WO2011022285A2 - Hair removal device - Google Patents
Hair removal device Download PDFInfo
- Publication number
- WO2011022285A2 WO2011022285A2 PCT/US2010/045270 US2010045270W WO2011022285A2 WO 2011022285 A2 WO2011022285 A2 WO 2011022285A2 US 2010045270 W US2010045270 W US 2010045270W WO 2011022285 A2 WO2011022285 A2 WO 2011022285A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- removal device
- hair removal
- lubricating composition
- solid lubricating
- hair
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q9/00—Preparations for removing hair or for aiding hair removal
- A61Q9/02—Shaving preparations
-
- 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
- A61K8/73—Polysaccharides
- A61K8/738—Cyclodextrins
-
- 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
- A61Q9/00—Preparations for removing hair or for aiding hair removal
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/56—Compounds, absorbed onto or entrapped into a solid carrier, e.g. encapsulated perfumes, inclusion compounds, sustained release forms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
- A61K2800/81—Preparation or application process involves irradiation
Definitions
- the present invention concerns the provision of a hair removal device comprising robust solid lubricating compositions.
- Hair removal devices comprising a soap composition are known - reference is made to WO 07/056509.
- WO 07/056509 also variously teaches to include a small amount of polymer, such as polyoxyethylene, and fatty alcohol, such as behenyl alcohol, within the soap composition.
- a hair removal device incorporating a skin-engaging composition comprising large quantities of hydrophilic polymers, such as polyethylene oxide, to lubricate the skin.
- a disadvantage of the compositions of '116 and '117 is that they may be prone to disintegrate in water and therefore be unsuited to provide lubrication for more than a few shaves.
- a hair removal device comprising a solid lubricating composition, the solid lubricating composition comprising:
- ii. has a molecular weight of less than or equal to 8,000,000, preferably from 100,000 to 3,000,000;
- composition of one or more fatty alcohols selected from Ci 2 - C 3O fatty alcohols.
- Figure 1 is a graph of PEG released into a solvent as discussed in the Disintegration/dissolution Test, below. DETAILED DESCRIPTION OF THE INVENTION
- the present invention overcomes problems associated with prior art hair removal devices incorporating comprise a solid lubricating composition comprising hydrophilic lubricating polymer.
- a solid lubricating composition comprising hydrophilic lubricating polymer.
- the inclusion of the defined fatty alcohols renders the compositions more resistant to dissolution in water and therefore enhances their longevity - in other words, it enables them to provide lubrication for a greater number of uses than would otherwise be the case.
- STP Standard Temperature and Pressure
- the hair removal device may be any hair removal device, such as, but not limited to, a razor or a hair removal device comprising a light source to degrade or destroy the hair.
- the hair removal device comprises a light source
- the light source is advantageously a source of laser light.
- the hair removal device is a razor.
- the solid lubricating composition may advantageously be provided on the razor cartridge, and is preferably as a strip located before and/or after the blade(s) in the direction of cutting.
- WO 97/02116 illustrates locations in which such a strip may be placed.
- the solid lubricating composition may comprise from 3 to 50%, preferable from 5 to 25% by weight of the solid lubricating composition of one or more fatty alcohols selected from Cn - C30, preferably Ci 2 - C 22 fatty alcohol. More preferably, the fatty alcohol comprises cetyl, stearyl, or behenyl alcohol or mixtures thereof.
- the presence of the defined amount of fatty alcohol may enhance the life of the composition by reducing its tendency to disintegrate by dissolution in water, as illustrated in Figure 1, discussed below. If too much fatty alcohol is present, however, then the solid lubricating composition may become too hydrophobic and the water soluble lubricating polymer may be prevented from performing its intended function.
- the solid lubricating composition comprises a water-soluble lubricating polymer.
- the water- soluble lubricating polymer may achieve lubrication by a number of mechanisms, such as binding water to form a gel. In order to be effective, the polymer must be solid at STP and have a molecular weight of less than 8,000,000.
- Suitable water-soluble lubricating polymers include polyalkylene glycol; cellulosic polymers, including hydroxypropyl cellulose; hydroxypropyl methylcellulose (HPMC);
- polyalkylene glycol is synonymous with “polyalkane oxide", although some sources have, in the past, referred to lower molecular weight variants as “polyalkylene glycol” and higher molecular weight variants as “polyalkane oxide”.
