AP608A - Pharmaceutical or veterinary composition comprising a cream base. - Google Patents
Pharmaceutical or veterinary composition comprising a cream base. Download PDFInfo
- Publication number
- AP608A AP608A APAP/P/1996/000798A AP9600798A AP608A AP 608 A AP608 A AP 608A AP 9600798 A AP9600798 A AP 9600798A AP 608 A AP608 A AP 608A
- Authority
- AP
- ARIPO
- Prior art keywords
- weight
- composition
- mineral oil
- alcohol
- pharmaceutical
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 45
- 239000006071 cream Substances 0.000 title claims abstract description 15
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 claims description 16
- 239000002480 mineral oil Substances 0.000 claims description 15
- 235000010446 mineral oil Nutrition 0.000 claims description 15
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 claims description 14
- 150000002148 esters Chemical class 0.000 claims description 13
- MINDHVHHQZYEEK-UHFFFAOYSA-N (E)-(2S,3R,4R,5S)-5-[(2S,3S,4S,5S)-2,3-epoxy-5-hydroxy-4-methylhexyl]tetrahydro-3,4-dihydroxy-(beta)-methyl-2H-pyran-2-crotonic acid ester with 9-hydroxynonanoic acid Natural products CC(O)C(C)C1OC1CC1C(O)C(O)C(CC(C)=CC(=O)OCCCCCCCCC(O)=O)OC1 MINDHVHHQZYEEK-UHFFFAOYSA-N 0.000 claims description 11
- 239000003814 drug Substances 0.000 claims description 11
- 229960003128 mupirocin Drugs 0.000 claims description 11
- 229930187697 mupirocin Natural products 0.000 claims description 11
- 229940124597 therapeutic agent Drugs 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims description 9
- 150000002191 fatty alcohols Chemical class 0.000 claims description 9
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 claims description 8
- 229960000541 cetyl alcohol Drugs 0.000 claims description 7
- 239000004094 surface-active agent Substances 0.000 claims description 7
- -1 polyoxyethylene Polymers 0.000 claims description 6
- FDCJDKXCCYFOCV-UHFFFAOYSA-N 1-hexadecoxyhexadecane Chemical compound CCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCC FDCJDKXCCYFOCV-UHFFFAOYSA-N 0.000 claims description 5
- 230000003115 biocidal effect Effects 0.000 claims description 5
- 229940051841 polyoxyethylene ether Drugs 0.000 claims description 5
- 229920000056 polyoxyethylene ether Polymers 0.000 claims description 5
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 claims description 4
- 239000003242 anti bacterial agent Substances 0.000 claims description 4
- 159000000007 calcium salts Chemical class 0.000 claims description 4
- 229960005323 phenoxyethanol Drugs 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- 235000019445 benzyl alcohol Nutrition 0.000 claims description 3
- 239000004615 ingredient Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 150000004683 dihydrates Chemical class 0.000 claims description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
- 239000003755 preservative agent Substances 0.000 claims description 2
- 238000002560 therapeutic procedure Methods 0.000 claims description 2
- DDHVILIIHBIMQU-YJGQQKNPSA-L mupirocin calcium hydrate Chemical compound O.O.[Ca+2].C[C@H](O)[C@H](C)[C@@H]1O[C@H]1C[C@@H]1[C@@H](O)[C@@H](O)[C@H](C\C(C)=C\C(=O)OCCCCCCCCC([O-])=O)OC1.C[C@H](O)[C@H](C)[C@@H]1O[C@H]1C[C@@H]1[C@@H](O)[C@@H](O)[C@H](C\C(C)=C\C(=O)OCCCCCCCCC([O-])=O)OC1 DDHVILIIHBIMQU-YJGQQKNPSA-L 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 1
- 230000002335 preservative effect Effects 0.000 claims 1
- HAXVBVDETFUQGV-LNQHITRNSA-L mupirocin calcium (anhydrous) Chemical compound [Ca+2].C[C@H](O)[C@H](C)[C@@H]1O[C@H]1C[C@@H]1[C@@H](O)[C@@H](O)[C@H](C\C(C)=C\C(=O)OCCCCCCCCC([O-])=O)OC1.C[C@H](O)[C@H](C)[C@@H]1O[C@H]1C[C@@H]1[C@@H](O)[C@@H](O)[C@H](C\C(C)=C\C(=O)OCCCCCCCCC([O-])=O)OC1 HAXVBVDETFUQGV-LNQHITRNSA-L 0.000 description 9
- 230000000699 topical effect Effects 0.000 description 6
