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== Side effects ==
== Side effects ==
Hydrazine sulfate is toxic and [[carcinogen]]ic,<ref name="EPA">{{citation | publisher = [[U.S. Environmental Protection Agency]] | title = Hydrazine Hazard Summary | date = January 2000 | url = http://www.epa.gov/ttn/atw/hlthef/hydrazin.html}}.</ref><ref name="EHC">Section 9.2.1, {{citation | publisher = [[International Programme on Chemical Safety]] | url = http://www.inchem.org/documents/ehc/ehc/ehc68.htm | title = Environmental Health Criteria for Hydrazine | year = 1987}}.</ref> as are many mainstream cancer treatments. Nevertheless, the side-effects reported in the various clinical trials are remarkably mild:<ref name="Black">{{citation | author = Black, M.; Hussain, H. | year = 2000 | title = Hydrazine, Cancer, the Internet, Isoniazid, and the Liver | url = http://www.annals.org/cgi/reprint/133/11/911.pdf | journal = Annals of Internal Medicine | volume = 133 | issue = 11 | pages = 911–13 | pmid = 11103062}}.</ref> minor nausea and vomiting, dizziness and excitement, [[Neuritis|polyneuritis]] (inflammation of the nerves) and difficulties in fine muscle control (such as writing). However, more serious, even fatal side-effects have been reported in rare cases: one patient who developed fatal liver and kidney failure,<ref name="Hainer">{{citation | author = Hainer, M. I. ''et al.'' | title = Fatal hepatorenal failure associated with hydrazine sulfate | url = http://www.annals.org/cgi/reprint/133/11/877.pdf | journal = Annals of Internal Medicine | volume = 133 | pages = 877–80 | year = 2000 | pmid = 11103057}}.</ref> another with serious symptoms of neurotoxicity.<ref>{{citation | author = Nagappan, R.; Riddell, T. | title = Pyridoxine therapy in a patient with severe hydrazine sulfate toxicity | journal = Critical Care in Medicine | volume = 28 | pages = 2116–18 | year = 2000 | pmid = 10890675}}.</ref> In the report of the single case of fatal liver and kidney failure, however, there was no documentation of the substance taken ("We could not obtain samples of the product ingested"), nor was there a blood test done to verify that the patient had ever taken hydrazine sulfate.<ref name="Hainer"> These serious side effects are consistent with other reports of hydrazine toxicity,<ref name="EPA" /><ref name="EHC" /> and with toxic reactions to the [[antibiotic]] [[isoniazid]], which is though to be metabolized to hydrazine in the body.<ref name="Black" />
Hydrazine sulfate is toxic and [[carcinogen]]ic,<ref name="EPA">{{citation | publisher = [[U.S. Environmental Protection Agency]] | title = Hydrazine Hazard Summary | date = January 2000 | url = http://www.epa.gov/ttn/atw/hlthef/hydrazin.html}}.</ref><ref name="EHC">Section 9.2.1, {{citation | publisher = [[International Programme on Chemical Safety]] | url = http://www.inchem.org/documents/ehc/ehc/ehc68.htm | title = Environmental Health Criteria for Hydrazine | year = 1987}}.</ref> as are many mainstream cancer treatments. Nevertheless, the side-effects reported in the various clinical trials are remarkably mild:<ref name="Black">{{citation | author = Black, M.; Hussain, H. | year = 2000 | title = Hydrazine, Cancer, the Internet, Isoniazid, and the Liver | url = http://www.annals.org/cgi/reprint/133/11/911.pdf | journal = Annals of Internal Medicine | volume = 133 | issue = 11 | pages = 911–13 | pmid = 11103062}}.</ref> minor nausea and vomiting, dizziness and excitement, [[Neuritis|polyneuritis]] (inflammation of the nerves) and difficulties in fine muscle control (such as writing). However, more serious, even fatal side-effects have been reported in rare cases: one patient who developed fatal liver and kidney failure,<ref name="Hainer">{{citation | author = Hainer, M. I. ''et al.'' | title = Fatal hepatorenal failure associated with hydrazine sulfate | url = http://www.annals.org/cgi/reprint/133/11/877.pdf | journal = Annals of Internal Medicine | volume = 133 | pages = 877–80 | year = 2000 | pmid = 11103057}}.</ref> another with serious symptoms of neurotoxicity.<ref>{{citation | author = Nagappan, R.; Riddell, T. | title = Pyridoxine therapy in a patient with severe hydrazine sulfate toxicity | journal = Critical Care in Medicine | volume = 28 | pages = 2116–18 | year = 2000 | pmid = 10890675}}.</ref> In the report of the single case of fatal liver and kidney failure, however, there was no documentation of the substance taken ("We could not obtain samples of the product ingested"), nor was there a blood test done to verify that the patient had ever taken hydrazine sulfate.<ref name="Hainer"/> These serious side effects are consistent with other reports of hydrazine toxicity,<ref name="EPA" /><ref name="EHC" /> and with toxic reactions to the [[antibiotic]] [[isoniazid]], which is though to be metabolized to hydrazine in the body.<ref name="Black" />