- the polyalkylene glycol (polyalkane oxide) comprises polyethylene glycol (which may also be referred to herein as "PEG”), polypropylene glycol, or mixtures thereof and more preferably it comprises polyethylene glycol.
- the solid lubricating composition preferably comprises from 40 to 95%, preferably from 45 to 85%, by weight of water-soluble lubricating polymer.
- the water-soluble lubricating polymers comprise polyethylene oxides generally known as POLYOX (available from the Dow Chemical Company) or
- these particular polyethylene oxides will have molecular weights of about 100,000 to about 6 million, preferably from about 300,000 to about 5 million and the polyethylene oxide comprises a blend of polyethylene oxide having an average molecular weight of about 5 million and polyethylene oxide having an average molecular weight of about 300,000.
- the solid lubricating composition comprises less than 2%, preferably less than 1% and more preferably 0% of water-soluble surfactant, by weight of the solid lubricating composition.
- water-soluble surfactant refers to surfactant which fulfils the following condition: at 25°C, Ig of the surfactant dissolves in 1000ml or less of water. For completeness, one requires more than 10,000ml of water at 25°C in order to dissolve Ig of magnesium stearate or Ig of cetyl alcohol.
- the solid lubricating compositions may comprise a hydrophobic binder. The presence of such a component may enhance the life of the composition by reducing its tendency to be mechanically eroded.
- the hydrophobic binder is solid at STP.
- Suitable hydrophobic binders include divalent metal cation stearate, preferably magnesium stearate, calcium stearate, zinc stearate, or mixtures thereof, more preferably magnesium stearate; ethyl cellulose; polycaprolactone; polyethylene; polypropylene; polystyrene; butadiene-styrene copolymer (e.g. medium and high impact polystyrene); polyacetal; acrylonitrilebutadiene- styrene copolymer; ethylene vinyl acetate copolymer and blends such as polypropylene/polystyrene blend; and mixtures thereof.
- the solid lubricating composition In the event that the solid lubricating composition is cold-pressed, then it preferably comprises from 1 to 20% and more preferably from 5 to 15% hydrophobic binder, by weight of the solid lubricating composition. In the event that the solid lubricating composition is manufactured by an extrusion process, as discussed below, then it preferably comprises from 10 to 50%, more preferably from 15 to 40% and yet more preferably 20 to 35% hydrophobic binder, by weight of the solid lubricating composition.
- perfume oils may volatilize and boil off. During a cold-pressing process, the perfume may be squeezed out during compaction and lost as well. Furthermore, perfume oils are usually fairly hydrophobic and may be repelled by hydrophilic materials, such as the water-soluble lubricating polymers disclosed herein. The result tends to be an unsatisfactorily perfumed product.
- perfume oils comprised within the solid lubricating compositions according to the invention may be releasably encapsulated within a powder.
- Any powder which permits perfume release in use, such as on contact with water, may suitably be used.
- the powder comprises a cyclic oligosaccharide, which may encapsulate the perfume.
- cyclic oligosaccharide means a cyclic structure comprising six or more saccharide units.
- Preferred for use herein are cyclic oligosaccharides having six, seven or eight saccharide units and mixtures thereof, more preferably six or seven saccharide units and even more preferably seven saccharide units. It is common in the art to abbreviate six, seven and eight membered cyclic oligosaccharides to ⁇ , ⁇ and ⁇ respectively.
- Cyclic oligosaccharides for use herein may comprise any suitable saccharide or mixtures of saccharides.
- suitable saccharides include, but are not limited to, glucose, fructose, mannose, galactose, maltose and mixtures thereof, preferably glucose.
- the preferred cyclic oligosaccharides for use herein are ⁇ -cyclodextrins or ⁇ - cyclodextrins, or mixtures thereof, and the most preferred cyclic oligosaccharides for use herein are ⁇ -cyclodextrins.
- the cyclic oligosaccharides for use herein may be substituted by any suitable substituent or mixture of substituents.
- mixture of substituents means that two or more different suitable substituents can be substituted onto one cyclic oligosaccharide.
- the derivatives of cyclodextrins consist mainly of molecules wherein some of the OH groups have been substituted.
