EP4355292A1 - Produit cosmétique constitué d'un matériau d'emballage et d'une préparation contenant des diesters de propylène-glycol - Google Patents

Produit cosmétique constitué d'un matériau d'emballage et d'une préparation contenant des diesters de propylène-glycol

Info

Publication number
EP4355292A1
EP4355292A1 EP22734245.8A EP22734245A EP4355292A1 EP 4355292 A1 EP4355292 A1 EP 4355292A1 EP 22734245 A EP22734245 A EP 22734245A EP 4355292 A1 EP4355292 A1 EP 4355292A1
Authority
EP
European Patent Office
Prior art keywords
inci
propylene glycol
preparation
cosmetic according
oil
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.)
Pending
Application number
EP22734245.8A
Other languages
German (de)
English (en)
Inventor
Claudia Müller
Jette Mareike NEBEN
Sabrina Diekert
Astrid Albrecht
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beiersdorf AG
Original Assignee
Beiersdorf AG
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 Beiersdorf AG filed Critical Beiersdorf AG
Publication of EP4355292A1 publication Critical patent/EP4355292A1/fr
Pending legal-status Critical Current

Links

Classifications

    • 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
    • A61K8/37Esters of carboxylic acids
    • A61K8/375Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • 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
    • A61K2800/87Application Devices; Containers; Packaging

Definitions

  • the present invention relates to a cosmetic made from a cosmetic preparation containing propylene glycol diester and a packaging material made from HDPE, LDPE, PP or PET.
  • the cleansing of the skin serves to remove dirt, sweat and the remains of dead skin particles, which form an ideal breeding ground for pathogens and parasites of all kinds.
  • Skin care products are mostly used to moisturize and moisturize the skin. Active ingredients are often added to them, which regenerate the skin and, for example, prevent and reduce its premature aging (e.g. the development of fine lines, wrinkles).
  • Skin care products are usually stored in packaging in the form of bottles, tubes or jars. These consist mainly of glass (glass jars) or plastics such as high-density polyethylene (HDPE), low-density polyethylene (LDPE), polypropylene (PP) or polyethylene terephthalate (PET).
  • HDPE high-density polyethylene
  • LDPE low-density polyethylene
  • PP polypropylene
  • PET polyethylene terephthalate
  • a disadvantage of such packaging which is actually very cheap and extremely hygienic, is the fact that this packaging is not particularly sustainable/environmentally friendly, since it is made from petroleum products and/or natural gas and, when it is thermally recycled (combustion in the waste incineration plant), ultimately carbon dioxide from fossil fuels sources is released.
  • these packaging materials In order to conserve natural resources, attempts are therefore being made to make these packaging materials as thin as possible and to recycle them after the preparation has been used.
  • these thin-walled packaging materials have the disadvantage that, if the cosmetic preparation filled in them contains one or more oil components, they are not particularly stable in storage, but rather swell on contact with the oil, since the oil is "sucked up” and absorbed by the plastic.
  • the products can oil out.
  • the oil in the plastic means that the inscriptions printed on the packaging can smudge and become detached.
  • the oil absorbed by the packaging makes it more difficult to recycle the plastic because the oil has to be separated from the polymer in a laborious process before new packaging can be made from the polymer plastic.
  • oil-free preparations e.g. toothpaste
  • packaging has to be coated or sealed on the inside facing the cosmetic, which is a complex process.
  • protective barriers made of ethylene vinyl alcohol are known from the prior art, which are relatively expensive and also less easy to recycle than pure polyolefin packaging materials.
  • a cosmetic made from a) a packaging material made of high-density polyethylene (HDPE), low-density polyethylene (LDPE), polypropylene (PP) or polyethylene terephthalate (PET), and b) a cosmetic preparation containing propylene glycol diester.
  • HDPE high-density polyethylene
  • LDPE low-density polyethylene
  • PP polypropylene
  • PET polyethylene terephthalate
  • the packaging means a is formed from high-density polyethylene (HDPE).
  • HDPE high-density polyethylene
  • the packaging a has a wall thickness (thickness) of 1 to 8 mm.
  • the advantageous embodiments of the present invention according to the invention are characterized in that the packaging has no protective layer (e.g. made of ethylene vinyl alcohol) on the inside facing the preparation.
  • the packaging has no protective layer (e.g. made of ethylene vinyl alcohol) on the inside facing the preparation.
  • Embodiments of the present invention that are advantageous according to the invention are characterized in that the propylene glycol diester is one or more compounds from the group of propylene glycol diheptanoate (INCI: propylene glycol diheptanoate), propylene glycol dicaprate (INCI: propylene glycol dicaprate), propylene glycol dicaprylate/dicaprate (INCI: propylene glycol dicaprylate/dicaprate) and propylene glycol dibenzoate (INCI: Propylene Glycol Dibenzoate) can be used.
  • the propylene glycol diester is one or more compounds from the group of propylene glycol diheptanoate (INCI: propylene glycol diheptanoate), propylene glycol dicaprate (INCI: propylene glycol dicaprate), propylene glycol dicaprylate/dicaprate (INCI: propylene glycol dicaprylate/dicaprate) and propylene glycol dibenzoate
  • propylene glycol diheptanoate (INCI: Propylene Glycol Diheptanoate) is used as the propylene glycol diester.
  • Embodiments of the present invention that are advantageous according to the invention are also obtained in that the preparation is free from dimethicone (INCI: Dimethicone).
  • the preparation is free from silicone oil, mineral oil, paraffin wax, microcrystalline wax, shellac wax and polyethylene wax.
  • the preparation is free from polyacrylates, crosslinked acrylate/C10-C30 alkyl acrylate polymers and vinylpyrrolidone/hexadecene copolymers and free from 3-(4-methylbenzylidene)camphor, 2-hydroxy-4-methoxybenzophenone (INCI: oxybenzone), 2-ethylhexyl 4-methoxycinnamate (INCI octyl methoxycinnamate), ethylhexyl 2-cyano-3,3-diphenyl acrylate (INCI: octocrylene), parabens (particularly methyl, propyl and butyl paraben), methylisothiazolinone, chloromethylisothiazolinone and DMDM hydantoin, polyethylene glycol ethers or polyethylene glycol esters
  • the cosmetic preparation is in the form of an emulsion. It is preferred according to the invention if the cosmetic preparation is in the form of an oil-in-water emulsion (O/W emulsion). It is advantageous according to the invention if the cosmetic preparation contains propylene glycol diester in a concentration of 0.1 to 10% by weight, based on the total weight of the preparation. A use concentration of 0.1 from 5 to 5% by weight, based on the total weight of the preparation, is preferred according to the invention. These use concentrations relate to the total amount of propylene glycol diesters used. If only one propylene glycol diester (eg propylene glycol diheptanoate) is used, this is the advantageous or preferred use concentration for this one compound.
  • propylene glycol diester eg propylene glycol diheptanoate
  • the total amount of propylene glycol diesters in the oil phase of the preparation is at least 3% by weight, based on the total weight of the oil phase.
  • Embodiments that are advantageous according to the invention are also characterized in that the preparation contains one or more oils selected from the group consisting of the compounds octyldodecanol, caprylic/capric acid triglycerides (INCI: caprylic/capric triglycerides), coconut glycerides (INCI: cocoglycerides), tridecyl stearate (INCI: tridecyl stearate) , tridecyl trimelliate (INCI: Tridecyl Trimelliate).
  • the preparation contains one or more oils selected from the group consisting of the compounds octyldodecanol, caprylic/capric acid triglycerides (INCI: caprylic/capric triglycerides), coconut glycerides (INCI: cocoglycerides), tridecyl stearate (INCI: tridecyl stearate) , tridecyl trimelliate (INCI: Tride
  • the preparation contains one or more oils selected from the group of compounds containing polycitronellol (INCI: polycitronellol), polycitronellol acetate (INCI: polycitronellol acetate), triolein, ethylhexyl acetoxystearate (INCI: ethylhexyl acetoxystearate), acetylethylhexyl polyhydroxystearate (INCI: acetyl ethylhexyl polyhydroxystearate).
  • the preparation contains one or more oils selected from the group consisting of almond oil (INCI: Prunus Amygdalus Dulcis Oil) and/or sunflower oil (INCI: Helianthus Annuus Seed Oil), hydrogenated castor oil (INCI: Hydrogenated Castor Oil) contains.
  • almond oil INCI: Prunus Amygdalus Dulcis Oil
  • sunflower oil INCI: Helianthus Annuus Seed Oil
  • hydrogenated castor oil INCI: Hydrogenated Castor Oil
  • the preparation contains tocopherol.
  • the preparation according to the invention can contain the ingredients customary for cosmetics and be composed accordingly. comparison tests
  • the penetration of the following cosmetic oils into the packaging material HDPE was examined.
  • the product “Hostalen ACP 5831 D” from Lyondellbasell was used as the HDPE.
  • Raw materials or components of the cosmetic preparation have migrated into the packaging material if the weight of the die-cut m1 is greater than the weight of mO.
  • Weight increase (%) (m1 - mO) / mO
  • the formula (m1 - m0)/m0 is used to determine the increase in weight (%) of the raw material or cosmetic preparation that has migrated into the packaging material.
  • the mean value [%] and standard deviation [%] of the triple determination are also calculated.
  • Example 1 O/W lotion
  • Example 2 W/O lotion
  • Example 3 O/W cream

