2015-10-05

We use a unique delivery system which moves minerals, such as Zinc and Copper, through the epidermal layers across semipermeable membranes very quickly to immediately be absorbed by diseased or healthy tissues at very low concentrations.

The Krebs cycle is a charting of the metabolic pathways that healthy plant or animal cells must follow to perform all functions supporting life. There are approximately thirty-two (32) steps in the process. The steps allow healthy cells to expel excessive amounts of toxic materials continuously, including minerals and other nutrients unless totally overwhelmed.

Diseased and/or mutated cells (such as cancer cells) do not follow the Krebs cycle. Rather they follow an alternative metabolic cycle with only about 18 steps to absorb all foods (particularly sugars). The diseased cells will also take up excessive amounts of minerals such as Zinc and Copper (in our formulation) in amounts that are toxic to them, causing the diseased cells to die. The surrounding healthy tissues (following the Krebs cycle’s 32 steps) take up only the amounts of Zinc and Copper needed to function and excrete the excess minerals. Following the Krebs 32 steps versus the 18 steps that cancer and other diseases follow saves normal healthy tissue while killing the diseased cells.

Now we can treat mutated cells, non-functioning cells and non-typical cells diseased as well as viral, bacterial and fungal diseases in conjunction with or without other drugs, surgery chemotherapy or radiation.

In summary, we are able to transport our highly available Zinc and Copper to our target diseased cells (including cancer cells) and kill ONLY the diseased cells, leaving the healthy normal cells surrounding them functioning without disruption.

Further, a sheath of bacterial cells (also non-Krebs cycle) often surrounds a mass of mutated cells. The highly bioavailable Zinc and Copper will penetrate and kill the bacterial cells in this shield. The mass of mutated cells are then exposed to the immune system and are destroyed.

This is an uncomplicated explanation of a highly complex system that was very difficult to develop. It took many years of study to devise a strategy that is efficacious and easy to apply. My hopes and dreams are that it will save many people afflicted by several terrible diseases.

Respectfully,

John W. Kennedy, Scientist/Developer

Bioavailable Ionic Minerals for Disease Mitigation

There is no such thing as a silver bullet. A personalized consultation with Dr. Darrell Wolfe Ac.PhD. to ensure the success of this program is important when it comes to the proper nutritional support and detoxification for healing to take place. It is also important for all patients to follow up with Dr. Wolfe every few days; there are no silly symptoms or silly questions. Call 1 855 900 4544 to book your consultation by phone, Skype or in person.

Abstract

STRUCTURED ATOMIC REDOX SPRAY is a bioavailable immunotherapy technology for mitigating infectious and other diseases. This technology targets cells which do not follow the Krebs metabolic cycle by delivering a lethal dose of minerals (zinc and copper) to those cells. Because cancer cells follow an anaerobic, non-Krebs metabolism, it is predicted to target cancer cells precisely. Normal, healthy cells which follow the Krebs cycle should absorb the minerals that they need and reject the rest. Because bacteria and fungi follow non-Krebs metabolic cycles, the product may also be capable of treating a variety of infections.

The formulation uses highly bioavailable cations through inorganic coordination complexes formed by the coordinate bond formation between an electropositive mineral cation and molecular groups that pose unshared electron pairs. A salicylic acid preparation can enhance transport of free zinc and copper ions systemically through tissue via an artificial superoxide dismutase (SOD) radical.

A topical version has been tested on over 100 volunteer subjects during eight years of informal trials on a variety of diseases. Results reported have been extremely positive. Cancer patients using the topical formulation reported that dead cancer cells were excreted by the body via the skin, stool, or urine. Although many experienced pain and other effects, subjects reported that the effects ended upon conclusion of the treatment. The treatment has also been tested on MRSA and ALS patients with promising results. The product is currently undergoing additional pre-clinical doctor-supervised case studies on several types of diseases.

* Prepared with the assistance of the Cancer Cell Treatment Support Network, www.cancer-cell-treatment.com.

The Science



The Krebs cycle, also known as the citric acid cycle or the tricarboxylic acid cycle (TCA cycle), describes the metabolic pathways of the higher-order plants and animals in which available fuels, oxygen, water, and other essentials to life are utilized in an aerobic mode. The metabolic system is a well-documented and familiar process involving the basic steps to produce a “higher” form of life. The protection provided by at least 32 steps in the process provides a system that protects the oxygen-driven plants and animals.

Lower-order organisms are not near as complex in their metabolic pathways as higher-order organisms such as a tree or a human. The cycle followed by organisms such as bacteria and fungi, as well as certain diseased cells in higher-order life forms, follow a less complicated process that allows the disease to multiply at an almost exponential rate in an anaerobic cycle that has far fewer steps. Warburg1 first observed the unique metabolic cycle of cancer cells and their ravenous appetite. The disease utilizes all available minerals, sugars, fats, and proteins to fuel the reproduction of cells using the abbreviated anaerobic cycle. The higher the rate of replication, the less oxygen is available for healthy tissues surrounding the disease. Reduced oxygen aids in the fermentation process that is part of the favorable conditions required for the exponential growth of cells and organisms employing the anaerobic cycle, including infections and abnormal cells.

Our bioavailable ionic minerals (Zinc-Copper) formulation, a free radical oxygen scavenger technology named STRUCTURED ATOMIC REDOX SPRAY, exploits a flaw in the exponential expansion mechanism of the disease organism. Specifically, it exploits the mineral-gathering mechanism of the organism against itself2. Lower orders of disease organisms gather the necessary minerals and other building blocks in an amount proportional to their availability in the environment. This differs from the metabolic processes of higher organisms that only gather enough of the elements and building blocks to satisfy the requirements of the Krebs cycle.

Higher organisms will only incorporate minerals and other nutrients at a rate necessary for survival, while lower organisms and certain diseased cells will accumulate minerals in an amount that is toxic. Therefore, providing a high concentration of ionic minerals to a disease area could result in a toxic level of the mineral to disease organisms and allow survival of higher organisms so long as the dosage rate of the ionic minerals is below the toxic level for the higher organism.

