food additives and food supplements for human consumption.

* * *

Liquid zeolite is a brand new health supplement that uses a unique manufacturing process that not only removes all impurities from the starting zeolite mineral but "activates" the free-floating cages or boxes so that they are preloaded with magnesium, calcium, and phosphorous ions which not only exchange easily with heavy metals but are also healthy for the body. The supplement is so efficient that just 100 drops has the equivalent toxin absorption area of nearly 8m²! There is no other health supplement on the market that is as pure or as effective at detoxifying the body.

Oral liquid zeolite was the brainchild of Harvey Kaufman who spent fourteen years in its development and application. The manufacturing process uses the same top grade zeolite used by NASA as a starting material, sourced from mines in Montana and Texas known for their zeolite purity, before putting the rock through a liquidation, purification and activation process that involves heating it in an acid solution for a couple of hours at a temperature of 100C (212F). Kaufman’s invention was sold to biochemist Rik Deitsch who now licenses it to an MLM company selling selling it as a branded liquid health supplement. (No doubt, more brands of liquid zeolites will be developed in the near future as this supplement is so remarkably beneficial.)

There are 14 key reasons why liquid zeolite is such a unique and extraordinary food supplement:

1) Extremely safe and non-toxic: Liquid zeolite is completely non-toxic and is safely and completely eliminated after 5 to 7 hours. It can be used long-term, and even children, babies and pregnant women have safely supplemented with it. And toxins that it captures in its cage are effectively deactivated so that there are no side-effects from those toxins as they are eliminated from the body — except possibly slight dehydration which is why it is important to drink plenty of water (8 to 10 glasses a day) when taking zeolite. And because most pharmaceuticals are negatively charged chemicals, liquid zeolite tends to leave these alone (although always check with your doctor though if you are on medication).

2) Removes heavy metals: Liquid zeolite has the perfect molecular structure for latching on to and then removing heavy metals (including radioactive ones) from the body, including mercury, cadmium, lead, arsenic, aluminium, strontium and excess iron. Some heavy metals, such as mercury, have a huge affinity to the zeolite, which is why they are dragged out of the body first, before the zeolite moves on to slightly less reactive metals such as lead or aluminium. Heavy metal toxins, therefore, are removed stepwise, following the reactivity series of the metals — with the most reactive first to go. The elimination of each level of the reactivity series is relatively fast, with liquid zeolite taking under a week, for example, to remove mercury before moving on to cadmium and then lead. The whole available heavy metal removal process can take a few months in total, although there are always more being added to the body by external sources and by release from internal non-available sources such as fat cells.

3) Helps remove pesticides, herbicides & dioxins: Although liquid zeolite is unable to remove these directly due to their negative or neutral charge, by reducing the toxic load to the liver, liver-induced glucuronidation, which is their main means of removal, is increased. As these chamicals are prime candidates for triggering cancer and disrupting hormone balances, even in low levels, it is very important that they are removed from the body as quickly as possible.

4) Reduces viral load: once the heavy metal concentration is significantly reduced, liquid zeolite then latches on to viral components. Viruses reproduce by first manufacturing viral components before assembling these components into a complete virus. It captures these components before they can be assembled into viruses, helping to reduce our viral load. This can help relieve some of the symptoms of viral diseases and infections.

5) Reduces absorption of nitrosamines: These substances can be found in processed meats and are linked with pancreatic, stomach and colon cancer, as well as Type II diabetes. Liquid zeolite helps to neutralizes these toxins in the digestive tract by capturing them in its molecular cages before they can be absorbed into the body. The spent zeolite is then safely eliminated in by the body in the normal way.

6) Helps buffer body pH to a healthy alkalinity: by trapping excess protons, liquid zeolite acts like a pH buffer, helping to prevent the acidic conditions in our blood and cellular fluids that encourage disease states and low immunity. A slightly alkaline environment in our bodies (pH 7.35 – 7.45) promotes optimum immune function, and liquid zeolite helps us to reach this ideal.

7) Helps to buffer blood sugar: in the same way that liquid zeolite can buffer excess protons and thus help balance body pH, it can also buffer excess glucose by its negative charge and therefore helps reduce blood sugar spikes.

8) Helps reduce cancer risk: evidence is accumulating that liquid zeolite not only removes toxins that can cause cancer (75% or more of cancers may be toxin related) but can also destroy cancer cells directly by triggering the P21 tumour repressor gene in cancer cells that it encounters. Even the liquid zeolite patent is for epithelial cancer cell destruction. [N.B. This does not mean that liquid zeolite is a cancer treatment per se, but rather that it is a useful supplement to integrate into a cancer treatment program supervised by a medical practitioner.]

