WO1983001196A1 - Mixture for human supply of selenium as a trace substance and the use thereof in solutions for storage of organs, in media for cell cultivation and in nutritive solutions for storage of blood components - Google Patents
Mixture for human supply of selenium as a trace substance and the use thereof in solutions for storage of organs, in media for cell cultivation and in nutritive solutions for storage of blood components Download PDFInfo
- Publication number
- WO1983001196A1 WO1983001196A1 PCT/SE1982/000304 SE8200304W WO8301196A1 WO 1983001196 A1 WO1983001196 A1 WO 1983001196A1 SE 8200304 W SE8200304 W SE 8200304W WO 8301196 A1 WO8301196 A1 WO 8301196A1
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- selenium
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N1/00—Preservation of bodies of humans or animals, or parts thereof
- A01N1/02—Preservation of living parts
- A01N1/0205—Chemical aspects
- A01N1/021—Preservation or perfusion media, liquids, solids or gases used in the preservation of cells, tissue, organs or bodily fluids
- A01N1/0226—Physiologically active agents, i.e. substances affecting physiological processes of cells and tissue to be preserved, e.g. anti-oxidants or nutrients
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N1/00—Preservation of bodies of humans or animals, or parts thereof
- A01N1/02—Preservation of living parts
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K33/00—Medicinal preparations containing inorganic active ingredients
- A61K33/04—Sulfur, selenium or tellurium; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
- C12N5/0018—Culture media for cell or tissue culture
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N2500/00—Specific components of cell culture medium
- C12N2500/05—Inorganic components
Definitions
- the invention concerns a composition designed to ingest the trace element selenium into human beings.
- trace elements i.e. elements which are absolutely vital to the human organism, albeit in minute amounts.
- trace elements i.e. elements which are absolutely vital to the human organism, albeit in minute amounts.
- many diseases and states of ill-health are a consequence of deficiencies of one or several of such trace elements.
- certain heavy metals such as cadmium
- acid such as through acid rains
- Animal tests have shown that cadmium-induced high blood-pressure conditions may be normalized by selenium compounds. Ingestion of the heavy metal cadmium in animals are inducive to damages to the endothelium.
- selenium-deficit areas are oppositely correlated to some forms of cancer, such as cancer of the breast, stomach, colon and rectum.
- Animal tests have shown that selenium compounds (Na 2 SeO 3 , seleno-methionine) have a protective effect against selected mammary-carcinogenic, colon -carcinogenic and liver-carcinogenic compounds.
- Mutagenic studies of carcinogens likewise show that selenium is effective in reducing significantly the mutagenic activity. It is therefore probable that the diet should contain certain amounts of selenium compounds in order to protect human beings against cancer. The protection could exist at several levels: 1) protection against nucleotide peroxides;
- the daily intake should be higher than that recommended by RDA, which is 50-200 ⁇ g Se/day. To obtain a cancer-inhibitory efrect it is considered that the intake should be about 200-350 ⁇ g Se/day.
- the purpose of the invention is to provide a formula by means of which selenium may be ingested in such a form that the body is capable of absorbing selenium as a trace element.
- the invention concerns a composition for human ingestion of selenium as a trace element but also for normalizing imbalance in the mineral status of the body.
- This composition is characterised in that it contains a selenium (IV) compound or such a compound in combination with seleno-methionine in an amount corresponding to between 50 and 500 ⁇ g of selenium, Vitamin E in amounts of between 10 and 100 mg, Vitamin B 2 in amounts of between 1 and 5 mg, Vitamin B 6 in amounts between 2 and 10 mg and Vitamin B 12 in amounts between 1 and 5 ⁇ g .
- the body absorbs selenium Se(lV) and seleno -methionine.
- composition is to have a certain formulation when intended for pharmaceutical uses.
- the purpose of the invention is also to prevent selenium deficiency, in which case the compo sition in accordance with the invention is to be ingested as food supplementation and preferably be formulated in accordance with the teachings of Claim 2.