STRUCTURED ATOMIC REDOX SPRAY uses highly bio-available ionic minerals at a rate that will kill the lower organism without impairing the function of the higher organism. This formulation transports all the minerals systemically to a plant, animal, or human with assistance of an artificial superoxide dismutase (SOD) carrier. The artificial SOD carrier causes the disease-causing cell or organism to uptake an amount of ionic mineral that is toxic, which results in death of the disease cell or organism. Additionally, many diseases follow an anaerobic fermentation process which oxygen will impair thereby suggesting a secondary mechanism for destroying the disease.[1] STRUCTURED ATOMIC REDOX SPRAY also contains sulfur, which may further aid in destroying disease and relief of pain. However, the prime mode of action is the uptake of minerals in a highly biologically available formulation.

The general principle of STRUCTURED ATOMIC REDOX SPRAY is rapid entry into the aerobic biological system of a plant or animal using a mineral complex carrier in an ionic form, which penetrates and migrates toward an anaerobic disease system if present. The product is capable of penetrating the barrier zone between the aerobic and anaerobic tissues if the disease is internal. Other mineral formulations are not as bioavailable, being unable to pass through cellular tissues as easily as the STRUCTURED ATOMIC REDOX SPRAY. The unique quality of the formulation is thus its penetration of the membrane and the movement of large amounts of ionic minerals into the disease area.

Diseases have three vulnerable sites that can be attacked by treatment:

Penetrating the outer membrane of the disease

Destroying the internal components that drive the cells metabolism

Destroying the gene pool that may provide a future defense (resistance) against the introduced substance

Minerals that are not in the bioavailable form will not be able to eliminate or otherwise disable the disease cells because the minerals cannot pass through the membrane coating the outer surface of the disease cells and/or cannot travel in an extracellular fashion. The bioavailable minerals will attack all of the vulnerable targets in the disease cells because of the systemic capabilities of the formulation. When using the bioavailable formulation, the cell membrane should be easily trans-versed and possibly ruptured, the inner cell compromised because of the Krebs cycle (aerobic vs. anaerobic) as described above, and the genetic code of the disease cell destroyed by apoptosis. There should be no further deviations from the genetic code to produce new strains that may be resistant to the STRUCTURED ATOMIC REDOX SPRAY. In fact, there are no known resistances to plant and/or animal disease when the primary source of the product being used is a mineral.

Complex Ion Formation of Mineral Complex Bonds

The complex ions and inorganic coordination complexes are formed by the coordinate bond formation between an electropositive mineral cation (positive) and molecular groups that possesses unshared electron pairs (ammonia). Every metal ion has at least one coordination sphere which determines the number of coordinate bonds possible for each mineral atom. The coordinate bonds attract negatively charged ions possessing unshared electron pairs. All cations except those in periodic table Groups IA and IIA exist as complex cations with a definite number of coordinating groups bound to them. The cations use the unshared pair in attempting to fill gaps in the outer electron orbitals where those electron shells are incomplete. The bonds formed between the cation and the unshared pair of electrons are mineral complex bonds.

An exemplary compound can be produced, as a result of the acid-base reaction when sulfuric acid is combined with ammonia sulfate is ammonia (NH3). Ammonia is one of the compounds having an unshared pair of electrons that enables mineral complex bond formation between itself and the free cation in solution. The nitrogen atom includes an unshared pair of electrons. Ammonia is very reactive in mineral complex bonding due to its respectively small size, and the unshared pair of electrons. The two hydrogen atoms cannot equalize the charge due to repulsion between the electron pair making ammonia polar. Therefore, for example, ammonia may enter into the following two complexes:

Cu+2 (Copper ion) + 4NH3→[Cu(NH3)4]+2

Zn+2 (Zinc ion) + 4NH3→[Zn(NH3)4]+2

The number of ammonia molecules is double the metallic ion valence, and the valence charge does not change. The unshared pair of electrons forms the mineral complex bonds, the complex system supplying both the unshared electrons. The resulting compound is a plurality of ammonia molecules bonded to a single molecule of ionic mineral forming an encapsulated mineral surrounded by ammonia “mineral complex bonds.” This molecular diagram is shown for purpose of example only and the zinc cation may be substituted by any of the cation ions.



This compound, including ammonia encapsulating a bioactive mineral cation, is hereinafter referred to as a “mineral complex system.” Additionally, urea may be included in the formulation resulting in mineral complex bonding of the cations with the urea. In this composition, the bioavailable minerals could be formulated with the urea producing a spray containing higher than anticipated mineral content than is normally expected in the formulations.

Examples of the mineral complex compounds are:

Zinc:            Zn[(NH3)4]+2

Copper:        Cu[(NH3)4]+2

As another example, in aqueous solutions without complexing agents, cobalt+2 is the favored state. In the presence of complexing agents such as ammonia, NH3, complexes of cobalt+3 have greater stability and are more stable in basic media than acid media. Additionally, compound bonding is conducive to maintain the abundance of hydrogen ions. The resulting solution has a very low pH reading (at or near zero) because of the combined bonded mineral ions. STRUCTURED ATOMIC REDOX SPRAY does not act as a conventional acid because of the stability of the mixture. The pH of the products is not indicative of the expected acid characteristics one might imagine at a pH of 1.0 or below. The solution can only be reduced by non-heat evaporation to a certain volume.

The efficiency of STRUCTURED ATOMIC REDOX SPRAY is in direct relation to the amount of free zinc ions. The complex ion and/or inorganic coordination complexes using zinc is prepared by combining and agitating zinc sulfate (ZnSO4) with a mixture of ammonium hydrogen sulfate (NH4HSO4) and water. The result is a zinc mineral complex system that has the ability to penetrate through cell membranes without being blocked. The complex has a strong positive charge and is readily accepted into the cell.