- Suitable substituents include, but are not limited to, alkyl groups; hydroxyalkyl groups; dihydroxyalkyl groups; (hydroxyalkyl) alkylenyl bridging groups such as cyclodextrin glycerol ethers; aryl groups; maltosyl groups; allyl groups; benzyl groups; alkanoyl groups; cationic cyclodextrins such as those containing 2-hydroxy-3- (dimethylamino) propyl ether; quaternary ammonium groups; anionic cyclodextrins such as carboxyalkyl groups,
- the substituents may be saturated or unsaturated, straight or branched chain.
- Preferred substituents include saturated and straight chain alkyl groups, hydroxyalkyl groups and mixtures thereof.
- Preferred alkyl and hydroxyalkyl substituents are selected from C1-C8 alkyl or hydroxyalkyl groups or mixtures thereof, more preferred alkyl and hydroxyalkyl substituents are selected from C1-C6 alkyl or hydroxyalkyl groups or mixtures thereof, even more preferred alkyl and hydroxyalkyl substituents are selected from C1-C4 alkyl or hydroxyalkyl groups and mixtures thereof.
- Especially preferred alkyl and hydroxyalkyl substituents are propyl, ethyl and methyl, more especially hydroxypropyl and methyl and even more preferably methyl.
- cyclic oligosaccharides for use in the present invention are unsubstituted, or are substituted by only saturated straight chain alkyl, or hydroxyalkyl substituents. Therefore, preferred examples of cyclic oligosaccharides for use herein are ⁇ -cyclodextrin, ⁇ -cyclodextrin, methyl- ⁇ -cyclodextrin, methyl- ⁇ -cyclodextrin, and hydroxypropyl- ⁇ -cyclodextrin.
- the solid lubricating composition comprised within the hair removal device according to the invention may be manufactured in a number of ways. Traditionally, such a composition may be manufactured using an extrusion method, such as is disclosed in WO 97/02116 and WO 97/02117, referred to above. If the solid lubricating composition comprises a temperature- sensitive component, such as a fragrance oil, then the solid lubricating composition may advantageously be a cold-pressed composition, as exemplified in Examples 1 to 3 below. By cold-pressing, temperature-sensitive components may be better retained within the composition and not lost by boiling off, degradation, and the like. As discussed above, if the composition is cold-pressed, then it advantageously does not comprise more than 20% and preferably less than 15% of fatty alcohol by weight of the solid lubricating composition.
- a temperature-sensitive component such as a fragrance oil
- the term "cold-pressed” means that the formulation has been manufactured by process involving a compression step, without any active heating and the term “cold-pressing” should be interpreted accordingly. For the avoidance of doubt, heat generated by the compression step itself is not regarded as being active heating.
- temperature-sensitive component refers to materials which have a boiling point, undergo significant sublimation, or which undergo a change in chemical structure at temperatures above ambient temperatures and below 100 0 C.
- Materials having a boiling point in this range are known to the skilled person and include many low boiling point perfume oils.
- Low boiling perfume oils, or top notes are those that provide the initial burst of fragrance following application to the skin, because they boil off quickly when exposed to body heat.
- the skilled person is similarly familiar with materials which undergo significant sublimation in the present temperature range.
- An example of a commonly used sensate which sublimes in this temperatures range is menthol.
- Materials whose chemical structures change at temperatures within the cited range are known to the skilled person.
- One example of such a material is L-ascorbic acid, which oxidizes at an increasing rate as the temperature rises.
- ⁇ olyoxTM WSR-N750 powder a polyethylene glycol with molecular weigh about 300,000 manufactured by Dow Chemicals
- compositions of Examples 1 -3 are manufactured by placing the materials into a blending device and blending until the mixture is entirely homogeneous. Once homogenised, the mixture is pressed into the desired shape using an appropriate mould tool / punch.
- An example of a suitable device is the GEA Courtoy R253-27 tablet press. The powder is compressed using a force of 1 x 10 10 - I x 10 12 Nm "2 . The resultant tablet is ejected from the mould in the desired shape.
- the above composition is manufactured by extruding the blend through a Haake System 90, 0.019m ( 3 A inch) diameter extruder with a barrel pressure of about 68.9 - 137.8 bar (1000-2000 psi), a rotor speed of about 10 to 50 rpm, and a temperature of about 150-185"C and a die temperature of about 170- 185 "C.