- compositions in accordance with the subject invention also has efficient therapeutic effects in relieving and healing inflammatory conditions, that is, to strengthen the body's natural resistance against inflammations of the skin, the effects of surgical operations, microorganism-induced inflammations, virus attacks, and so on.
- the invention is not limited to only the formulations indicated herein but that obviously the addition thereto of further trace elements is possible, in which case it should be understood that it is necessary to ensure that such added elements are compatible with the rest of the substances making up the composition.
- admixture of additives facilitating the metal-ion balance in metal-ion-depending enzymes lies within the scope of the subject invention, examples of such additives being manganese, chromium, magnesium and zinc.
- Vitamin E ( ⁇ . -tocopheryl acetate) 10 mg
- Vitamin B 2 sodium riboflavine phosphate
- Vitamin B 6 pyridoxine chloride
- Vitamin B 12 (cyancobolamin) 1 ⁇ g
- Fillers such as magnesium stearate
- Vitamin E ⁇ -tocopheryl acetate 100 mg Vitamin B 2 (sodium riboflavine phosphate) 2 mg Vitamin B 6 (pyridoxin ⁇ chloride) 2 mg
- Vitamin B 12 (cyancobolamin) 1 ⁇ g
- Fillers such as magnesium stearate Dosage: 1 to 2 tablets/day according to need. 500 ⁇ g Se/day should not be exceeded unnecessarily in oases of prolonged therapy.
- Vitamin B 12 should be removed from the composition and be administered according to need as per special prescription.
- the tablets should be taken together with food for optimal effect. Large amounts of juice (Vitamin C) should not be taken together with the tablets. Juice may be taken after the absorption of the tablets.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Biomedical Technology (AREA)
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- Organic Chemistry (AREA)
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- Genetics & Genomics (AREA)
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- Pharmacology & Pharmacy (AREA)
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- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Engineering & Computer Science (AREA)
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- Epidemiology (AREA)
- Inorganic Chemistry (AREA)
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- General Chemical & Material Sciences (AREA)
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- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
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Abstract
A composition for human ingestion of selenium as a trace element and comprising a selenium (IV) compound or seleno-methionine + a selenium (IV) compound. The admixture into the composition of Vitamins E, B2?, B6? and B12? allows the body to assimilate selenium. The composition may also be used in solutions for storage of organs, in media for cell cultivation and in nutritive solutions for storage of blood components.
Description
MIXTURE FORHUMAN SUPPLY OF SELENIUM AS ATRACE SUBSTANCE AND THE USE THEREOF IN SOLUTIONS FOR STORAGE OF ORGANS INMEDIAFOR CELLCULTIVATION ANDINNUTRITIVE SOLUTIONSFORSTORAGE OF BLOODCOMPONENTS. The invention concerns a composition designed to ingest the trace element selenium into human beings.
In later years, increasing interest has been drawn to the substances known as trace elements, i.e. elements which are absolutely vital to the human organism, albeit in minute amounts. There are clear indications that many diseases and states of ill-health are a consequence of deficiencies of one or several of such trace elements. For example, there are reasons to suspect that certain heavy metals, such as cadmium, which are dissolved upon their contact with acid, such as through acid rains, cause a rise of the blood pressure. Animal tests have shown that cadmium-induced high blood-pressure conditions may be normalized by selenium compounds. Ingestion of the heavy metal cadmium in animals are inducive to damages to the endothelium. This, jointly with an increased blood-pressure and changes in the cholesterol pattern in the blood are considered the primary factors of arteriosclerosis. According to an American study, individuals having a high blood-pressure showed cadmium contents in erythrocytes which ware double those found in a control group. Expositions in industry to heavy metals together with an excess ingestion of cadmium present in food in combination with a selenium -depleted diet may play important parts in the pathoganesis in this regard. Animal tests (on rats) have shown that iron (aluminium) may trigger off epileptic attacks. When selenium (IV) was ingested with drinking water, no such attacks were triggered off. Patients suffering from epilepsy proved to have low selenium contents in urine. The iron contents in plasma in one patient was considerably increased while the selenium
contents were somewhat below the reference amounts. Since high iron contents are considered to start off lipid pβroxidation, supplementation of selenium should reduce this disorder. In cases of prolonged total parenteral nutrition (TPN) food diets having low contents of selenium have proved to cause muscular pain. Ingestion of selenium under certain conditions as will be explained in closer detail in the following, removed these pains completely. Tests have also shown that such muscular diseases as muscular dystrophy, non-specified muscular pains and myositis in many cases are selenium responsive. Also in some multiple-sclerosis patients remarkable improvements from selenium therapy (auto-therapy) have been found. Additionally, attempts to alleviate rheumatoid arthritis by selenium supplementation have given interesting results. Patients suffering from this disease have increased contents of copper in serum whereas the selenium contents are reduced. In selenium therapy (for instance using Mixture 3) care should be taken to ensure that the treatment continues over a prolonged period, allowing saturation of any metallic ion surplus. Copper has an inhibitory effect on the selenium enzyme (GSH-Px), which means that in an initial stage the activity may increase only slowly.