Other products containing zinc only produce a limited amount of ionic zinc. Zinc oxide, for example, releases zinc ions depending on the acidity of the product. Zinc sulphate has a weaker bonding structure than does zinc oxide. It generates complex cations and inorganic coordination complexes, which allow the ions to act independently without a counter-balance at a cell membrane and can be translocated throughout the body, passing through healthy cells with no effect. Without being processed properly, zinc sulphate will be rejected at the cell membrane and only a small amount of zinc ions will enter the cell, making this method highly ineffective.

Secondary Active Complex

The formulation includes a high level of sulfur, which functions as a secondary active complex. This complex can operate synergistically with the mineral complex by accelerating the treatment of the affected cells. The high level of free sulfur can be transported to various locations and may speed reconstitution of damaged tissue affected by the disease. Sulfur is a non-metallic acidic macro mineral usually consumed as part of a larger compound (zinc, copper, etc.) and is not usually expressed as an aid to the mitigation of disease. However, the benefits of sulfur are well known and the formulation that combines a high-sulfur content (NH4HSO4) base with the minerals with radicals that contain sulfur (zinc sulfate, etc.) will provide an abundance of free sulfur that may accumulate in those regions of the human body that require attention. The preferred mineral radical would be a sulfate for that reason but is not necessary for the success of the free sulfur. The benefits of sulfur include boosting the immune system and providing pain relief to targeted cells. The mechanism by which free sulfur produced in this mixture operates similarly to the operative mode of glucosamine sulfate, chondroitin sulfate, and methylsulfonylmethane (MSM).

Superoxide Dismutase (SOD)

Superoxide dismutases (SOD) are essential enzymes that eliminate superoxide radical (O2-) and thus protect cells from damage induced by free radicals. The active O2– production and low SOD activity in cancer cells may render the malignant cells highly dependent on SOD for survival and sensitive to inhibition of SOD.

STRUCTURED ATOMIC REDOX SPRAY also contains a mineral complex of ammonia ligands in combination with the zinc and copper forming a Super Oxide Dismutase (SOD) that is a highly effective anti-inflammatory agent and has strong antiviral properties. SOD is an oxygen scavenger that may be effective in renewing tissue damaged by disease, mechanical damage such as cuts, and may even be effective against radiation damage by the Sun. Our artificial SOD has a relatively low molecular weight compared to natural SODs, which should increase its bioavailability.

A deficiency of cytochrome oxidase is a metabolic defect of cancer cells that causes a blockage of cellular respiration or oxidative energy production. Bioavailable copper and a SOD make copper and zinc available to the cytochrome oxide enzyme that is copper dependent. The process can be exemplified by the use of salicylic acid in the formulation and produce an effect similar to the use of an aspirin to relieve pain where the salicylate combines with the available copper and that residing in the stomach lining and transported to the site of the pain.



The STRUCTURED ATOMIC REDOX SPRAY, with its bioavailable Cu/Zn SOD, counteracts the effects of overproduction of superoxide by utilizing a mineral complex system, which can permeate into the affected tissues and countering of the overproduction of superoxide. A Cu/Zn superoxide dismutase (SOD) is used that neutralizes the debilitating effects suffered by individuals that are producing excessive superoxide causing the symptoms of neural disorders, suggesting that its effects on ALS3 and similar diseases. A patent addressing that particular disease has been submitted. SOD is also known as an anti-inflammatory treatment for traumas it is considered over 3000 times stronger than vitamin C as a nutrient. Thus a key attribute of STRUCTURED ATOMIC REDOX SPRAY is not only its ionic minerals but its SOD, both highly bioavailable.

Mode of Action

As described above, STRUCTURED ATOMIC REDOX SPRAY uses ionic mineral complexes that are predicted to be capable of penetrating tissue, benefitting normal cells, and destroying diseased or mutant cells. A Superoxide Dismutase (SOD) carrier provides for extracellular transport of the ionic minerals systemically throughout the region of topical application. The method of action on disease described herein stems from both the scientific theory (section above) and test results (section below).

The ionic mineral complexes are believed capable of penetrating cell membranes at a rapid pace. The formulation thus may present highly bioavailable minerals to cells. The minerals should be blocked from excess absorption by normal cells following the Krebs cycle, which will not allow entry of an abnormally high concentration of minerals. Instead, the excess minerals should travel through the cells without disrupting normal cell functions. Cells, which do not follow the Krebs cycle, do not have the regulatory capabilities of the Krebs cycle. These non-normal cells receive an overload of minerals, resulting in mineral toxicity. The process of destruction of the diseased and other non-normal cells is in some cases may be aided by the added effect of oxidation of the anaerobic disease fermentation process. Once the targeted cells die, testing has observed that the body’s natural capabilities expel the dead cells through the skin, urine, or feces.

Another mode of action is the effect of the ionic mineral complex on bacteria or other pathogens or saprophytic organisms that surround and act to encapsulate a disease region such as a tumor. Tumors are typically surrounded by a sheath containing the disease (including cancer), immune system cells, bacteria, viruses, and/or other organisms. High numbers of bacteria, etc. have been identified in the protective membrane and may be responsible for the membrane’s existence. The bioavailable ionic mineral complexes in STRUCTURED ATOMIC REDOX SPRAY are predicted to have antimicrobial properties and be able to freely move among and through cells. These complexes may thus be capable of reaching the interface between the healthy and diseased tissues and destroying the organisms that exist in the protective membrane.

Cancer is typically not recognized as a threat by the immune system of the body. The composition exposes the cancer as a foreign body to the immune system, which attacks the cancer, activates the immune response, and causing the body to destroy the cancer and/or expel and/or absorb the cancer. Additionally, in animals without an immune system, the composition will not be able to promote immune response. However, the formulation may have cytotoxic effects that may kill the cancer in immune-resistant hosts.

We believe that building a strong immune system to fight off diseases and an immune system that is challenged by disease will improve effectiveness of STRUCTURED ATOMIC REDOX SPRAY. It is important that the proper vitamin, minerals and other support directed at building an immune response be pursued. We also believe that the use of botanicals will support the treatment via use of complementary modes of action.

