GB2107715A - Micronised beclomethasone dipropionate monohydrate and powder inhalation compositions containing it - Google Patents
Micronised beclomethasone dipropionate monohydrate and powder inhalation compositions containing it Download PDFInfo
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- GB2107715A GB2107715A GB08229740A GB8229740A GB2107715A GB 2107715 A GB2107715 A GB 2107715A GB 08229740 A GB08229740 A GB 08229740A GB 8229740 A GB8229740 A GB 8229740A GB 2107715 A GB2107715 A GB 2107715A
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- United Kingdom
- Prior art keywords
- beclomethasone dipropionate
- water
- monohydrate
- micronised
- dipropionate monohydrate
- Prior art date
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- 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
- A61K9/007—Pulmonary tract; Aromatherapy
- A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
- A61K9/0075—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy for inhalation via a dry powder inhaler [DPI], e.g. comprising micronized drug mixed with lactose carrier particles
-
- 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
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J5/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
- C07J5/0046—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa
- C07J5/0061—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa substituted in position 16
- C07J5/0069—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa substituted in position 16 by a saturated or unsaturated hydrocarbon group
- C07J5/0076—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond substituted in position 17 alfa substituted in position 16 by a saturated or unsaturated hydrocarbon group by an alkyl group
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Organic Chemistry (AREA)
- Otolaryngology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Abstract
Beclomethasone dipropionate in the form of its micronised monohydrate substantially free from water other than water of crystallization. Pharmaceutical compositions containing the compound may be in the form of powder inhalation cartridges especially suitable for the treatment and/or prophylaxis of asthma; and may also contain isoprenaline, salbutamol, atropine or sodium cromoglycate.
Description
SPECIFICATION
Improvements in or relating to a steroid compound and pharmaceutical compositions containing it
This invention relates to improvements in or relating to pharmaceutical compositions comprising 9a-ch loro-l 1 ss-hydroxy-16ss-methyl-17a,21 -dipropionyl-oxypregna-1 ,4-diene-3,20-dione, which is known as beclomethasone dipropionate.
Beclomethasone dipropionate is a corticosteroid which exhibits a high topical antiinflammatory activity, and is described and claimed in U.K. Patent Specification No. 1.047,519. The compound may be formulated into preparations suitable for topical administration as, for example, lotions, creams, ointments and the like.
In the management of asthma it has been found effective to spray the corticosteroid into the bronchial system prophylactically. Formulations containing beclomethasone dipropionate for the treatment of asthma include aerosol formulations consisting of a suspension of the micronised corticosteroid in a chlorofluorohydrocarbon propellant. Such formulations are dispensed using conventional pressurised aerosols or inhalers.
It has been found, however, that when micronised beclomethasone dipropionate is formulated with aerosol propellants, the active compound exhibits crystal growth which results in the formation of particles having a size above 20 um. Medicaments for administration by inhalation desirably have a controlled particle size. The optimum particle size for inhalation into the bronchial system is usually 1-10 1 -101lm preferably 2-5 Fm.
Particles having a size above 20 um are generally too large when inhaled to reach the small airways. U.K.
Patent Specification No. 1429184 describes a method of converting an anti-inflammatory steroid, such as beclomethasone dipropionate, exhibiting crystal growth in aerosol propellants, into a form which does not exhibit such growth, whereby the steroid is contacted with a halogenated hydrocarbon to form a crystalline solvate therewith, the crystalline material so formed being reduced to a particle size permitting inhalataion into the human bronchial system when dispersed as an aerosol.
Similrly, German Offenlegungsschrift 3018550 describes ethyl acetate solvates of antiinflammatory steroids (particularly beclomethasone dipropionate) and South African Patent Specification No. 80/2601 describes solvates of beclomethasone dipropionate with alkanes having from 5 to 8 carbon atoms, both for use in aerosol formulations. All these solvates appear to have essentially the same type of crystal structure.
