Pharmaceutical composition for oral administration of chelating

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Radical -xh acid – or anhydride – acid halide or salt thereof...

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514566, A61K 31195

Patent

active

061143871

ABSTRACT:
A solid pharmaceutical composition for the oral administration of chelating agents to an individual consists essentially of: at least 100 milligrams of ethylenediaminetetraacetic acid (EDTA) or a molar equivalent amount of pharmaceutically acceptable salts or hydrated salts of EDTA, at least 75 milligrams of N-acetyl-L-cysteine, and an appropriate amount of at least one pharmaceutical formulating agent.

REFERENCES:
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patent: 5114974 (1992-05-01), Rubin
Schroeder, "A Practical Method For the Reduction of Plasma Cholesterol in Man", Journal of Chronic Diseases, 1956, vol. 4. No. 5, pp. 461-468.
Banner, W., et al, "Experimental Chelation Therapy in Chromium, Lead, and Boron Intoxication With N-Acetylcysteine and Other Compounds", Toxicology and Applied Pharmacology, 1986, vol. 83, pp. 142-147.
Peters, Henry, et al., "Turkish Epidemic Hexachlorobenzene Porphyria: A 30-Year Study", Annals of the New York Academy of Sciences, (Mechanisms of Chemical--Induced Porphyrinopathies), 1987, vol. 514, pp. 183-189.
Brumas, V., et al., "Can N-Acetyl-L-cysteine Affect Zinc Metabolism When Used as a Paractamol Antidote", Agents Actions, 1992, vol. 36, pp. 278-188.
Kelation PlusWeb Page, Jan. 27, 2000.
Vibrant Life Web Page, Jan. 19, 2000.

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