WO2009129943A1 - Formulierung mit reduzierter hygroskopizität - Google Patents
Formulierung mit reduzierter hygroskopizität Download PDFInfo
- Publication number
- WO2009129943A1 WO2009129943A1 PCT/EP2009/002691 EP2009002691W WO2009129943A1 WO 2009129943 A1 WO2009129943 A1 WO 2009129943A1 EP 2009002691 W EP2009002691 W EP 2009002691W WO 2009129943 A1 WO2009129943 A1 WO 2009129943A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- formulation
- formulations
- hygroscopic
- hygroscopic solid
- solvent
- Prior art date
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
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5005—Wall or coating material
- A61K9/5015—Organic compounds, e.g. fats, sugars
-
- 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
- A61K9/145—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 compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
Definitions
- the invention relates to formulations of hygroscopic solids with a lipophilic coating layer, and to a process for their preparation.
- a variety of fabrics, e.g. used as a pharmaceutical agent are hygroscopic. That the substances tend to absorb water, e.g. from the ambient air.
- Some of these substances are absorbed by the absorption of water but in their property, e.g. as a pharmaceutical agent, adversely affected. For example, there is a chemical decomposition of the active ingredient.
- one way of stabilizing these substances is, for example, to provide a formulation of these substances which comprises at least one further substance which has an even higher affinity for the absorption of water than the active ingredient, so that the A substance to be present as an active ingredient in the formulation which will not be exposed to moisture until the substance with the higher affinity to absorb water has reached a degree of saturation.
- adsorbent resins are disclosed, for example.
- WO 2007/142628 discloses copovidone (Plasdone® S-630) as a potential substance for uptake of water.
- WO 2007/142628 further discloses a formulation comprising a moisture-sensitive active substance with at least one adjuvant, wherein the adjuvant is preferably a binder.
- the disclosed method of making this formulation involves wet granulation of the active ingredient together with the binder.
- the resulting formulation thus comprises a matrix material of at least one excipient and the active ingredient.
- the formulation and the process for its preparation are disadvantageous because it does not prevent moisture from entering the formulation.
- the disclosure that more stable formulations are obtained when solvents with 95% ethanol are used in the course of granulation instead of solvents with higher levels of water, that the stabilization of the active ingredient in such formulations are narrow limits. It can be assumed that stabilization of the active ingredient takes place only as long as the saturation of the at least one auxiliary with water does not occur Measure achieves that the affinity of the active ingredient for receiving water is similar to that of the excipient.
- EP 1 161 941 discloses a formulation of active ingredients and a process for their preparation which provides a surface coating of powders of active ingredients.
- the desired technical effect relates to the ability to improve the flowability of the powders through the surface coating to allow dry granulation or direct tableting of the dry matter.
- the active ingredients suitable for such formulation also include typical hygroscopic substances such as calcium carbonate and magnesium oxide.
- the surface coating is carried out by granulation of the likewise pulverulent coating material with the active ingredient.
- the coating material may also include hygroscopic substances such as calcium carbonate.
- EP 1 161 941 is unfavorable with regard to the possibility of achieving stabilization of the active ingredient, since granulation of the active ingredient takes place with the coating material. As a result, agglomerates are generated which have a porosity as intrinsic property. This porosity leads to the fact that penetration of moisture into the core of the formulation can not be prevented, so that a stabilization of the active ingredient can not be done safely.
- the object is therefore to develop formulations of hygroscopic, solid substances and a process for their preparation which overcomes the disadvantages of the prior art, so that the formulations of the hygroscopic, solid substances are no longer hygroscopic.
- a lipophilic envelope surrounding the nucleus comprises, wherein the core and shell are connected by ionic interaction, can be solved.
- a substance is considered to be hygroscopic if, under standard conditions, it has a relative mass increase over a period of 24 hours, based on its initial weight of at least 3%, by taking up water from the moisture contained in the environment. All substances which have lower mass increase under normal conditions are considered to be non-hygroscopic in connection with the present invention.
- Normal conditions in connection with the present invention refer to a pressure of 1013 hPa, room temperature (20 ° C.), and a relative air humidity of 100%.
- the hygroscopic, solid substances are usually active ingredients and / or fillers.
- active substances are usually substances which find pharmaceutical use or can be used in crop protection.
