WO2013107687A2 - Compositions dermo-cosmétiques à base d'une association synergique d'argent colloïdal et d'acide désoxyribonucléique - Google Patents
Compositions dermo-cosmétiques à base d'une association synergique d'argent colloïdal et d'acide désoxyribonucléique Download PDFInfo
- Publication number
- WO2013107687A2 WO2013107687A2 PCT/EP2013/050422 EP2013050422W WO2013107687A2 WO 2013107687 A2 WO2013107687 A2 WO 2013107687A2 EP 2013050422 W EP2013050422 W EP 2013050422W WO 2013107687 A2 WO2013107687 A2 WO 2013107687A2
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- WO
- WIPO (PCT)
- Prior art keywords
- colloidal silver
- dna
- silver
- compositions according
- ppm
- Prior art date
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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
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0241—Containing particulates characterized by their shape and/or structure
-
- 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
-
- 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
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4953—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom containing pyrimidine ring derivatives, e.g. minoxidil
-
- 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
- A61K8/60—Sugars; Derivatives thereof
- A61K8/606—Nucleosides; Nucleotides; Nucleic acids
-
- 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
- A61Q19/08—Anti-ageing preparations
-
- 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
- A61K2800/10—General cosmetic use
-
- 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
- A61K2800/41—Particular ingredients further characterized by their size
- A61K2800/413—Nanosized, i.e. having sizes below 100 nm
-
- 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
- A61K2800/52—Stabilizers
- A61K2800/522—Antioxidants; Radical scavengers
-
- 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
- A61K2800/60—Particulates further characterized by their structure or composition
- A61K2800/65—Characterized by the composition of the particulate/core
- A61K2800/651—The particulate/core comprising inorganic material
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/14—Preparations for removing make-up
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- 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
- A61Q19/001—Preparations for care of the lips
-
- 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
- A61Q19/004—Aftersun preparations
-
- 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
- A61Q19/005—Preparations for sensitive skin
-
- 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
- A61Q19/008—Preparations for oily skin
-
- 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
- A61Q19/10—Washing or bathing preparations
Definitions
- Dermo-cosmetic compositions based on a synergistic combination of colloidal silver and deoxyribonucleic acid.
- the present invention relates to dermo-cosmetic compositions according to claim 1 and the use of such compositions in cosmetology according to claim 12.
- the present invention relates to novel topical formulations for use in dermo-cosmetology and more particularly in the treatment of physiological and actinic cutaneous senescence.
- formulations are based on a combination of active ingredients that potentiate the regeneration of collagen, as well as protection against free radicals.
- the active ingredients consist mainly of colloidal silver and deoxyribonucleic acid (DNA), possibly in combination with caffeine.
- DNA deoxyribonucleic acid
- the first manifestation that appears around 30 years affects the elastic fibers of the papillary dermis.
- the second stage appears towards 50 years concerning the collagen fibers of the deep dermis.
- the sun accentuates wrinkles and causes pigmented spots on the skin.
- the dermo-cosmetic compositions are defined in claim 1 of the present invention and the use of such compositions in cosmetology is defined in claim 12 of the present invention.
- the dermo-cosmetic compositions contain, as active ingredients, a synergistic combination of colloidal silver and deoxyribonucleic acid and are characterized in that the colloidal silver is more particularly an aqueous solution of electro colloidal silver.
- compositions according to the present invention may contain caffeine.
- the electro colloidal silver of the compositions according to the present invention can contain from 80 to 96% of silver ions and 4 to 20% of silver particles.
- the size of the silver particles can range from 0.0008 to 0.04 microns.
- the colloidal silver solution can contain from 5 to 20 ppm of silver.
- the colloidal silver solution can contain 10 ppm silver.
- compositions according to the present invention may contain from 1 to 90% colloidal silver.
- the deoxyribonucleic acid of the compositions according to the present invention may be more particularly highly polymerized deoxyribonucleic acid (HP DNA).
- HP DNA deoxyribonucleic acid
- the highly polymerized DNA is more particularly HP DNA in the form of sodium salt.