Finland like Sweden is a selenium-deficit area. The death rate in cardio-vascular diseases in Finland is one of the highest in the world. Exposition to heavy metals, such as cadmium (smoking, food), dietary habits can in these cases reduce the contents of selenium in the throrabocytes. Cardio-vascular patients show lower GSH-Px-values in the throrabocytes. This could be expected, in view of the fact that the throrabocytes are the species in the human body that are the richest in selenium. The hypothesis that also myocardial infarction is selenium-deficiency induced lies near at hand.
One of the reasons for selenium deficiency probably is the increased acidification of the environment, which causes leaching of the food that normally supplies the body with selenium in edible form, for instance in the form of Se(lV) or seleno-methionine. As mentioned above, acidification causes leaching but some investigations indicate that selenium absorption is reduced also as a consequence of "sulfur competition". Uraemia patients show changed trace element contents in blood, depending on impaired kidney function but. also on contamination from e.g. utensils (cadmium, aluminium) in haemodialysis therapy. An excess mortality rate in coronary-vascular diseases is found in this category of patients. Supplementation of trace elements prior to or after dialysis should reduce the mineral imbalance in the body of uraemia patients.
Epidemiological studies have shown that selenium-deficit areas are oppositely correlated to some forms of cancer, such as cancer of the breast, stomach, colon and rectum. Animal tests have shown that selenium compounds (Na2SeO3, seleno-methionine) have a protective effect against selected mammary-carcinogenic, colon -carcinogenic and liver-carcinogenic compounds. Mutagenic studies of carcinogens likewise show that selenium is effective in reducing significantly the mutagenic activity. It is therefore probable that the diet should contain certain amounts of selenium compounds in order to protect human beings against cancer. The protection could exist at several levels: 1) protection against nucleotide peroxides;
2) prevention of imbalance in metal ions;
3) improvement of the infection and immunity defence;
4) facilitation of the microsomale detoxifi cation;
5) anti-oxidant protection against lipid peroxides;
6) radical modulator.
The daily intake should be higher than that recommended by RDA, which is 50-200 μg Se/day. To obtain a cancer-inhibitory efrect it is considered that the intake should be about 200-350μg Se/day.
Treatment of various cancer forms with anticancer compounds, e.g. adriamycine, has considerable negative effects, such as a high cardiac toxicity. Since selenium compounds (Na2SeO3, seleno-methionine) have a beneficial effect on some muscular diseases, selenium supplementation (storing) prior to and during treatment with anticancerous preparations felso in combination with radiology treatment) should be effective in reducing some of the negative effects of anticancer coumpounds. Considering that the microsoraal function is affected by selenium deficiency an indrease of the selenium level will contribute additionally to reducing the toxic effect of the carcinocidal substances.
Patients suffering from diabetic cataract have been successfully treated with selenium plus Vitamin E. Animal tests have shown that seleno-methionine is preferable to sodium selenite to treat cataract. Selenium deficiency is assumed to increase the lipid peroxidation and thus result in an increase of pigmentation. Selenium therapy tested on cataract patients in Sweden has given positive results.