An alternative inhalation form of beclomethasone dipropionate is a form suitable for powder inhalation especially valuable for treating patients who are unable to use the pressurised inhalers effectively or who might use them incorrectly. In this form the contents of a cartridge are inhaled using an inhalation device which releases the drug from the cartridge when the patient inhales. Such drug delivery systems are more reliable for many patients.
We have found that when pharmaceutical powder compositions which contain beclomethasone dipropionate contained in conventional gelatin inhalation cartridges are stored in adverse conditions the particle size distribution of the powder changes. Thus the fraction of fine particles having the desired 1-10 um size may decrease to such an extent that an unsatisfactory product may result.
We have now found that in pharmaceutical dry powder compositions for use in powder inhalation cartridges, the above problem can be overcome by using beclomethazone dipropionate in the form of its monohydrate. We have found that the particle size of the micronised monohydrate in such powder compositions remains substantially constant even after storage for extended periods. Beclomethasone dipropionate monohydrate, which differs in its crystal structure from the previously described solvates referred to above, has never been proposed for use in powder formulations for bronchial inhalation.
According to one aspect of the invention we provide beclomethasone dipropionate monohydrate substantially free from water other than water of crystallisation, at least 90% by weight of the particles thereof having an effective particle size below 10 um, preferably between 2-5 um.
The crystalline monohydrate has been subjected to X-ray powder diffraction studies. A sample of the monohydrate was exposed to Cu Ka radiation of wavelength 1 .54051A in a Nonius Guinier X-ray powder diffraction camera. The line intensities were compared against a set of standards to give the relative intensities shown in the following Table:
TABLE d( ) Intensity d( ) Intensity d( ) Intensity
9.6 VS 5.8 VS 3.8 MD
7.7 VS 4.9 S 3.7 M
6.8 VS 4.7 S 3.4 W
6.3 VS 4.6 VS 3.4 W
6.2 M 4.5 W 3.3 S
6.0 M 4.2 S 3.2 M
3.9 M 3.1 MD
2.8 M
2.4 M (VS = very strong; S = strong; M = medium; W = weak; D = diffuse)
The new monohydrate of the invention has also been characterised by its infrared spectrum.The infrared spectrum of a sample of the monohydrate as a mull in mineral oil is shown in the Figure of the accompanying drawing.
The principal absorption bands are at 3560, 3510, 3300, 1730,1710,1663,1630, 1285,1190,1120,1090, 1053,973,940,890,810, 785 and 700 cm-1.
The invention further provides a pharmaceutical dry powder composition comprising micronised beclomethasone dipropionate monohydrate in association with at least one pharmaceutically acceptable powder carrier or excipient.
The monohydrate may be conveniently prepared by crystallisation from a mixed solvent system consisting of water and a water-miscible organic solvent. For example, the monohydrate may be prepared by slowly adding a solution of beclomethasone dipropionate in a water-miscible organic solvent to water, whereafter the monohydrate is crystallised.The beclomethasone dipropionate is conveniently first dissolved in the organic solvent at an elevated temperature e.g. at a temperature of from 40 to 80"C, for example, at about 60"C. The organic solvent solution is then added slowly to water, preferably with stirring, while maintaining the solution at a temperature of e.g. 40 to 80"C, preferably about 60"C. Upon cooling, of the resulting suspension, the crystalline monohydrate is formed.
Water-miscible organic solvents which may be used in such a process include, for example, methanol, ethanol, acetone and dioxan.
After crystallisation, the monohydrate may be isolated by, for example, filtration and washed and dried in conventional manner. For example, the monohydrate may be dried by air drying, drying under reduced pressure, or drying in the presence of a sterile inert gas.
The beclomethasone dipropionate monohydrate may be micronised to the desired particle size range by conventional techniques, for example using a ball mill or fluid energy mill or by ultrasonic means. The desired fraction may be separated out by air classification or sieving. The compositions may be prepared by intimately mixing the ingredients together, for example, in a high shearfluidising mixer. The compositions according to the invention may conveniently be filled into gelatin, plastics or other capsules. Such capsules may be conventional two-part capsules or may be sealed. In general, No 3 size hard gelatin two-part capsules are preferred.