Hydrazine sulfate is claimed to be a [[monoamine oxidase inhibitor]] (MAOI), and so to be incompatible with [[Ethanol|alcohol]], tranquilizers and sleeping pills ([[benzodiazepine]]s and [[barbiturate]]s), and other psycho-active drugs, with [[pethidine]] (meperidine, Demerol), and with foods containing significant amounts of the amino acid [[tyrosine]], such as most cheeses, raisins, avocados, processed and cured fish and meats, fermented products, and others.
Hydrazine sulfate is claimed to be a [[monoamine oxidase inhibitor]] (MAOI), and so to be incompatible with [[Ethanol|alcohol]], tranquilizers and sleeping pills ([[benzodiazepine]]s and [[barbiturate]]s), and other psycho-active drugs, with [[pethidine]] (meperidine, Demerol), and with foods containing significant amounts of the amino acid [[tyrosine]], such as most cheeses, raisins, avocados, processed and cured fish and meats, fermented products, and others.

Revision as of 06:35, 2 June 2009

Hydrazine sulfate
Names
IUPAC name
Hydrazinium hydrogen sulfate
Other names
Hydrazine sulphate
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.030.088 Edit this at Wikidata
EC Number
  • 233-110-4
  • NN.OS(=O)(=O)O
Properties
H6N2O4S
Molar mass 130.12 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Hydrazine sulfate is the salt of hydrazine and sulfuric acid. Known by the trade name Sehydrin, it is a chemical compound that has been used as an alternative medical treatment for the loss of appetite (anorexia) and weight loss (cachexia) which is often associated with cancer.[1][2][3][4] It has never been approved as a mainstream drug, although it is approved for use in clinical trials by the U.S. Food and Drug Administration (FDA) and is marketed in the United States as a dietary supplement.[5] It is also used in palliative care for terminal cancer patients in Russia and other countries of the former Soviet Union.[6]

The use of hydrazine sulfate as a cancer remedy was popularized by the magazine Penthouse in the mid 1990s, when Kathy Keeton, wife and business partner of the magazine's publisher Bob Guccione, used it to treat her metastatic breast cancer.[7] Keeton and other supporters of hydrazine sulfate treatment accused the U.S. National Cancer Institute (NCI) of deliberately hiding the beneficial effects of the compound, and threatened to launch a class action law suit.[8][9] The NCI denies the claims,[10] and says that there is little to no evidence that hydrazine sulfate has any beneficial effects whatsoever.[5] The position of the NCI was supported by an inquiry held by the General Accounting Office.[11]

A review of the clinical research concluded that hydrazine sulfate has never been shown to act as an anticancer agent; patients do not experience remissions or regressions of their cancer; and patients do not live longer than non-treated patients.[5][12][13]

Chemistry

Hydrazine sulfate is a commercially available form of hydrazine. It is a white solid, prepared by reacting an aqueous solution of hydrazine with sulfuric acid:[14] it is soluble in water, and the original hydrazine can be reformed by simply adjusting the pH. It has a number of laboratory uses in analytical chemistry and organic synthesis.