The purpose of the invention is to provide a formula by means of which selenium may be ingested in such a form that the body is capable of absorbing selenium as a trace element. For this purpose the invention concerns a composition for human ingestion of selenium as a trace element but also for normalizing imbalance in the mineral status of the body.
This composition is characterised in that it contains a selenium (IV) compound or such a compound in combination with seleno-methionine in an amount corresponding to between 50 and 500 μg of selenium, Vitamin E in amounts of between 10 and 100 mg, Vitamin B2 in amounts of between 1 and 5 mg, Vitamin B6 in amounts between 2 and 10 mg and Vitamin B12 in amounts between 1 and 5 μg . Owing to this formulation of the composition the body absorbs selenium Se(lV) and seleno -methionine.
As apparent from the dependent claims the composition is to have a certain formulation when intended for pharmaceutical uses. The purpose of the invention is also to prevent selenium deficiency, in which case the compo sition in accordance with the invention is to be ingested as food supplementation and preferably be formulated in accordance with the teachings of Claim 2.
The amounts specified in the claims are intended daily doses for adults of normal weight, and some modifi cation of the daily amounts therefore is possible and sometimes also recαmmendable. The amounts specified therefore are to be regarded as an indication of the mutual relationship between the substances of which the mixture is composed. Tests have further shown that a composition in accordance with the subject invention also has efficient therapeutic effects in relieving and healing inflammatory conditions, that is, to strengthen the body's natural resistance against inflammations of the skin, the effects of surgical operations, microorganism-induced inflammations, virus attacks, and so on.
Much remains to be understood as regards the exact mechanisms connected with Se(lV) and seleno-methionine, but research carried out to date indicate that selenium is of extremely great importance as a trace element in the body and this research suggests that the importance of selenium extends also to many other
functions of the body, among them the enzyme production and the effects of enzymes.
Finally, it should be pointed out that the invention is not limited to only the formulations indicated herein but that obviously the addition thereto of further trace elements is possible, in which case it should be understood that it is necessary to ensure that such added elements are compatible with the rest of the substances making up the composition. For instance, admixture of additives facilitating the metal-ion balance in metal-ion-depending enzymes lies within the scope of the subject invention, examples of such additives being manganese, chromium, magnesium and zinc.
The following examples of the composition of tablets are to be regarded as illustrative of the invention and in no way to limit the latter. Food supplementation Example 1 Sodium selenite (Na2SeO3.5H2O) 50 μg(Se(lV))
Vitamin E (α. -tocopheryl acetate) 10 mg
Vitamin B2 (sodium riboflavine phosphate) 2 mg Vitamin B6 (pyridoxine chloride) 2 mg
Vitamin B12 (cyancobolamin) 1μg
Fillers, such as magnesium stearate
Dosage: 1 tablet/day. Children, adults Example 2 Sodium selenite (Na2SeO3.SH2O) 25 μg Se
Seleno-methionine 25 μg Se
Vitamin E 10 mg
Vitamin B2 2 mg
Vitamin B6 2 mg
Vitamin 31 2 1 μ g
Fillers, such as magnesium stearate Dosage: 1 tab let/day . Child ren , adu lts
Therapy Example 1 Sodium se lenite (Na2SeO3 . 5H2O ) 200 μ g Se
Vitamin E (α -tocopheryl acetate) 100 mg Vitamin B2 (sodium riboflavine phosphate) 2 mg Vitamin B6 (pyridoxinβ chloride) 2 mg
Vitamin B12 (cyancobolamin) 1 μg
Fillers, such as magnesium stearate Dosage: 1 to 2 tablets/day according to need. 500 μg Se/day should not be exceeded unnecessarily in cases of prolonged therapy. Therapy Example 2 Sodium selenite (Na2SeO3.SH2O) 100 μg Se
Selena methionine 100 μg Se
Vitamin E 100 mg
Vitamin B2 2 mg
Vitamin B6 2 mg
Vitamin B12 1 μg
Fillers, such as magnesium stearate Dosage: 1 to 2 tablets/day according to need. 500 μg Se/day should not be exceeded unnecessarily in oases of prolonged therapy.
In cases of pernicious anaemia or leukaemia
(leukaemian conditions) Vitamin B12 should be removed from the composition and be administered according to need as per special prescription.