In summary, when the mineral complex system is introduced into a cell, we predict that the minerals will dissociate from the complex and be highly bioavailable to the cell. These minerals are predicted to kill the cancer, bacteria, and fungi cells through the different modes of action causing degradation of the growth and death of the cancer cells, much like antibodies do to any foreign body during an immune response. Other aids to building the immune response and botanicals can be of assistance in treating the diseases.

Testing

STRUCTURED ATOMIC REDOX SPRAY is considered experimental and has not undergone formal clinical trials. However, there have been extensive informal tests by volunteers on the treatment, as described below. Formal testing on the treatment has been limited.

Testing has primarily used a topic skin spray consisting of concentrations of STRUCTURED ATOMIC REDOX SPRAY varying from 7.5 – 10%. The topical formulation has undergone successful skin irritation testing4 and is currently being laboratory tested against a number of pathogens. Doctors are also currently testing the product in case studies in several countries as a form of pre-clinical trials on a number of diseases such as skin cancer and MRSA. One physician plans to test an injectable formulation, which might allow a higher rate of effects on internal tumors than is achieved via topical application.

Based on the results of these pre-clinical case studies, it is expected that the topical formulation may enter clinical trials for targeted diseases. Other limited-claim pathways to early markets, such as a disinfectant, are being explored.

Past Testing

STRUCTURED ATOMIC REDOX SPRAY has gone through years of development, starting with various animals over eight years ago. Over the years of testing and reformulation, numerous informal human studies have shown remarkable successes. The diversity of these case studies is summarized below.

Disease

Studies

Disease

Studies

ALS

3

Lung Cancer

2

Breast Cancer

4

Lymphoma

2

Colon Cancer

1

Throat Cancer

1

Ovarian Cancer

2

MRSA

4

Brain Tumor

2

Skin Ulcers

3

Stomach Cancer

1

Skin Infections

15

Non-melanoma

14

Fungal Infections

3

Melanoma

2

Myomas

1

Prostate Cancer

1

Dental Infection

3

Testicular Cancer

1

In studies performed using this composition, the bioavailable minerals appeared to have penetrated the sheath, which surrounds malignant tumors, destroyed the bacteria, and dissolved the sheath in addition to killing the tumor. This was evidenced in several case studies by rejection of entire tumors from the body in a sheath-like mass, which was transported from an internal area of the body through the epidermis. In other cases, patients reported white streaks in their stool and/or white specks in urine, which are hypothesized to be dead cancer cells being expelled.

From studies conducted to date, an area will react to this treatment according to the type of lesion present. Cancer will be detected when a strong reaction takes place at the suspect site. No pronounced reaction will take place if the lesion is not cancerous. If cancer is present, the reaction will be pronounced, with swelling and redness in the area or white cloudy material in urine and/or stools. Tumors may be transported to the surface dead with a bluish color indicative of Cu/Zn abundance. A red rash indicates additional cancer cell being transported. Black scabs and nodules that are typical of toxins indicate their transport to the surface. The swelling and redness will persist and the skin may develop a boil that may break and be absorbed into the body. Patients may experience pain, particularly when tumors are expelled via the skin. The process from treatment to the final disappearance may take from anywhere from 10 days to several months depending on the location and stage of the tumor and the health of the patient. In nearly all case studies, at the conclusion of treatment, all locations became cancer-free and the skin healed with minimal scarring.

The treatment has also been able to detect locations of skin cancer in some patients. After application of the topical formulation to a known skin cancer location, other locations of previously unknown skin cancer began to present.

Personalized Protocol for STRUCTURED ATOMIC REDOX SPRAY Treatment

The Personalized Protocol provides information for physicians and patients who are trialing the STRUCTURED ATOMIC REDOX SPRAY in physician-supervised studies. The STRUCTURED ATOMIC REDOX SPRAY is used as a personalized treatment plan and is adjusted by the care provider after considering the patient’s condition, the type and severity of disease, past and concurrent treatments. The safety and efficacy of the STRUCTURED ATOMIC REDOX SPRAY allows it to be used for prevention, detection, targeted therapy, complementary and/or standalone treatment.

Patient Instructions

Possible Expected Reactions

If the STRUCTURED ATOMIC REDOX SPRAY is being used to treat a condition, which involves the structure and/or the function of cells either on or beneath your skin or a viral or bacterial infection, then the use of this Formula may produce one or more of the following common reactions:

Redness, stinging, itching and/or scabbing of the skin (some with white halos around them)

Skin nodules of various sizes colors

Extreme or mild fatigue (depending upon seriousness of condition, age and strength of the immune system)

Bowel and/or urine incontinence and/or white cloudy material in urine and/or stools

Itchy foot bottoms

Unusual body and/or stool/urine odors

Metallic taste in the mouth

Flu-like symptoms

Sensitivity to direct sunlight

Manageable to severe localized pain

All of these conditions should resolve themselves with no residual effect or scarring.

Areas of Application

Origin of the Disease

The treatment involves topical administration to targeted areas, starting with the skin areas surrounding the known origin of the disease. Additional applications are applied to the regional lymph nodes serving the area.

Prevention and Detection

Treating the sentinel lymph nodes and organs (collecting ducts) of the lymphatic system such as the thymus and spleen may reduce the potential of current or future metastasis of non-normal cells.

Boosting the Immune System

A strong immune system enhances the effect of the STRUCTURED ATOMIC REDOX SPRAY Treatment.  A consultation is important along with the proper nutritional support, which depends on the condition of the patient with continual guidance by a health care provider.

Vitamin and Mineral Supplements

Bioavailable Minerals or BAMs will greatly improve general health. Nutrient bioavailability is the proportion of a nutrient that is absorbed from the diet. The bioavailability of a nutrient is governed by external and internal factors. Daily allowances of both vitamins and minerals can be obtained through a healthy diet, but when an individual’s immune system is compromised and they are facing some major disease, supplementing the food intake is vital to the mitigation of the disease.

Mineral supplements will be necessary in traditional forms to meet minimum daily requirements when boosting the strength of the immune system. It is true that the daily allowances for both vitamins and minerals can be obtained through a healthy diet, but when an individual’s immune system is compromised and they are facing some major disease, supplementing the food intake is vital to the mitigation of the disease.

