WO2006102004A2 - Formulation d'emulsion aqueuse stable comportant de l'uree et de l'acide salicylique et son procede d'utilisation - Google Patents
Formulation d'emulsion aqueuse stable comportant de l'uree et de l'acide salicylique et son procede d'utilisation Download PDFInfo
- Publication number
- WO2006102004A2 WO2006102004A2 PCT/US2006/009568 US2006009568W WO2006102004A2 WO 2006102004 A2 WO2006102004 A2 WO 2006102004A2 US 2006009568 W US2006009568 W US 2006009568W WO 2006102004 A2 WO2006102004 A2 WO 2006102004A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- stable formulation
- formulation
- agent
- stable
- salicylic acid
- Prior art date
Links
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- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
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- 229940008099 dimethicone Drugs 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
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- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
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- 238000005187 foaming Methods 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 230000002068 genetic effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 208000016354 hearing loss disease Diseases 0.000 description 1
- 201000003636 hereditary ataxia Diseases 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 239000008309 hydrophilic cream Substances 0.000 description 1
- 239000008311 hydrophilic ointment Substances 0.000 description 1
- 208000018548 hypothalamic dysfunction Diseases 0.000 description 1
- 230000002989 hypothyroidism Effects 0.000 description 1
- 208000003532 hypothyroidism Diseases 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 208000027866 inflammatory disease Diseases 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 230000007803 itching Effects 0.000 description 1
- 230000001530 keratinolytic effect Effects 0.000 description 1
- 150000004715 keto acids Chemical class 0.000 description 1
- 208000017169 kidney disease Diseases 0.000 description 1
- 229940099367 lanolin alcohols Drugs 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 210000005075 mammary gland Anatomy 0.000 description 1
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- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
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- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
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- 230000037311 normal skin Effects 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 229960002446 octanoic acid Drugs 0.000 description 1
- 239000003883 ointment base Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000003711 photoprotective effect Effects 0.000 description 1
- KASDHRXLYQOAKZ-ZPSXYTITSA-N pimecrolimus Chemical compound C/C([C@H]1OC(=O)[C@@H]2CCCCN2C(=O)C(=O)[C@]2(O)O[C@@H]([C@H](C[C@H]2C)OC)[C@@H](OC)C[C@@H](C)C/C(C)=C/[C@H](C(C[C@H](O)[C@H]1C)=O)CC)=C\[C@@H]1CC[C@@H](Cl)[C@H](OC)C1 KASDHRXLYQOAKZ-ZPSXYTITSA-N 0.000 description 1
- 229960005330 pimecrolimus Drugs 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229960004839 potassium iodide Drugs 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 229940095574 propionic acid Drugs 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
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- 238000009877 rendering Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical group 0.000 description 1
- 201000000306 sarcoidosis Diseases 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 230000037307 sensitive skin Effects 0.000 description 1
- 206010040882 skin lesion Diseases 0.000 description 1
- 231100000444 skin lesion Toxicity 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
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- 241000894007 species Species 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 229960001967 tacrolimus Drugs 0.000 description 1
- QJJXYPPXXYFBGM-SHYZHZOCSA-N tacrolimus Natural products CO[C@H]1C[C@H](CC[C@@H]1O)C=C(C)[C@H]2OC(=O)[C@H]3CCCCN3C(=O)C(=O)[C@@]4(O)O[C@@H]([C@H](C[C@H]4C)OC)[C@@H](C[C@H](C)CC(=C[C@@H](CC=C)C(=O)C[C@H](O)[C@H]2C)C)OC QJJXYPPXXYFBGM-SHYZHZOCSA-N 0.000 description 1
- 229960004214 tioconazole Drugs 0.000 description 1
- 238000011200 topical administration Methods 0.000 description 1
- 239000006208 topical dosage form Substances 0.000 description 1
- 239000012049 topical pharmaceutical composition Substances 0.000 description 1
- UJMBCXLDXJUMFB-UHFFFAOYSA-K trisodium;5-oxo-1-(4-sulfonatophenyl)-4-[(4-sulfonatophenyl)diazenyl]-4h-pyrazole-3-carboxylate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-UHFFFAOYSA-K 0.000 description 1
- 229960002703 undecylenic acid Drugs 0.000 description 1
- 229960003726 vasopressin Drugs 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000003871 white petrolatum Substances 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/365—Hydroxycarboxylic acids; Ketocarboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
- A61K8/064—Water-in-oil emulsions, e.g. Water-in-silicone emulsions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/342—Alcohols having more than seven atoms in an unbroken chain
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/86—Polyethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/007—Preparations for dry skin
Definitions
- “emollient” refers to an agent, when applied locally onto skin, would increase tissue moisture content, thereby rendering the skin softer and more pliable;
- % refers to % wt; and % wt refers to % of weight of respective component with respect to the total weight of the composition.