- compositions according to the present invention may contain from 0.1 to 5% of HP DNA.
- compositions according to the present invention may contain from 0.1 to 3% caffeine.
- compositions according to the present invention can be used in cosmetology in the treatment of aging disorders and more particularly for anti-wrinkle activity.
- colloidal silver or silver colloid You should know that there are four different products on the market called colloidal silver or silver colloid.
- the first type is the classic product used in our formulations, called electro colloidal silver.
- This product is prepared by the electric arc method in deionized water, or by the low voltage electrolysis method in distilled water. This product is usually found in a concentration of 3 to 20 ppm. It is formed of microscopic particles of elemental pure silver suspended in water. Each silver particle has a positive electrical charge. The silver colloid thus prepared is totally transparent.
- the second is called protein silver colloid, this chemical product attaches microscopic silver particles to a protein molecule.
- the third is the group of silver salts, for example silver citrate.
- the fourth is sometimes called "silver powder". This product was developed by the Russians and results from a pure silver wire that is disintegrated by a high voltage electrical discharge. This microscopic dust is collected and dissolved in water. Electro colloidal silver is considered colloidal because of particle size and ionic as a function of its positive charge.
- compositions of the present invention contain from 1 to 90% colloidal silver.
- Colloidal silver has an anti-radical action.
- Dr. BECKER in 1985, studies the mechanism by which silver ions regenerate tissues. Silver ions form a complex with living cells to produce stem cells responsible for tissue regeneration. Antibacterial activity:
- Electro colloidal silver was more effective than silver nitrate, silver chloride and silver sulfadiazine, for its ability to act as a germicide with broad spectrum of activity and on all species of bacteria and fungi.
- Jason HENRY tested colloidal silver on a pathogenic yeast (S.cerivisae) and reports that a single application of the product dosed at 10 ppm, was able to stop the development of yeast for 24 hours, which allowed the immune system to have time to react.
- Sovereign Silver colloidal silver marketed by Natural Immunogenics at 10 ppm, has been tested in an FDA-approved laboratory (Covance Laboratories Inc.). This toxicological study confirms the perfect tolerance and the safety of this product (report of March 20, 2003).
- DNA Deoxyribonucleic acid
- the DNA used in our formulations is more particularly the highly polymerized DNA in the form of its sodium salt marketed by JAVENECH.
- This macromolecule of marine origin is in the form of long white fibers. This fibrous appearance is characteristic of the super-double-helix organization of this bio-polymer.
- the extraction of HP DNA (highly polymerized) by non-denaturing techniques ensures a perfect protection of the molecular structure preserving its physiological activity.
- HP DNA is an excellent moisturizing agent for the skin. Thus at the cellular level, when they diffuse the HP DNA molecules bind to a volume of aqueous solution greater than 10,000 times their own volume.
- compositions of the present invention contain from 0.1 to 5% HP DNA.
- the HP DNA biomolecule By trapping the OH radicals within the double helix.
- the HP DNA biomolecule has the advantage over most other substances of the same activity, does not generate, after capture of free radicals, a derivative likely to alter other constituents of proximity.
- the OH radical is fixed on the bases of the molecule, in particular on guanine, giving a stable compound: 8-hydroxyguanoside.
- anti-lipoperoxidant properties can be used to protect the oxidation of membrane lipids in the skin, as well as in creams, in order to protect the skin. oily phase.
- HP DNA is also likely to inhibit the elastases and more particularly the elastase fibroblasts of human skin, mainly responsible for the lysis of elastic fibers of the dermis during aging.
- HP DNA In addition to the biological effects of HP DNA, an important physical characteristic reinforces its protective role of cutaneous structures. At a thickness of 1 mm, a solution of 1% HP DNA absorbs all of the low intensity UV radiation, between 200 and 300 nm, which is the one that damages the cellular DNA.
- Caffeine This product is used in our formulations, for its lipolytic action, more particularly in the formulations "eye contour" which confer an effective action anticernes.
- compositions of the present invention contain from 0.1 to 3% caffeine.
- Lipid peroxidation is a typical case of a radical induced chain reaction.
