High Dose Vitamin C Therapy

High Dose Vitamin C Intravenous Therapy

High dose Vitamin C IV therapy challenges cancer cells at a metabolic level.

High Dose Vitamin C Intravenous Therapy

IV High Dose Vitamin C IV Therapy

High dose vitamin C IV therapy challenges cancer cells at a metabolic level while at the same time does no damage whatsoever to normal functioning health cells. Also, to clear up any confusion on whether or not there is any scientific research to prove this there are over ninety-one thousand publications on PubMed regarding the effect it has on cancer.

Cancer cells, unlike healthy human cells, are both flawed and primeval.

Cancer cells are lacking in many enzymes that normal healthy cells have in copious amounts and also, they are not able to use oxygen to metabolize glucose into energy production. One example of a particular enzyme that transforms oxygen and water into hydrogen peroxide is catalase.

Hydrogen peroxide production in and outside the cells results from high doses of vitamin C (ascorbic acid). Hydrogen peroxide is used by normal cells for specific metabolic needs and whatever is not needed is converted in oxygen and water which is healthy stuff.

Here’s the good news, cancer cells have very small amounts of catalase, so they aren’t able to convert the hydrogen peroxide into water and oxygen and as a result, they are oxidized and killed off. So, what does this tell us, well, it tells us that ascorbic acid or high dose vitamin C IV therapy is very good for healthy cells and very bad for the cancer cells.

The National Institute of Health (NIH), the National Cancer Institute (NCI) and the Food and Drug Administration (FDA)  have finally confirmed the research findings that Linus Pauling, Ph.D., Hugh Riordan, MD and many other scientists and physicians over the past few decades have conducted regarding the therapeutic utility of treating cancer with vitamin C.

The NIH study confirms in vitro, the hypotheses described by Riordan et al in “Intravenous Ascorbate as a Chemotherapeutic and Biologic Response Modifying Agent”:

  1. Tumor cells are more susceptible to the effects of high-dose, ascorbate-induced peroxidation products because of a relative catalase deficiency.
  2. Concentrations of ascorbate high enough to kill tumor cells can be achieved in humans.

Neil H. Riordan Ph.D. commented on the study, “It is gratifying to have our research on vitamin C and cancer confirmed by scientists at the prestigious National Institutes of Health.”

For even more information about Vitamin C and Cancer, click here to go to our blog page Treating Cancer with Vitamin C https://www.anoasisofhealing.com/treating-cancer-with-vitamin-c/ 

High Dose Vitamin C IV Therapy

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Want to know more about Vitamin C and Cancer?  Click the links below to go to our many informative blogs.

Listed below are several, peer-reviewed references regarding vitamin C therapy as it pertains to the treatment of cancer:

Pharmacologic ascorbic acid concentrations selectively kill cancer cells: Action as a pro-drug to deliver hydrogen peroxide to tissuesQi Chen *, Michael Graham Espey, Murali C. Krishna, James B. Mitchell, Christopher P. Corpe *, Garry R. Buettner, Emily Shacter, and Mark Levine * Reference Link

*Molecular and Clinical Nutrition Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892; Radiation Biology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892; Free Radical and Radiation Biology Program, University of Iowa, Iowa City, IA 52242-1101; and Laboratory of Biochemistry, Center for Drug Evaluation and Research, Food and Drug Administration, Bethesda, MD 20892 PNAS | September 20, 2005 | vol. 102 | no. 38 | 13604-13609

Orthomolecular Oncology Review: Ascorbic Acid and Cancer 25 Years LaterBy Michael J. González, Jorge R. Miranda-Massari, Edna M. Mora, Angelik Guzmán, Neil H. Riordan, Hugh D. Riordan, Joseph J. Casciari, James A. Jackson, and Angel Romá-Franco, from Integrative Cancer Therapies 4(1); 2005 pp.32-44

Intravenous Ascorbic Acid: Protocol for its Application and UseBy Hugh D. Riordan, Ronald E. Hunninghake, Neil H. Riordan, James A. Jackson, Xiao LongMeng, Paul Taylor, et al, from Puerto Rico Health Sciences Journal (2003) 22:3, 287-290

The Effect of Alternating Magnetic Field Exposure and Vitamin C on Cancer CellsBy N. Mikirova, J.A. Jackson, J.P. Casciari and H.D. Riordan, from Journal of Orthomolecular Medicine (2001) 3, 177-182

Cytotoxicity of Ascorbate, Lipoic Acid, and Other Antioxidants In Hollow Fibre In Vitro TumoursBy J.P. Casciari, N.H. Riordan, T.L. Schmidt, XL Meng, J.A. Jackson, and H.D. Riordan, from British Journal of Cancer (2001) 84:11, 1544-1550

Clinical and Experimental Experiences with Intravenous Vitamin C By N.H. Riordan, H.D. Riordan, J.A. Jackson, and J.P. Casciari, from Journal of Orthomolecular Medicine (2000) 15:4, 201-213

Different Fatty Acid Composition Between Normal and Malignant Cell LinesBy X.L. Meng, N.H. Riordan, H.D. Riordan, J.A. Jackson, et al, from BioMedicina, (1999) 2:4, 5-7

Rethinking Vitamin C and Cancer: An Update on Nutritional OncologyBy M.J. Gonzalez, E. Mora, N.H. Riordan, H.D. Riordan, and P. Mojica, from Cancer Prevention International (1998) 3, 215-224

Intravenous Ascorbate as a Chemotherapeutic and Biologic Response Modifying AgentBio-Communications Research Institute (1997)

Intravenous Vitamin C in a Terminal Cancer PatientBy N.H. Riordan, J.A. Jackson, and H.D. Riordan, from Journal of Orthomolecular Medicine (1996) 11, 80-82

High-Dose Intravenous Vitamin C and Long-Time Survival of a Patient with Cancer of Head of the PancreasBy J.A. Jackson, H.D. Riordan, R.E. Hunninghake and N.H. Riordan, from Journal of Orthomolecular Medicine (1995) 10, 87-88

Intravenous Ascorbate as a Tumor Cytotoxic Chemotherapeutic AgentBy N.H. Riordan, H.D. Riordan, X. Meng, Y. Li and J.A. Jackson, from Medical Hypotheses (1995) 44, 207-213

Case Study: High-Dose Intravenous Vitamin C in the Treatment of a Patient with Adenocarcinoma of the KidneyBy H.D. Riordan, J.A. Jackson and Mavis Schultz, from Journal of Orthomolecular Medicine (1990) 5:1, 5-7

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