The tablets should be taken together with food for optimal effect. Large amounts of juice (Vitamin C) should not be taken together with the tablets. Juice may be taken after the absorption of the tablets.
Claims
1. A composition for human ingestion of selenium as a trace element, c h a r a c t e r i s e d i n t h a t the composition contains a selenium (lV) compound or seleno methionine + a selenium (IV) compound in amounts corresponding to between 50 and 500 μg selenium, Vitamin E in amounts of between 10 and 100 mg, Vitamin B2 in amounts of between 1 and 5 mg,
Vitamin B6 in amounts of between 2 and 10 mg, and preferably
Vitamin B12 in amounts between 1 and 5 μg.
2. A composition according to claim 1 for use as food supplementation, c h a r a c t e r i s e d i n t h a t it contains Se(lV) in an amount corresponding to 100 μg selenium,
Vitamin E in an amount of 10 mg, Vitamin B2 in an amount of 1.5 mg,
Vitamin B6 in an amount of 2 mg, and preferably
Vitamin B12 in an amount of 2 μg.
3. A composition according to claim 1 for therapeutical uses, c h a r a c t e r i s e d i n t h a t the composition contains Se(lV) or Se(lV) + seleno methionine in an amount corresponding to 200μg selenium, Vitamin E in an amount of 10 mg, Vitamin B2 in an amount of 1.5 mg,
Vitamin B6 in an amount of 2 mg, and preferably
Vitamin B12 in an amount of 2 μg.
4. A composition according to any one of the preceding claims, c h a r a c t e r i s e d i n t h a t selenium (lV) is present as Na2SeO3.
5. A composition according to any one of the preceding claims, c h a r a c t e r i s e d i n t h a t it contains anti-inflammatory preparations.
6. A composition according to any one of the preceding claims, c h a r a c t e r i s e d i n t h a t it also contains anticancer compounds.
7. Use of the composition according to any one of the preceding claims in solutions for storage of organs.
B. Use of the composition according to any one of claims 1 - 6 in cell-cultivation media. 9. Use of the composition according to any one of claims 1 - 6 in nutritive solutions for storage of blood components.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE8282903001T DE3268851D1 (en) | 1981-10-06 | 1982-09-30 | Mixture for human supply of selenium as a trace substance |
AT82903001T ATE17651T1 (en) | 1981-10-06 | 1982-09-30 | MIXTURE FOR HUMAN ADMINISTRATION OF SELENIUM AS A TRACE ELEMENT. |
DK2496/83A DK249683D0 (en) | 1981-10-06 | 1983-06-02 | MIXING TO HUMAN SUPPLY OF SELEN AS A TRUST, AND ITS APPLICATION IN SOLUTIONS FOR STORAGE ORGANIC MEDIA FOR CELL CULTIVATION AND IN NUTRITIONAL SOLUTIONS FOR STORAGE OF BLOOD COMPONENTS |
FI831979A FI831979L (en) | 1981-10-06 | 1983-06-02 | BLANDNING FOER HUMAN TILLFOERSEL AV SELEN SOM SPAORAEMNE |
HK953/88A HK95388A (en) | 1981-10-06 | 1988-11-24 | Mixture for human supply of selenium as a trace substance |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE8105887A SE8105887L (en) | 1981-10-06 | 1981-10-06 | MIXING FOR HUMAN SUPPLY OF SELEN AS A SUBSTANCE |
SE8105887-7811006 | 1981-10-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1983001196A1 true WO1983001196A1 (en) | 1983-04-14 |
Family
ID=20344709
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/SE1982/000304 WO1983001196A1 (en) | 1981-10-06 | 1982-09-30 | Mixture for human supply of selenium as a trace substance and the use thereof in solutions for storage of organs, in media for cell cultivation and in nutritive solutions for storage of blood components |
Country Status (11)
Country | Link |
---|---|