9) Improves nutrient absorption: By promoting a healthy gut environment, liquid zeolite is able to not only increase nutrient absorption but helps promote healthy gut micro-organisms, increasing immunity to stomach bugs and infections. In this way, liquid zeolite also helps reduce the incidents of diarrhoea, which is why zeolites can now be found in the latest diarrhoea drugs.

10) Acts as a powerful antioxidant: The cage-like structure of liquid zeolite can also trap free radical molecules, making it an effective antioxidant. [N.B. This does not mean that liquid zeolite is a substitute for more conventional antioxidants such as Vitamins C, E and A, lutein and selenium, all of which have other vital roles to play in the body.]

11) Reduces symptoms of allergies: Liquid zeolite can capture some of the the antigens that cause allergies, migraines, and asthma, and in so doing it helps to reduce the symptoms.

12) Increases immune system function: Because of all of the above — with decreased toxic and viral loads in the body, many of which depress immune function and interfere with hormones — the immune system of those taking liquid zeolite is rapidly optimised. Zeolite is not stimulating the immune system but removing those chemicals and conditions that interfere with it. This also means that we regain youthful energy and vitality.

13) Helps prevent premature ageing: The main reason that many of us age prematurely is due to the build up of toxins in our system that interfere with optimum metabolic function and cellular repair. By removing the toxic load with liquid zeolite, our body’s normal repair and regeneration mechanisms are freed up to work efficiently.

14) Extremely easy and pleasant to take: Most serious detox solutions are difficult to take (many are injected or given as an enima, or must be taken away from meals), taste unpleasant, and can leave a person feeling drained because they indiscriminantly remove healthy metal ions as well. By contrast, liquid zeolite is a small bottle of tasteless liquid that can be taken with or without food and that removes only unhealthy ions.

Just one or two of the the above features would define a useful new food supplement, but take all ten features together and you begin to understand why leading-edge health and rejuvenation pioneers are raving about this product. Dr. Gabriel Cousins at The Tree of Life Rejuvenation Center in New Mexico describes liquid zeolite as "simple, elegant, extraordinary, and necessary for maintaining healthy living in today’s modern toxic world." It is also being used by Brian Clements at the famed Hippocrates Health Institute in Florida.

Of course, no product can be used in every single situation. Dr. Rik Deitsch, the biochemist who has done research on liquid zeolite, states that it may conflict with metal containing medication such as lithium and carboplatin and so should not be taken by those on these drugs. This is because it could potentially deactivate them by removing the metal ions.

That said, liquid zeolite is certainly one of the safest health supplements on the market today and one that is essential for anybody wanting to find and maintain optimum health in a toxic world.

* * *

Toxicity, acidic conditions and viral load, all of which suppress the immune system and interfere with normal cellular metabolism, are behind a whole array of conditions that plague humanity — from cancer and other serious chronic illnesses, to low energy and a susceptibility to colds and flu. Because liquid zeolite is able to help remove the root cause of immune suppression and metabolic imbalance, it has been accredited with not only bringing relief to a broad spectrum of different disease conditions (have a look at some of testimonies in the index) but also helping healthy individuals reach new levels of vitality. Such a spectrum of benefit can raise skepticism in those who do not appreciate common causes of ill health, but the science behind liquid zeolite is pretty sold and supports its unique mechanism of action. By removing fundamental disease causes in the ways outlined above, liquid zeolite is able to catalyze the body’s innate healing mechanisms, bringing important and life-changing health benefits to those who take it, some unexpected.

The question is: what would happen to you if you liberated your body from its accumulating toxic burden, a burden that has been depressing your immune system, degrading your body’s natural cellular regeneration and repair mechanisms, slowing your mitochondrial energy production, and disrupting your hormone balance for practically your whole life? What would happen if you unleashed the natural healing powers of this miracle that stands before you in the mirror? There is only one way to find out…

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There are a number of people on the internet putting all kinds of things into their liquid zeolite but the biggest travesty on the internet is Robert Sopias in his "report" which he now charges nearly $30 for. In this report which is entitled  "11 Natural Therapies for Conquering Cancer".  He used to give this report away on his site cancerfightingstrategies.com but he found that people would google his ‘recommendations’ and he would lose sales when people found the truth. Now he sells the book, and gives you a discount on product if you buy from him. Slick deal for him, but what about all the cancer patients he is taking money from?

