US20020071853A1

US20020071853A1 - Cosmetic products compatible with cutaneous ecology and methods for their use

Info

Publication number: US20020071853A1
Application number: US10/006,389
Authority: US
Inventors: Jean-Noel Thorel
Original assignee: Individual
Current assignee: Individual
Priority date: 1997-01-21
Filing date: 2001-12-10
Publication date: 2002-06-13
Also published as: DE69805812D1; US6342236B1; CA2278226A1; KR20000070249A; FR2758458B1; FR2758458A1; AU5993798A; CN1112175C; ES2176955T3; EP1009376A1; WO1998031337A1; KR100528088B1; CN1244117A; JP2001508789A; EP1009376B1; DE69805812T2; CA2278226C

Abstract

A cosmetic or corporal hygiene composition may comprise 98-100% by weight biodermal constituents including at least two different biodermal constituents, each biodermal constituent being cytocompatible with skin; and 0-2% by weight of at least one non-biodermal constituent that is compatible with skin. This composition may be used in a cosmetic method. The cosmetic method may comprise: (a) starting from the living epidermis as an ecological medium; (b) choosing biodermal constituents that are each cytocompatible and biomimetic with a component of the skin; (c) choosing non-biodermal constituents that are biocompatible with the skin; (d) formulating a composition for topically use, which comprises 98-100% by weight of the biodermal constituents, including at least one component in a major amount and at least one component in a minor amount, and 0-2% by weight of the non-biodermal constituents, so that the composition is stable and exhibits at least one non-systemic topical beneficial activity; and (e) applying the composition on a superficial part of the human body so as to maintain the functional biological equilibria of the living epidermis ecological medium.

Description

The present invention relates to cosmetology, body-hygiene, topical dermotherapeutics and, in general, any product intended for the skin, or for surface parts of the human body, in the region of the epidermis, such as nails and hair.

Traditionally, a cosmetic or dermatological product comprises one or more active principles and an excipient or vehicle in which the active principle(s) is (are) distributed or dispersed, the whole being formulated for topical application, for example in the form of a gel or cream.

The term “active principle” means any compound, any composition or any product which exerts biomechanical, biophysical, physiological or biological activity on the skin, and in particular on the epidermis, and which has any physicochemical form or nature required for the treatment or action chosen or selected with respect to the skin.

The active principle(s) selected, of chemical type, is (are) in the great majority foreign to the skin; cf. EP-0,475,851. In certain cases, these active principles are natural products, i.e. products obtained from products or substances of nature, for example in the plant kingdom, cf. EP-0,477,833. In other cases, these active principles are products or constituents found in the skin; cf. WO-94/18945 and EP-0,627,223.

Moreover, cosmetic or dermopharmaceutical products are known which comprise no excipient or vehicle per se, but in the form of a complex, combining various products; cf EP-0,379,846. In certain examples, one or more components, but not all of them, are natural components; cf. WO-89/05629.

At the present time, to the Applicant's best knowledge, nobody has been concerned, for cosmetic or therapeutic purposes, in the skin, and in particular the epidermis, considered as an ecological medium or system whose equilibrium should be respected, with the exception of certain studies relating only to the ecology of the cutaneous bacterial flora.

This is the subject of the present invention.

In its general aspect, the invention proposes a new generation of cosmetic or corporal hygiene or dermotherapeutic products which comprise, to at least 98% by weight, biodermal constituents, each chosen for their biocompatibility and cytocompatibility with skin cells, and preferably biomimetic with a component of the skin, in particular of the epidermis. These biodermal constituents are chosen and formulated, on the one hand, in order together to express at least one topical biological activity, which is identical to or different from the biological activity of at least one biodermal constituent, and, on the other hand, in order to give the product a composition in topical pharmaceutical form which is stable, as regards the mode of administration considered, for example gel, milk, cream, lotion or make-up remover, for a body hygiene or cosmetic product.