US (1) | US4784852A (en) |
EP (1) | EP0089997B1 (en) |
JP (1) | JPS58501676A (en) |
AT (1) | ATE17651T1 (en) |
CY (1) | CY1449A (en) |
DE (1) | DE3268851D1 (en) |
DK (1) | DK249683D0 (en) |
FI (1) | FI831979L (en) |
HK (1) | HK95388A (en) |
SE (1) | SE8105887L (en) |
WO (1) | WO1983001196A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3421644A1 (en) * | 1984-06-09 | 1985-12-12 | Richard 7880 Bad Säckingen Hau | DIET DIAGRAM |
EP0287896A1 (en) * | 1987-04-21 | 1988-10-26 | Walter Huber | Process and apparatus for isolating endocrine islets from a donor organ, and use of the islets in the treatment of metabolic diseases |
EP0519876A1 (en) * | 1991-06-18 | 1992-12-23 | Istituti Fisioterapici Ospitalieri | Pharmaceutical preparation to be used as adjuvant treatment of the seborrheic dermatitis even in HIV positive subjects |
WO1995029684A1 (en) * | 1994-05-02 | 1995-11-09 | Abbott Laboratories | Inhibition of atherosclerosis by antioxidants |
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US5639482A (en) * | 1993-11-10 | 1997-06-17 | Crary; Ely J. | Composition for control and prevention of diabetic retinopathy |
US5531989A (en) | 1994-10-28 | 1996-07-02 | Metagenics, Inc. | Immunoglobulin and fiber-containing composition for human gastrointestinal health |
US6241983B1 (en) | 1994-10-28 | 2001-06-05 | Metagenics, Inc. | Bacteria-and fiber-containing composition for human gastrointestinal health |
US6197295B1 (en) * | 1996-09-25 | 2001-03-06 | Viva America Marketing Corporation | Dietary supplementation with, and methods for administration of yeast-derived selenium product |
GB9722361D0 (en) * | 1997-10-24 | 1997-12-17 | Pharma Nord Uk Ltd | Pharmaceutical formulation for treating liver disorders |
WO1999064022A1 (en) * | 1998-06-10 | 1999-12-16 | Crum Albert B | Prophylactic and therapeutic nutritional supplement for creation/maintenance of health-protective intestinal microflora and enhancement of the immune system |
US6667063B2 (en) | 1998-06-10 | 2003-12-23 | Albert Crum | Nutritional or therapeutic supplement and method |
US7648699B2 (en) | 2000-06-02 | 2010-01-19 | Caridianbct Biotechnologies, Llc | Preventing transfusion related complications in a recipient of a blood transfusion |
US7714006B1 (en) | 2001-12-03 | 2010-05-11 | King Pharmaceuticals Research & Development, Inc. | Methods of modifying the bioavailability of metaxalone |
US6407128B1 (en) | 2001-12-03 | 2002-06-18 | Elan Pharmaceuticals, Inc. | Method for increasing the bioavailability of metaxalone |
EP1809101B1 (en) * | 2004-11-12 | 2016-11-02 | Organoflush B.V. | Composition for cold preservation and perfusion of organs |
CN103608006B (en) * | 2011-04-01 | 2017-07-07 | 伊亚索梅股份公司 | Combination comprising N acetyl group L cysteines and application thereof |
US10874098B2 (en) | 2015-04-03 | 2020-12-29 | Tx Innovations B.V. | Organ preservation composition |
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FR2100669A1 (en) * | 1970-05-20 | 1972-03-24 | American General Entrepr | Ant-ageing lung-protecting compns |
FR2244468A1 (en) * | 1973-07-31 | 1975-04-18 | Passwater Richard | Anticarcinogenic food supplements - contg antioxidants and S-contg amino acids |
US3928578A (en) * | 1967-04-28 | 1975-12-23 | Chromalloy Pharmaceutical Inc | Composition for control of white muscle disease |
GB1444024A (en) * | 1973-07-20 | 1976-07-28 | Passwaterr A | Food and feed supplents |
EP0000670A1 (en) * | 1977-08-02 | 1979-02-07 | Lundy Research Laboratories, Inc. | Therapeutic selenium compositions and the use thereof |