- 239000002202 Polyethylene glycol Substances 0.000 description 5
- 229940057995 liquid paraffin Drugs 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 229920001223 polyethylene glycol Polymers 0.000 description 5
- IQXJCCZJOIKIAD-UHFFFAOYSA-N 1-(2-methoxyethoxy)hexadecane Chemical compound CCCCCCCCCCCCCCCCOCCOC IQXJCCZJOIKIAD-UHFFFAOYSA-N 0.000 description 4
- 229950009789 cetomacrogol 1000 Drugs 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000000230 xanthan gum Substances 0.000 description 4
- 229920001285 xanthan gum Polymers 0.000 description 4
- 229940082509 xanthan gum Drugs 0.000 description 4
- 235000010493 xanthan gum Nutrition 0.000 description 4
- 239000008213 purified water Substances 0.000 description 3
- 229920001214 Polysorbate 60 Polymers 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 239000002674 ointment Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- HZXURXPUHRWIIT-UHFFFAOYSA-N [Ca].O(C1=CC=CC=C1)C(C)O Chemical compound [Ca].O(C1=CC=CC=C1)C(C)O HZXURXPUHRWIIT-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 239000006172 buffering agent Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002194 fatty esters Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229940059904 light mineral oil Drugs 0.000 description 1
- MINDHVHHQZYEEK-HBBNESRFSA-N mupirocin Chemical compound C[C@H](O)[C@H](C)[C@@H]1O[C@H]1C[C@@H]1[C@@H](O)[C@@H](O)[C@H](C\C(C)=C\C(=O)OCCCCCCCCC(O)=O)OC1 MINDHVHHQZYEEK-HBBNESRFSA-N 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 1
- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 1
- 229940113124 polysorbate 60 Drugs 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
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
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/02—Local antiseptics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- 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
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
-
- 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
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
-
- 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
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Dermatology (AREA)
- Communicable Diseases (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cosmetics (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Pharmaceutical or veterinary compositions are having a cream base comprising from
Description
NOVEL COMPOSITION
This invention is concerned with novel compositions for use as carriers for therapeutic compounds. In particular it is concerned with so-called creams used as vehicle for topical application of active therapeutic agents, such as antibiotics.
EP-A-0 069 423 (Gist-Brocades) discloses so-called fatty-creams for pharmaceutical topical compositions which comprise from 50 to 80% by weight of fatty materials, 1.5 to 5% by weight of hydrophilic, non-ionic surfactant and a therapeutic agent. Preferred compositions comprise cetyl stearyl alcohol, liquid paraffin, white soft paraffin and cetomacrogol 1000.
EP-A-0 251 434 (Beecham Group) discloses inter alia various cream formulations containing the antibiotic mupirocin. One embodiment comprises 1 to 3% by weight 15 of mupirocin (or a salt thereof), 25 to 60% by weight of liquid paraffin, 20 to 50% by weight of water and 3 to 30% by weight of emulsifier. Example 6 thereof discloses a cream comprising liquid paraffin (42%), stearyl alcohol (16.4%) and cetomacrogol 1000 (3.6%).
Topical antibacterial compositions comprising mupirocin are marketed in the UK by Beecham Research Laboratories under the trade names Bactroban Ointment and Bactroban Nasal. The first product is an ointment comprising a water soluble polyethylene glycol base whilst the second product comprises the calcium salt of mupirocin in a white soft paraffin based ointment containing a glycerin ester.