- the oxidation of membrane lipids results in the formation of lipoperoxides which break down into different fragmentation products, some of which are very toxic and aggressive to the skin.
- MDA malone dialdehyde
- the Applicant proposes a combination of colloidal silver and HP DNA.
- each of the two active agents has been subjected to the lipid peroxidation initiation treatment according to:
- Example 1 The formulation of Example 1 was tested clinically using a method of assessing anti-wrinkle activity.
- the method used is the fingerprint technique associated with macro-photographic analysis.
- the Applicant proposes cosmetic compositions based on a synergistic combination of colloidal silver and HP DNA useful in the treatment of physiological skin aging and actinic, possibly in combination with caffeine.
- the colloidal silver used is an electro colloidal silver containing from 80 to 96% of Ag + ionic silver and 4 to 20% of particles.
- the size of the silver particles ranges from 0.0008 microns to 0.04 microns.
- the ppm content (part per million) of the colloidal silver solution is between 5 ppm and 20 ppm.
- colloidal silver solution can significantly reduce the rate of preservatives in our cosmetic formulations.
- the colloidal silver used is more particularly that marketed by the company Natural Immunogenics dosed at 10 ppm.
- the DNA used is more particularly the highly polymerized (HP) DNA in the form of sodium salt marketed by JAVENECH.
- Active ingredients 10 ppm colloidal silver solution 70 to 80 ml
- Organic sweet almond oil 1 to 5%
- Organic argan oil 1 to 5%
- Oily extract of organic aloe vera 1 to 5%
- cetearylalcohol cetearylglucoside: 5 to 10%
- Hydrogenated vegetable glycerides 1 to 5%
- Glycerin 1 to 5%
- Dicaprylyl carbonate 1 to 5%
- Caprylic / caprictriglycerides 1 to 5%
- Tocopheryl acetate less than 1%
- Xanthan gum less than 1%
- hypoallergenic fragrance less than 1%
- Active ingredients 10 ppm colloidal silver solution 60 to 80 ml
- hypoallergenic fragrance less than 1%
- hypoallergenic fragrance less than 1%
- hypoallergenic fragrance less than 1%
- Active ingredients 10 ppm solution of colloidal silver 70 to 80 ml HP DNA: 250 mg
- hypoallergenic fragrance less than 1%
- Active ingredients 10 ppm colloidal silver solution 60 to 80 ml
- HP DNA 1000 to 1200 mg
- Caffeine 500 to 800 mg
- Active ingredients 20 ppm colloidal silver solution 2 to 5 ml
- hypoallergenic fragrance less than 1%
- Active ingredients 20 ppm colloidal silver solution 70 to 90 ml
- HP DNA 300 to 500 mg
- Caffeine 300 to 500 mg
- hypoallergenic fragrance less than 1%
- Active ingredients 15 ppm solution of colloidal silver 1 to 5 ml
- hypoallergenic fragrance less than 1%
- Active ingredients 10 ppm colloidal silver solution 60 to 90 ml
- HP DNA 200 to 500 mg
- hypoallergenic fragrance less than 1%
- Active ingredients 10 ppm colloidal silver solution 70 to 90 ml
- HP DNA 100 to 200 mg
- hypoallergenic fragrance less than 1%
- Active ingredients 10 ppm colloidal silver solution 65 to 85 ml
- HP DNA 500 to 1000 mg
- Active ingredients 10 ppm colloidal silver solution 1 to 3 ml
- hypoallergenic fragrance less than 1%
- Active ingredients 10 ppm colloidal silver solution 65 to 80 ml
- hypoallergenic fragrance less than 1%
- Active ingredients 15 ppm colloidal silver solution 70 to 80 ml
- hypoallergenic fragrance less than 1%
