WO2015000470A1 - Gel for producing a coating for a finger nail - Google Patents

Gel for producing a coating for a finger nail Download PDF

Info

Publication number
WO2015000470A1
WO2015000470A1 PCT/DE2014/100231 DE2014100231W WO2015000470A1 WO 2015000470 A1 WO2015000470 A1 WO 2015000470A1 DE 2014100231 W DE2014100231 W DE 2014100231W WO 2015000470 A1 WO2015000470 A1 WO 2015000470A1
Authority
WO
WIPO (PCT)
Prior art keywords
gel
gel according
resin
fingernail
weight
Prior art date
Application number
PCT/DE2014/100231
Other languages
German (de)
French (fr)
Inventor
Hans HUBRICH
Thomas Beyerlein
Elena REICHERT
Jürgen Burkhardt
Original Assignee
Polystone-Chemical Gmbh
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Polystone-Chemical Gmbh filed Critical Polystone-Chemical Gmbh
Priority to DE112014003112.7T priority Critical patent/DE112014003112A5/en
Publication of WO2015000470A1 publication Critical patent/WO2015000470A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q3/00Manicure or pedicure preparations
    • A61Q3/02Nail coatings
    • AHUMAN NECESSITIES
    • A45HAND OR TRAVELLING ARTICLES
    • A45DHAIRDRESSING OR SHAVING EQUIPMENT; EQUIPMENT FOR COSMETICS OR COSMETIC TREATMENTS, e.g. FOR MANICURING OR PEDICURING
    • A45D31/00Artificial nails
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/042Gels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/39Derivatives containing from 2 to 10 oxyalkylene groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/55Phosphorus compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/80Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/95Involves in-situ formation or cross-linking of polymers

Definitions

  • the invention relates to a gel for producing a coating for a fingernail, in particular for producing an artificial fingernail, which comprises a resin, a reactive diluent and a photopolymerization catalyst.
  • the invention further relates to a use of the gel for the production of a coating for a fingernail.
  • Such gels are known for use in the manufacture of artificial fingernails.
  • the gels are usually applied to a carrier layer of UV-polymerized plastic, which is provided for better adhesion of the gel on the natural fingernail. After 2 to 3 weeks, the carrier layer and the gel are filed off the nail again.
  • the problem is that both the carrier layer and the known gels contain toxic or / and irritating substances.
  • the invention has for its object to provide a gel of the type mentioned, which can be applied healthily without any concern directly on the fingernail.
  • the problem solving gel according to the invention is characterized in that the reactive diluent is formed from monomers having a molecular weight> 300 g / mol.
  • such a reactive diluent can not or only very slightly penetrate into the nail and into the skin because of the size of the molecules. It will achieved such a good compatibility of the gel with the skin, so that the gel can be provided for immediate placement on the fingernail.
  • a particularly high level of safety against nail and skin intolerance is achieved if the reactive diluent is formed from monomers having a molecular weight> 500 g / mol.
  • the reactive diluent which is preferably present in a proportion of 10 to 40% by weight, preferably 20 to 30% by weight, in the gel, is formed by a monomer having at least one ethylenically unsaturated group.
  • Tetraethylene glycol dimethacrylate-based monomers have proven particularly effective for the application; Alternatively or additionally, however, would also be a reactive diluent in question, the lauryl methacrylate, polypropylene glycol monomethacrylate, phenethoxymethacrylate, propoxylated trimethylolpropane trimethacrylate, trimethylolpropane ethoxylate triacrylate, polyethylene glycol 200 Dimetha- crylate and / or polyethylene glycol 400 dimethacrylates or consists thereof.
  • the resin is free of hydroquinone (HQ) and free of p-hydroxyanisole (HQME).
  • HQ hydroquinone
  • HQME p-hydroxyanisole
  • the resin comprises an acrylic resin.
  • the acrylic resin is expediently formed by at least one, preferably aliphatic, urethane acrylate resin and / or at least one, preferably aliphatic, methacrylate resin.
  • the gel for improving the mechanical properties further comprises an epoxy acrylate or an epoxy methacrylate, preferably in a proportion of 1 to 30 wt .-%, particularly preferably 5 to 20 wt .-%.
  • isopropylidenediphenyl can be bisoxyhydroxypropyl
  • Methacrylates bisphenol A glycerolate (l-glycerol / phenol) dimethacrylate
  • bisphenol A glycerolate l-glycerol / phenol dimethacrylate
  • the urethane-acrylic resin is suitably present in a proportion of 20 to 60% by weight, preferably 30 to 50% by weight, in the gel.
  • the methacrylate resin is expediently present in a proportion of 10 to 40% by weight, preferably 20 to 30% by weight, in the gel.
  • the resin comprises di-HEMA trimethylhexyl dicarbamate.
  • an epoxy acrylate, polyester acrylate or polyester methacrylate would also be suitable.
  • the gel is formed such that it is soluble by means of a solvent, preferably by means of acetone.
  • the gel is expediently provided with a cellulose compound as swelling agent for detaching the coating formed from the gel from the fingernail by means of the solvent, preferably the acetone.
  • the quenching agent is expediently present in a proportion of 0-2% by weight in the gel.
  • Cellulose acetate butyrate has proven to be a particularly suitable swelling agent, but cellulose nitrate and / or sucrose benzoate are also suitable.
  • the gel of the invention after it has been cured to the artificial fingernail, as conventional nail polish by means of a solvent from the fingernail remove.
  • a mechanical removal of the artificial fingernail by filing is not necessary. Damage to the natural fingernail is avoided.
  • the gel contains the photopolymerization catalyst in an amount of 1 to 10% by weight, preferably 2 to 6% by weight.
  • the photopolymerization catalyst comprises phenylbis (2,4,6-trimethylbenzoyl) phosphine oxide and / or ethylphenyl (2,4,6-trimethylbenzoyl) phenylphosphinate, whereupon the phenyl bis (2,4, 6- trimethylbenzoyl) phosphine oxide is preferably present in the gel at from 0.5 to 3% by weight and / or the ethylphenyl (2,4,6-trimethylbenzoyl) phenyl phosphinate at from 2 to 6% by weight.
  • Bis (the ⁇ hylamino) phenone, dibenzosuberone, dihydroxybenzophenone and / or thioxanthenone.
  • the gel comprises silica by means of which pigments and / or dyes are stabilized to color the gel in the gel.
  • the proportion of silica in the gel is preferably 0.5 to 3% by weight.
  • a further constituent in the gel is a defoaming agent, preferably ethylhexyl acrylate, which is preferably present at a maximum of 1% by weight.
  • the defoaming agent preferably also contains a polysiloxane, preferably with a proportion of at most 0.5 wt .-%.
  • the gel further contains polyether-modified siloxane, preferably in a proportion of at most 1% by weight, by means of which the pigments in the gel are stabilized.
  • the pigments and / or the dyes for coloring the gel are expediently present in a proportion of 0.1 to 10 wt .-%, preferably 0.1 to 5 wt .-%, before.
  • Butylated hydroxytoluene, if appropriate as a constituent of the resin, is expediently contained in a proportion of not more than 0.5% by weight as stabilizer for the resin in the gel.
  • a gel according to the invention has the following composition:
  • Another gel according to the invention has the following composition:
  • Another gel according to the invention has the following composition

