DE504183C - Process for the preparation of therapeutically valuable, sterile and durable solutions of p-dialkylaminoarylphosphinous acid salts suitable for injections - Google Patents
Process for the preparation of therapeutically valuable, sterile and durable solutions of p-dialkylaminoarylphosphinous acid salts suitable for injectionsInfo
- Publication number
- DE504183C DE504183C DEI33982D DEI0033982D DE504183C DE 504183 C DE504183 C DE 504183C DE I33982 D DEI33982 D DE I33982D DE I0033982 D DEI0033982 D DE I0033982D DE 504183 C DE504183 C DE 504183C
- Authority
- DE
- Germany
- Prior art keywords
- dialkylaminoarylphosphinous
- sterile
- injections
- solutions
- acid salts
- 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
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/02—Inorganic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Dermatology (AREA)
- Inorganic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
Description
Verfahren zur Darstellung therapeutisch wertvoller, steriler und haltbarer, zu Injektionen geeigneter Lösungen von p-dialkyiaminoarylphosphinigsauren Salzen Lösungen von dialkylaminoarylphosphinigsauren Salzen sind nicht haltbar. Besonders unangenehm tritt diese Unbeständigkeit in Erscheinung bei dem Versuch, solche Lösungen zu sterilisieren. In vielen Fällen tritt schon nach kurzem Erhitzen auf Sterilisationstemperatur Zersetzung ein unter Abscheidung des betreffenden Arylamins, in anderen Fällen färben sich die sterilisierten Lösungen nach kurzem Lagern und scheiden einen blauvioletten Niederschlag aus.Process for the preparation of therapeutically valuable, sterile and durable, for injections of suitable solutions of p-dialkyiaminoarylphosphinous acid salts Solutions of dialkylaminoarylphosphinous acid salts are not stable. Particularly This instability becomes unpleasant when trying to find such solutions to sterilize. In many cases, sterilization temperature occurs after a short period of heating Decomposition one with deposition of the arylamine in question, in other cases color the sterilized solutions after a short storage and excrete a blue-violet Precipitation from.
Es wurde nun gefunden, daß man durch Zusatz säurebindender Substanzen zu den neutral reagierenden Lösungen vollkommen beständige und sterilisierbare Lösungen erhält, die - in Form von subkutanen, intravenösen oder intramuskulären Injektionen angewandt -sich als hervorragende, völlig ungiftige und reizlose Roborantia, Stoffwechsel-Stimulantia und Antirachitica erwiesen haben.It has now been found that by adding acid-binding substances Completely stable and sterilizable solutions in addition to the neutral reacting solutions receives that - in the form of subcutaneous, intravenous or intramuscular injections Applied as an excellent, completely non-toxic and irritant-free Roborantia, metabolic stimulant and Antirachitica have proven.
Die Ausführung des Verfahrens kann in der Weise geschehen, da.ß man die gelösten Komponenten zusammenbringt und dann sterilisiert oder daß man sie in festem Zustande mischt, die Mischung löst und hierauf sterilisiert.The procedure can be carried out in such a way that one the dissolved components are brought together and then sterilized or that they are in solid state mixes, the mixture dissolves and then sterilized.