It results from the above definition, by difference with the traditional cosmetic or dermatological products, that it is no longer possible in particular to distinguish between active principle(s) and excipient or vehicle. In practice, a product according to the present invention behaves both as one or more active principles and as an excipient. Furthermore, each biodermal constituent must be considered equally as a constituent of the skin and/or an active principle and/or a pharmaceutical agent, for example a thickener or a surfactant.

The composition of a product according to the present invention in practice excludes any non-biodermal excipient other than water or an aqueous phase.

It results from the above definition that a product according to the present invention cannot be likened to:

one or more biodermal, including biomimetic, active principles formulated in a stable pharmaceutical form, with a traditional excipient or vehicle

a complex of natural products, in general without excipient or vehicle per se, since it in practice comprises, as a whole, specific natural products, i.e. biodermal constituents.

According to the above definition, any product limited to one or more biodermal active principles, distributed in one way or another in water or in an aqueous phase, which is predominant by weight in the total composition of the product is also excluded; this product being, for example, a lotion obtained by dispersing a glycosaminoglycan in an aqueous phase.

Preferably, biodermal constituents which are cytocompatible with the skin represent the entire weight composition of the product considered.

Preferably, each biodermal constituent, which is biomimetic with a component of the skin, has a weight content in the said product (expressed as a weight percentage, for example) which is different from that of the said component in the skin.

By way of example, a product according to the invention comprises two biodermal and biomimetic constituents, the major one of which is a constitutive component of the epidermis and the minor of which is a skin nutrient.

Advantageously, the biodermal constituent is chosen from the biological, mineral, organic or biochemical species or entities of which the epidermis or the dermis is composed. By way of example, one of the biodermal constituents is chosen from skin nutrients.

A product in accordance with the invention is two-phase or single-phase or constitutes several emulsion or non-emulsion phases, to obtain any suitable topical form, for example cream, emulsion, lotion, serum, milk, gel, fluid, etc.

The terms “excipient” and “vehicle” conventionally mean any compound or composition, such as a diluent, dispersant or solvent, which is adapted to form the topical form required, for example a cream, a gel, an oil, a lotion, etc. This composition is completed with various adjuvants that are well known to those skilled in the art, such as wetting agents, astringents, humidifying agents, emollients, etc.

The term “interactive” refers to the property by which the composition of a product according to the invention maintains all the functional biological equilibria of the skin, without inhibiting or exacerbating them, this being in addition to the topical biological activity of the said composition, resulting from the synergistic or non-synergistic biological activity on the skin of one or more biodermal constituents.

A product according to the invention thus has three functions. A first function consists in both protecting and maintaining, or even in restoring, the main biological and physiological cutaneous equilibria. A second function consists in creating a suitable stable pharmaceutical form (milk, cream, etc.). A third function consists in treating the skin by providing it with one or more topical benefits, in particular therapeutic or cosmetic benefits.

The term “pharmaceutical form” means any form or presentation, adapted to the mode of administration selected, which allows the product to exert functional activity on the skin.

The term “biodermal constituent” means any component or product forming part of the composition of the skin, in particular of the epidermis, it being understood that this constituent is considered in isolated form, in a form identical to its natural form, or modified relative to its natural form, but remaining cytocompatible with the skin, irrespective of the method by which it is obtained or produced, in particular by separation from live skin products, by biosynthesis, by a biotechnology process or by genetic recombination.

The term “biologically active” refers to the fact that the component or constituent considered itself displays biological activity in the epidermis, or alternatively participates in any biological process, such as metabolism, in the epidermis.

The term “topical activity” refers to the fact that, globally, the cutaneous interactive base exhibits or manifests, via the topical route, a cosmetic or therapeutic benefit on the skin, for example on the epidermis.

The expression “cytocompatible with the skin” refers to the property by which the biodermal constituent selected has a cytotoxicity of less than 10% with respect to a cell culture of human keratinocytes, i.e. it remains virtually neutral with respect to the cellular viability and morpho-differentiation of the keratinocytes.