Abstract

The invention relates to a gel for producing a coating for a finger nail, in particular for producing an artificial fingernail, comprising a resin, a reactive diluent and a photopolymersation catalyst. According to the invention, the reactive diluent is formed from monomers which have a molecular weight of 300g/mol. Said reactive diluent comprises a monomer having at least one ethylenically unsaturated group, preferably tetraethylene glycol dimethacrylate-based monomers. In a preferred embodiment of the invention, the resin is devoid of both hydroquinone (HQ) and p-hydroxyanisole (HQME). Advantageously, the gel has a cellulose compound as a source agent for detaching the coating, formed from the gel, from the fingernail.

Description

Beschreibung:  Description:
"Gel zur Herstellung eines Überzugs für einen Fingernagel" "Gel for making a cover for a fingernail"
Die Erfindung betrifft ein Gel zur Herstellung eines Überzugs für einen Fingernagel, insbesondere zur Herstellung eines künstlichen Fingernagels, das ein Harz, einen Reaktivverdünner und einen Photopolymerisationskatalysator aufweist. The invention relates to a gel for producing a coating for a fingernail, in particular for producing an artificial fingernail, which comprises a resin, a reactive diluent and a photopolymerization catalyst.
Die Erfindung betrifft ferner eine Verwendung des Gels zur Herstellung eines Überzugs für einen Fingernagel. The invention further relates to a use of the gel for the production of a coating for a fingernail.
Solche Gele sind für die Herstellung künstlicher Fingernägel durch Benutzung bekannt. Die Gele werden normalerweise auf eine Trägerschicht aus unter UV- Strahlung polymerisiertem Kunststoff aufgetragen, die zur besseren Haftung des Gels auf dem natürlichen Fingernagel vorgesehen wird. Nach 2 bis 3 Wochen werden die Trägerschicht und das Gel wieder vom Nagel abgefeilt. Problematisch ist, dass sowohl die Trägerschicht als auch die bekannten Gele giftige oder/und reizende Stoffe enthalten. Such gels are known for use in the manufacture of artificial fingernails. The gels are usually applied to a carrier layer of UV-polymerized plastic, which is provided for better adhesion of the gel on the natural fingernail. After 2 to 3 weeks, the carrier layer and the gel are filed off the nail again. The problem is that both the carrier layer and the known gels contain toxic or / and irritating substances.
Wegen der chemischen und mechanischen Beanspruchung beim Aufbringen und Abfeilen der künstlichen Fingernägel wird der natürliche Fingernagel angegriffen. Because of the chemical and mechanical stress when applying and filing the artificial fingernail, the natural fingernail is attacked.
Der Erfindung liegt die Aufgabe zugrunde, ein Gel der eingangs genannten Art zu schaffen, das gesundheitlich bedenkenlos direkt auf den Fingernagel aufge- bracht werden kann. The invention has for its object to provide a gel of the type mentioned, which can be applied healthily without any concern directly on the fingernail.
Das diese Aufgabe lösende Gel nach der Erfindung ist dadurch gekennzeichnet, dass der Reaktivverdünner aus Monomeren gebildet ist, die ein Molgewicht > 300 g/mol aufweisen. The problem solving gel according to the invention is characterized in that the reactive diluent is formed from monomers having a molecular weight> 300 g / mol.
Vorteilhaft kann ein solcher Reaktivverdünner wegen der Größe der Moleküle nicht oder nur sehr geringfügig in den Nagel und in die Haut eindringen. Es wird eine derart gute Verträglichkeit des Gels mit der Haut erreicht, sodass das Gel zur unmittelbaren Anordnung auf dem Fingernagel vorgesehen werden kann. Advantageously, such a reactive diluent can not or only very slightly penetrate into the nail and into the skin because of the size of the molecules. It will achieved such a good compatibility of the gel with the skin, so that the gel can be provided for immediate placement on the fingernail.
Eine besonders hohe Sicherheit gegen Nagel- und Hautunverträglichkeit wird erreicht, wenn der Reaktivverdünner aus Monomeren gebildet ist, die ein Mol- gewicht > 500 g/mol aufweisen.  A particularly high level of safety against nail and skin intolerance is achieved if the reactive diluent is formed from monomers having a molecular weight> 500 g / mol.
In einer Ausführungsform der Erfindung ist der Reaktivverdünner, der vorzugsweise in einem Anteil von 10 bis 40 Gew-%, bevorzugt 20 bis 30 Gew-%, in dem Gel vorliegt, durch ein Monomer mit mindestens einer ethylenisch ungesättigten Gruppe gebildet. Als besonders wirkungsvoll für die Anwendung haben sich Tetraethylengiycoldimethacrylat-basierte Monomere erwiesen; alternativ oder ergänzend käme aber auch ein Reaktivverdünner infrage, der Laurylmethacrylat, Polypropylenglycolmonomethacrylat, Phenethoxymethacrylat, propoxyliertes Trimethylolpropantrimetha-crylat, Trimethylolpropane ethoxylate triacrylate, Polyethylene Glycol 200 Dimetha-crylate und/oder Polyethylene Glycol 400 Dimethacrylate aufweist oder daraus besteht. In one embodiment of the invention, the reactive diluent, which is preferably present in a proportion of 10 to 40% by weight, preferably 20 to 30% by weight, in the gel, is formed by a monomer having at least one ethylenically unsaturated group. Tetraethylene glycol dimethacrylate-based monomers have proven particularly effective for the application; Alternatively or additionally, however, would also be a reactive diluent in question, the lauryl methacrylate, polypropylene glycol monomethacrylate, phenethoxymethacrylate, propoxylated trimethylolpropane trimethacrylate, trimethylolpropane ethoxylate triacrylate, polyethylene glycol 200 Dimetha- crylate and / or polyethylene glycol 400 dimethacrylates or consists thereof.