So who is Robert Sopias? On his website he says this about himself:

Hello, My name is Robert Sopias and I have set up this site just for you. I’m not a medical professional. However, I’ve studied cancer and its treatment every day for the last seven (7) years. The information I give you is exactly "what I would do if I had your cancer." It’s not a prescription. You can "take it or leave it."

I wonder what he means by "studied cancer and it’s treatment". Do you think he means he looked up products on the internet that he could sell to cancer patients and make money?

So what is  this "Zeolite Enhanced with DHQ" that "not a medical professional" Robert Sopias recommends? Well DHQ is an anti-oxidant of the bioflavinoid family. Much like green tea extract. What do you think that would do to a zeolite molecule?? NOTHING. That’s right. Nothing.

Anyone can say that their product is 10 times, 100 times or even 1000 times better. Is it? Robert Sopias isn’t a medical professional. He also hasn’t has cancer. He’s an internet marketer who makes money selling products to cancer patients. Remember that.

If you want more information on zeolite, even just for a balance of view-points, I recommend http://www.theliquidzeolitebook.com Don’t buy the products. Just read the book.

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Recently I learned that preliminary research has been done taking Zeolite with a chemotherapy drug, Cyclophosphamine. Apparently this drug causes a toxin called “acrolene” when ingested which has toxic side effects. When the Activated Liquid Zeolite is taken in conjunction with the drug, the toxic effects are eliminated.  This is preliminary research and it will be many years before this connection is proven by published scientific papers. It may explain why some people have less side effects from treatment when they are taking the Activated Liquid Zeolite as well.

In an article titled “Natural zeolite clinoptilolite: new adjuvant in anticancer therapy” published in the Journal of Molecular Medicine Volume 78, Number 12 / February 2001, research is detailed with Mice, Dogs and Rats, indicating the use of Zeolite reduces skin cancer tumour growth.

It states, “In vitro tissue culture studies showed that finely ground clinoptilolite inhibits protein kinase B (c-Akt), induces expression of p21WAF1/CIP1 and p27KIP1 tumor suppressor proteins, and blocks cell growth in several cancer cell lines. These data indicate that clinoptilolite treatment might affect cancer growth by attenuating survival signals and inducing tumor suppressor genes in treated cells”.

While this is not a study on humans, it does indicate that the use of Zeolite has some function at least in animals in tumour suppression. The p21 gene is known by scientists to suppress tumours and one of the great scientific debates is how to trigger this gene in cancer patients.

The following information is quoted on many websites. To my knowledge, it has not been substantiated or published, and the study was done by Lifelink Pharmaceuticals, of which Rik Deitsch is a director. It therefore must be taken with a grain of salt!

Although only one small human trial has been conducted, the results were intriguing: 78% full remission for stage 4 cancer patients (with various types of cancer). The study was an open-label trial conducted by the researchers at LifeLink Pharmaceuticals in Ohio. Although one small study is not grounds for leaping to solid conclusions about cancer, this result is promising enough to warrant additional investigation. Any anti-cancer effect is probably due to NCD’s ability to induce tumor suppressor genes that cause the body to not only halt the growth of tumor cells, but actually destroy such tumors.

There are some other areas where Liquid Zeolite could definitely help with many disease states. One is the area of body pH. Studies done invitro (in a test tube) indicate that with a pH of 7.4 or higher, cancer cells become dormant. This would indicate that if the body’s pH can be raised to this level, it is possible that it could slow down or even stop the spread of cancer.

Dr. William Kelley, in an article titled, “Cancer – Self Treatment”, suggests that “There is research indicating that cancer grows slowly in a highly acid environment (because the acids cause it to partially destroy itself) and may actually grow more quickly as your body becomes more alkaline prior to reaching the healthy pH slightly above 7.4 where the cancer becomes dormant. Therefore, you will want to get your pH above 7.4 as quickly as possible by every means available.”

This would indicate that when raising pH, it is important that it is done as quickly as possible and that as pH rises, cancer activity can increase for a while. So, one would have to be really convinced that a pH of 7.4 does effectively stop the spread of the disease before considering this action.

Often there is a challenge with Natural Remedies in that sometimes indications get worse before they normalise. This leads many physicians to recommend against the use of such products, because they see any worsening of the situation as alarming. Again, you will have to make your own mind up about this. The question then is to research alternate pathways and decide the likely outcome in each case!

Liquid Zeolite  taken regularly, will raise pH into the 7.4 zone and keep it there, which I think is a good thing!