It may be preferred over pure hydrazine or hydrazine hydrate for laboratory use because it is easily purified if necessary (by recrystallization from water),[14] and it is less volatile and less susceptible to atmospheric oxidation on storage. These same properties make it the preferred form of hydrazine for dietary supplements and pharmaceutical trials. It is relatively inexpensive, with 100 grams of analytical grade hydrazine sulfate costing about USD20, and 100 tablets or capsules (60 milligrams hydrazine sulfate) costing USD20–60.

Background

Hydrazine sulfate was specifically developed as a result of a theoretical paper by Joseph Gold, M.D., indicating cancer glycolysis and normal-body gluconeogenesis to constitute a systemic (whole-body) energy-losing cycle as the biochemical and thermodynamic cause of cancer cachexia and postulating the inhibition of gluconeogenesis at the enzymic site of PEP CK to be an effective treatment for cancer cachexia.[15] It was also postulated that if tumor energy gain (glycolysis) and host-energy loss (gluconeogenesis) were functionally interrelated, inhibition of gluconeogenesis at PEP CK could result in actual tumor regression in addition to reversal or arrest of cancer cachexia.[16] Hydrazine sulfate is thought to act as a gluconeogenic blocking agent irreversibly inhibiting the enzyme phosphoenolpyruvate carboxykinase (PEP CK).

Investigational

Early clinical trials indicated efficacy and safety in about 50 percent of all patients. Efficacy and safety were expressed in terms of appetite and weight improvements, performance status increase, decrease or disappearance of pain and weakness, tumor stabilization and regression and increased survival time. These multicentric Phase II and randomized, double-blind Phase III clinical trials were carried out at the Petrov Research Institute of Oncology in St. Petersburg over a period of 17 years,[6][12] and at the Harbor-UCLA Medical Center in California over period of 10 years, respectively. Later trials failed to find any improvement in survival time or weight gain.

Side effects

Hydrazine sulfate is toxic and carcinogenic,[17][18] as are many mainstream cancer treatments. Nevertheless, the side-effects reported in the various clinical trials are remarkably mild:[19] minor nausea and vomiting, dizziness and excitement, polyneuritis (inflammation of the nerves) and difficulties in fine muscle control (such as writing). However, more serious, even fatal side-effects have been reported in rare cases: one patient who developed fatal liver and kidney failure,[20] another with serious symptoms of neurotoxicity.[21] In the report of the single case of fatal liver and kidney failure, however, there was no documentation of the substance taken ("We could not obtain samples of the product ingested"), nor was there a blood test done to verify that the patient had ever taken hydrazine sulfate.[20] These serious side effects are consistent with other reports of hydrazine toxicity,[17][18] and with toxic reactions to the antibiotic isoniazid, which is though to be metabolized to hydrazine in the body.[19]

Hydrazine sulfate is claimed to be a monoamine oxidase inhibitor (MAOI), and so to be incompatible with alcohol, tranquilizers and sleeping pills (benzodiazepines and barbiturates), and other psycho-active drugs, with pethidine (meperidine, Demerol), and with foods containing significant amounts of the amino acid tyrosine, such as most cheeses, raisins, avocados, processed and cured fish and meats, fermented products, and others.