Zweckmäßigerweise ist das Harz frei von Hydrochinon (HQ) und frei von p-Hydroxy- anisol (HQME). Diese Stoffe, die bisher in den Harzen, die in Gelen zur Herstellung von künstlichen Fingernägeln verwendet werden, vorhanden sind, sind gesundheitsschädlich und ätzend. Die Anwesenheit der letztgenannten Stoffe ist rechtlich durch den Beschluss des„Scientific Committee on cosmetic products and non- food products intended for consumers" (SCC NFP/0486/01 ) geregelt und schreibt vor, dass kosmetische Produkte, die die Stoffe enthalten, nur für den professio- nellen Gebrauch z.B. in Kosmetikstudios freigegeben sind, nicht aber zum privaten Gebrauch an den Endverbraucher abgegeben werden dürfen. Da das erfindungsgemäße Gel die Stoffe nicht enthält, ist es zur direkten Abgabe an den Endverbraucher geeignet. In der bevorzugten Ausführungsform der Erfindung ist das Gel ferner frei von Lösemitteln. Dadurch wird die Verträglichkeit für den Nagel und die Haut weiter verbessert. Conveniently, the resin is free of hydroquinone (HQ) and free of p-hydroxyanisole (HQME). These substances, which hitherto are present in the resins used in gels for the production of artificial fingernails, are harmful and corrosive. The presence of these latter substances is legally regulated by the decision of the Scientific Committee on cosmetic products and non-food products intended for consumers (SCC NFP / 0486/01) and requires that cosmetic products containing the substances be used only for Since the gel according to the invention does not contain the substances, it is suitable for direct delivery to the end consumer, which in the preferred embodiment of the invention is suitable for use in private households Gel is also solvent-free, further improving nail and skin compatibility.
In einerweiteren Ausführungsform der Erfindung weist das Harz ein Acrylharz auf . Zweckmäßigerweise ist das Acrylharz durch zumindest ein, vorzugsweise aliphatisches, Urethanacrylatharz und/oder zumindest ein, vorzugsweise aliphatisches, Methacrylatharz, gebildet. In einer Ausgestaltung der Erfindung weist das Gel zur Verbesserung der mechanischen Eigenschaften ferner ein Epoxyacrylate oder ein Epoxymethacrylate auf, vorzugsweise in einem Anteil von 1 bis 30 Gew.-%, besonders bevorzugt 5 bis 20 Gew.-%. Beispielsweise kann Isopropylidenediphenyl Bisoxyhydroxypropyl In another embodiment of the invention, the resin comprises an acrylic resin. The acrylic resin is expediently formed by at least one, preferably aliphatic, urethane acrylate resin and / or at least one, preferably aliphatic, methacrylate resin. In one embodiment of the invention, the gel for improving the mechanical properties further comprises an epoxy acrylate or an epoxy methacrylate, preferably in a proportion of 1 to 30 wt .-%, particularly preferably 5 to 20 wt .-%. For example, isopropylidenediphenyl can be bisoxyhydroxypropyl
Methacrylate (Bisphenol-A-glycerolat-(l-glycerol/phenol)-dimethacrylat) vorgesehen sein. Methacrylates (bisphenol A glycerolate (l-glycerol / phenol) dimethacrylate) may be provided.
Das Urethanacrylharz liegt zweckmäßigerweise in einem Anteil von 20 bis 60 Gew- %, bevorzugt 30 bis 50 Gew.-%, in dem Gel vor. Das Methacrylatharz liegt zweck- mäßigerweise in einem Anteil von 10 bis 40 Gew-%, bevorzugt 20 bis 30 Gew.-%, in dem Gel vor. In einer Ausführungsform der Erfindung umfasst das Harz Di-HEMA Trimethylhexyl Dicarbamate. Alternativ oder ergänzend käme aber auch ein Epoxyacrylat, Polyesteracrylat oder Polyestermethacrylat infrage. In einer bevorzugten Ausgestaltung der Erfindung ist das Gel derart gebildet, dass es mittels eines Lösemittels, vorzugsweise mittels Aceton, lösbar ist. The urethane-acrylic resin is suitably present in a proportion of 20 to 60% by weight, preferably 30 to 50% by weight, in the gel. The methacrylate resin is expediently present in a proportion of 10 to 40% by weight, preferably 20 to 30% by weight, in the gel. In one embodiment of the invention, the resin comprises di-HEMA trimethylhexyl dicarbamate. Alternatively or additionally, however, an epoxy acrylate, polyester acrylate or polyester methacrylate would also be suitable. In a preferred embodiment of the invention, the gel is formed such that it is soluble by means of a solvent, preferably by means of acetone.
Zweckmäßigerweise ist das Gel mit einer Celluloseverbindung als Quellmittel zur Ablösung des aus dem Gel gebildeten Überzugs vom Fingernagel mittels des Lösemittels, vorzugsweise des Acetons, versehen. Das Queflmittel liegt zweckmäßiger- weise in einem Anteil von 0-2 Gew-% in dem Gel vor.  The gel is expediently provided with a cellulose compound as swelling agent for detaching the coating formed from the gel from the fingernail by means of the solvent, preferably the acetone. The quenching agent is expediently present in a proportion of 0-2% by weight in the gel.
Als besonders geeignetes Quellmittel hat sich Cellulose Acetat Butyrat erwiesen, es kommt aber auch Cellulosenitrat und/oder Succrosebenzoat infrage.  Cellulose acetate butyrate has proven to be a particularly suitable swelling agent, but cellulose nitrate and / or sucrose benzoate are also suitable.