Summary

STRUCTURED ATOMIC REDOX SPRAY is an experimental product, which transports highly bioavailable zinc and copper ions systemically. It is hypothesized that these ions will kill cells, including non-normal cells, bacteria, fungi, and viral cells which do not follow the Krebs metabolic cycle, through a mineral overdose. It is also hypothesized that it will leave unaffected or enhanced those healthy cells, which strictly follow the Krebs cycle. Cancer cells, being anaerobic, do not follow the Krebs cycle, nor do most infectious pathogens.

STRUCTURED ATOMIC REDOX SPRAY formulated as a topical spray has undergone informal studies with remarkable success on skin cancer, internal cancer, MRSA, and several other diseases on plants, animals and humans.

Many in the bio pharma industry have discovered immunotherapy technologies, which have yielded a number of compounds that hold promise for cancer sufferers. However, we believe that this potential solution offers a delivery system, non-invasive characteristics, and mode of action, which may eliminate the non-functioning cells associated with many serious diseases.

Treatment Protocol

This section provides information for physicians and researchers who are testing the product.

Phases and Duration of Treatment

The length of treatment depends widely on the location and severity of the condition and the strength of the immune system.   Phases of the treatment can be considered as follows:

Initial treatment without any reactions (days to weeks)

Reactions increase, showing that the treatment is beginning to work (weeks to months)

Reactions decrease, showing the treatment is nearly complete (days to months)

Maintenance mode. Reactions cease, indicating that the treatment was successful (permanent use of reduced quantity is recommended)

Some skin conditions can be treated in days. Some subjects with internal conditions have treated for as long as four weeks before a noticeable reaction (which shows that the treatment is working) has developed. Some subjects with advanced diseases have used the treatment three times per day until reactions subside. Thereafter use twice each week may help to discover and/or prevent a reoccurrence of the condition.

Possible Expected Reactions

Users with cancer, infections, or other abnormal cells should expect reactions. These are signs that the treatment is working.

Redness, stinging, itching, crusting, and/or scabbing of the skin

Small black and/or red “pinpoint” spots (some with white halos around them),

Skin nodules of various sizes colors,

Bowel and/or urine incontinence and/or white cloudy material in urine and/or stools

Itchy foot bottoms

Unusual body and/or stool/urine odors

Metallic taste in the mouth

Flu-like symptoms

Mild to severe pain.

Mild to extreme fatigue (depending upon seriousness of condition, age, and strength of the immune system)

Sensitivity to direct sunlight.

All of these conditions should resolve themselves with no residual effect or scarring.

These effects indicate that the treatment is working and that the body is expelling the dead disease cells. Users should not stop treatment because of the effects listed above. Treatment should not be stopped until after these effects stop.

Directions for Application

Shake vigorously before each application. Spray STRUCTURED ATOMIC REDOX SPRAY liberally and evenly over the affected area. Apply three (3) times a day until any reactions subside and two (2) times a day thereafter. Allow the formula to be absorbed into the skin naturally; it is not necessary to “rub” it into the skin; it should be completely absorbed within minutes. Do not rinse or wash the treated area or shower for at least two (2) hours. Store this product out of direct sunlight at 40F-90F.

Warnings and Indications

Keep out of eyes and sensitive membranes; this formula may contain a lower pH than normal topical preparations and if you have sensitive skin, do a patch test on your arm for 2 to 4 hours. Do not use this formula if you are pregnant or on children under 12 years of age. Avoid contact with eyes and mucous membranes. If you do get the product in your eyes, rinse thoroughly with water. Do not swallow or use internally.

Ingredients

Structured Water, Cetearyl Alcohol, Dicetyl Phosphate, Shea Butter, Dimethyl Isosorbide, Caprylic/Capric Triglyceride, Ammonium Sulfate, Ceteth-10 Phosphate, Zinc Sulfate, Cetyl Alcohol, Sodium Hyaluronate, Farnesol, Copper Sulfate, Phenyl Dimethicone, Citric Acid, Sodium Hydroxide, Silver Citrate. Base Ingredients: Asea Liquid and Manuka Honey. All ingredients are classified as Generally Regarded as Safe (“GRAS”).

Area of Application

The area of application can be different for each disease that is being treated. A general application to the location or region of the infection, non-normal cells, or cancer is applied as described in the directions. Additionally lymph node areas that serve the diseased area should also receive applications of the STRUCTURED ATOMIC REDOX SPRAY. This will help treat the surrounding area and help the immune system remove infection and non-normal cells that may have possibly migrated to the lymph system.

Complementary Treatments

Mitigation includes the prevention of diseases, and includes the use of the above methods of administering doses of the bioavailable minerals with other supplements such as vitamins and botanicals to provide a healthy body. It is important to understand that the bioavailable minerals can act independently, but for the best results in the most difficult cases include the use of proper detoxification, nutrition and Whole Plant Based Superfoods for support in the mitigation effort. For example, ‘Doc of Detox’ Daily Cleansing Tea, Structured and Hydrogen-Enriched Water, Curcumin-Cayenne 5000 Plus, FibroClear Systemic Enzymes, Vitamin D, Iodine and Zija® SmartMix. A consultation with Dr. Wolfe is advisable. Other supportive therapies are CanSave Essential Oil, Infrared Sauna, Core Twisting, Rebounding and Sonic Vibration. If scabbing occurs, use Structured Moringa Oil, RENU 28 and Asea Liquid Spray.

During treatment with the STRUCTURED ATOMIC REDOX SPRAY, it is important to also build the immune system. Treatments with radiation and chemotherapy may adversely impact the immune system, the only real defense that the body has against cancer. The treatments do kill cancer, but the fine line between the elimination of the cancer and destruction of the immune system becomes critical, especially for individuals whose immune systems have been challenged to a large extent before. The highly bioavailable minerals of this formula maintain and boost the immune system. However, other immune reinforcements by Dr. Wolfe should be use with this protocol.