- Active ingredients 20 ppm colloidal silver solution 5 to 10 ml
- HP DNA 300 to 500mg
- hypoallergenic fragrance less than 1%
- Active ingredients 10 ppm colloidal silver solution 65 to 80 ml
- HP DNA 300 to 500 mg
- hypoallergenic fragrance less than 1%
- Active ingredients 5 ppm solution of colloidal silver 30 to 50 ml
- HP DNA 100 to 250mg
- hypoallergenic fragrance less than 1%
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Chemical & Material Sciences (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Gerontology & Geriatric Medicine (AREA)
- Dermatology (AREA)
- Inorganic Chemistry (AREA)
- Cosmetics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP13700114.5A EP2747739B1 (fr) | 2012-01-16 | 2013-01-10 | Compositions dermo-cosmétiques à base d'une association synergique d'argent colloïdal et d'acide désoxyribonucléique |
CN201380005376.5A CN104053425B (zh) | 2012-01-16 | 2013-01-10 | 基于胶体银和脱氧核糖核酸的协同组合的医学护肤组合物 |
RU2014119440A RU2609867C1 (ru) | 2012-01-16 | 2013-01-10 | Дерматокосметологические композиции, основанные на синергетическом сочетании коллоидного серебра и дезоксирибонуклеиновой кислоты |
BR112014017448-2A BR112014017448B1 (pt) | 2012-01-16 | 2013-01-10 | Composição dermocosmética contendo como princípio ativo, uma combinação sinérgica de prata coloidal e ácido desoxirribonucleico e seu uso |
US14/371,818 US9486397B2 (en) | 2012-01-16 | 2013-01-10 | Dermocosmetic compositions based on a synergistic combination of colloidal silver and deoxyribonucleic acid |
ES13700114.5T ES2553055T3 (es) | 2012-01-16 | 2013-01-10 | Composiciones dermocosméticas basadas en una asociación sinérgica de plata coloidal y ácido desoxirribonucleico |
JP2014551617A JP6267653B2 (ja) | 2012-01-16 | 2013-01-10 | コロイド銀とデオキシリボ核酸との相乗的組み合わせに基づく皮膚化粧用組成物 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR1200122A FR2985662B1 (fr) | 2012-01-16 | 2012-01-16 | Compositions dermo-cosmetiques a base d'une association synergique d'argent colloidal et d'acide desoxyribonucleique |
FR12/00122 | 2012-01-16 |
Publications (3)
Publication Number | Publication Date |
---|---|
WO2013107687A2 true WO2013107687A2 (fr) | 2013-07-25 |
WO2013107687A3 WO2013107687A3 (fr) | 2014-04-03 |
WO2013107687A4 WO2013107687A4 (fr) | 2014-05-30 |
Family
ID=47522703
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2013/050422 WO2013107687A2 (fr) | 2012-01-16 | 2013-01-10 | Compositions dermo-cosmétiques à base d'une association synergique d'argent colloïdal et d'acide désoxyribonucléique |
Country Status (9)
Country | Link |
---|---|
US (1) | US9486397B2 (fr) |
EP (1) | EP2747739B1 (fr) |
JP (1) | JP6267653B2 (fr) |
CN (1) | CN104053425B (fr) |
BR (1) | BR112014017448B1 (fr) |
ES (1) | ES2553055T3 (fr) |
FR (1) | FR2985662B1 (fr) |
RU (1) | RU2609867C1 (fr) |
WO (1) | WO2013107687A2 (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3188706A4 (fr) * | 2014-09-02 | 2018-05-02 | American Silver, LLC | Toxine botulique et particules colloïdales d'argent |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9511034B1 (en) * | 2013-12-09 | 2016-12-06 | Bio-Silicote, Inc. | Method for applying a skin treatment |