Vorteilhaft lässt sich das erfindungsgemäße Gel, nachdem es zu dem künstlichen Fingernagel ausgehärtet worden ist, wie herkömmlicher Nagellack mittels eines Lösemittels vom Fingernagel entfernen. Ein mechanisches Abtragen des künstlichen Fingernagels durch Feilen ist nicht notwendig. Beschädigungen des natürlichen Fingernagels werden vermieden.  Advantageously, the gel of the invention, after it has been cured to the artificial fingernail, as conventional nail polish by means of a solvent from the fingernail remove. A mechanical removal of the artificial fingernail by filing is not necessary. Damage to the natural fingernail is avoided.
Zweckmäßigerweise enthält das Gel den Photopolymeristaionskatalysator in einem Anteil von 1 bis 10 Gew-%, vorzugsweise 2 bis 6 Gew.-%. Der Photopolymerisationskatalysator weist in einer Ausführungsform der Erfindung Phenyl- bis(2,4,6-trimethylbenzoyl)-phosphinoxid und/oder Ethylphenyl (2,4,6- trimethylbenzoyl)phenyl-phosphinat auf, wobei das Phenyl-bis (2,4,6- trimethylbenzoyl)-phosphinoxid bevorzugt mit 0,5 bis 3 Gew-% und/oder das Ethyl- phenyl(2,4,6-trimethylbenzoyl)phenyl-phosphinat mit 2 bis 6 Gew.-% in dem Gel enthalten ist. Bis(Die†hylamino)phenon, Dibenzosuberon, Dihydroxybenzophenon und/oder Thioxanthenon verwendet werden. Conveniently, the gel contains the photopolymerization catalyst in an amount of 1 to 10% by weight, preferably 2 to 6% by weight. In one embodiment of the invention, the photopolymerization catalyst comprises phenylbis (2,4,6-trimethylbenzoyl) phosphine oxide and / or ethylphenyl (2,4,6-trimethylbenzoyl) phenylphosphinate, whereupon the phenyl bis (2,4, 6- trimethylbenzoyl) phosphine oxide is preferably present in the gel at from 0.5 to 3% by weight and / or the ethylphenyl (2,4,6-trimethylbenzoyl) phenyl phosphinate at from 2 to 6% by weight. Bis (the † hylamino) phenone, dibenzosuberone, dihydroxybenzophenone and / or thioxanthenone.
In einerweiteren Ausgestaltung der Erfindung weist das Gel Siliziumdioxid auf, mittels dessen Pigmente und/oder Farbstoffe zur Färbung des Gels in dem Gel stabilisiert sind. Der Anteil des Siliziumdioxid in dem Gel beträgt vorzugsweise 0,5 bis 3 Gew.-%.  In a further aspect of the invention, the gel comprises silica by means of which pigments and / or dyes are stabilized to color the gel in the gel. The proportion of silica in the gel is preferably 0.5 to 3% by weight.
Ferner ist in einer weiteren Ausführungsform der Erfindung als weiterer Bestandteil in dem Gel ein Entschäumungsmittel, vorzugsweise Ethylhexylacrylat, enthalten, das vorzugsweise mit maximal 1 Gew.-% vorliegt. Das Entschäumungsmittels enthält vorzugsweise ferner ein Polysiloxan, bevorzugt mit einem Anteil von maximal 0,5 Gew.-%. Furthermore, in a further embodiment of the invention, a further constituent in the gel is a defoaming agent, preferably ethylhexyl acrylate, which is preferably present at a maximum of 1% by weight. The defoaming agent preferably also contains a polysiloxane, preferably with a proportion of at most 0.5 wt .-%.
Zweckmäßigerweise ist in dem Gel ferner polyethermodifiziertes Siloxan, vorzugsweise mit einem Anteil von maximal 1 Gew.-%, enthalten, mittels dessen die Pigmente in dem Gel stabilisiert werden. Conveniently, the gel further contains polyether-modified siloxane, preferably in a proportion of at most 1% by weight, by means of which the pigments in the gel are stabilized.
Die Pigmente und/oder die Farbstoffe zur Färbung des Gels liegen zweckmäßigerweise in einem Anteil von 0,1 bis 10 Gew.-%, vorzugsweise 0,1 bis 5 Gew.-%, vor. Butyliertes Hydroxytoluol ist, ggf. als Bestandteil des Harzes, zweckmäßigerweise in einem Anteil von maximal 0,5 Gew.-% als Stabilisator für das Harz in dem Gel enthalten. The pigments and / or the dyes for coloring the gel are expediently present in a proportion of 0.1 to 10 wt .-%, preferably 0.1 to 5 wt .-%, before. Butylated hydroxytoluene, if appropriate as a constituent of the resin, is expediently contained in a proportion of not more than 0.5% by weight as stabilizer for the resin in the gel.
Folgende Tabelle gibt eine Übersicht über Stoffzusammensetzungen mit Anteilsbereichen, die für das erfindungsgemäße Gel verstellbar sind: The following table gives an overview of compositions with proportion ranges which are adjustable for the gel according to the invention:
Figure imgf000006_0001
Figure imgf000006_0001
Tabelle 1  Table 1
wobei in which
INCI: Nomenklatur gemäß„International Nomenclature Cosmetic  INCI: Nomenclature according to "International Nomenclature Cosmetic
ingredients"  ingredients "
CAS: Registernummer des„Chemical Abstracts Service" CAS: Registration number of the "Chemical Abstracts Service"
EINECS: Registernummer des„European Inventory of Existing Commercial chemical Substances" Ein erfindungsgemäßes Gel hat folgende Zusammensetzung: EINECS: Register number of the "European Inventory of Existing Commercial chemical Substances" A gel according to the invention has the following composition:
Beispiel 1 :Example 1 :
Figure imgf000007_0001
Figure imgf000007_0001
Tabelle 2 Table 2
Ein weiteres erfindungsgemäßes Gel hat folgende Zusammensetzung: Another gel according to the invention has the following composition:
Beispiel 2:Example 2:
Figure imgf000008_0001
Figure imgf000008_0001
Tabelle 3 Table 3
Ein weiteres erfindungsgemäßes Gel hat folgende Zusammensetzung; Another gel according to the invention has the following composition;
Beispiel 3:Example 3:
Figure imgf000009_0001
Figure imgf000009_0001
Tabelle 4  Table 4