Within ±e broad range of compositions disclosed by the above prior an, we have now discovered a narrow band of formulations that exhibit improved cosmetic properties over the prior an formulations.
According to the present invention there is provided a pharmaceutical or veterinary composition comprising a cream base and a therapeutic agent characterised in that the cream base comprises:
to 60%, preferably 50 to 55%. by weight of a mineral oil;
to 15%, preferably 5 to 10% by weight of one or more fatty alcohols or fatty esters;
4 to 8%, preferably 5 to 7% by weight of a polyoxyethylene ether or ester surfactant;
and to 35%, preferably 25 to 35% by weight of water.
- 1 8 6 / 0 0 / 9 6 /d/dV
AP.00608
The percentages in the above composition are based on the total weight of the composition which typically also contains from 1 to 3% by weight of a therapeutic agent, such as an antibiotic.
Suitably, the mineral oil and fatty alcohol or ester together compromise from 50 to 75%, preferably 55 to 70%, more preferably from 55 to 65%, by weight of the composition. Suitably, the ratio of mineral oil to fatty alcohol or ester is in the range of from 1:3 to 1:12, prefreably from 1:5 to 1:11, by weight.
The therapeutic agent may be any such agent which is effective in topical application. C As an antibiotic suitable for topical use there may be mentioned in particular ζ- mupirocin, especially its calcium salt, in particular, the dihydrate thereof. Suitably, mupirocin or a salt thereof is present in from 1 to 3% by weight of the formulation, typically about 2% (expressed as the weight of the free acid).
The term mineral oil as used herein includes any that is suitable for use in a topical pharmaceutical or veterinary composition and includes mineral oil USP, light mineral oil NF, liquid paraffin BP and light liquid paraffin BP. The mineral oil known as mineral oil USP is especially suitable.
As fatty alcohol or ester there may be used any of such materials conventionally used in pharmaceutical or veterinary compositions such as stearyl alcohol, cetyl alcohol, θ cetyl stearyl alcohol, myristyl alcohol and glycerin monostearate. Suitably, a mixture θ 25 of stearyl alcohol and cetyl alcohol is used.
The polyoxyethylene ester or alcohol used in this invention is one which will function as a non-ionic surfactant. As indicated in EP-A-0 069 423 cited above, it may be advantageous for the surfactant to have an HLB value of 14 or above. Suitable materials include polyoxyethylene glycol monocetyl ethers, such as the material sold under the trade name Cetomacrogol 1000, and polyoxyethlene sorbitan monostearates, such as the material sold under the trade name Polysorbate 60, or polyoxyethylene sorbitan monoleates, as sold under the trade name Tween 80.
The composition of this invention may also include minor amounts of conventional additives such as viscosity modifiers, for example xanthan gum, and preservatives, such as phenoxyethanol or benzyl alcohol, including mixtures thereof. Also for some
AP/P/ 9 6 / ft 0 7 9 8
-2AP.00608 therapeutic agents it may be necessary to incorporate buffering agents to maintain a suitable pH.
Preferred compositions within the present invention comprise from 50 to 55% by 5 weight of a mineral oil, suitably mineral oil USP; from 5 to 10% by weight of a fatty alcohol or ester, suitably cetyl alcohol or stearyl alcohol or a mixture thereof; from 5 to 7% of a polyoxyethylene ether or ester surfactant, suitably a polyethylene glycol monocetyl ether such as cctomacrogol 1000; from 25 to 35% by weight of water and from 1 to 3%, suitably about 2% by weight (expressed as the weight of free acid) of the calcium salt of mupirocin, in particular the dihydrate salt thereof.
The cream base may be prepared by conventional techniques well known to those skilled in the an. Generally, a suitable process comprises admixing the various ingredients of the cream in appropriate relative amounts in any order that is 15 convenient and thereafter, and if necessary, adjusting the pH to the final desired value. For example, the components of the base may be mixed together at an elevated temperature, for example 60-70°C, until an emulsion has formed. The therapeutic agent may be added after cooling the emulsified cream base, or during mixing, if it is stable to the temperatures employed.