Vic Shayne, PhD in an article called’  “Ignoring the Link Between Toxins and Cancer”  states, “With all of the cancer information and disinformation broadcasted continually through the major news media, rarely do we hear a mention of the greatest threat to our health – and the most prevalent cause of cancer: toxins.”

More evidence is emerging every day that there is a relationship between environmental toxins and cancer. A recent article in the Vancouver Sun stated, ” Banned pesticides and other toxic chemicals lingering in the environment put people at an increased risk of developing non-Hodgkin lymphoma, according to a B.C. Cancer Agency study”.

We are rapidly approaching a point where there is little doubt that toxins are affecting our health in a negative way. In 1907 there were less than 7% of deaths from cancer. At that time no chemicals were used in agriculture. Today the death rate from cancer is over 30% and of course we have thousands of toxic substances in our food, water and air. Is this a coincidence? You decide!

Liquid Zeolite, is effective in removing toxins, particularly heavy metals and organic chemicals such as dioxin, deildrin and benzene. We have done hair analysis tests before and after using the product, and although this is not a scientific controlled study, the results are documented by lab reports and are quite impressive.

Research was published in an article titled,  “Zeolite Binds to Benzene” (Active Crystallography 1996). This shows how in a laboratory, the Zeolite molecules combine with benzene to remove it from the body.

Conclusion. In summary, we know that Activated Liquid Zeolite increases heavy metal secretion by 8-20 times baseline. We know that it increases pH to the 7.4 range. We know that it removes toxins and heavy metals from the body.

Liquid Zeolite is a good choices for cancer patients.

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Toxins poison our air, our water, our food , and our bodies. According to the EPA, 70,000 chemicals are used commercially in the U.S., 65,000 of which are potentially hazardous to our health. The Environmental Defense Council reports that more than four billion pounds of toxic chemicals are released into the environment each year, including 72 million pounds of known carcinogens.

Cancer fatalities account for approximately 12 percent of all deaths worldwide each year. Across the globe, 10.9 million people are diagnosed with cancer annually and 6.7 million die because of it. According to the World Health Organization, global cancer rates could increase by 50 percent in the next 15 years. The U.S. ranks in the top three countries with the highest cancer rate in both men and women.

The toxic onslaught doesn’t stop with carcinogens. A joint study by Mt. Sinai School of Medicine, Commonweal, and the Environmental Working Group in 2003 identified a total of 167 hazardous compounds in the blood and urine of American adults (with an average of 91 per person tested), including 76 known to cause cancer, 94 that are toxic to the nervous system, 82 that damage the lungs, 86 that affect hormone function, and 79 that cause birth defects. A study by the Environmental Working Group in 2004 found a total of 287 industrial chemicals in babies’ umbilical-cord blood, including 180 known to cause cancer, 217 that are toxic to the brain and nervous system, and 208 that cause birth or developmental defects in animals.

A s many as 25 percent of Americans are estimated to suffer from some degree of heavy metal poisoning , particularly from mercury, lead, cadmium, and arsenic. We are also exposed to a significant amount of radiation and increasing viral attacks. Our immune systems are further compromised by poor nutrition and unhealthy lifestyles, and most of us suffer from an excessively acidic pH level, which creates an internal environment in which cancer – as well as viral, bacterial, and fungal infections – can thrive.

What it Is

In my work to develop a detoxification system for prospective mothers to enable them to bring non-toxic babies into the world, I have searched for a simple, natural remedy that could serve as a practical antidote for toxicity. Recently , I learned about zeolite, a naturally occurring, negatively charged mineral, with a unique crystalline structure. Zeolite is formed from the fusion of volcanic lava and ocean water, and combines the four elements – air, earth, water, and fire.

It has been used for 800 years throughout Asia as a traditional remedy to promote overall health and well-being, and for 30 years in the U.S. in animal feed. It has also undergone 13 years of pharmaceutical research in the U.S. with humans. Zeolite is included on the Food and Drug Administration’s GRAS list (generally recognized as safe) and thus is considered to be “completely safe.”

A biochemist from a small pharmaceutical company in Ohio researched and purified zeolite, was amazed by its potential, and was granted a patent (U.S. #6,288,045). That patent is now held by a nutritional and research biochemist, who leases it to the company that markets purified zeolite.

Zeolite may well be one of the most potent natural preventatives and treatments for cancer ever discovered. Life Link Pharmaceuticals recently completed a preliminary, 14-month, open-label study of 65 level-four, terminal-stage cancer patients. These people had various types of cancer, and all of them had been sent home to die. After taking purified zeolite, 51 of them (78 percent) experienced complete remission, which means that their cancer disappeared. This preliminary research suggests that purified and activated zeolite may be effective in treating all forms of cancer, leukemia, and lymphoma.