- Active ingredients which find pharmaceutical use are, for example, active substances which can be used in the field of healing and alleviating diseases of the animal and of man, such as e.g. Acidosetherapeutika, Analeptika / Antihypoxämika, Analgesika / Antirheumatika, Antacide, Antiallergika, Antianämika, Antiarryhtmika, Antibiotik / Antiin Stammiva, Antidementiva, Antidiabetic, Antidota, Antiepileptika, Antihypertonika, Antihyperglyhimmika, Antihypotonika, Antikoagulantia, Antifungal, Antiparasitic, Antiphlogizinga, Arteriosklerosestoff, Broncholytika / Anti - asthmatics, cholagogues and biliary tract therapeutics, cholinergics, corticoids, dermatics, diuretics, circulation-promoting agents, agents for the treatment of addictions, enzyme inhibitors, fibrinolytics, geria
- Active substances that can be used in crop protection are, in the context of the present inventions, substances from the classes of herbicides, fungicides, Insecticides, acaricides, nematicides, bird repellants, plant nutrients and soil conditioners.
- Fillers in the context of the present invention are all substances which are authorized together with active substances either for pharmaceutical use or, accordingly, for use in a plant protection product.
- Preferred fillers are the carbonate and phosphate salts and oxides and / or hydroxides of the alkali and alkaline earth metals, such as calcium carbonate, calcium phosphate, calcium oxide, or cellulose derivatives such as hydroxypropylmethylcellulose (HPMC), hydroxypropylcellulose (HPC), etc.
- Preferred are active ingredients and / or or fillers that can be used as antacids or gastrointestinal agents. Particularly preferred are oxides and / or hydroxides of alkaline earth metals.
- the present invention is not limited to the above-mentioned preferred substances in terms of the hygroscopic solids. Rather, these substances are often characterized by the fact that they may not lose their properties as an active ingredient even after prolonged storage by the absorption of water, so that the subject of the present invention has a particularly positive effect here.
- a limitation of the invention exists only in that the hygroscopic solid must have at least one chemical group which allows the formation of the ionic interaction with the lipophilic shell.
- the formation of an ionic interaction between the hygroscopic, solid substance and the lipophilic shell is particularly advantageous because this results in an orientation of the lipophilic substances with their lipophilic portion is achieved to the outside, so that even thin layers of the cladding layer already achieve the positive technical effects of the envelope , This is on the one hand economically advantageous because less shell material must be used, on the other hand, the properties of the hygroscopic solid, which correlate with its particle size, are not greatly affected.
- the aerodynamic diameter of the formulation according to the invention remains approximately the same, so that a narrowing of the range of use, for example inhalation products, etc., does not result.
- the hygroscopic solid comprises at least one positively charged chemical group.
- the lipophilic shell surrounding the core usually comprises a salt of the at least one hygroscopic solid with at least one organic acid which is characterized by a lipophilic portion and at least one acid group.
- a lipophilic portion of an organic acid is referred to as that portion of an organic acid molecule comprising at least four non-ring carbon atoms and optionally having one or more multiple bonds between the at least four non-ring carbon atoms.
- Preference is given to organic acids of the homologous series of alkanes, alkenes and alkynes having at least four carbon atoms.
- Acid group in the context of the present invention refers to that part of an organic acid molecule which leads to a lowering of the aqueous medium in the aqueous by dissociation of a proton (H + ) present in it.
- Preferred are acid groups of the carboxylates, sulfonates and phosphates.
- the organic acids may have one or more acid groups. Preference is given to organic acids having only one acid group or mixtures of different organic acids having only one acid group. Particular preference is given to carboxylates of alkanes or alkenes having only one acid group and at least twelve carbon atoms or mixtures of different carboxylates of alkanes or alkenes having only one acid group.
- alkanecarboxylic acids e.g. Capric acid, undecanoic acid, lauric acid, tridecanoic acid, myristic acid, pentadecanoic acid, palmitic acid, margarine acid, stearic acid, nonadecanoic acid and arachic acid, or alkene carboxylic acids such as linoleic acid, linolenic acid and arachidonic acid, or mixtures thereof.
- solubility in water is the mass of the hygroscopic, solid substance which can be dissolved in water at room temperature (20 ° C.) and atmospheric pressure (1013 hPa) at most in water.
- the solubility of the formulation preferably does not decrease by more than 10% compared with the formulated substance. Most preferably, it does not change.
- pH value when dissolved in water referred to in the context of the present invention, the measurable pH after one hour in an aqueous solution with a concentration of 0.1 wt.% Of a substance or its formulation.