Compositions of the invention are intended for pharmaceutical or veterinary use. Compositions may optionally be provided in sterile condition, by incorporating a conventional sterilisation step into the above procedure. Alternatively, sterile ingredients may be mixed under aseptic conditions.
In a further aspect, the present invention provides pharmaceutical or veterinary compositions for use in therapy.
In addition, in another aspect of this invention, the cream base per se as described 30 may be used as a moisturising cream or emollient without the presence of a therapeutic agent.
The following examples illustrate compositions in accordance with the invention:
AP/P/ 9 6 / 0 0 7 98
-3AP.0 0 6 0 8
Example 1
Mineral Oil USP
Polyethylene glycol (1000) monocetyl ether* 5 Stearyl Alcohol NF
Cetyl Alcohol NF Phenoxyethanol Calcium Mupirocin Xanthan Gum
Purified Water * Cetomacrogol 1000
Example 2
Mineral Oil USP
Polyethylene glycol (1000) monocetyl ether Stearyl Alcohol NF Cetyl Alcohol NF
Phenoxyethanol Benzyl Alcohol Calcium Mupirocin Xanthan Gum Purified Water
Example 3
Mineral Oil USP
Polyethylene glycol (1000) monocetyl ether
Stearyl Alcohol NF Cetyl Alcohol NF Phenoxyethanol Benzyl Alcohol Calcium Mupirocin
Xanthan Gum Purified Water
Claims (16)
1. A pharmaceutical or veterinary composition comprising a cream base and a therapeutic agent characterised in that the cream base comprises:
5 45 to 60% by weight of a mineral oil;
5 to 15% by weight of one or more fatty alcohols or esters;
4 to 8% by weight of a polyoxyethylene ether or ester surfactant; and 20 to 35% by weight of water.
*·,
10
2. A composition as claimed in claim 1 comprising from 50 to 55% by weight of mineral oil.
3. A composition as claimed in claim 1 or 2 comprising from 5 to 10% by weight of one or more fatty alcohols or esters.
4. A composition as claimed in any one of claims 1 to 3 in which the fatty alcohols are a mixture of stearyl alcohol and cetyl alcohol.
5. A composition as claimed in any one of claims 1 to 4 comprising from 5 to 7% by
20 weight of a polyoxyethylene ether or ester surfactant
6. A composition as claimed in any one of claims 1 to 5 in which the surfactant is a polyoxyethylene glycol monocetyl ether.
25
7. A composition as claimed in any one of claims 1 to 6 comprising from 25 to 35% by weight of water.
8. A composition as claimed in any one of claims 1 to 7 comprising from 1 to 3% by weight of a therapeutic agent.
9. A composition as claimed in claim 8 in which the therapeutic agent is an antibiotic.
10. A composition as claimed in claim 9 in which the antibiotic is mupirocin or a salt 35 thereof.
AP/P/ 9 6 / 0 0 7 98
11. A composition as claimed in claim 10 in which the salt is calciom mupirocin
-5AP.00608 dihydrate.
12. A composition as claimed in any one of claims 1 to 11 further comprising a preservative selected from phenoxyethanol or benzyl alcohol or a mixture thereof.
13. A pharmaceutical or veterinary composition comprising from 50 to 55% by weight of a mineral oil; from 5 to 10% by weight of a fatty alcohol or ester; from 5 to 7% of a polyoxyethylene ether or ester surfactant; from 30 to 35% by weight of water and from 1 to 3% by weight (expressed as the weight of free acid) of the calcium salt
10 of mupirocin.
£
14. A composition as defined in any one of the preceding claims for use in therapy.
C 15. A process for preparing a composition as defined in any one of claims 1 to 13
15 which process comprises admixing the various ingredients thereof in appropriate relative amounts in any order that is convenient and thereafter, and if necessary, adjusting the pH to the final desired value.