How it Works

Zeolite’s mechanism of action against cancer cells is unique and unlike that of any other substance I have studied. Theoretically, it has the rare ability to take in a tremendous amount of positively charged toxins, indirectly neutralizing their effect in causing cancer. In the process, the zeolite develops a slight positive charge. It is then attracted to and pulled right into the negatively charged membrane of the cancer cell. When the zeolite moves inside the cancer cell, the cell’s P21 gene is activated. This gene acts as a tumor suppressor through its ability to control cell-cycle progression. The activation of P21 appears to halt the growth of tumors by directly suppressing growth signals.

During in-vitro studies using zeolite, all cancer cells tested were destroyed within 72 hours (Life Link Pharmaceuticals, U.S. Patent #6288045, 2001). This is a claim that cannot be made about any other substance. However, because it is still in the preliminary research phase, it is too soon to declare that zeolite is a cure for cancer.

What we can say is that zeolite has a chelation-like effect in removing heavy metals, pesticides, herbicides, and other positively charged toxins from the system. Zeolite’s negatively charged crystalline structure is what makes this possible. Its crystals act as “cages,” inside of which are positive ions. These positive ions switch places with positively charged toxins in the body, tightly bind them, and excrete them completely. One of the benefits of binding toxins in this manner is that they are 100 percent excreted. Heavy metals, pesticides, and herbicides all leave the system; they do not get deposited elsewhere in the body. Forty percent of zeolite binds heavy metals in the gastrointestinal tract, and 60 percent binds toxins in the bloodstream and at the cellular level. Zeolite’s binding power was proven during the Chernobyl disaster, when tons of it were used to remove radioactive cesium and strontium-90 before they contaminated local water systems. Acting primarily as a chelator, zeolite trapped these radioactive minerals within its crystalline cage structure.

Zeolite appears to remove toxins from the body in a hierarchical order. It first acts strongly to remove lead, mercury, cadmium, and arsenic. This first phase may take one to four weeks or longer. Zeolite then removes second-priority toxins, including pesticides, herbicides, and plastics. Zeolite appears to increase the rate of glucuronization in the liver, activating phase II of the glucuronidase function.  This in turn removes pesticides, herbicides, and xeno-estrogens from the body, releasing them through the urine. Interestingly, it also appears to neutralize the aflatoxin poison.

A third function of zeolite is to trap pre-virus components, preventing the replication of viruses and their ability to make us sick. In this way, zeolite may play an important role as a broad-spectrum anti-viral. Viruses are produced in parts as on a production line, at the end of which the virus is fully constructed. Zeolite absorbs viral parts into the pores of the mirconized zeolite aggregates (not into the chelating-like cages described above). This explains why zeolite seems to block the development of many viral infections , including herpes virus 1, coxsachie virus B-5, ecco-virus 7, and adeno virus 5.

Forty anecdotal cases of herpes zoster have reportedly been cured, with sufferers becoming pain-free in one to three days after beginning to take zeolite.

Anecdotal testimony also reports that it is effective in alleviating or curing the flu, colds, hepatitis C, viral or heavy-metal induced multiple sclerosis, and rheumatoid arthritis. Zeolite’s effect as an anti-viral appears to be a preventative function that builds up over time, beginning after approximately four to six weeks of use, when heavy metals, pesticides, and herbicides have been mostly eliminated. There is anecdotal evidence, however, that in some cases its anti-viral effect seems to be immediate.

Zeolite also is a unique antioxidant. A traditional antioxidant works by absorbing excess free radicals into its system because it has an unpaired electron. In contrast, zeolite traps free radicals in its complex structure, inactivating and eliminating them. In this way, it acts as a complement to traditional antioxidants.

In addition, zeolite buffers the system towards slight alkalinity by establishing pH levels of 7.35 to 7.45, which is the optimum pH for the human body. The body’s pH level influences both immunity and brain function. An acid blood pH (7.34 or lower) creates a precondition for cancer. In an acid environment, brain cell function can also be impaired, causing depression, anxiety, stupor, paranoia, delusions, hallucinations, or even psychosis.

Zeolite also appears to balance the immune system , either up- or down-regulating it as needed. Although the precise mechanism for this is not entirely understood, this function is clearly very important in a world in which most people’s immune systems are seriously compromised.

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