- a further subject of the present invention is a process for the preparation of formulations of hygroscopic solids which consist of a core of at least one hygroscopic solid and of a lipophilic shell, characterized by the steps of a) providing a solution A of at least one acid in a solvent or solvent mixture 1; b) mixing the solution A with a hygroscopic, solid material below
- the at least one organic acid of solution A of step a) comprises the organic acids already described in connection with the formulation according to the invention, as well as mixtures of these.
- the solvent or solvent mixture 1 of the solution A of step a) according to the method of the invention comprises non-polar solvents or mixtures thereof having a maximum polarity of 1.5 Debye.
- Non-limiting examples include aniline, anisole and toluene, as well as their mixtures and mixtures with solvents of lower polarity.
- solvents or solvent mixtures having a polarity of less than 0.5 Debye Preference is given to solvents or solvent mixtures having a polarity of less than 0.5 Debye.
- Non-conclusive examples are hexane, cyclohexane, benzene, Carbon disulfide, tetrachloroethene, carbon tetrachloride or mixtures thereof with solvents of higher polarity called.
- the at least one hygroscopic, solid substance of the dispersion B of step b) according to the method according to the invention comprises the hygroscopic solid substances already described in connection with the formulation according to the invention, which are further characterized in that they are in the form of a powder for the process.
- the powder has an average particle size of 0.1-200 microns, more preferably, this powder has an average particle size of 0.1-20 microns.
- step c) of the method according to the invention is usually carried out by the skilled worker for this well-known methods such as decantation, filtration, centrifugation, etc.
- inventive method can with a step d) in the form of aftertreatment, or be carried out without aftertreatment.
- a post-treatment is carried out.
- the aftertreatment according to step d) of the process according to the invention usually comprises drying and / or washing of the solids content. If a washing is carried out, the washing is preferably carried out together with a subsequent further separation according to step c) of the process according to the invention.
- the washing is carried out with a solvent for the acid used.
- solvents are, for example, water or alcohols or mixtures of water with alcohols.
- Carrying out a wash is particularly advantageous because it allows the solid content to be freed from residues of the free acid, thus making the solids content more usable, for example for pharmaceutical applications.
- Drying may be carried out under ambient pressure (1013 hPa) or under reduced pressure relative to ambient pressure. Further, the drying is usually a thermal drying.
- Thermal drying in the context of the present invention, means drying under elevated temperature conditions. Preferably, drying is carried out at temperatures approximately equal to the evaporation temperature of the solvent or solvent mixture 1 at the pressure during drying.
- the evaporation temperatures of the solvents or solvent mixtures 1 under certain pressures are generally known to the person skilled in the art, for example from tables such as the VDI-Wärmeatlas.
- the temperature of the thermal drying at ambient pressure (1013 hPa) is preferably 100 ° C.
- formulations according to the invention or the formulations according to the method of the invention are particularly suitable for use in connection with therapeutic methods on mammals, preferably humans or domestic animals.
- the formulations according to the invention or the formulations according to the process of the invention preferably find use as fillers or auxiliaries of other formulations which are used as medicaments.
- FIG. 1 shows the course of the relative change in weight in% of a formulation according to the invention (F) and pure magnesium hydroxide (Mg) when stored under air at 100% relative humidity and at 30 ° C.
- FIG. 2 shows the course of the pH of a formulation (F) according to the invention and of magnesium hydroxide (Mg) recorded according to Example 3.
- Example 1 as well as magnesium hydroxide were added and the increase in the pH was recorded (pH meter: Knick® Calimatic 766).
- pH meter Knick® Calimatic 766.
- FIG. 2 summarized. It can be seen that, after a time of about 1800 s, the same final pH value is established in the case of pure magnesium hydroxide (Mg), as is the case in formulation (F) according to the invention.
- FIG. 2 the delayed release of the magnesium hydroxide from the formulation according to the invention with approximately the same gradient as when releasing the pure magnesium hydroxide. The time offset here was about 300 s.
