WO2001012151A1 - Produit de soin pour la peau - Google Patents
Produit de soin pour la peau Download PDFInfo
- Publication number
- WO2001012151A1 WO2001012151A1 PCT/GB2000/003083 GB0003083W WO0112151A1 WO 2001012151 A1 WO2001012151 A1 WO 2001012151A1 GB 0003083 W GB0003083 W GB 0003083W WO 0112151 A1 WO0112151 A1 WO 0112151A1
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- WO
- WIPO (PCT)
- Prior art keywords
- composition
- component
- vitamin
- skin
- inhibitor
- Prior art date
Links
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-
- 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
- A61K2800/92—Oral administration
Definitions
- This invention relates to a skin care product. At least some embodiments provide skin care products for delaying or preventing skin ageing. At least some embodiments improve the physical appearance of persons afflicted with skin ageing. The invention further provides a cosmetic method of improving the appearance of a person suffering from skin ageing.
- Skin ageing appears to involve two pathways; extrinsic and intrinsic. Extrinsic factors are important. 80% or more of skin ageing may be due to extrinsic factors. A major extrinsic factor is photic ageing. Photic ageing is cumulative damage due to repeated exposure to the ionising radiation content of sunlight. Such ionising radiation is thought, but again we do not wish to be bound by this theory, to trigger the release of free radicals. The free radicals are thought to cause damage in a number of ways. Very high levels may cause acute cell death. This leads to sloughing of the skin and the loss of generative cells in the lower dermis. Lower levels of free radicals may cause DNA damage.
- MMPs matrix metalloproteases
- the extracellular matrix is subject to two competing processes; catabolism and anabolism, which may be categorised as tissue wear and renewal respectively.
- catabolic process is slightly greater than the anabolic process, and there is a gradual nett loss of tissue integrity, which results in the gradual appearance of ageing.
- a large part of the catabolic or damaging process is caused by free radical damage caused by exposure to light. Extensive exposure to sunlight increases the rate of catabolism, resulting in accelerated ageing. It follows therefore that skin appearance can be improved by either slowing photic ageing, or increasing the rate of tissue renewal, or preferably both.
- a skin care composition for reducing the photic ageing of skin by degradation of extracellular matrix comprising: i) at least one inhibitor of catabolism of the extracellular matrix; and ii) at least one anabolic or pro-anabolic factor for the extracellular matrix.
- a cosmetic method of improving the appearance of a mammal afflicted with photic skin ageing comprising administering to the afflicted mammal the skin care composition of the invention.
- compositions of the invention can include inhibitors of catabolism.
- Catabolism inhibitors fall into several classes.
- the invention may provide one or more members of one or more classes.
- UV-blocking agent UV-blocking agents reduce the amount of high energy radiation reaching the skin. Since a reduced amount of radiation reaches the skin the potential for damage is reduced.
- suitable UV- blocking agents include metal oxides such as titanium dioxide and zinc oxide which are opaque to a wide range of wavelengths and unsaturated compounds which have strong UV absorbency such as esters of cinnamic acid. The UV blocking agent will generally be applied topically.
- Free radical quenchers destroy free radicals before substantial damage occurs.
- the free radical quenchers fall into two sub-groups.
- the first such as vitamin E, and carotenoids such as ⁇ -carotene and lycopene are lypophilic and thus tend to penetrate the dermis.
- the second sub-group such as vitamin C are hydrophilic and tend to be most effective in extracellular fluids.
- the free radical quenchers can be applied topically, orally or both.
- MMP Inhibitors Free radicals may promote the release of MMPs which cause inflammation and hence damage.
- Some embodiments of the invention comprise MMP inhibitors. Examples include flavonoids such as those obtain from bilberry, elderberry or chokeberry. These flavonoids may also inhibit glycosylation of macromolecules which may also be implanted in degeneration of the extracellular matrix. These materials may be administered orally or topically or both.
- Anti-inflammatories include flavonoids such as those obtain from bilberry, elderberry or chokeberry. These flavonoids may also inhibit glycosylation of macromolecules which may also be
- Anti-inflammatories are thought to reduce the damage caused by MMPs.
- fatty acids such as omega 3 polyunsaturated fatty acids and cis- linoleic acid.
- Purified fatty acids may be used but relatively impure forms such as certain fish oil or preferably plant oils may be used instead.
- Application may be oral, topical or both.