The monohydrate may also be prepared by comminuting beclomethasone dipropionate in the presence of water, for example, in a ball mill or by ultrasonic means.
The compositions according to the invention exhibit the high topical antiinflammatory activity of beclomethasone dipropionate. As indicated above, we have found that the particle size of the crystalline monohydrate remains substantially constant even after storage for extended periods.
These properties render the monohydrate of value in the preparation of the pharmaceutical powder compositions and their packaging in containers or packs.
The compositions according to the invention are conveniently in the form of inhalation cartridges which may be used with an inhalation device, for example that described in U.K. Patent Specification No. 1561835 or British Patent Application No.80 39174 (Publication No.2064336).
For use in the pharmaceutical powder compositions such as inhalation cartridges, the monohydrate is micronised, preferably such that at least 90% by weight of the particles have an effective particle size below 10 Fm and preferably between 2 to 5 lim. Thus in a preferred embodiment we provide pharmaceutical powder compositions such as inhalation cartridges, which comprise micronised beclomethasone dipropionate monohydrate, in which at least 90% by weight of the particles have an effective particle size below 10 urn, preferably between 2-5 urn, and at least one pharmaceutically acceptable dry powder carrier or excipient.
The carrier may be selected from diluents such as, for example, lactose, mannitol, arabinose or dextrose, but is preferably lactose. The carrier or excipient may be commercially available in the desired particle size range or may also be separated by air classification or sieving. The compositions may also additionally contain a bronchodilator such as iosprenaline or salbutamol or an anticholinergic such as atropine or a drug used in the prophylaxis of allergic conditions such as sodium cromoglycate.
The amount of the composition contained in the capsule will to some extent depend on the desired dosage.
The compositions are conveniently in the form of dosage units (e.g. inhalation cartridges) containing beclomethasone dipropionate monohydrate equivalent to from 10-10001l9 and preferably from 50-500 9 (e.g. 20-250 yg) of beclomethasone dipropionate and from 10-100 mg by weight and more especially from 25-50 mg by weight of the carrier. Most preferably unit dosages of the compositions are such as to provide 100 to 300 ug usually 200,ug of beclomethasone dipropionate.
The average daily dosage of beclomethasone dipropionate monohydrate will depend on the age, weight and condition of the patient to be treated. In general, average daily dosages lie in the range of 200 to 2000 ug, preferably 400 to 800 yg, of beclomethasone dipropionate. In the case of high dosage compositions, the daily dosage can be approximately about 4 mg of beclomethasone dipropionate.
The invention will now be illustrated with reference to the following non-limiting Examples. All temperatures are in "C "Hplc" is high-pressure liquid chromatography, and "gc" is gas chromatography.
Example 1
Beclomethasone dipropionate (0.5g), which had been previously dried to constant weight at 1000, was dissolved in 15ml ethanol. Water (100ml) was added, with stirring, causing clouding followed by crystallisation. The crystalline hydrate in the form of long thin laths was removed by filtration and air-dried.
Yield 0.5g.
The sample had the IR spectrum indicated in the figure of the accompanying drawing.
The crystals were subsequently micronised in a fluid energy mill to the particle size 2-5 urn.
Example 2
Beclomethasone dipropionate (550g) was dissolved in 3.2 litres of hot methanol and filtered. The filtrate held at a temperature of about 60 was added with stirring to 33 litres of deionised water, also at 600. The mixture was cooled to 20 and the resulting crystalline monohydrate was removed by filtration, washed with water (1.0 litre) and air-dried. Yield 506g.
Analytical data
Beclomethasone dipropionate (hplc) 96.4% w/w
Water (gc) 3.8% w/w
Loss on drying (105 ) 3.5%w/w
The sample had the l.R. spectrum shown in the figure of the accompanying drawing.
The crystals were subsequently micronised in a fluid energy mill to the particle size 2-5 urn.