DE2811222A1 (en) * | 1978-03-15 | 1979-09-27 | Geb Meier Elfriede Juergens | Invigorating and disease-preventing foodstuff - contg. vitamin=E, vitamin=A, a vitamin=B, hawthorn, juniper, silica, garlic, yeast, minerals and trace elements |
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1981
- 1981-10-06 SE SE8105887A patent/SE8105887L/en not_active Application Discontinuation
-
1982
- 1982-09-30 WO PCT/SE1982/000304 patent/WO1983001196A1/en active IP Right Grant
- 1982-09-30 AT AT82903001T patent/ATE17651T1/en not_active IP Right Cessation
- 1982-09-30 EP EP82903001A patent/EP0089997B1/en not_active Expired
- 1982-09-30 DE DE8282903001T patent/DE3268851D1/en not_active Expired
- 1982-09-30 JP JP57503038A patent/JPS58501676A/en active Pending
-
1983
- 1983-06-02 DK DK2496/83A patent/DK249683D0/en not_active Application Discontinuation
- 1983-06-02 FI FI831979A patent/FI831979L/en not_active Application Discontinuation
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1986
- 1986-11-12 US US06/930,077 patent/US4784852A/en not_active Expired - Lifetime
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1988
- 1988-11-24 HK HK953/88A patent/HK95388A/en not_active IP Right Cessation
-
1989
- 1989-03-10 CY CY1449A patent/CY1449A/en unknown
Patent Citations (6)
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US3928578A (en) * | 1967-04-28 | 1975-12-23 | Chromalloy Pharmaceutical Inc | Composition for control of white muscle disease |
FR2100669A1 (en) * | 1970-05-20 | 1972-03-24 | American General Entrepr | Ant-ageing lung-protecting compns |
GB1444024A (en) * | 1973-07-20 | 1976-07-28 | Passwaterr A | Food and feed supplents |
FR2244468A1 (en) * | 1973-07-31 | 1975-04-18 | Passwater Richard | Anticarcinogenic food supplements - contg antioxidants and S-contg amino acids |
EP0000670A1 (en) * | 1977-08-02 | 1979-02-07 | Lundy Research Laboratories, Inc. | Therapeutic selenium compositions and the use thereof |
DE2811222A1 (en) * | 1978-03-15 | 1979-09-27 | Geb Meier Elfriede Juergens | Invigorating and disease-preventing foodstuff - contg. vitamin=E, vitamin=A, a vitamin=B, hawthorn, juniper, silica, garlic, yeast, minerals and trace elements |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3421644A1 (en) * | 1984-06-09 | 1985-12-12 | Richard 7880 Bad Säckingen Hau | DIET DIAGRAM |
EP0287896A1 (en) * | 1987-04-21 | 1988-10-26 | Walter Huber | Process and apparatus for isolating endocrine islets from a donor organ, and use of the islets in the treatment of metabolic diseases |
EP0519876A1 (en) * | 1991-06-18 | 1992-12-23 | Istituti Fisioterapici Ospitalieri | Pharmaceutical preparation to be used as adjuvant treatment of the seborrheic dermatitis even in HIV positive subjects |
US5290809A (en) * | 1991-06-18 | 1994-03-01 | Istituto Fisioterapici Ospitalieri | Methods for the treatment of seborrheic dermatitis |
WO1995029684A1 (en) * | 1994-05-02 | 1995-11-09 | Abbott Laboratories | Inhibition of atherosclerosis by antioxidants |
Also Published As
Publication number | Publication date |
---|---|
FI831979A0 (en) | 1983-06-02 |
DK249683A (en) | 1983-06-02 |
ATE17651T1 (en) | 1986-02-15 |
DE3268851D1 (en) | 1986-03-13 |
HK95388A (en) | 1988-12-02 |
CY1449A (en) | 1989-03-10 |
EP0089997A1 (en) | 1983-10-05 |
FI831979L (en) | 1983-06-02 |
EP0089997B1 (en) | 1986-01-29 |
JPS58501676A (en) | 1983-10-06 |
US4784852A (en) | 1988-11-15 |
SE8105887L (en) | 1983-04-07 |
DK249683D0 (en) | 1983-06-02 |
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