This cytocompatibility can be evaluated by means of the following routine test. [0028]
Normal human keratinocytes obtained from plastic surgery are cultured in sub-emerged condition in defined medium (MCDB 153) supplemented with 10 ng/ml of an epidermal growth factor, 5 μg/ml of insulin, 0.1 mM ethanolamine, 0.1 mM phosphoethanolamine and 2% of non-essential amino acids. This medium allows keratinocytes to be cultured without the presence either of serum or of live nourishing cells (3T3 fibroblasts); its low calcium content (0.1 mM) promotes cell growth. [0029]
The biodermal constituents are evaluated as regards their capacity to induce cytopathic effects on sub-confluent cultures. The contact times are 6 hours, 12 hours, 24 hours and 36 hours. [0030]
The cell viability is measured quantitatively by indirect counting of the live cells after labeling them with a vital dye. The neutral red system (3-amino-7-dimethylamino-2-methylphenasine hydrochloride) measures the activity of passage of the dye across the plasma membrane and of storage in the lysosomes of the viable cells. [0031]
The total incorporation of the neutral red is proportional to the number of live cells in culture. [0032]
The dye incorporated is extracted with an acetic acid/ethanol solvent and quantified by spectrophotometric measurement. The results are compared qualitatively, relative to culture standards, and are expressed as optical density (OD) and/or percentage of optical density relative to the negative control (untreated culture). [0033]
Within the variation limits of the strains used, a percentage of greater than or equal to 90% optical density for a culture placed in contact with the test biodermal constituent, relative to the negative control, indicates that the said constituent is cytocompatible with the skin. [0034]
The term “biomimetic” refers to the fact that the biodermal constituent selected has the structure and/or exerts the biomechanical, biophysical, physiological or biological function or activity of any skin component, i.e. of any skin component which can be isolated or separated by fractionating the dermis and/or the epidermis, or alternatively of any component whose existence can be characterized or demonstrated in the dermis and/or the epidermis, or alternatively of any component which can be assimilated by the skin and serve, if need be, as a nutrient for the constituent cells of the skin. [0035]
In other words, the skin, as a live biological medium, cannot distinguish between its own biodermal constituents. [0036]
Preferably, the biodermal constituents are chosen from biological, inorganic, organic or biochemical species or entities which constitute the skin, irrespective of the effective origin of the constituents brought onto or into the skin. [0037]
The biodermal constituents can be chosen from the constituent molecules of the epidermis and of the dermis. By way of example, the following will be selected: [0038]
various fluid or solid lipids, such as oleic acid, essential fatty acids, mono-, di- and triglycerides, linoleic acid, squalene, stearic acid or glyceryl monostearate, [0039]
solid lipids, such as stearic acid, cholesterol, ceramides, cholesterol ester or sulphate, or saturated diglycerides, [0040]
nucleic acids, [0041]
mucopolysaccharides such as hyaluronic acid, [0042]
collagens. [0043]
The biodermal constituent can also be chosen from skin nutrients, i.e. compounds or compositions which can be metabolized by skin cells. [0044]
By way of example, mention will be made of all the elements, or fragments of foods, which are useful for the metabolism of the skin, such as cutaneous acids, fatty acids, vitamins, peptone, casein, caseinates, immunoglobulin glycoproteins, complex lipids, amino acids, trace elements and lactoserum. [0045]
If necessary, the composition of a cosmetic, corporal hygiene or dermopharmaceutical product according to the present invention can be supplemented, to a maximum amount of 2%, with non-biodermal constituents which are cytocompatible with the latter, and which are necessary for the pharmaceutical formulation of the said product, and/or to supplement the topical biological activity of the product. By way of example, mention will be made mainly of fragrances, and quite incidentally and exceptionally certain minor adjuvants required for the correct maintenance of the stability and purity of the cosmetic or dermotherapeutic product. [0046]
The biodermal constituents forming virtually all, if not all, of a product according to the invention are formulated and obtained according to traditional techniques, for example in two-phase form, consisting of a water-in-oil or oil-in-water dispersion. [0047]
Tables 1 to 3 collate examples of biodermal constituents for formulating an oily phase, and/or an aqueous phase, and supplementing the formulations depending on the applications of the cosmetic product. In these tables, the left-hand column indicates a recommendation, it being understood that, as stated previously, each of the biodermal constituents is by nature cytocompatible with the skin, and biomimetic with the latter. The other columns indicate the class to which the said component belongs, according to the following classification: [0048]
Class 1: [0049]
Substantially cytocompatible and/or bio-assimilable components, present in constitutional form in the skin (water, amino acids, trace elements, vitamins, etc.). [0050]
Class 2: [0051]
Macromolecules obtained by biotechnological means, synthesis or extraction process, which are identical or virtually identical to the constituents of the skin (sodium salt of DNA, sodium hyaluronate, etc.) in composition and structure. These compounds are cytocompatible with the skin, but they can exhibit metabolic interactions in the context of biological or physiological processes. However, their biological action is comparable to that of the components naturally present in the skin (biomimetism). [0052]
The components of classes 1 and 2 are interactive, i.e. they act both as active agents and as excipients. [0053]
Class 3: [0054]
Components which are useful to and assimilable by the skin, if possible of food or dietary origin, or alternatively authorized in foodstuffs, but they must be cytocompatible. These components are interactive: they act both as “dermo-dietary” agents and as excipients. [0055]
Class 4: [0056]