- the inhibitor In view of the large number of proteases in the body it is generally preferred to apply the inhibitor topically. However in the case of the Birket-Bowman protease inhibitor and other inhibitors which are present in foods, and which are frequently ingested, oral application may be preferable.
- the above components alone or in conjunction may reduce the rate of photic ageing.
- At lease some embodiments of the invention seek to enhance the rate of microfibre formation. It is believed that in many people microfibre formation is reduced due to micronutrient deficiency. Consequently administration of the micronutrients may enhance formation of micro fibres in the extracellular matrix.
- Collagen formation may be stimulated by oral administration of vitamin C, vitamin B6, zinc ions and/or copper ions.
- Formation of the aminosugar polymer component can be facilitated by glucosamine which will generally be administered orally as a physiologically acceptable salt such as the sulphate or, more preferably the hydrochloride.
- glucosamine which will generally be administered orally as a physiologically acceptable salt such as the sulphate or, more preferably the hydrochloride.
- manganese is considered to be an important co-factor in glucosamine polymerisation, manganese ions will also be included in the formulation.
- a two part composition is employed.
- a first part is for oral administration and a second for topical administration.
- suitable compositions are as follows: Oral Components
- Vitamin C 0.1 -5g, preferably 0.5-2g, especially 1 g in divided doses, more preferably in sustained release form; Vitamin B6 1 - 10 x RDI (Recommended Daily Input), preferably 5x RDI ;
- Zinc in bioavailable form, e.g. as a chelate or organic or inorganic salt
- -lOOmg preferably 5-20mg, especially lOmg; Copper (in bioavailable form, e.g. as a chelate or organic or inorganic alt) 1-lOOmg preferably 1-1 Omg, especially 5mg; Glucosamine (as hydrochloride) 0.1 - 1 Og preferably 0.5-2g, especially 1 g
- Titanium dioxide finely divided or other UV filter Vitamin E - max permitted load Vitamin C (ascorbyl palmitate) - max permitted load OPC flavonoids
- the oral component may be presented in powdered, tablet, encapsulated or liquid form and may optionally include colourings, flavourings and other materials.
- the topical component will generally be presented in the form of a cream or lotion and may include colourings and perfumes
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Botany (AREA)
- Biotechnology (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Dermatology (AREA)
- Gerontology & Geriatric Medicine (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cosmetics (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP00951735A EP1207847A1 (fr) | 1999-08-12 | 2000-08-10 | Produit de soin pour la peau |
AU64587/00A AU6458700A (en) | 1999-08-12 | 2000-08-10 | Skin care product |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9919079.5 | 1999-08-12 | ||
GBGB9919079.5A GB9919079D0 (en) | 1999-08-12 | 1999-08-12 | Skin care product |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2001012151A1 true WO2001012151A1 (fr) | 2001-02-22 |
Family
ID=10859055
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB2000/003083 WO2001012151A1 (fr) | 1999-08-12 | 2000-08-10 | Produit de soin pour la peau |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP1207847A1 (fr) |
AU (1) | AU6458700A (fr) |
GB (2) | GB9919079D0 (fr) |
WO (1) | WO2001012151A1 (fr) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10126396A1 (de) * | 2001-05-31 | 2002-12-05 | Beiersdorf Ag | Verwendung von Glucosamin zur Herstellung von kosmetischen oder dermatologischen Zubereitungen zur Prophylaxe und Behandlung von entzündlichen Hautzuständen und/oder zum Hautschutz bei empfindlich determinierter und trockener Haut |
EP1314420A1 (fr) * | 2001-11-23 | 2003-05-28 | Cognis Iberia, S.L. | Compositions contre le vieillissement |