- the extruded strip of composite is cooled and sliced to the appropriate size.
- a lO ⁇ l drop of extraction solvent (Deuterium oxide) was placed at the bottom of a glass vial and the strip of solid lubricant placed on the drop of solvent.
- the vial was then placed into an oven at 50 0 C for two minutes which 'glued' the fragment to the vial.
- lOOO ⁇ l of extraction solvent (Deuterium oxide) was added to the vial and it was tumble mixed for 20 minutes. After 20 minutes, 200ul of the solution was extracted from the top of the vial for NMR analysis of PEG levels.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Dermatology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Lubricants (AREA)
- Laser Surgery Devices (AREA)
- Radiation-Therapy Devices (AREA)
Abstract
Description
Claims
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| MX2012002173A MX2012002173A (en) | 2009-08-21 | 2010-08-12 | Hair removal device. |
| CA2770836A CA2770836A1 (en) | 2009-08-21 | 2010-08-12 | Hair removal device |
| RU2012102689/15A RU2485934C1 (en) | 2009-08-21 | 2010-08-12 | Device for hair removal |
| JP2011536633A JP5173034B2 (en) | 2009-08-21 | 2010-08-12 | Hair removal device |
| AU2010284467A AU2010284467B2 (en) | 2009-08-21 | 2010-08-12 | Hair removal device |
| CN2010800369887A CN102481240A (en) | 2009-08-21 | 2010-08-12 | hair removal device |
| BR112012003751A BR112012003751A2 (en) | 2009-08-21 | 2010-08-12 | hair removal device |
| ZA2012/01081A ZA201201081B (en) | 2009-08-21 | 2012-02-14 | Hair removal device |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09168358.1 | 2009-08-21 | ||
| EP09168358 | 2009-08-21 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2011022285A2 true WO2011022285A2 (en) | 2011-02-24 |
| WO2011022285A3 WO2011022285A3 (en) | 2011-04-14 |
Family
ID=42026183
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2010/045270 Ceased WO2011022285A2 (en) | 2009-08-21 | 2010-08-12 | Hair removal device |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20110041865A1 (en) |
| EP (1) | EP2286788A3 (en) |
| JP (1) | JP5173034B2 (en) |
| CN (1) | CN102481240A (en) |
| AU (1) | AU2010284467B2 (en) |
| BR (1) | BR112012003751A2 (en) |
| CA (1) | CA2770836A1 (en) |
| MX (1) | MX2012002173A (en) |
| RU (1) | RU2485934C1 (en) |
| WO (1) | WO2011022285A2 (en) |
| ZA (1) | ZA201201081B (en) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL2537511T3 (en) * | 2011-06-24 | 2017-07-31 | The Gillette Company Llc | Hair removal device comprising erodable moisturizer |
| US20130042482A1 (en) * | 2011-08-16 | 2013-02-21 | Valerie Jean Bradford | Skin Engaging Member Comprising An Anti-Irritation Agent |
| EP2559418A1 (en) * | 2011-08-17 | 2013-02-20 | The Procter & Gamble Company | Fragrant depilatory article |
| AU2015325131B2 (en) * | 2014-09-30 | 2020-11-05 | Edgewell Personal Care Brands, Llc | Erodible anhydrous polyethylene oxide film |
| MX2017008210A (en) * | 2014-12-18 | 2017-10-06 | Gillette Co Llc | Lubricating members having hydrophobic components for razor cartridges. |
| AU2016285816A1 (en) * | 2015-06-30 | 2018-01-18 | The Gillette Company Llc | Lubricating members for razor cartridges |
| US10898425B2 (en) * | 2016-11-17 | 2021-01-26 | The Gillette Company Llc | Skin engaging member comprising ethylene vinyl acetate and a fragrance |
| US11872711B2 (en) | 2019-05-10 | 2024-01-16 | The Gillette Company Llc | Lubricating member for razor cartridges |
| US20210322290A1 (en) | 2020-04-10 | 2021-10-21 | The Procter & Gamble Company | Rheological Solid Composition for Use in Shaving |