Als Lösungsmittel dient reines Wasser; es können aber auch in manchen Fällen mit Vorteil sogenannte physiologische Lösungen, wie physiologische Kochsalzlösung, Ringer-L östing u. dgl., verwendet werden. Beispiel 1,25 kg i-dimethylamino-3-methylbenzol-4-phosphinigsaures Natrium (vgl. Patentschrift 397 813 der Klasse i2q, Beispiel 2) werden in ioo 1 Wasser gelöst. Man fügt 4o g Natrium carbonicum siccum (D. A. B. 6) zu und sterilisiert bei ioo° G i Stunde lang in strömendem Wasserdampf. Die Lösung bleibt vollkommen klar und wasserhell und ist unbegrenzte Zeit haltbar, während eine ohne Zusatz von Natrium carbonicum siccum, aber sonst in gleicher Weise bereitete Lösung nach dem Sterilisieren zersetzt ist unter Abscheidung von Öltropfen, die im wesentlichen aus Dimethylm-toluidin bestehen.Pure water is used as the solvent; In some cases, however, so-called physiological solutions, such as physiological saline solution, Ringer's dissolving and the like, can also be used with advantage. Example 1.25 kg of i-dimethylamino-3-methylbenzene-4-phosphinous acid sodium (cf. patent specification 397 813 of class i2q, example 2) are dissolved in 100 l of water. 40 g of sodium carbonicum siccum (DAB 6) are added and sterilized at 100 ° G for 1 hour in flowing steam. The solution remains completely clear and water-white and can be kept indefinitely, while a solution prepared without the addition of sodium carbonicum siccum, but otherwise prepared in the same way, is decomposed after sterilization with the separation of oil droplets, which essentially consist of dimethylm-toluidine.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEI33982D DE504183C (en) | 1928-03-30 | 1928-03-30 | Process for the preparation of therapeutically valuable, sterile and durable solutions of p-dialkylaminoarylphosphinous acid salts suitable for injections |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEI33982D DE504183C (en) | 1928-03-30 | 1928-03-30 | Process for the preparation of therapeutically valuable, sterile and durable solutions of p-dialkylaminoarylphosphinous acid salts suitable for injections |
Publications (1)
Publication Number | Publication Date |
---|---|
DE504183C true DE504183C (en) | 1930-08-07 |
Family
ID=7188581
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEI33982D Expired DE504183C (en) | 1928-03-30 | 1928-03-30 | Process for the preparation of therapeutically valuable, sterile and durable solutions of p-dialkylaminoarylphosphinous acid salts suitable for injections |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE504183C (en) |
-
1928
- 1928-03-30 DE DEI33982D patent/DE504183C/en not_active Expired
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE963184C (en) | Process for the preparation of durable solutions of salts of 1-dialkylaminoalkoxy-3-alkyl-isoquinolines | |
DE151036C (en) | ||
DE504183C (en) | Process for the preparation of therapeutically valuable, sterile and durable solutions of p-dialkylaminoarylphosphinous acid salts suitable for injections | |
DE1617871A1 (en) | Process for the production of a stable aqueous solution | |
CH142019A (en) | Process for the preparation of therapeutically valuable, sterile and durable solutions of dialkylaminoarylphosphinous acid salts. | |
DE539403C (en) | Process for the preparation of N-haloacylarylsulfamides | |
DE951756C (en) | Process for the production of concentrated, long-lasting aqueous solutions of furanochromones | |
DE700113C (en) | Process for the production of stable, sterilizable emulsions of clot-activating phosphatides | |
DE739912C (en) | Process for the production of concentrated calcium gluconate solutions | |
DE384688C (en) | Process for the preparation of durable guaiacol preparations in aqueous solution | |
DE752784C (en) | Production of durable liquid suspensions of water-soluble antimony compounds | |
DE305228C (en) | ||
DE557519C (en) | Process for the preparation of easily soluble alkali salts of acylaminophenolar acids | |
DE321616C (en) | Process for the preservation of hydrogen peroxide solutions | |
DE726635C (en) | Process for the production of rich, durable solutions of calcium gluconate or lactate | |
AT162289B (en) | Process for the preparation of esters of 1-alkyl-4-oxypiperidine | |
DE472346C (en) | Process for the preparation of a concentrated calcium solution which remains clear for a long time and which can be injected intramuscularly without tissue irritation | |
DE763310C (en) | Process for the production of quaternary ammonium compounds | |
DE708768C (en) | Process for the preparation of acidic esters of the alkylated 1,4-naphthohydroquinones | |
DE672494C (en) | Process for the production of hexamethylenetetramine preparations | |
DE694679C (en) | Process for the production of durable solutions of the condensation products from 4,4'-diaminophenyl sulfones and aldoses | |
AT81069B (en) | Process for the preservation of extracts from drugs Processes for the preservation of extracts from drugs. en. | |
DE423821C (en) | Process for the production of non-toxic, strongly bactericidal cerium solutions | |
AT133143B (en) | Process for the preparation of readily soluble sodium salts of 4-oxy-3-acylaminobenzolaric acids (1) or their substitution products. | |
DE855614C (en) | Process for the preparation of penicillin solutions with long-lasting effects |