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Emergency Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

Produit cosmétique constitué a) d'un matériau d'emballage en polyéthylène haute densité (HDPE), polyéthylène basse densité (LDPE), polypropylène (PP) ou polyéthylène téréphtalate (PET), et b) d'une préparation cosmétique contenant des diesters de propylène-glycol.
EP22734245.8A 2021-06-14 2022-06-09 Produit cosmétique constitué d'un matériau d'emballage et d'une préparation contenant des diesters de propylène-glycol Pending EP4355292A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102021206043.9A DE102021206043A1 (de) 2021-06-14 2021-06-14 Kosmetikum aus einem Packmittel und einer Zubereitung enthaltend Propylenglycoldiester
PCT/EP2022/065646 WO2022263271A1 (fr) 2021-06-14 2022-06-09 Produit cosmétique constitué d'un matériau d'emballage et d'une préparation contenant des diesters de propylène-glycol

Publications (1)

Publication Number Publication Date
EP4355292A1 true EP4355292A1 (fr) 2024-04-24

Family

ID=82258549

Family Applications (1)

Application Number Title Priority Date Filing Date
EP22734245.8A Pending EP4355292A1 (fr) 2021-06-14 2022-06-09 Produit cosmétique constitué d'un matériau d'emballage et d'une préparation contenant des diesters de propylène-glycol

Country Status (3)

Country Link
EP (1) EP4355292A1 (fr)
DE (1) DE102021206043A1 (fr)
WO (1) WO2022263271A1 (fr)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102762661B (zh) * 2010-02-12 2014-06-18 花王株式会社 包装体成型用材料、包装体、制品以及防止吸附的方法

Also Published As

Publication number Publication date
WO2022263271A1 (fr) 2022-12-22
DE102021206043A1 (de) 2022-12-15

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