GB887872A - Improvements in or relating to pharmaceutical preparations - Google Patents
Improvements in or relating to pharmaceutical preparationsInfo
- Publication number
- GB887872A GB887872A GB15720/59A GB1572059A GB887872A GB 887872 A GB887872 A GB 887872A GB 15720/59 A GB15720/59 A GB 15720/59A GB 1572059 A GB1572059 A GB 1572059A GB 887872 A GB887872 A GB 887872A
- Authority
- GB
- United Kingdom
- Prior art keywords
- soluble
- water
- toxic
- polyethylene glycol
- molecular weight
- 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
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/2031—Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyethylene oxide, poloxamers
-
- 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
- A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2095—Tabletting processes; Dosage units made by direct compression of powders or specially processed granules, by eliminating solvents, by melt-extrusion, by injection molding, by 3D printing
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)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
A pharmaceutical base suitable for shaping by extrusion comprises a solid polyethylene glycol of molecular weight from about 4,000 to about 6,000; a liquid polyethylene glycol soluble in the solid polyethylene glycol; a non-toxic, non-ionic solid oil-soluble surface-active agent; spermaceti; a non-toxic, non-ionic solid water-soluble surface-active agent; and a non-toxic, solid carrier mixture of which between about 80% and 90% by weight is water-soluble. Preferred oil-soluble surface-active agents are polyoxyethylene sorbitan mono- and tri-stearates. Water-soluble surface-active agents preferred have the formula HO(C2H4O) (C3H6O) (C2H4O)H with a polypropyleneoxy base molecular weight of about 1,750 and a total molecular weight of about 8,750. Also suitable are polyoxyethylene stearate and palmitate. In the carrier beta lactose, sucrose, dextrose, sodium chloride or sodium sulphate may form the water-soluble part and the balance may be starch with which methylcellulose, guar gum or purified wood cellulose may be mixed. A number of medicinal ingredients for mixing with the base are listed (see Group VI).ALSO:A pharmaceutical preparation contains a medicament and a base suitable for shaping by extrusion-moulding comprising a polyethylene glycol having a molecular weight between about 4000 and about 6000; a liquid polyethylene glycol soluble in the solid polyethylene glycol; a non-toxic non-ionic solid oil-soluble surface-active agent; spermaceti; a non-toxic non-ionic solid water-soluble surface-active agent; and a non-toxic solid carrier mixture of which between about 80% and about 90% is water-soluble. Preferred oil-soluble surface-active agents are polyoxyethylene mono- and di-stearates. Water-soluble surface-active agents preferred have the formula HO(C2H4O)(C3H6O)(C2H4O)H with a polypropylene oxy base molecular weight of about 1750 and a total molecular weight of about 8750. Also suitable are polyoxyethylene stearate and palmitate. In the carrier beta lactose, sucrose, dextrose, sodium chloride, or sodium sulphate may form the water-soluble part and the balance may be starch with which methylcellulose, guar gum or purified wood cellulose may be mixed. Shaped preparations for nasal, urethral, vaginal and rectal application are prepared. As medicinal ingredients there can be incorporated: steroids, for example, estrone, testosterone, progesterone, hydrocortisone, prednisolone, 6-methyl prednisolone, and their therapeutically active derivatives; hypnotics and sedatives, for example phenobarbital, pentobarbital and amobarbital; antibiotics, for example, neomycin, bacitrocin, polymyxin, erythromycin, tyrothricin, gramicidin; diuretics, for example, aminophylline and theophylline; trichomonicides, for example, phenylmercuric acetate, sodium lauryl sulphate, oxyquinoline benzoate; antiseptics and bactericidal agents, for example, hexachlorophene, hexylresorcinol, nitrofurazone, myristyl g -picolinium chloride, sulfadiazine, phenol, secondary amyl tricresols; anaesthetics, for example, benzocaine, procaine, tetracaine; vasoconstrictors, for example, epinephrine, phenylephrine; analgesics, for example, caffeine and ergotamine tartrate, acetylsilicylic acid, acetophenetidin, N-acetyl-p-amino-phenol; narcotitizing medicaments, for example, morphine, dihydromorphinone, scopolamine and codeine.