Eutectic mixtures in personal care compositions

a technology of eutectic mixtures and compositions, applied in the field of eu, can solve the problems of difficult formulation of personal care compositions and destroying textur

Inactive Publication Date: 2015-10-22
CONOPCO INC D B A UNILEVER
View PDF6 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present inventors have discovered that a mixture of 12-HSA and L-menthol has a lower melting point than pure 12-HSA. This invention is about a new mixture of three chemicals (L-menthol, L-menthyl lactate, and 12-hydroxystearic acid) that have a lower melting point than each individual chemical and also have some unique properties. This mixture can be used in personal care products such as skincare products. It has a lower melting point, which makes it easier to apply the product to skin and easier to spread the product. The invention is a new way to make skincare products that are easier to apply and spread.

Problems solved by technology

Unfortunately, 12-HSA is a solid having a melting point of about 72 to 77 degrees Celsius, has no water solubility and limited oil solubility.
Because of the high melting temperature it is difficult to formulate in a personal care composition, often requiring elevated temperatures or solvents.
Another drawback associated with the high melting point of 12-HSA is that it may re-crystallize upon storage after being incorporated in a personal care product in non-solid form like e.g. in a solvent.
Such re-crystallization may cause the undesired gellation of such personal care products thereby destroying the texture thereof.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0081]Mixtures of L-menthol, L-menthyl lactate and 12-HSA where prepared as follows, using the ingredients as in Table 1 and the amounts mentioned in Tables 2A and 2B.

[0082]The three components L-menthol, L-menthyl lactate and 12-HSA were weighed and then mixed by grinding in a mortar and pestle until a homogenous mixture was obtained. Mixtures that started to melt at room temperature were mixed by grinding until a transparent liquid was formed.

TABLE 1Ingredients of ternary eutectic mixturesIngredientPurityCAS#Supplier12-HSA95%106-14-9Alfa AesarL-menthol99.5% 2216-51-5Damas-betaL-menthyl lactate99%69-72-7Sigma

[0083]The melting point of these mixtures was measured and the results are shown in Tables 2A and 2B. It is clearly shown that specific mixtures have a lower melting temperature. The lowest melting point of about −52 degrees Celsius was determined for a eutectic composition of L-menthol and L-menthyl lactate in a weight ratio of 4:6 and a 12-HSA concentration of 1 wt % with res...

example 2

[0084]A personal care composition (PCC 1) according to Table 3A comprising a pre-formed mixture of L-menthol, L-menthyl lactate and 12-HSA was prepared using the following protocol.[0085]1. Phase A was prepared by mixing the ingredients and heating the mixture to 70 degrees Celsius to dissolve the ingredients.[0086]2. Phase B was prepared by mixing sodium polyacrylate and 1,3-butylene glycol and adding them to Phase A. Glycerin was used to flush the beaker and decanted into phase A. The same was repeated with water.[0087]3. Phase C was prepared by mixing the ingredients at 75 degrees Celsius under manual stirring until the phase was transparent.[0088]4. Phase D was prepared by mixing the ingredients in a mortar and pestle until a transparent liquid was obtained. This liquid was added to Phase C.[0089]5. The ingredients of phase E and F were mixed separately and added at 75 degrees Celsius to the mixture obtained after step 4) and stirred manually.[0090]6. Phase G was added to the mi...

example 3

[0095]Personal care compositions according to Table 3B comprising were prepared using the following protocol. PCC 2 comprises 12-HSA, but no L-menthol and L-menthyl lactate. In PCC 3, L-menthol, L-menthyl lactate and 12-HSA were added separately (i.e. not added as a pre-formed eutectic mixture).[0096]1. Phase A was prepared by mixing the ingredients and heating the mixture to 70 degrees Celsius to dissolve the ingredients.[0097]2. Phase B was prepared by mixing sodium polyacrylate and 1,3-butylene glycol and adding them to Phase A. Glycerine was used to flush the beaker and decanted into phase A. The same was repeated with water.[0098]3. Phase C was prepared by was prepared by mixing the ingredients at 75 degrees Celsius under manual stirring until the phase was transparent. For PCC 3, 12-HSA, L-menthol and L-menthyl lactate were added to the dispersion one by one as the last ingredients.[0099]4. The ingredients of phase D and E were mixed separately and then added to the mixture ob...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention relates to active eutectic mixtures of L-menthol, L-menthyllactate and 12-hydroxystearic acid, personal care products comprising such active eutectic mixtures, a method for preparing such personal care composition and a method of applying to human skin such personal care compositions.

Description

FIELD OF THE INVENTION[0001]The present invention relates to eutectic mixtures of L-menthol, L-menthyl lactate and 12-hydroxystearic acid; and personal care compositions comprising such eutectic mixtures.BACKGROUND OF THE INVENTION[0002]12-hydroxystearic acid (hereinafter “12-HSA”) is reported to have a wide variety of beneficial cosmetic effects on skin. It is a known PPAR-alpha (peroxisome proliferator activated receptors sub-type alpha) activator, skin lightening agent, and a sebum secretion inhibitor. See e.g. Alaluf et al. U.S. Pat. No. 6,423,325, Mayes et al. U.S. Pat. No. 6,713,051, WO2006 / 056283 (Hindustan Lever), Madison US 2009 / 0317341, Minami et al. U.S. Pat. No. 6,197,343, Granger et al. US2004 / 0043044.[0003]As such, cosmetic products containing 12-HSA are highly desirable.[0004]JP 09-048962 describes the use of 12-HSA or its salt as an effective constituent of a solidification inhibitor, to inhibit solidification of a liquid detergent or a liquid cosmetic; all the examp...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(United States)
IPC IPC(8): A61K8/37A61K8/365A61K8/67A61Q5/12A61Q19/10A61Q19/00A61Q9/02A61Q1/06A61Q1/02A61Q17/04A61Q5/02A61K8/34A61Q15/00
CPCA61K8/37A61K2800/24A61K8/365A61K8/67A61Q5/12A61Q19/10A61Q15/00A61Q9/02A61Q1/06A61Q1/02A61Q17/04A61Q5/02A61Q19/007A61K2800/59A61K8/34A61K8/675A61Q19/00A61K2800/244
Inventor KHOSHDEL, EZATSCHUMM, STEPHAN GEORGYAO, YINFANGZHANG, QIQING
Owner CONOPCO INC D B A UNILEVER
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products