Claims

Patentansprüche: claims:
1. Gel zur Herstellung eines Überzugs für einen Fingernagel, insbesondere zur Herstellung eines künstlichen Fingernagels, das ein Harz, einen Reakfivverdünner und einen Photopolymerisationskatalysator aufweist, A gel for producing a fingernail coating, in particular for producing an artificial fingernail, comprising a resin, a reactive diluent and a photopolymerization catalyst,
dadurch gekennzeichnet,  characterized,
dass der Reaktivverdünner aus Monomeren gebildet ist, die ein Molgewicht > 300 g/mol aufweisen.  that the reactive diluent is formed from monomers having a molecular weight> 300 g / mol.
2. Gel nach Anspruch 1 , 2. Gel according to claim 1,
dadurch gekennzeichnet,  characterized,
dass der Reaktivverdünner in ienem anteil von 10 bis 40 Gew.-%, vorzugsweise 20 - 30 Gew.-%, vorliegt.  the reactive diluent is present in the proportion of from 10 to 40% by weight, preferably from 20 to 30% by weight.
3. Gel nach Anspruch 1 oder 2, 3. Gel according to claim 1 or 2,
dadurch gekennzeichnet,  characterized,
dass der Reaktivverdünner ein Monomer mit mindestens einer ethylenisch ungesättigten Gruppe aufweist, vorzugsweise etraethylenglycoldimethacrylat- basierte Monomere, Laurylmethacrylat, Polypropylenglycolmonomethacrylat, Phenethoxymethacrylat, propoxyliertem Trimethylolpropantrimethacrylat, the reactive diluent comprises a monomer having at least one ethylenically unsaturated group, preferably ethylene glycol dimethacrylate-based monomers, lauryl methacrylate, polypropylene glycol monomethacrylate, phenethoxymethacrylate, propoxylated trimethylolpropane trimethacrylate,
Trimethylolpropane Ethoxylat Triacrylat, Polyethylen Glycol 200 Dimefhacrylat und/oder Polyethylen Glycol 400 Dimefhacrylat. Trimethylolpropane ethoxylate triacrylate, polyethylene glycol 200 dimethacrylate and / or polyethylene glycol 400 dimethacrylate.
4. Gel nach einem Ansprüche 1 bis 3, 4. Gel according to claims 1 to 3,
dadurch gekennzeichnet,  characterized,
dass das Harz frei von Hydroquinon (HQ) und frei von p-Hydroxyanisol (HQME) ist.  that the resin is free of hydroquinone (HQ) and free of p-hydroxyanisole (HQME).
5. Gel nach einem der Ansprüche 1 bis 4, 5. Gel according to one of claims 1 to 4,
dadurch gekennzeichnet,  characterized,
dass das Gel frei von Lösemitteln ist.  that the gel is free of solvents.
6. Gel nach einem der Ansprüche 1 bis 5, 6. Gel according to one of claims 1 to 5,
dadurch gekennzeichnet,  characterized,
dass das Harz ein Acrylharz aufweist.  the resin has an acrylic resin.
7. Gel nach einem der Ansprüche 1 bis 6, 7. Gel according to one of claims 1 to 6,
dadurch gekennzeichnet, dass das Harz zumindest ein Urethanacrylatharz und/oder zumindest ein Methacrylatharz aufweist, wobei vorzugsweise das Urethanacrylharz in einem Anteil von 20 bis 60 Gew.-%, besonders bevorzugt 30 bis 50 Gew.-% vorliegt und/oder das Methacrylatharz in einem Anteil von 10 bis 40 Gew.-%, vorliegt. characterized, the resin comprises at least one urethane acrylate resin and / or at least one methacrylate resin, the urethane-acrylic resin preferably being present in an amount of from 20 to 60% by weight, particularly preferably 30 to 50% by weight and / or the methacrylate resin in a proportion of 10 to 40 wt .-%, is present.
8. Gel nach einem der Ansprüche 1 bis 7, 8. Gel according to one of claims 1 to 7,
dadurch gekennzeichnet,  characterized,