| US11554087B2 (en) | 2020-11-05 | 2023-01-17 | The Gillette Company Llc | Shaving aid comprising an antioxidant |
| DE102021131291A1 (en) | 2020-12-29 | 2022-06-30 | The Gillette Company Llc | SHAVING AID COMPRISING AN ACTIVE INGREDIENT |
| EP4587128A1 (en) | 2022-09-14 | 2025-07-23 | The Gillette Company LLC | Lubricating member comprising polyglutamic acid |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997002117A1 (en) | 1995-06-30 | 1997-01-23 | The Gillette Company | Shaving aid composite with an inclusion complex of a skin-soothing agent and cyclodextrin |
| WO1997002116A1 (en) | 1995-06-30 | 1997-01-23 | The Gillette Company | Shaving aid composite with a non-volatile cooling agent |
| WO2007056509A1 (en) | 2005-11-09 | 2007-05-18 | The Gillette Company | Molded shaving aid compositions, components and methode of manufacture |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5113585A (en) * | 1990-09-28 | 1992-05-19 | The Gillette Company | Shaving system |
| US5910472A (en) * | 1994-12-03 | 1999-06-08 | The Procter & Gamble Company | Cleansing compositions |
| DE60101151T2 (en) * | 2000-02-18 | 2004-09-02 | The Gillette Co., Boston | SHAVING AID STRIP FOR RAZOR BLADE UNIT |
| US6763590B2 (en) * | 2002-10-21 | 2004-07-20 | Eveready Battery Company, Inc. | Razor assembly having a clutch controlled shaving aid delivery system |
| AU2009223548B2 (en) * | 2008-03-07 | 2015-01-29 | Edgewell Personal Care Brands, Llc | Shaving aid material |
| IN2012DN01371A (en) * | 2009-08-21 | 2015-06-05 | Gillette Co |
-
2010
- 2010-08-12 CA CA2770836A patent/CA2770836A1/en not_active Abandoned
- 2010-08-12 WO PCT/US2010/045270 patent/WO2011022285A2/en not_active Ceased
- 2010-08-12 RU RU2012102689/15A patent/RU2485934C1/en not_active IP Right Cessation
- 2010-08-12 MX MX2012002173A patent/MX2012002173A/en unknown
- 2010-08-12 JP JP2011536633A patent/JP5173034B2/en not_active Expired - Fee Related
- 2010-08-12 CN CN2010800369887A patent/CN102481240A/en active Pending
- 2010-08-12 AU AU2010284467A patent/AU2010284467B2/en not_active Expired - Fee Related
- 2010-08-12 BR BR112012003751A patent/BR112012003751A2/en not_active IP Right Cessation
- 2010-08-16 EP EP10172938A patent/EP2286788A3/en not_active Withdrawn
- 2010-08-17 US US12/858,120 patent/US20110041865A1/en not_active Abandoned
-
2012
- 2012-02-14 ZA ZA2012/01081A patent/ZA201201081B/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1997002117A1 (en) | 1995-06-30 | 1997-01-23 | The Gillette Company | Shaving aid composite with an inclusion complex of a skin-soothing agent and cyclodextrin |
| WO1997002116A1 (en) | 1995-06-30 | 1997-01-23 | The Gillette Company | Shaving aid composite with a non-volatile cooling agent |
| WO2007056509A1 (en) | 2005-11-09 | 2007-05-18 | The Gillette Company | Molded shaving aid compositions, components and methode of manufacture |
Also Published As
| Publication number | Publication date |
|---|---|
| RU2485934C1 (en) | 2013-06-27 |
| CN102481240A (en) | 2012-05-30 |
| MX2012002173A (en) | 2012-05-29 |
| CA2770836A1 (en) | 2011-02-24 |
| JP5173034B2 (en) | 2013-03-27 |
| ZA201201081B (en) | 2015-08-26 |
| AU2010284467B2 (en) | 2014-10-02 |
| US20110041865A1 (en) | 2011-02-24 |
| EP2286788A3 (en) | 2012-10-24 |
| EP2286788A2 (en) | 2011-02-23 |
| BR112012003751A2 (en) | 2016-04-12 |
| AU2010284467A1 (en) | 2012-03-15 |
| JP2012508088A (en) | 2012-04-05 |
| WO2011022285A3 (en) | 2011-04-14 |
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