16. A composition as defined in claim 1 substantially as hereinbefore defined with 20 reference to any one of the Examples.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB939321876A GB9321876D0 (en) | 1993-10-22 | 1993-10-22 | Novel composition |
| GB939322288A GB9322288D0 (en) | 1993-10-29 | 1993-10-29 | Novel composition |
| PCT/US1994/012026 WO1995010999A1 (en) | 1993-10-22 | 1994-10-20 | Novel composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AP9600798A0 AP9600798A0 (en) | 1996-04-30 |
| AP608A true AP608A (en) | 1997-08-28 |
Family
ID=26303736
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| APAP/P/1996/000798A AP608A (en) | 1993-10-22 | 1994-10-20 | Pharmaceutical or veterinary composition comprising a cream base. |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US6025389A (en) |
| EP (1) | EP0727979B1 (en) |
| JP (1) | JPH09506865A (en) |
| KR (1) | KR100374462B1 (en) |
| CN (1) | CN1102410C (en) |
| AP (1) | AP608A (en) |
| AT (1) | ATE202467T1 (en) |
| AU (1) | AU692486B2 (en) |
| BG (1) | BG62912B1 (en) |
| BR (1) | BR9407840A (en) |
| CA (1) | CA2174658C (en) |
| CZ (1) | CZ292223B6 (en) |
| DE (1) | DE69427589T2 (en) |
| DK (1) | DK0727979T3 (en) |
| ES (1) | ES2157996T3 (en) |
| FI (1) | FI116931B (en) |
| GR (1) | GR3036591T3 (en) |
| HU (1) | HU221853B1 (en) |
| NO (1) | NO313446B1 (en) |
| NZ (1) | NZ275282A (en) |
| OA (1) | OA10361A (en) |
| PL (1) | PL177592B1 (en) |
| PT (1) | PT727979E (en) |
| RO (1) | RO112987B1 (en) |
| SK (1) | SK280222B6 (en) |
| UA (1) | UA39896C2 (en) |
| WO (1) | WO1995010999A1 (en) |
Families Citing this family (38)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20000048812A (en) * | 1996-10-01 | 2000-07-25 | 스튜어트 알. 수터, 스티븐 베네티아너, 피터 존 기딩스 | Use of Mupirocin for the Manufacture of a Medicament for the Treatment of Bacterial Infections Associated with Colonisation of the Nasopharynx by Pathogenic Organisms |
| CO4910145A1 (en) * | 1996-10-01 | 2000-04-24 | Smithkline Beecham Corp | USE |
| WO1999012520A1 (en) * | 1997-09-11 | 1999-03-18 | Smithkline Beecham Plc | Compositions adapted for prolonged residence in the nasal pharynx |
| IL123143A (en) * | 1998-02-02 | 2001-08-26 | Agis Ind 1983 Ltd | Pharmaceutical compositions containing mupirocin |
| GB9808470D0 (en) | 1998-04-22 | 1998-06-17 | Smithkline Beecham Plc | Novel process and apparatus |
| IL137363A (en) * | 2000-07-18 | 2005-12-18 | Agis Ind 1983 Ltd | Pharmaceutical compositions containing mupirocin |
| IL150907A (en) * | 2002-07-25 | 2007-07-04 | Stephan Cherkez | Process for the preparation of stable amorphous calcium pseudomonate |
| EP1619947A4 (en) * | 2003-05-01 | 2006-05-31 | Replidyne Inc | Antibacterial methods and compositions |
| US20050123575A1 (en) * | 2003-12-03 | 2005-06-09 | Eilon Asculai | Spreadable compositions for topical use, an improved process of making same and methods of using same |
| WO2008007182A2 (en) * | 2006-07-07 | 2008-01-17 | Glenmark Pharmaceuticals Limited | Topical pharmaceutical compositions of mupirocin or pharmaceutically acceptable salts or esters thereof |
| HUE041512T2 (en) | 2010-03-30 | 2019-05-28 | Helperby Therapeutics Ltd | Novel combination and use |