dass das Gel zur Verbesserung der mechanischen Eigenschaften ein  that the gel to improve the mechanical properties
Epoxyacrylat oder/und ein Expoxymethacrylat aufweist, vorzugsweise in einem Anteil von 1 bis 30 Gew.-%, bevorzugt 5 bis 20 Gew.-%.  Epoxy acrylate and / or an epoxy methacrylate, preferably in a proportion of 1 to 30 wt .-%, preferably 5 to 20 wt .-%.
9. Gel nach einem der Ansprüche 1 bis 8, 9. Gel according to one of claims 1 to 8,
dadurch gekennzeichnet,  characterized,
dass das Gel mittels eines Lösemittels, vorzugsweise mittels Aceton, lösbar ist.  that the gel is soluble by means of a solvent, preferably by means of acetone.
10. Gel nach einem der Ansprüche 1 bis 9, 10. Gel according to one of claims 1 to 9,
dadurch gekennzeichnet,  characterized,
dass das Gel mit einer Celluloseverbindung als Quellmittel zur Ablösung des aus dem Gel gebildeten Überzugs vom Fingernagel versehen ist.  that the gel is provided with a cellulose compound as a swelling agent for detachment of the gel-formed coating from the fingernail.
11. Gel nach Anspruch 10, 11. Gel according to claim 10,
dadurch gekennzeichnet,  characterized,
dass die Celluloseverbindung Cellulose Acetat Butyrat, Cellulosenitrat und/ oder Sucrosebenzoat umfasst.  the cellulose compound comprises cellulose acetate butyrate, cellulose nitrate and / or sucrose benzoate.
12. Gel nach einem der Ansprüche 1 bis 1 1 , 12. Gel according to one of claims 1 to 1 1,
dadurch gekennzeichnet,  characterized,
dass das Gel als der Photopolymeristaionskatalysator Phenyl-bis(2,4,6-trimethyl benzoyl)-phosphinoxid und/oder Ethylphenyl[2A6- trimethylbenzoyl)phosphinat, Methylbenzoylformiat, Benzophenon,  that the gel as the photopolymerization catalyst is phenylbis (2,4,6-trimethylbenzoyl) phosphine oxide and / or ethylphenyl [2A6-trimethylbenzoyl) phosphinate, methylbenzoylformate, benzophenone,
Camporquinon, Acetophenon, Anthrachinon, Bis(Diethylamino)phenon, Dibenzosuberon, Dihydroxybenzophenon und/oder Thioxanthenon aufweist.  Camporquinone, acetophenone, anthraquinone, bis (diethylamino) phenone, dibenzosuberone, dihydroxybenzophenone and / or thioxanthenone.
13. Gel nach einem der Ansprüche 1 bis 9, 13. Gel according to one of claims 1 to 9,
dadurch gekennzeichnet,  characterized,
dass das Gel Pigmente zur Färbung aufweist, wobei die Pigmente  that the gel has pigments for coloring, the pigments
vorzugsweise in einem Anteil von 0,1 bis 10 Gew.-%, bevorzugt 0,1 bis  preferably in a proportion of 0.1 to 10 wt .-%, preferably 0.1 to
5 Gew.-%, vorliegen. 5 wt .-%, are present.
14. Gel nach einem der Ansprüche 1 bis 9, 14. Gel according to one of claims 1 to 9,
dadurch gekennzeichnet,  characterized,
dass das Gel zur unmittelbaren Anordnung auf dem Fingernagel vorgesehen ist.  that the gel is intended for direct placement on the fingernail.
15. Verwendung des Gels nach einem der Ansprüche 1 bis 14 zur Herstellung eines Überzugs für einen Fingernagel, vorzugsweise zur Herstellung eines künstlichen Fingernagels. 15. Use of the gel according to any one of claims 1 to 14 for the preparation of a coating for a fingernail, preferably for the production of an artificial fingernail.
PCT/DE2014/100231 2013-07-04 2014-07-04 Gel for producing a coating for a finger nail WO2015000470A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DE112014003112.7T DE112014003112A5 (en) 2013-07-04 2014-07-04 Gel for making a cover for a fingernail