Example 3
Beclomethasone dipropionate (0.5g) and water (25 ml) were ball milled for 36 hours in a glass bottle with steatite balls. The solid in the form of fine particles of 2-5 urn size was removed by filtration and air dried to give the monohydrate with the l.R. spectrum shown in the figure of the accompanying drawing.
Example 4
Deionised water (16.5 1) was heated to 60 and beclomethasone dipropionate (250 g) dissolved in hot methanol (1.6 1) was added slowly at about 60 over a period of 2.5 minutes with stirring. The mixture was cooled to room temperature to give the precipitated hydrate which was collected by filtration, washed with water and dried in vacuo (ca 150 mmHg/40"). The product (253 g) had the I.R. spectrum indicates in the figure. Loss on drying (105 ) 3.19%w/w.
The crystals were subsequently micronised in a fluid energy mill to the particle size 2-5 urn.
Example 5
Beclomethazone dipropionate monohydrate : inhalation cartridges for use in a powder inhalation device
Per cartridge
Beclomethasone dipropionate
monohydrate, micronised 114 or 228 ug Lactose to 25 mg.
The active ingredient and lactose are intimately mixed in a high shearfluidising mixer. The blend is encapsulated in No. 3 size hard gelatin capsules using an automatic machine. Each cartridge contains the equivalent of 110 us or 220 ug of beclomethasone dipropionate.
Example 6
Beclomethasone dipropionate monohydrate and salbutamol: inhalation cartridges for use in a powder inhalation device
Per cartridge
Beclomethasone dipropionate 228 9 monohydrate, micronised
Salbutamol sulphate, micronised 528 9 Lactose to 25 mg
The active ingredients and lactose are intimately mixed as before and the blend is encapsulated in No. 3 size hard gelatin capsules using an automatic machine. Each cartridge contains the equivalent of 220 R9 of beclomethasone dipropionate and 440 9 of salbutamol.
Claims (19)
1. Beclomethasone dipropionate monohydrate substantially free from water other than water of crystallisation, at least 90% by weight of the particles thereof having an effective particle size below 10 urn.
2. Beclomethasone dipropionate monohydrate according to claim 1 which exhibits the infrared spectrum as shown in the Figure of the accompanying drawing.
3. Beclomethasone dipropionate monohydrate according to claim 1 which yields the following data when subjected to an X-ray powder diffraction study with a Nonius Guinier X-ray powder diffraction camera
under exposure with Cu Ka radiation of wavelength 1.54051 :- d( ) Intensity d( ) Intensity d( ) Intensity
9.6 VS 5.8 VS 3.8 MD
7.7 VS 4.9 S 3.7 M
6.8 VS 4.7 S 3.4 W
6.3 VS 4.6 VS 3.4 W
6.2 M 4.5 W 3.3 S
6.0 M 4.2 S 3.2 M
3.9 M 3.1 MD
2.8 M
2.4 M
(VS = very strong; S = strong; M = medium; W = weak; D = diffuse)
4. A pharmaceutical dry powder composition comprising micronised beclomethasone dipropionate monohydrate in association with at least one pharmaceutically acceptable dry powder carrier or excipient.
5. A composition according to claim 4 wherein the carrier comprises lactose.
6. A composition according to either of claims 4 and 5 wherein at least 90% by weight of the micronised beclomethasone dipropionate monohydrate has an effective particle size below 10 urn.
7. A composition according to claim 6 wherein at least 90% by weight of the micronised beclomethasone dipropionate monohydrate has an effective particle size between 2 to 5 urn.
8. A composition according to any one of claims 4 to 7 in the form of a dosage unit comprising a powder inhalation cartridge.
9. A composition according to claim 8 wherein the dosage unit contains beclomethasone dipropionate monohydrate equivalent to from 10 to 1000 wig of beclomethasone dipropionate.
10. A composition according to claim 8 wherein the dosage unit contains beclomethasone dipropionate monohydrate equivalent to from 50 to 500 ug of beclomethasone dipropionate.