Minerals are also important in normal physiology, including digestion, brain function, and physical exertion, and performance of the minerals is dependent on the synergistic relationship with vitamins and botanicals. Vitamins act in a synergistic fashion and are not absolutely necessary, but are used in a support mode. An integrated system of bioavailable minerals, vitamins, botanicals, and amino acids contribute to the total health of an individual along with exercise, rest, etc.

Elemental zinc accumulates in different portions of the body and is used on as needed basis by different bodily regions for general health and maintenance of the body. Additionally, zinc cations are utilized by the cells of the body to combat specific diseases.

Urea or carBIMide is an organic compound with the chemical formula CO(NH2)2, Urea serves an important role in the metabolism of nitrogen-containing compounds by humans and animals. For example, urea breaks down the hydrophobic bonds of cancer cells when injected into and/or around cancers. The watery structure surrounding the cancer breaks and the cancer cells are unable to feed, and the cells become unprotected and exposed to attack by the body’s immune system. The immune system then attacks the cancer cells. Urea also forms mineral complex bonds much like the ammonia that aid in increasing the bioavailability of the minerals. The addition of the urea in STRUCTURED ATOMIC REDOX SPRAY provides for a two-prong attack, and is also a factor in transporting the cations as mineral complex bonds throughout the system.

Frequently Asked Questions

Does the product provide a permanent cure for any medical condition?

The manufacturer does not believe nor does it claim that this product is a permanent cure to any medical condition or disease. The treatment is not considered a permanent “cure” for any disease as it is possible that the removal of existing cellular tumors or other non-productive cells does not preclude the possibility of a future return of new mutated cells or tumors. Therefore, it is possible and even probable that re-treatments may be indicated.

Non-clinical trials have indicated that the product impacts several types of viral, bacterial and/or non-typical cell related conditions. However, these diseases may return and the manufacturer recommends a continuing “maintenance program” of treatment by applying the formula twice per day to various parts of the body.

What kinds of reactions might I expect?

Reactions are expected and indicate that the treatment is working. See above for a list of possible expected reactions. These reactions indicate that your body is expelling the dead disease cells. Treatment should not be stopped until after these effects stop. If you are taking prescription drugs, read the information which accompanied those drugs to ensure that there are no contraindications of the ingredients, listed below, to those drugs; if in doubt, ask your doctor or pharmacologist.

Is there any pain or discomfort involved with the use of this formula?

While many users experience no discomfort, the risk of discomfort or moderate pain due to the use of the formula is possible, depending on the severity of the affliction of mutated cells present in the skin or body. A few subjects have experienced extreme pain; however there is limited experience with all types of diseases and severe pain may only be typical with certain diseases. Users have observed that the disease cells are typically killed and expelled by the body, either via the skin, urine, or feces. Subjects have experienced ulcerations and moderate to severe pain where tumors have come through the skin to be expelled after tumor cells were killed by the treatment. In most cases, this left no noticeable scars.

Should I discuss the STRUCTURED ATOMIC REDOX SPRAY Treatment with my doctor?

Yes, you should discuss this with your doctor before beginning the treatment and throughout the treatment period. If you have a reaction, which is not on the list above of expected reactions, talk to your doctor. If you experience pain during treatment, your doctor may be able to help you manage the pain. This information is not intended to replace a one-on-one relationship with a qualified healthcare professional and is not intended as medical advice. If any instructions which you receive from this paper or website conflict with those from your physician, your physician’s instructions should always be followed.

Can I overdose or over use the formula?

No clinical trials have been performed yet with this treatment. The manufacturer has conducted several years of non-clinical trials with the formula. No subjects reported any adverse effects from liberal and/or long-term use of the formula. This does not preclude the possibility of side effects from the prolonged use of extraordinary amounts of the formula and more research is required to make a final determination. Blood tests on one patient who used large doses of the treatment did not show elevated mineral levels. As with any experimental treatment, dosing levels are uncertain and risk of overdosing cannot be eliminated. Formal dosage studies have not yet taken place.

How does the formula get to internal parts of my body?

The ionic minerals are highly bioavailable and can penetrate the skin. Users have reported that the formula is systemic (affecting the region where applied and potentially the entire body). Systemic therapies employ carrier agents, which travel through the body’s fluids and can affect cells throughout the body.

Is the product approved as a medicine by any government agencies?

STRUCTURED ATOMIC REDOX SPRAY is still in the experimental or pre-clinical stage. The manufacturer has not applied for approval as a drug in any country. Thus those distributing the product are prohibited from claiming that it treats or cures any disease and no such claims may be made on the label.

The risk of sickness or serious illness due to the use of this formula is considered minimal by the manufacturer, because all ingredients are considered Generally Regarded as Safe (“GRAS”) under United States 40 CFR 180.1001 entitled the “Exemption from the Requirements of a Tolerance.” The key mineral components in the formulation are considered nutritional elements for plants and animals. There have been no adverse effects reported by any of the over 100 of users during over eight years of non-clinical trials.

The concentrations of each ingredient in the STRUCTURED ATOMIC REDOX SPRAY are below the maximum permissible levels established by the European Union for cosmetics. Thus is it considered safe for application to the skin? The product has successfully passed formal skin irritation and microbial testing. Some of the ingredients are concentrated minerals that are readily expelled from the body when assimilated in excess of the normal daily nutritional requirements. More research is required to develop a complete understanding of all of the possible benefits and consequences of the use of this formula.

What is the difference between your formula and other mineral compounds that are on the market?

This formula contains a patent-pending technology, which makes its key ingredients much more bioavailable than others. The manufacturer believes that this will deliver minerals directly into non-typical cells, which adversely impact the health of humans, other animals, and plants. These minerals are pharmaceutical-grade, balanced, ionic minerals, which have been combined with a unique delivery technology “Mineral Complex System”.

Should I refrigerate the container?

Store this product out of direct sunlight at 60O Fahrenheit – 80 O Fahrenheit or 15.5 O Celsius – 26.7 O Celsius. Do not refrigerate or freeze.