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102013107030.2A DE102013107030A1 (en) 2013-07-04 2013-07-04 Gel for making a cover for a fingernail
DE102013107030.2 2013-07-04

Publications (1)

Publication Number Publication Date
WO2015000470A1 true WO2015000470A1 (en) 2015-01-08

Family

ID=51392014

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/DE2014/100231 WO2015000470A1 (en) 2013-07-04 2014-07-04 Gel for producing a coating for a finger nail

Country Status (2)

Country Link
DE (2) DE102013107030A1 (en)
WO (1) WO2015000470A1 (en)

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69512007T2 (en) * 1994-12-13 2000-01-27 Macdermid Imaging Technology Soft relief photopolymer printing plates for flexography
WO2001043579A1 (en) * 1999-12-17 2001-06-21 Gel Products, Inc. Radiation curable nail coatings and methods of using same
GB2452566A (en) * 2007-09-08 2009-03-11 Chemence Ltd A radiation curable, nail coating composition
US20100008876A1 (en) * 2008-07-10 2010-01-14 Hisaki Tanaka Artificial nail composition having improved curability
WO2011031578A1 (en) * 2009-09-08 2011-03-17 Creative Nail Design, Inc. Removable color gel basecoat for artificial nail coatings and methods therefore
US20120247496A1 (en) * 2011-03-29 2012-10-04 Tammy Taylor Fingernail and toenail base coat composition and method of applying the same
WO2012130600A1 (en) * 2011-03-15 2012-10-04 L'oreal Photo-crosslinkable nail varnishes free of unsaturated monomers
WO2013154845A1 (en) * 2012-04-10 2013-10-17 Esschem, Inc. Curable nail enhancements
WO2014028020A1 (en) * 2012-08-16 2014-02-20 L'oreal Nail compositions
WO2014130729A1 (en) * 2013-02-20 2014-08-28 O P I Products, Inc. Suspending medium for glitter or pigments in urethane (meth)acrylates