- the term "about” refers to +/- 10 % of a specified value.
- the present stable aqueous-based emulsion formulation may include a photoprotectant or antioxidant such as genestein, vitamin C, vitamin E, avobenzone, octinoxate, and the like.
- Photoprotectant is an agent that prevents UV penetration into skin. The amount of photoprotectant or antioxidant is present at a therapeutic amount to render photoprotection and antioxidation of skins.
- the stable aqueous-based emulsion formulation composition as disclosed in this example was prepared in the following manner.
- oil phase components i.e., glyceryl stearate and PEG 100 stearate, cetyl alcohol, stearyl alcohol, mineral oil light and stearic acid were heated to 70 ⁇ 3°C.
- the water phase components i.e., purified water
- Urea and glycerin were then added and mixed.
- Xanthan gum was slowly added with the homogenizer ON at 2,000 RPM and with a gap setting of 2.5-3.0.
- Benzyl alcohol, propylene glycol, polysorbate 80 and simethicone emulsion were added to the water phase.
- the water phase components were mixed at 39 RPM and the temperature was maintained at 68 ⁇ 3°C.
- Example 1 The following table summarizes additional consistent assay results of salicylic acid urea and benzyl alcohol of the cream formulation as prepared in Example 1.
- the stability was conducted at 35 0 C and 60% relative humidity (RH).
- the stable aqueous-based emulsion formulation was prepared in a commercial scale-manufacturing kettle.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Emergency Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Dermatology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
La présente invention a trait à une formulation d'émulsion aqueuse stable comportant de l'urée et de l'acide salicylique et son procédé de préparation. En particulier, la présente invention a trait à un procédé de traitement d'une condition de la peau comprenant l'étape d'administration topique d'une forme stable d'une formulation comportant de l'urée et de l'acide salicylique.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06738606A EP1863434A4 (fr) | 2005-03-16 | 2006-03-16 | Formulation d'emulsion aqueuse stable comportant de l'uree et de l'acide salicylique et son procede d'utilisation |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US66250805P | 2005-03-16 | 2005-03-16 | |
US60/662,508 | 2005-03-16 | ||
US74808405P | 2005-12-07 | 2005-12-07 | |
US60/748,084 | 2005-12-07 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2006102004A2 true WO2006102004A2 (fr) | 2006-09-28 |
WO2006102004A3 WO2006102004A3 (fr) | 2007-01-11 |
Family
ID=37024396
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2006/009568 WO2006102004A2 (fr) | 2005-03-16 | 2006-03-16 | Formulation d'emulsion aqueuse stable comportant de l'uree et de l'acide salicylique et son procede d'utilisation |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP1863434A4 (fr) |
WO (1) | WO2006102004A2 (fr) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1867322A1 (fr) * | 2006-06-12 | 2007-12-19 | M. Cristina Fernández Rodríguez | Composition topique pour le traitement du psoriasis |
EP2100586A1 (fr) * | 2008-03-11 | 2009-09-16 | L'Oréal | Composition cosmétique comprenant un composé d'acide ascorbique ou d'acide salicylique |
FR2928541A1 (fr) * | 2008-03-11 | 2009-09-18 | Oreal | Composition cosmetique comprenant un compose d'acide salicylique |
JP2016515525A (ja) * | 2013-03-15 | 2016-05-30 | メディシス ファーマシューティカル コーポレイション | フルニソリドの局所用組成物および治療方法 |
US9775851B1 (en) * | 2009-08-31 | 2017-10-03 | Dr. Reddy's Laboratories, Ltd. | Topical formulations comprising a steroid |
US11179465B2 (en) | 2014-03-11 | 2021-11-23 | Primus Pharmaceuticals, Inc. | Topical compositions comprising a corticosteroid |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110180032A (zh) * | 2019-06-12 | 2019-08-30 | 东华大学 | 一种载药控释的同轴静电纺丝纳米纤维支架及其制备方法和应用 |
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FR2586692B1 (fr) * | 1985-08-30 | 1988-03-11 | Oreal | Nouveaux polyaminoamides filtrant le rayonnement ultraviolet, leur procede de preparation et leur utilisation pour proteger la peau et les cheveux |
US5167950A (en) * | 1991-03-28 | 1992-12-01 | S. C. Johnson & Son | High alcohol content aerosol antimicrobial mousse |