Will the formula stain or discolor clothing?

Possibly, there have been instances where users reported discolored clothing and/or cloth.

How long do I wait, after applying the formula, before I can shower or bathe?

For maximum absorption, do not shower or bathe for at least two hours after applying the treatment.

Should I take nutritional supplements while using this product?

Nutritional supplementation supports the healing; a consultation with Dr. Wolfe is advisable. Call 1 855 900 4544 to book a consultation.

There is no such thing as a silver bullet. A personalized consultation with Dr. Darrell Wolfe Ac.PhD. to ensure the success of this program is important when it comes to the proper nutritional support and detoxification for healing to take place. It is also important for all patients to follow up with Dr. Wolfe every few days; there are no silly symptoms or silly questions. Call 1 855 900 4544 to book your consultation by phone, Skype or in person.

Follow us on Facebook: www.facebook.com/drdarrellwolfe

References

Footnotes

1Cancer’s Molecular Sweet Tooth and the Warburg Effect

http://cancerres.aacrjournals.org/content/66/18/8927.long

Kim and Dang, 10.1158/0008-5472.CAN-06-1501 Cancer Res September 15, 2006 66; 8927

2Mitigation of Animal and Plant Diseases Using Bioavailable Minerals

http://www.cancer-cell-treatment.com/images/PDF-Files/CCFormula-International-Patent-World-Filing-WO2009058857A1.pdf

W. Kennedy, US patent application, publication number US20120171130 A1, application number US 11/932,260. Publication date: Jul 5, 2012, Filing date: Oct 31, 2007

3Copper/Zinc Superoxide Dismutase (SOD) Formulation for the Treatment of Traumas Including Amyotropic Lateral Sclerosis

http://www.cancer-cell-treatment.com/images/PDF-Files/CCFormula-ALS-Patent.pdf

W. Kennedy, US patent application, Filing date Apr 3, 2014, to be published

4Certified Human Safety Report on the CC Formula

http://www.cancer-cell-treatment.com/en/testimonials/certified-human-safety-report-on-the-cc-formula

Cencon Centro de Control Microbiology Laboratorio, Puebla, Col. Roma, D.F., Mexico

For Further Reading

Activation of superoxide dismutases: Putting the metal to the pedal

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1633718/

Department of Environmental Health Sciences, Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD 21205, USA and Department of Chemistry and Department of Biochemistry, Molecular Biology and Cell Biology, Northwestern University, Evanston, IL 60208-3113, USA

Aerobic vs. Anaerobic Respiration

http://www.diffen.com/difference/Aerobic_Respiration_vs_Anaerobic_Respiration

Article presented by Nikhilesh Jasuja, Pooja Sehgal. Diffen.com. Diffen LLC, USA, Web. 21 Jun 2014.

Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase.

http://www.ncbi.nlm.nih.gov/pubmed/8351519/

Department of Neurology, Northwestern University Medical School, Chicago, IL 60611, USA

Anaerobic respiration using a complete oxidative TCA cycle drives multicellular swarming in Proteus mirabilis

http://www.ncbi.nlm.nih.gov/pubmed/23111869

Department of Microbiology and Immunology, University of Michigan Medical School, West Medical Center Drive, Ann Arbor, MI, USA.

Antimicrobial effects of copper(II) bis(thiosemicarbazonato) complexes provide new insight into their biochemical mode of action

http://www.ncbi.nlm.nih.gov/pubmed/24435165

School of Chemistry and Molecular Biosciences and Australian Centre for Infectious Diseases Research, University of Queensland, Bdg 76 Cooper Road, St Lucia, QLD 4127, Australia

Antioxidant Effects of Sulfur-Containing Amino Acids

http://ymj.or.kr/Synapse/Data/PDFData/0069YMJ/ymj-45-776.pdf

Dr. Gulizar Atmaca, Department of Physiology, Trakya University, Medical Facility, 22030 Edirne, Turkey

Antioxidant Enzymes and Human Diseases

http://www.biblioteca.uma.es/bbldoc/articulos/16689835.pdf

Department of Molecular Biology and Biochemistry, Faculty of Sciences, University of Ma´ laga, Campus de Teatinos, s/n 29071 Malaga, Spain

Cancer and Inflammation: Promise for Biological Therapy

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2941912/

Michael T. Lotze, MD Professor of Surgery University of Pittsburgh Cancer Institute 5117 Centre Avenue, Suite G.27a Pittsburgh, PA 15213, USA

Cellular and Infection Microbiology Mechanisms of copper homeostasis in bacteria

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817396/

José M. Argüello, Department of Chemistry and Biochemistry, Worcester Polytechnic Institute, 100 Institute Road, Worcester, MA 01609, USA

Cellular Biology Overview of the Krebs Cycle or referred to as the Citric Acid Cycle

https://www.khanacademy.org/science/biology/cellular-respiration/v/krebs—citric-acid-cycle

Biology and Cellular respiration Khan Academy PO Box 1630, Mountain View, CA 94042

Copper as a key regulator of cell signaling pathways.

http://www.ncbi.nlm.nih.gov/pubmed/24849048

Department of Pathology, the University of Melbourne, Parkville, Victoria 3010, Australia.

Correlation between superoxide dismutase 1 and 2 polymorphisms and susceptibility to oral squamous cell carcinoma.

http://www.ncbi.nlm.nih.gov/pubmed/24348785

State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan, P.R. China; Department of Head and Neck Oncology Surgery

Gene disruption using zinc finger nuclease technology

http://www.ncbi.nlm.nih.gov/pubmed/24839030

Surgical Sciences Domain, Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho, Campus de Gualtar, Braga, 4710-057, Portugal

Genetics Reference SOD1 Gene

http://ghr.nlm.nih.gov/gene/SOD

U.S. National Library of Medicine, 8600 Rockville Pike, Bethesda, MD 20894

Glucosamine and chondroitin sulfate as therapeutic agents for knee and hip osteoarthritis.

http://www.ncbi.nlm.nih.gov/pubmed/17658908

WHO Collaborating Center for Public Health Aspect of Osteoarticular Disorders, University of Liège, Liege, Belgium.