11. A composition according to any one of claims 4to 10 additionally containing salbutamol.
12. A composition according to any one of claims 4 to 11 additionally containing sodium cromoglycate.
13. A pharmaceutical dry powder composition as claimed in claim 4 substantially as herein described.
14. A pharmaceutical composition as claimed in any one of claims 4 to 13 in association with a powder inhalation device.
15. A powder inhalation device containing a pharmaceutical composition as defined in any one of claims 4 to 13.
16. Beclomethasone dipropionate monohydrate for use in the preparation of a pharmaceutical dry powder composition as defined in claim 4.
17. A process for the preparation of micronised beclomethasone dipropionate monohydrate which comprises contacting beclomethasone dipropionate with water and micronising to form beclomethasone dipropionate monohydrate substantially free from water other than water of crystallisation, at least 90% by weight of the particles thereof having an effective particle size below 10 .
18. A process according to claim 17 wherein beclomethasone dipropionate monohydrate is crystallised from a mixed solvent system consisting of water and a water-miscible organic solvent and subsequently micronised.
19. A process according to claim 17 wherein beclomethasone dipropionate is micronised in the presence of water.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB08229740A GB2107715B (en) | 1981-10-19 | 1982-10-18 | Micronised beclomethasone dipropionate monohydrate and powder inhalation compositions containing it |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8131425 | 1981-10-19 | ||
| GB08229740A GB2107715B (en) | 1981-10-19 | 1982-10-18 | Micronised beclomethasone dipropionate monohydrate and powder inhalation compositions containing it |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| GB2107715A true GB2107715A (en) | 1983-05-05 |
| GB2107715B GB2107715B (en) | 1985-11-13 |
Family
ID=26281006
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB08229740A Expired GB2107715B (en) | 1981-10-19 | 1982-10-18 | Micronised beclomethasone dipropionate monohydrate and powder inhalation compositions containing it |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB2107715B (en) |
Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2519989A1 (en) * | 1982-01-18 | 1983-07-22 | Squibb & Sons Inc | STEROID MONOHYDRATES, FORMULATIONS CONTAINING SAME, AND PROCESS FOR PREPARING SAME |
| EP0172672A1 (en) * | 1984-07-25 | 1986-02-26 | Hovione Inter Ltd. | Preparation and use of new solvates of beclomethasone 17,21-diproprionate |
| WO1986003750A1 (en) * | 1984-12-19 | 1986-07-03 | Riker Laboratories, Inc. | Physically modified beclomethasone dipropionate suitable for use in aerosols |
| FR2588474A1 (en) * | 1985-10-16 | 1987-04-17 | Cird | SYNERGETIC ANTI-INFLAMMATORY COMPOSITIONS BASED ON A CORTICOSTEROID AND AN AGONIST BETA |
| EP0416951A1 (en) * | 1989-09-08 | 1991-03-13 | Glaxo Group Limited | Medicaments comprising salmeterol and fluticason |
| EP0416950A1 (en) * | 1989-09-08 | 1991-03-13 | Glaxo Group Limited | Medicaments |
| US5208226A (en) * | 1989-09-08 | 1993-05-04 | Glaxo Group Limited | Medicaments |
| WO1993015741A1 (en) * | 1992-02-06 | 1993-08-19 | Glaxo Group Limited | Medicaments |
| US5270305A (en) * | 1989-09-08 | 1993-12-14 | Glaxo Group Limited | Medicaments |