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69512007T2 (en) * 1994-12-13 2000-01-27 Macdermid Imaging Technology Soft relief photopolymer printing plates for flexography
WO2001043579A1 (en) * 1999-12-17 2001-06-21 Gel Products, Inc. Radiation curable nail coatings and methods of using same
GB2452566A (en) * 2007-09-08 2009-03-11 Chemence Ltd A radiation curable, nail coating composition
US20100008876A1 (en) * 2008-07-10 2010-01-14 Hisaki Tanaka Artificial nail composition having improved curability
WO2011031578A1 (en) * 2009-09-08 2011-03-17 Creative Nail Design, Inc. Removable color gel basecoat for artificial nail coatings and methods therefore
WO2012130600A1 (en) * 2011-03-15 2012-10-04 L'oreal Photo-crosslinkable nail varnishes free of unsaturated monomers
US20120247496A1 (en) * 2011-03-29 2012-10-04 Tammy Taylor Fingernail and toenail base coat composition and method of applying the same
WO2013154845A1 (en) * 2012-04-10 2013-10-17 Esschem, Inc. Curable nail enhancements
WO2014028020A1 (en) * 2012-08-16 2014-02-20 L'oreal Nail compositions
WO2014130729A1 (en) * 2013-02-20 2014-08-28 O P I Products, Inc. Suspending medium for glitter or pigments in urethane (meth)acrylates

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
"Harz (Material)", 30 October 2014 (2014-10-30), XP002732931, Retrieved from the Internet <URL:http://de.wikipedia.org/wiki/Harz_%28Material%29> [retrieved on 20141119] *
"Reaktivverdünner", 16 August 2014 (2014-08-16), XP002732932, Retrieved from the Internet <URL:http://de.wikipedia.org/wiki/Reaktivverd%C3%BCnner> [retrieved on 20141119] *

Also Published As

Publication number Publication date
DE112014003112A5 (en) 2016-04-21
DE102013107030A1 (en) 2015-01-08

Similar Documents

Publication Publication Date Title
CN102639578B (en) Removable protective topcoat for artificial nail coatings and methods therefore
CN102781921B (en) Comprise the composition of Polymerizable ionic liquid mixture and goods and curing
ES2559027T3 (en) Removable colored gel base coat layer for artificial nail coatings and procedures for it
US8492454B2 (en) Removable color layer for artificial nail coatings and methods therefore
Morães et al. Improved dental adhesive formulations based on reactive nanogel additives
KR101700010B1 (en) Nail lacquer composition with hyposensitivity
EP0011735B1 (en) Dental Röntgen-opaque products based on organic synthetics in paste form
DE102007009590A1 (en) Shiny and scratch-resistant nail polish by adding sol-gel systems
EP0029957A1 (en) Process for producing protecting layers for photographic materials
JP2015189668A (en) Artificial nail coating composition improved in removability
DE102007013285A1 (en) Conditioning agent and method for bonding curable mixtures of molded articles made of filled high-temperature resistant plastics
DE10240855A1 (en) Photopolymerizable dental coating composition
WO2015000470A1 (en) Gel for producing a coating for a finger nail
DE102012022693A1 (en) Two component system, useful for preparing hypoallergenic plastic dental base, comprises a solid impact-modified component A and a solid impact-modified component B, where the components contain an additive
CN111065665B (en) Color protectant compositions
CN109486404A (en) A kind of ultraviolet-curing paint of elastic tactility
KR20220041274A (en) Modified metal oxide nano particle dispersion composition prepared using the same and method for preparing the same
DE1952721A1 (en) Coating agent for use on humans or animals
DE10228540A1 (en) Dental materials based on hydroxyalkylacrylamides
RU2015121435A (en) METHOD OF NAIL DESIGN USING PHOTO-SELLING COMPOSITIONS OF VARNISH
RU2015121713A (en) METHOD FOR PROCESSING NAILS WITH USE OF PHOTO-SELLING COMPOSITIONS OF VARNISH
DE10137372A1 (en) Polymerizable dental material based on chromophoric xerogels
EP2615121B1 (en) Composition and method for correcting a split nail
US10744348B2 (en) Photocurable nail compositions containing inorganic gelling agent
DE102020128570A1 (en) Process for applying artificial eyelashes

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 14754997

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 112014003112

Country of ref document: DE

REG Reference to national code

Ref country code: DE

Ref legal event code: R225

Ref document number: 112014003112

Country of ref document: DE

122 Ep: pct application non-entry in european phase

Ref document number: 14754997

Country of ref document: EP

Kind code of ref document: A1