GB475291A - Process of preparing nutritive amino-acid preparations - Google Patents
Process of preparing nutritive amino-acid preparationsInfo
- Publication number
- GB475291A GB475291A GB2107636A GB2107636A GB475291A GB 475291 A GB475291 A GB 475291A GB 2107636 A GB2107636 A GB 2107636A GB 2107636 A GB2107636 A GB 2107636A GB 475291 A GB475291 A GB 475291A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- water
- calcium
- heated
- acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
A nutritive amino - acid preparation for injection is prepared by converting total amino-acids obtained by acid or alkaline hydrolysis into their calcium, sodium, potassium or magnesium salts, heating with a monosaccharide and neutralizing the product. Amino-acids from casein, for example, may be heated with water and calcium carbonate on a water bath to give a weakly alkaline solution which is evaporated to obtain the calcium salts. These are dissolved in water and heated at 75--100 DEG C. with glucose. The solution is neutralized with alkali, filtered, diluted, sealed in ampoules and sterilized. Mannose, galactose, and fructose are other monosaccharides specified.ALSO:A nutritive amino-acid preparation for injection is prepared by converting total amino-acids obtained by acid or alkaline hydrolysis into their calcium, sodium, potassium or magnesium salts, heating with a monosaccharide and neutralizing the product. Amino-acids from casein, for example, may be heated with water and calcium carbonate on a water bath to give a weakly alkaline solution which is evaporated to obtain the calcium salts. These are dissolved in water and heated at 75-100 DEG C. with glucose. The solution is neutralized with alkali, filtered, diluted, sealed in ampoules, and sterilized. Mannose, galactose, and fructose are other monosaccharides specified.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2107636A GB475291A (en) | 1936-07-30 | 1936-07-30 | Process of preparing nutritive amino-acid preparations |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2107636A GB475291A (en) | 1936-07-30 | 1936-07-30 | Process of preparing nutritive amino-acid preparations |
Publications (1)
Publication Number | Publication Date |
---|---|
GB475291A true GB475291A (en) | 1937-11-17 |
Family
ID=10156795
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2107636A Expired GB475291A (en) | 1936-07-30 | 1936-07-30 | Process of preparing nutritive amino-acid preparations |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB475291A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2429596A (en) * | 1944-02-10 | 1947-10-28 | Harold A Abramson | Glycine-calcium carbonate antacid |
US2691617A (en) * | 1949-01-13 | 1954-10-12 | Hermann Siegwart | Choline gluconate medicament |
US2738299A (en) * | 1953-05-11 | 1956-03-13 | Abbott Lab | Stable nutritive amino acid compositions |
US2754296A (en) * | 1950-09-01 | 1956-07-10 | Schi Wa Chemisch Pharmazeutisc | Antihistaminic compounds |
EP0083993A1 (en) * | 1982-01-11 | 1983-07-20 | Massachusetts Institute Of Technology | Compositions for use in increasing brain tyrosine levels |
EP0183004A1 (en) * | 1984-11-27 | 1986-06-04 | Societe Des Produits Nestle S.A. | Methods for controlling the viscosity of protein hydrolysates |
-
1936
- 1936-07-30 GB GB2107636A patent/GB475291A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2429596A (en) * | 1944-02-10 | 1947-10-28 | Harold A Abramson | Glycine-calcium carbonate antacid |
US2691617A (en) * | 1949-01-13 | 1954-10-12 | Hermann Siegwart | Choline gluconate medicament |
US2754296A (en) * | 1950-09-01 | 1956-07-10 | Schi Wa Chemisch Pharmazeutisc | Antihistaminic compounds |
US2738299A (en) * | 1953-05-11 | 1956-03-13 | Abbott Lab | Stable nutritive amino acid compositions |
EP0083993A1 (en) * | 1982-01-11 | 1983-07-20 | Massachusetts Institute Of Technology | Compositions for use in increasing brain tyrosine levels |
EP0183004A1 (en) * | 1984-11-27 | 1986-06-04 | Societe Des Produits Nestle S.A. | Methods for controlling the viscosity of protein hydrolysates |
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