| WO2000053158A1 (en) * | 1999-03-05 | 2000-09-14 | Chiesi Farmaceutici S.P.A | Modified carrier particles for use in dry powder inhalers |
| WO2004046163A1 (en) * | 2002-11-08 | 2004-06-03 | Kaneka Corporation | Method of separating ergosterol |
| WO2004054545A1 (en) * | 2002-12-18 | 2004-07-01 | Chiesi Farmaceutici S.P.A. | Preparation of sterile aqueous suspensions comprising micronised crystalline active ingredients for inhalation |
| US8912174B2 (en) | 2003-04-16 | 2014-12-16 | Mylan Pharmaceuticals Inc. | Formulations and methods for treating rhinosinusitis |
| US9808471B2 (en) | 2003-04-16 | 2017-11-07 | Mylan Specialty Lp | Nasal pharmaceutical formulations and methods of using the same |
| CN115414321A (en) * | 2022-10-20 | 2022-12-02 | 山东新时代药业有限公司 | Beclomethasone dipropionate emulsifiable paste and preparation method thereof |
-
1982
- 1982-10-18 GB GB08229740A patent/GB2107715B/en not_active Expired
Cited By (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2519989A1 (en) * | 1982-01-18 | 1983-07-22 | Squibb & Sons Inc | STEROID MONOHYDRATES, FORMULATIONS CONTAINING SAME, AND PROCESS FOR PREPARING SAME |
| EP0172672A1 (en) * | 1984-07-25 | 1986-02-26 | Hovione Inter Ltd. | Preparation and use of new solvates of beclomethasone 17,21-diproprionate |
| WO1986003750A1 (en) * | 1984-12-19 | 1986-07-03 | Riker Laboratories, Inc. | Physically modified beclomethasone dipropionate suitable for use in aerosols |
| US4810488A (en) * | 1984-12-19 | 1989-03-07 | Riker Laboratories, Inc. | Physically modified beclomethasone dipropionate suitable for use in aerosols |
| FR2588474A1 (en) * | 1985-10-16 | 1987-04-17 | Cird | SYNERGETIC ANTI-INFLAMMATORY COMPOSITIONS BASED ON A CORTICOSTEROID AND AN AGONIST BETA |
| EP0223671A1 (en) * | 1985-10-16 | 1987-05-27 | Centre International De Recherches Dermatologiques Galderma - Cird Galderma | Medicament with a synergistic anti-inflammatory effect on the basis of a corticosteroid and a beta-agonist |
| AU584468B2 (en) * | 1985-10-16 | 1989-05-25 | Centre International De Recherches Dermatologiques C.I.R.D. | Pharmaceutical composition having a synergistic anti- inflammatory activity based on a combination of a corticosteroid and a `` agonist |
| EP0416950A1 (en) * | 1989-09-08 | 1991-03-13 | Glaxo Group Limited | Medicaments |
| EP0416951A1 (en) * | 1989-09-08 | 1991-03-13 | Glaxo Group Limited | Medicaments comprising salmeterol and fluticason |
| GB2235626A (en) * | 1989-09-08 | 1991-03-13 | Glaxo Group Ltd | Medicaments for treating respiratory disorders |
| FR2651677A1 (en) * | 1989-09-08 | 1991-03-15 | Glaxo Group Ltd | PHARMACEUTICAL COMPOSITION BASED ON SALMETEROL AND FLUTICASONE PROPIONATE. |
| FR2651678A1 (en) * | 1989-09-08 | 1991-03-15 | Glaxo Group Ltd | PHARMACEUTICAL COMPOSITION BASED ON SALMETEROL AND BECLOMETASONE DIPROPIONATE. |
| BE1003053A3 (en) * | 1989-09-08 | 1991-11-05 | Glaxo Group Ltd | PHARMACEUTICAL COMPOSITION BASED ON SALMETEROL AND FLUTICASONE PROPIONATE. |
| US5208226A (en) * | 1989-09-08 | 1993-05-04 | Glaxo Group Limited | Medicaments |
| USRE40045E1 (en) | 1989-09-08 | 2008-02-05 | Glaxo Group Limited | Medicaments |
| US5270305A (en) * | 1989-09-08 | 1993-12-14 | Glaxo Group Limited | Medicaments |
| GB2235626B (en) * | 1989-09-08 | 1994-02-09 | Glaxo Group Ltd | Inhalation medicaments for treating respiratory disorders |
| US5695744A (en) * | 1992-02-06 | 1997-12-09 | Glaxo Group Limited | Medicaments |