FR2728167A1 (fr) * | 1994-12-15 | 1996-06-21 | Cird Galderma | Composition cosmetique ou dermatologique sous forme d'une emulsion eau dans huile a teneur elevee en hydroxyacides |
US5804203A (en) * | 1994-12-21 | 1998-09-08 | Cosmederm Technologies | Topical product formulations containing strontium for reducing skin irritation |
US5567427A (en) * | 1995-03-17 | 1996-10-22 | Helene Curtis, Inc. | Emulsified, low ph cosmetic compositions having improved stability |
ZA962455B (en) * | 1995-03-31 | 1996-10-02 | B Eugene Guthery | Fast acting and persistent topical antiseptic |
EP0954278B8 (fr) * | 1996-11-12 | 2005-06-15 | Pharmacia & Upjohn Company LLC | Compositions pharmaceutiques contenant de l'huile de noix de kukui |
US6582711B1 (en) * | 1997-01-09 | 2003-06-24 | 3M Innovative Properties Company | Hydroalcoholic compositions thickened using polymers |
CA2353071A1 (fr) * | 1998-11-25 | 2000-06-02 | Sembiosys Genetics Inc. | Corps lipidiques servant d'excipient topique pour des agents actifs |
MXPA01012364A (es) * | 1999-06-03 | 2002-07-30 | Unilever Nv | Composiciones cosmeticas anti-secrecion sebacea para el cuidado de la piel. |
US20030104080A1 (en) * | 1999-09-07 | 2003-06-05 | Singh Parashu Ram | Topical urea composition |
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US6475526B1 (en) * | 2001-06-05 | 2002-11-05 | Jeffrey B. Smith | Zinc containing compositions for anti-viral use |
DE10133198A1 (de) * | 2001-07-07 | 2003-01-23 | Beiersdorf Ag | Kreatin enthaltende kosmetische und dermatologische Zubereitungen zur Behandlung und aktiven Prävention trockener Haut und anderer negativer Veränderungen der physiologischen Homöostase der gesunden Haut |
AU2002331001A1 (en) * | 2001-08-07 | 2003-02-24 | Dow Corning Corporation | Hair and skin care compositions containing siloxane-based polyamide copolymers |
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WO2003070161A2 (fr) * | 2001-12-19 | 2003-08-28 | Alwyn Company, Inc. | Composition de soins de beaute emulsifiee contenant de l'acide salicylique, de l'huile de lanoline, et du propyleneglycol |
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2006
- 2006-03-16 EP EP06738606A patent/EP1863434A4/fr not_active Withdrawn
- 2006-03-16 WO PCT/US2006/009568 patent/WO2006102004A2/fr active Application Filing
Non-Patent Citations (1)
Title |
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See references of EP1863434A4 * |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1867322A1 (fr) * | 2006-06-12 | 2007-12-19 | M. Cristina Fernández Rodríguez | Composition topique pour le traitement du psoriasis |
EP2100586A1 (fr) * | 2008-03-11 | 2009-09-16 | L'Oréal | Composition cosmétique comprenant un composé d'acide ascorbique ou d'acide salicylique |
EP2100585A1 (fr) * | 2008-03-11 | 2009-09-16 | L'Oréal | Composition cosmétique comprenant un composé d'acide ascorbique ou d'acide salicylique |
FR2928541A1 (fr) * | 2008-03-11 | 2009-09-18 | Oreal | Composition cosmetique comprenant un compose d'acide salicylique |
CN101530375B (zh) * | 2008-03-11 | 2012-01-11 | 莱雅公司 | 包含抗坏血酸或水杨酸化合物的化妆用组合物 |
US8980234B2 (en) | 2008-03-11 | 2015-03-17 | L'oreal | Cosmetic composition comprising an ascorbic acid or salicylic acid compound |
US9775851B1 (en) * | 2009-08-31 | 2017-10-03 | Dr. Reddy's Laboratories, Ltd. | Topical formulations comprising a steroid |
US10588914B2 (en) | 2009-08-31 | 2020-03-17 | Encore Dermatology, Inc. | Topical formulations comprising a steroid |
US10905697B2 (en) | 2009-08-31 | 2021-02-02 | Encore Dermatology, Inc. | Topical formulations comprising a steroid |
JP2016515525A (ja) * | 2013-03-15 | 2016-05-30 | メディシス ファーマシューティカル コーポレイション | フルニソリドの局所用組成物および治療方法 |
US10953021B2 (en) * | 2013-03-15 | 2021-03-23 | Lupin Limited | Topical compositions of flunisolide and methods of treatment |
US11179465B2 (en) | 2014-03-11 | 2021-11-23 | Primus Pharmaceuticals, Inc. | Topical compositions comprising a corticosteroid |
Also Published As
Publication number | Publication date |
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EP1863434A2 (fr) | 2007-12-12 |
EP1863434A4 (fr) | 2012-03-07 |
WO2006102004A3 (fr) | 2007-01-11 |
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