IT201700064400A1 (it) * | 2017-06-12 | 2018-12-12 | Elena Catalina Bistreanu | Composizione a base di argento colloidale e suo uso topico per il trattamento della psoriasi |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH678487A5 (en) * | 1989-05-23 | 1991-09-30 | Givenchy Parfums | Cosmetic compsn. for reviving skin - contg. placental extract, thymus peptide(s) high mol.wt. DNA, flavonoid(s) and saponin(s) |
FR2668063A1 (fr) * | 1990-10-17 | 1992-04-24 | Fabre Pierre Cosmetique | Liposomes d'eaux thermales stabilises dans un gel d'adn. |
RU2021804C1 (ru) * | 1991-12-17 | 1994-10-30 | Юрий Петрович Вайнберг | Крем для кожи лица |
JPH06100426A (ja) * | 1992-09-17 | 1994-04-12 | Mikimoto Pharmaceut Co Ltd | ヒアルロニダーゼ阻害剤 |
JP3187559B2 (ja) * | 1992-09-24 | 2001-07-11 | 御木本製薬株式会社 | 水中油型クリーム基剤 |
CA2515083A1 (fr) * | 2003-02-05 | 2004-08-26 | Amphora Discovery Corporation | Procede d'administration d'agents cosmetiques par application topique |
US20040191778A1 (en) * | 2003-03-28 | 2004-09-30 | Seiji Inaoka | Colloidal silver-biomolecule complexes |
JP2008063295A (ja) * | 2006-09-08 | 2008-03-21 | Dhc Co | 白金/銀コロイドを含有する皮膚外用剤 |
WO2008079898A1 (fr) * | 2006-12-20 | 2008-07-03 | Pharmwest, Inc. | Méthodes et formulations topiques comprenant un métal colloïdal servant à traiter ou prévenir des affections cutanées |
RU2338514C1 (ru) * | 2007-06-21 | 2008-11-20 | Общество с ограниченной ответственностью "Здоровье и Красота" | Косметическое средство для профилактики старения кожи |
FR2933584B1 (fr) * | 2008-07-10 | 2011-12-23 | Oreal | Procedes de traitement des matieres keratiniques et appareil pour la mise en oeuvre de tels procedes |
WO2011028847A1 (fr) * | 2009-09-01 | 2011-03-10 | Northwestern University | Conjugués de nanoparticule de polynucléotide polyvalente en tant que véhicules de distribution pour un agent chimiothérapique |
-
2012
- 2012-01-16 FR FR1200122A patent/FR2985662B1/fr active Active
-
2013
- 2013-01-10 BR BR112014017448-2A patent/BR112014017448B1/pt active IP Right Grant
- 2013-01-10 EP EP13700114.5A patent/EP2747739B1/fr active Active
- 2013-01-10 RU RU2014119440A patent/RU2609867C1/ru active
- 2013-01-10 ES ES13700114.5T patent/ES2553055T3/es active Active
- 2013-01-10 US US14/371,818 patent/US9486397B2/en active Active
- 2013-01-10 WO PCT/EP2013/050422 patent/WO2013107687A2/fr active Application Filing
- 2013-01-10 JP JP2014551617A patent/JP6267653B2/ja active Active
- 2013-01-10 CN CN201380005376.5A patent/CN104053425B/zh active Active
Non-Patent Citations (1)
Title |
---|
PHOTODERMATOLOGY, vol. 2, 1985, pages 15 - 26 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3188706A4 (fr) * | 2014-09-02 | 2018-05-02 | American Silver, LLC | Toxine botulique et particules colloïdales d'argent |
US11304973B2 (en) | 2014-09-02 | 2022-04-19 | American Silver, Llc | Botulinum toxin and colloidal silver particles |
Also Published As
Publication number | Publication date |
---|---|
BR112014017448A8 (pt) | 2017-07-04 |
CN104053425B (zh) | 2016-10-05 |
EP2747739A2 (fr) | 2014-07-02 |
JP2015503606A (ja) | 2015-02-02 |
BR112014017448A2 (pt) | 2017-06-13 |
US20140356436A1 (en) | 2014-12-04 |
WO2013107687A4 (fr) | 2014-05-30 |
JP6267653B2 (ja) | 2018-01-24 |
FR2985662B1 (fr) | 2014-10-17 |
ES2553055T3 (es) | 2015-12-03 |
FR2985662A1 (fr) | 2013-07-19 |
US9486397B2 (en) | 2016-11-08 |
BR112014017448B1 (pt) | 2019-06-25 |
EP2747739B1 (fr) | 2015-09-02 |
CN104053425A (zh) | 2014-09-17 |
WO2013107687A3 (fr) | 2014-04-03 |
RU2609867C1 (ru) | 2017-02-06 |
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