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US887872XA | 1958-06-25 | 1958-06-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB887872A true GB887872A (en) | 1962-01-24 |
Family
ID=22213459
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB15720/59A Expired GB887872A (en) | 1958-06-25 | 1959-05-07 | Improvements in or relating to pharmaceutical preparations |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB887872A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001028589A2 (en) * | 1999-10-15 | 2001-04-26 | Rainer Rogasch | Shaped body comprising an amphiphilic outer phase and a lipophilic inner phase |
US10010612B2 (en) | 2007-05-25 | 2018-07-03 | Indivior Uk Limited | Sustained delivery formulations of risperidone compounds |
US10022367B2 (en) | 2014-03-10 | 2018-07-17 | Indivior Uk Limited | Sustained-release buprenorphine solutions |
US10058554B2 (en) | 2005-09-30 | 2018-08-28 | Indivior Uk Limited | Sustained release small molecule drug formulation |
US10172849B2 (en) | 2010-06-08 | 2019-01-08 | Indivior Uk Limited | Compositions comprising buprenorphine |
US10198218B2 (en) | 2010-06-08 | 2019-02-05 | Indivior Uk Limited | Injectable flowable composition comprising buprenorphine |
-
1959
- 1959-05-07 GB GB15720/59A patent/GB887872A/en not_active Expired
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001028589A3 (en) * | 1999-10-15 | 2002-04-11 | Rainer Rogasch | Shaped body comprising an amphiphilic outer phase and a lipophilic inner phase |
US7541047B2 (en) * | 1999-10-15 | 2009-06-02 | Rainer Rogasch | Method for production of shaped body for treating wounds in milk producing animals |
WO2001028589A2 (en) * | 1999-10-15 | 2001-04-26 | Rainer Rogasch | Shaped body comprising an amphiphilic outer phase and a lipophilic inner phase |
US10058554B2 (en) | 2005-09-30 | 2018-08-28 | Indivior Uk Limited | Sustained release small molecule drug formulation |
US11110093B2 (en) | 2005-09-30 | 2021-09-07 | Indivior Uk Limited | Sustained release small molecule drug formulation |
US11013809B2 (en) | 2007-05-25 | 2021-05-25 | Indivior Uk Limited | Sustained delivery formulations of risperidone compound |
US10010612B2 (en) | 2007-05-25 | 2018-07-03 | Indivior Uk Limited | Sustained delivery formulations of risperidone compounds |
US11712475B2 (en) | 2007-05-25 | 2023-08-01 | Indivior Uk Limited | Sustained delivery formulations of risperidone compound |
US10376590B2 (en) | 2007-05-25 | 2019-08-13 | Indivior Uk Limited | Sustained delivery formulations of risperidone compound |
US10172849B2 (en) | 2010-06-08 | 2019-01-08 | Indivior Uk Limited | Compositions comprising buprenorphine |
US10558394B2 (en) | 2010-06-08 | 2020-02-11 | Indivior Uk Limited | Injectable flowable composition comprising buprenorphine |
US10592168B1 (en) | 2010-06-08 | 2020-03-17 | Indivior Uk Limited | Injectable flowable composition comprising buprenorphine |
US10198218B2 (en) | 2010-06-08 | 2019-02-05 | Indivior Uk Limited | Injectable flowable composition comprising buprenorphine |
US10517864B2 (en) | 2014-03-10 | 2019-12-31 | Indivior Uk Limited | Sustained-release buprenorphine solutions |
US10022367B2 (en) | 2014-03-10 | 2018-07-17 | Indivior Uk Limited | Sustained-release buprenorphine solutions |
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