| JP2013532716A (en) | 2010-08-05 | 2013-08-19 | ヘルパービー セラピューティクス リミテッド | A combination of a pyrroloquinoline compound and a β-lactam antimicrobial agent, mupirocin or chlorhexidine |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4847068A (en) * | 1987-08-06 | 1989-07-11 | Johnson & Johnson Consumer Products, Inc. | Skin care compositions |
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| US3758686A (en) * | 1971-12-07 | 1973-09-11 | American Cyanamid Co | Method of using steroid acetonides |
| US3934013A (en) * | 1975-02-21 | 1976-01-20 | Syntex (U.S.A.) Inc. | Pharmaceutical composition |
| NZ200918A (en) * | 1981-07-02 | 1985-07-31 | Gist Brocades Nv | Stable fatty oil-in-water emulsion cream for topical application |
| GB8530796D0 (en) * | 1985-12-13 | 1986-01-22 | Beecham Group Plc | Pharmaceutical composition |
| IE59628B1 (en) * | 1986-06-26 | 1994-03-09 | Beecham Group Plc | Treatment of fungal infections |
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1994
- 1994-10-20 AT AT94931943T patent/ATE202467T1/en active
- 1994-10-20 DK DK94931943T patent/DK0727979T3/en active
- 1994-10-20 AU AU80847/94A patent/AU692486B2/en not_active Expired
- 1994-10-20 PL PL94314038A patent/PL177592B1/en unknown
- 1994-10-20 BR BR9407840A patent/BR9407840A/en not_active Application Discontinuation
- 1994-10-20 RO RO96-00817A patent/RO112987B1/en unknown
- 1994-10-20 NZ NZ275282A patent/NZ275282A/en not_active IP Right Cessation
- 1994-10-20 CA CA002174658A patent/CA2174658C/en not_active Expired - Lifetime
- 1994-10-20 EP EP94931943A patent/EP0727979B1/en not_active Expired - Lifetime
- 1994-10-20 HU HU9601030A patent/HU221853B1/en active IP Right Grant
- 1994-10-20 WO PCT/US1994/012026 patent/WO1995010999A1/en not_active Ceased
- 1994-10-20 KR KR1019960702041A patent/KR100374462B1/en not_active Expired - Lifetime
- 1994-10-20 ES ES94931943T patent/ES2157996T3/en not_active Expired - Lifetime
- 1994-10-20 CN CN94194238A patent/CN1102410C/en not_active Expired - Lifetime
- 1994-10-20 UA UA96041570A patent/UA39896C2/en unknown
- 1994-10-20 DE DE69427589T patent/DE69427589T2/en not_active Expired - Lifetime
- 1994-10-20 AP APAP/P/1996/000798A patent/AP608A/en active
- 1994-10-20 SK SK495-96A patent/SK280222B6/en not_active IP Right Cessation
- 1994-10-20 CZ CZ19961120A patent/CZ292223B6/en not_active IP Right Cessation
- 1994-10-20 PT PT94931943T patent/PT727979E/en unknown
- 1994-10-20 JP JP7512208A patent/JPH09506865A/en active Pending
-
1996
- 1996-04-12 BG BG100501A patent/BG62912B1/en unknown
- 1996-04-19 FI FI961720A patent/FI116931B/en not_active IP Right Cessation
- 1996-04-19 NO NO19961588A patent/NO313446B1/en not_active IP Right Cessation
- 1996-04-22 OA OA60817A patent/OA10361A/en unknown
-
1997
- 1997-07-25 US US08/903,255 patent/US6025389A/en not_active Expired - Lifetime
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2001
- 2001-09-11 GR GR20010401448T patent/GR3036591T3/en unknown
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4847068A (en) * | 1987-08-06 | 1989-07-11 | Johnson & Johnson Consumer Products, Inc. | Skin care compositions |
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