WO2006022723A1 (fr) * | 2004-08-18 | 2006-03-02 | The Procter & Gamble Company | Moyen pour ameliorer l'aspect des cheveux et des ongles chez les mammiferes |
WO2004068970A3 (fr) * | 2003-01-31 | 2006-03-09 | Procter & Gamble | Moyen pour ameliorer l'aspect de tissus keratiniques de mammiferes |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7217690B2 (en) | 2003-10-07 | 2007-05-15 | Kimberly-Clark Worldwide, Inc. | Compositions of sunflower trypsin inhibitors |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2694692A1 (fr) * | 1992-08-13 | 1994-02-18 | Thorel Jean Noel | Préparation cosmétique de nutrition de la peau. |
FR2704390A1 (fr) * | 1993-04-29 | 1994-11-04 | Boiron | Complément nutritionnel absorbable per-os destiné à améliorer la peau. |
CN1120931A (zh) * | 1995-06-30 | 1996-04-24 | 张漪� | 一种美容保健护肤品 |
US5658580A (en) * | 1993-09-09 | 1997-08-19 | Chanel, Inc. | Skin cream composition |
FR2746008A1 (fr) * | 1996-03-14 | 1997-09-19 | Thorel Jean Noel | Composition a usage topique anti-vieillissement |
JPH11124311A (ja) * | 1997-10-20 | 1999-05-11 | Shiseido Co Ltd | 光毒性抑制剤 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
LU87145A1 (fr) * | 1988-02-26 | 1989-09-20 | Oreal | Methode pour ameliorer l'aspect esthetique de la peau a l'aide de melanges polyvitaminiques |
US5698206A (en) * | 1996-12-05 | 1997-12-16 | Swedish Herbal Systems, Inc. | Topical composition for the treatment of spider veins |
TWI234467B (en) * | 1997-06-04 | 2005-06-21 | Univ Michigan | Composition for inhibiting photoaging of skin |
AUPP229598A0 (en) * | 1998-03-11 | 1998-04-09 | Oldfield Family Holdings Pty Limited | Treatment of sunburn |
-
1999
- 1999-08-12 GB GBGB9919079.5A patent/GB9919079D0/en not_active Ceased
-
2000
- 2000-08-10 WO PCT/GB2000/003083 patent/WO2001012151A1/fr not_active Application Discontinuation
- 2000-08-10 AU AU64587/00A patent/AU6458700A/en not_active Abandoned
- 2000-08-10 EP EP00951735A patent/EP1207847A1/fr not_active Withdrawn
- 2000-08-10 GB GB0019702A patent/GB2355193A/en not_active Withdrawn
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2694692A1 (fr) * | 1992-08-13 | 1994-02-18 | Thorel Jean Noel | Préparation cosmétique de nutrition de la peau. |
FR2704390A1 (fr) * | 1993-04-29 | 1994-11-04 | Boiron | Complément nutritionnel absorbable per-os destiné à améliorer la peau. |
US5658580A (en) * | 1993-09-09 | 1997-08-19 | Chanel, Inc. | Skin cream composition |
CN1120931A (zh) * | 1995-06-30 | 1996-04-24 | 张漪� | 一种美容保健护肤品 |
FR2746008A1 (fr) * | 1996-03-14 | 1997-09-19 | Thorel Jean Noel | Composition a usage topique anti-vieillissement |
JPH11124311A (ja) * | 1997-10-20 | 1999-05-11 | Shiseido Co Ltd | 光毒性抑制剤 |
Non-Patent Citations (2)
Title |
---|
DATABASE WPI Week 199745, Derwent World Patents Index; AN 1997-481089, XP002154016 * |
DATABASE WPI Week 199929, Derwent World Patents Index; AN 1999-341587, XP002154015 * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10126396A1 (de) * | 2001-05-31 | 2002-12-05 | Beiersdorf Ag | Verwendung von Glucosamin zur Herstellung von kosmetischen oder dermatologischen Zubereitungen zur Prophylaxe und Behandlung von entzündlichen Hautzuständen und/oder zum Hautschutz bei empfindlich determinierter und trockener Haut |
EP1314420A1 (fr) * | 2001-11-23 | 2003-05-28 | Cognis Iberia, S.L. | Compositions contre le vieillissement |
WO2003043595A1 (fr) * | 2001-11-23 | 2003-05-30 | Cognis Iberia, S.L. | Agents anti-vieillissement |
WO2004068970A3 (fr) * | 2003-01-31 | 2006-03-09 | Procter & Gamble | Moyen pour ameliorer l'aspect de tissus keratiniques de mammiferes |
WO2006022723A1 (fr) * | 2004-08-18 | 2006-03-02 | The Procter & Gamble Company | Moyen pour ameliorer l'aspect des cheveux et des ongles chez les mammiferes |
Also Published As
Publication number | Publication date |
---|---|
EP1207847A1 (fr) | 2002-05-29 |
GB0019702D0 (en) | 2000-09-27 |
AU6458700A (en) | 2001-03-13 |
GB9919079D0 (en) | 1999-10-13 |
GB2355193A (en) | 2001-04-18 |
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