How does the metabolism of tumor cells differ from that of normal cells?

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3828821/

Instituto de Bioquímica Médica, Centro de Ciências da Saúde, Universidade Federal do Rio de Janeiro, Cidade Universitária, Av, Carlos Chagas Filho 373, Ilha do Fundão CEP 21941-590, Rio de Janeiro, Brazil

Metals in Medicine: Targets, Diagnostics, and Therapeutics

http://ods.od.nih.gov/attachments/Meeting%20report.doc

Report prepared by Peter C. Preusch, Ph.D., PPBC Division, NIGMS, NIH.

SOD1 (copper zinc superoxide dismutase 1) and ALS

http://www.alsa.org/research/about-als-research/sod1.html

The ALS Association, 1275 K Street NW Suite 250, Washington, DC 20005, USA

Red blood cell as a carrier of Superoxide Dismutase

http://www.ncbi.nlm.nih.gov/pubmed/11540441

Institute of Space Medico-Engineering, Beijing, China.

Sulfur in Human Nutrition & Applications in Medicine

http://www.thorne.com/altmedrev/.fulltext/7/1/22.pdf

Dr. Stephen Parcell, ND. Alternative Medicine Review Volume 7, Number 1, 2002 Thorne Research, Inc.

Superoxide dismutase as a target for the selective killing of cancer cells.

http://www.ncbi.nlm.nih.gov/pubmed/11014196

Department of Experimental Therapeutics, the University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA

The Application of CarBIMide (Urea) Therapy in Wound Healing

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1391326/

Hall G. Holder, M.D. and Eaton M. MacKay, M.D. San Diego, CA., USA

The bio-energetic theory of carcinogenesis

http://www.ncbi.nlm.nih.gov/pubmed/22809841

University of Puerto Rico, Medical Sciences Campus, School of Public Health and Pharmacy, RECNAC2 Program, San Juan, PR 00936-5067, USA

The Energy Derived from Glucose Oxidation and Glucose Metabolism of Cancer: The Warburg Effect

http://themedicalbiochemistrypage.org/glycolysis.php

Michael W King, PhD

The families of zinc (SLC30 and SLC39) and copper (SLC31) transporters

http://www.ncbi.nlm.nih.gov/pubmed/24745988

Institute for Muscle Biology & Growth, Leibniz Institute for Farm Animal Biology, Dummerstorf, Germany.

The Fate of Tumor Cells: Survival/Autophagy, Apoptosis, or Necrosis

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2941912/

Department of Surgery, University of Pittsburgh Cancer Institute, Pittsburgh, PA

Contact for Correspondence: Michael T. Lotze, MD Professor of Surgery University of Pittsburgh Cancer Institute 5117 Centre Avenue, Suite G.27a Pittsburgh, USA.

The Roles of Oxidative Stress and Antioxidant Treatment in Experimental Diabetic Neuropathy

http://diabetes.diabetesjournals.org/content/46/Supplement_2/S38.full.pdf

Low et. al., 10.2337/diab.46.2.S38 Diabetes September 1997 vol. 46 no. Supplement 2 S38-S42

The structural biochemistry of the superoxide dismutases

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098211/

J.A. Tainer, Department of Molecular Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.

Two-Photon Fluorescent Probes for Intracellular Free Zinc Ions in Living Tissue

http://onlinelibrary.wiley.com/doi/10.1002/ange.200800929/pdf

National Creative Research Initiative Center for Neurodynamics and Department of Physics, Korea University, Korea

Understanding Antimicrobial (Drug) Resistance and Methicillin-Resistant Staphylococcus aureus (MRSA)

http://www.niaid.nih.gov/topics/antimicrobialResistance/Understanding/Pages/default.aspx

National Institute of Allergy and Infectious Diseases – U.S. Department of Health and Human Services and National Institutes of Health

Universal Screening for Methicillin-Resistant Staphylococcus aureus at Hospital Admission and Nosocomial Infection in Surgical Patients

http://jama.jamanetwork.com/article.aspx?articleid=181604

Infection Control Program (Drs Harbarth, Sax, and Pittet and Mss Fankhauser and Bandiera-Clerc), Microbiology Laboratory (Dr Schrenzel and Mr Renzi), Department of Surgery (Drs Christenson and Gervaz), and Hospital Pharmacy (Dr Vernaz), University of Geneva Hospitals and Medical School, Geneva, Switzerland.

Zinc biochemistry: from a single zinc enzyme to a key element of life

http://www.ncbi.nlm.nih.gov/pubmed/23319127

King’s College London, Metal Metabolism Group, Division of Diabetes and Nutritional Sciences, School of Medicine, London, United Kingdom

Zinc Absorption from Zinc Oxide, Zinc Sulfate, Zinc Oxide + EDTA, or Sodium-Zinc EDTA Does Not Differ When Added as Fortificants to Maize Tortillas

http://jn.nutrition.org/content/135/5/1102.long

Centro de Investigación en Nutrición y Salud, Instituto Nacional de Salud Pública, Cuernavaca, Morelos, México;

U.S. Department of Agriculture Western Human Nutrition Research Center, University of California Davis, Davis, CA; and Children’s Hospital Research Center at Oakland, Oakland, CA

Zinc biochemistry: from a single zinc enzyme to a key element of life

http://www.ncbi.nlm.nih.gov/pubmed/23319127

King’s College London, Metal Metabolism Group, Division of Diabetes and Nutritional Sciences, School of Medicine, London, United Kingdom.

There is no such thing as a silver bullet. A personalized consultation with Dr. Darrell Wolfe Ac.PhD. to ensure the success of this program is important when it comes to the proper nutritional support and detoxification for healing to take place. It is also important for all patients to follow up with Dr. Wolfe every few days; there are no silly symptoms or silly questions. Call 1 855 900 4544 to book your consultation by phone, Skype or in person.

Follow us on Facebook: www.facebook.com/drdarrellwolfe

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