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- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Diabetes (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Anesthesiology (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/934,286 US20110021355A1 (en) | 2008-04-24 | 2009-04-11 | Formulation with reduced hygroscopicity |
CN2009801142789A CN102014875B (zh) | 2008-04-24 | 2009-04-11 | 吸湿性降低的制剂 |
EP09735236A EP2271319A1 (de) | 2008-04-24 | 2009-04-11 | Formulierung mit reduzierter hygroskopizität |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102008020701.2 | 2008-04-24 | ||
DE102008020701A DE102008020701A1 (de) | 2008-04-24 | 2008-04-24 | Formulierung mit reduzierter Hygroskopizität |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2009129943A1 true WO2009129943A1 (de) | 2009-10-29 |
WO2009129943A8 WO2009129943A8 (de) | 2010-11-18 |
Family
ID=40984892
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2009/002691 WO2009129943A1 (de) | 2008-04-24 | 2009-04-11 | Formulierung mit reduzierter hygroskopizität |
Country Status (5)
Country | Link |
---|---|
US (1) | US20110021355A1 (de) |
EP (1) | EP2271319A1 (de) |
CN (1) | CN102014875B (de) |
DE (1) | DE102008020701A1 (de) |
WO (1) | WO2009129943A1 (de) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103271895A (zh) * | 2012-03-14 | 2013-09-04 | 南京先宇科技有限公司 | 一种稳定的含有羟苯磺酸钙的药物组合物及其制备方法 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB505362A (en) * | 1937-03-01 | 1939-05-08 | Armour & Co | Improvements in compositions of matter containing anti-hygroscopic agents and processes of preparing the same |
WO2004060353A1 (en) * | 2002-12-19 | 2004-07-22 | Pharmacia Corporation | Solid dispersions comprising a hygroscopic and/or deliquescent drug |
WO2006021455A1 (en) * | 2004-08-27 | 2006-03-02 | Novartis Ag | Fast release composition including melt granules of a moisture sensitive drug and process for manufacturing thereof |
EP1864677A1 (de) * | 2006-06-02 | 2007-12-12 | Teva Pharmaceutical Industries Ltd | Stabile Zubereitung enthaltend eine feuchtigkeitsemphindliche aktive Substanz und Verfahren zur Herstellung der Zubereitung. |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2702747A (en) * | 1951-08-27 | 1955-02-22 | Phillips Petroleum Co | Noncaking fertilizers |
AU2944700A (en) | 1999-03-15 | 2000-10-04 | Kaken Pharmaceutical Co., Ltd. | Quickly disintegrating tablets and process for producing the same |
US6878693B2 (en) * | 2001-09-28 | 2005-04-12 | Solubest Ltd. | Hydrophilic complexes of lipophilic materials and an apparatus and method for their production |
AU2006278571B2 (en) * | 2005-08-05 | 2011-11-24 | 3M Innovative Properties Company | Compositions exhibiting improved flowability |
BRPI0621739A2 (pt) | 2006-06-02 | 2011-12-20 | Teva Pharma | formulação estável que consiste em drogas sensìveis à umectação e seu procedimento de fabricação |
-
2008
- 2008-04-24 DE DE102008020701A patent/DE102008020701A1/de not_active Withdrawn
-
2009
- 2009-04-11 EP EP09735236A patent/EP2271319A1/de not_active Withdrawn
- 2009-04-11 CN CN2009801142789A patent/CN102014875B/zh not_active Expired - Fee Related
- 2009-04-11 US US12/934,286 patent/US20110021355A1/en not_active Abandoned
- 2009-04-11 WO PCT/EP2009/002691 patent/WO2009129943A1/de active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB505362A (en) * | 1937-03-01 | 1939-05-08 | Armour & Co | Improvements in compositions of matter containing anti-hygroscopic agents and processes of preparing the same |
WO2004060353A1 (en) * | 2002-12-19 | 2004-07-22 | Pharmacia Corporation | Solid dispersions comprising a hygroscopic and/or deliquescent drug |
WO2006021455A1 (en) * | 2004-08-27 | 2006-03-02 | Novartis Ag | Fast release composition including melt granules of a moisture sensitive drug and process for manufacturing thereof |
EP1864677A1 (de) * | 2006-06-02 | 2007-12-12 | Teva Pharmaceutical Industries Ltd | Stabile Zubereitung enthaltend eine feuchtigkeitsemphindliche aktive Substanz und Verfahren zur Herstellung der Zubereitung. |
Also Published As
Publication number | Publication date |
---|---|
CN102014875A (zh) | 2011-04-13 |
CN102014875B (zh) | 2013-07-24 |
EP2271319A1 (de) | 2011-01-12 |
WO2009129943A8 (de) | 2010-11-18 |
DE102008020701A1 (de) | 2009-10-29 |
US20110021355A1 (en) | 2011-01-27 |
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