| AU667074B2 (en) * | 1992-02-06 | 1996-03-07 | Glaxo Group Limited | A pharmaceutical aerosol formulation |
| US5688782A (en) * | 1992-02-06 | 1997-11-18 | Glaxo Group Limited | Medicaments for treating respiratory disorders |
| AP419A (en) * | 1992-02-06 | 1995-10-24 | Glaxo Group Ltd | Pharmaceutical aerosol formulation comprising beclomethasone diproprionate monohydrate. |
| CN1048394C (en) * | 1992-02-06 | 2000-01-19 | 格拉克索公司 | Medicaments |
| WO1993015741A1 (en) * | 1992-02-06 | 1993-08-19 | Glaxo Group Limited | Medicaments |
| US7132115B2 (en) | 1999-03-05 | 2006-11-07 | Chiesi Farmaceutici S.P.A. | Modified carrier particles for use in dry powder inhalers |
| WO2000053158A1 (en) * | 1999-03-05 | 2000-09-14 | Chiesi Farmaceutici S.P.A | Modified carrier particles for use in dry powder inhalers |
| EP1312357A3 (en) * | 1999-03-05 | 2004-01-07 | CHIESI FARMACEUTICI S.p.A. | Pharmaceutical formulations for dry powder inhalers |
| EP1312357A2 (en) * | 1999-03-05 | 2003-05-21 | CHIESI FARMACEUTICI S.p.A. | Pharmaceutical formulations for dry powder inhalers |
| US6641844B1 (en) | 1999-03-05 | 2003-11-04 | Chiesi Farmaceutici S.P.A. | Modified carrier particles for use in dry powder inhalers |
| WO2004046163A1 (en) * | 2002-11-08 | 2004-06-03 | Kaneka Corporation | Method of separating ergosterol |
| US7884221B2 (en) | 2002-11-08 | 2011-02-08 | Kaneka Corporation | Method of separating ergosterol |
| CN100398095C (en) * | 2002-12-18 | 2008-07-02 | 奇斯药制品公司 | Preparation of sterile aqueous suspensions comprising micronised crystalline active ingredients for inhalation |
| US20070140980A1 (en) * | 2002-12-18 | 2007-06-21 | Chiesi Farmaceutici S.P.A. | Preparation of sterile aqueous suspensions comprising micronised crystalline active ingredients for inhalation |
| EA008122B1 (en) * | 2002-12-18 | 2007-04-27 | КЬЕЗИ ФАРМАЧЕУТИЧИ С.п.А. | Preparation of sterile aqueous suspensions comprising micronised crystalline active ingredients for inhalation |
| WO2004054545A1 (en) * | 2002-12-18 | 2004-07-01 | Chiesi Farmaceutici S.P.A. | Preparation of sterile aqueous suspensions comprising micronised crystalline active ingredients for inhalation |
| US8128909B2 (en) | 2002-12-18 | 2012-03-06 | Chiesi Farmaceutici S.P.A. | Preparation of sterile aqueous suspensions comprising micronised crystalline active ingredients for inhalation |
| HRP20050546B1 (en) * | 2002-12-18 | 2014-05-23 | Chiesi Farmaceutici S.P.A. | Preparation of sterile aqueous suspensions comprising micronised crystalline active ingredients for inhalation |
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| US9808471B2 (en) | 2003-04-16 | 2017-11-07 | Mylan Specialty Lp | Nasal pharmaceutical formulations and methods of using the same |
| CN115414321A (en) * | 2022-10-20 | 2022-12-02 | 山东新时代药业有限公司 | Beclomethasone dipropionate emulsifiable paste and preparation method thereof |
| CN115414321B (en) * | 2022-10-20 | 2023-06-20 | 山东新时代药业有限公司 | Beclomethasone dipropionate cream and preparation method thereof |
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| Publication number | Publication date |
|---|---|
| GB2107715B (en) | 1985-11-13 |
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| Date | Code | Title | Description |
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| PE20 | Patent expired after termination of 20 years |
Effective date: 20021017 |