References

  1. ^ Chlebowski, R. T.; Bulcavage, L.; Grosvenor, M.; et al. (1987), "Hydrazine Sulfate in Cancer Patients With Weight Loss. A Placebo-Controlled Clinical Experience", Cancer, 59 (3): 406–10, PMID 3791153 {{citation}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link).
  2. ^ Brauer, M.; Inculet, R. I.; Bratnager, G.; Marsh, G. D.; Driedger, A. A.; Thompson, R. T. (1994), "Insulin Protects against Hepatic Bioenergetic Deterioration by Cancer Cachexia. An in-Vivo 31P Magnetic Resonance Study", Cancer Research, 54 (24): 6383–86, PMID 7987832 {{citation}}: Cite has empty unknown parameter: |1= (help)CS1 maint: multiple names: authors list (link).
  3. ^ Chlebowski, R. T.; Bulcavage, L.; Grosvenor, M.; Oktay, E.; Block, J. B.; Chlebowski, J. S.; Ali, I.; Elashoff, R. (1990), "Hydrazine Sulfate Influence on Nutritional Status and Survival in Non-Small-Cell Lung Cancer", Journal of Clinical Oncology (8): 9–15, PMID 1688616{{citation}}: CS1 maint: multiple names: authors list (link).
  4. ^ Gold, J. (1999), "Long term complete response in patient with advanced, localized NSCLC with hydrazine sulfate, radiation and Carboplatin, refractory to combination chemotherapy", Proceedings of the American Association for Cancer Research (40): 642. Abstract.
  5. ^ a b c Questions and answers about hydrazine sulfate, National Cancer Institute, March 12, 2009
  6. ^ a b Filov, V. A.; Gershanovich, M. L.; Danova, L. A.; Ivin, B. A. (1995), "Experience of the Treatment with Sehydrin (Hydrazine Sulfate, HS) in the Advanced Cancer Patients", Investigational New Drugs, 13 (1): 89–97, PMID 7499115{{citation}}: CS1 maint: multiple names: authors list (link).
  7. ^ London, William M. (July 23, 2006), Penthouse's promotion of hydrazine sulfate
  8. ^ Goldberg, Burton (June 12, 2000), Holding the National Cancer Institute Accountable for Cancer Deaths
  9. ^ Goldberg, Burton; Trivieri, Larry; Anderson, John W., ed. (2002), Alternative medicine: the definitive guide (2nd ed.), Celestial Arts, pp. 50–51, 598, ISBN 1587611414{{citation}}: CS1 maint: multiple names: editors list (link).
  10. ^ Jenks, S. (1993), "Hydrazine Sulfate Ad Is "Offensive"", Journal of the National Cancer Institute, 85 (7): 528–29, doi:10.1093/jnci/85.7.528, PMID 8455198.
  11. ^ Nadel, M. V. (September 1995), "Cancer Drug Research—Contrary to Allegations, Hydrazine Sulfate Studies Were Not Flawed", Report to the Chairman and Ranking Minority Member, Human Resources and Intergovernmental Relations Subcommittee, House Committee on Government Reform and Oversight, Washington, D.C.: General Accounting Office, Document No. HEHS-95-141.
  12. ^ a b Kaegi, Elizabeth (1998), "Unconventional therapies for cancer: 4. Hydrazine sulfate. Task Force on Alternative Therapies of the Canadian Breast Cancer Research Initiative", Canadian Medical Association Journal, 158 (10): 1327–30, PMID 9614826.
  13. ^ Green, Saul (1997), "Hydrazine sulfate: is it an anticancer agent?", Scientific Review of Alternative Medicine, 1: 19–21
  14. ^ a b Adams, Roger; Brown, B. K. (1922). "Hydrazine sulfate". Organic Syntheses. 2: 37{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 1, p. 309.
  15. ^ Gold, J. (1968), "Proposed Treatment of Cancer by Inhibition of Gluconeogenesis", Oncology, 22 (2): 185–207, PMID 5688432.
  16. ^ Gold, J. (1974), "Cancer Cachexia and Gluconeogenesis", Annals of the New York Academy of Sciences, 230: 103–10, PMID 4522864.
  17. ^ a b Hydrazine Hazard Summary, U.S. Environmental Protection Agency, January 2000.
  18. ^ a b Section 9.2.1, Environmental Health Criteria for Hydrazine, International Programme on Chemical Safety, 1987.
  19. ^ a b Black, M.; Hussain, H. (2000), "Hydrazine, Cancer, the Internet, Isoniazid, and the Liver" (PDF), Annals of Internal Medicine, 133 (11): 911–13, PMID 11103062{{citation}}: CS1 maint: multiple names: authors list (link).
  20. ^ a b Hainer, M. I.; et al. (2000), "Fatal hepatorenal failure associated with hydrazine sulfate" (PDF), Annals of Internal Medicine, 133: 877–80, PMID 11103057 {{citation}}: Explicit use of et al. in: |author= (help).
  21. ^ Nagappan, R.; Riddell, T. (2000), "Pyridoxine therapy in a patient with severe hydrazine sulfate toxicity", Critical Care in Medicine, 28: 2116–18, PMID 10890675{{citation}}: CS1 maint: multiple names: authors list (link).
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