Inert components, i.e. components which do not bring about any chemical, biological or immunological effect on the skin: compounds remaining in the superficial cellular strata of the epidermis (for example petroleum jelly and other fatty substances of mineral origin, silicones, titanium dioxide, zinc oxide or mica).

TABLE 1


CUTANEOUS CYTOCOMPATIBILITY SCALE

NATURE OF THE
COMPONENTS	(1)	(2)	(3)	(4)

Fluid lipids	oleic acid (XX)		plant oils (XX or	liquid petroleum
	linoleic acid (XX)	triglycerides	XXX depending	jelly (XXX)
	squalene (XX)	(XXX)	on the oil used)
Solid lipids	stearic acid (XX)
	palmitic acid (XX)
	cholesterol (XX)
	cholesterol ester		palm oil (XX)	white petroleum
	(XX)		beeswax (XX)	jelly (XXX)
	cholesterol
	sulfate (XX)
	ceramides (X)
Radical-scavenging	tocopherols (XX)
antioxidants	citric acid (XX)		bioflavonoids (X)
	glutathione (XX)
	superoxide
	dismutase (X)
Preserving agent	taurine (X)

TABLE 2


NATURE OF THE
COMPONENTS	(1)	(2)	(3)	(4)

Surfactants	glycolipids (XX)
	lecithins (XX)
	glycosylceramides
	(XX)	sophorolipids (XX)	lipoproteins (XX)
	lysine stearate
	(XX)
	arginine stearate
	(XX)
	lysine oleate (XX)
Thickeners	hyaluronic acid	mucopolysaccharides	xanthan (XXXX)
Gelling agents	(X)	(XXX)	pectin (XX)	chitin (XX)
	DNA (XX)		starch (XX)
Wetting agents	glycerol (XX)
	urea (XX)
	serine (XX)		fructose (XX)
	glucose (XX)
Antiseptics	short-chain fatty
	acids (X)
	lactoferrin/		propolis (X)
	lactoperoxidase
	(X)

TABLE 3


NATURE OF THE
COMPONENTS	(1)	(2)	(3)	(4)

Dyes	vitamin B		carotenoids
	(X)		(X)
	flavins		caramel
	(X)		(X)
Sunscreens and	DNA
sunblocks	(XX)
	pyrimidine			titanium oxide
	bases			(X)
	(XX)			zinc oxide
	melanins			(XX)
	(XX)
Fragrances			honey
			(X)
Minerals	sodium
	(XX)
	calcium
	(XX)
	magnesium
	(XX)
Trace elements	iron, copper
	(X)
	zinc
	(XX)
	selenium
	(X)

The compositions of a number of cosmetic products according to the invention are given below.



PRODUCT 1: Nutrient and moisturizing gel

	PHASE A:
	nutrient composition (amino acids,	qs 100
	vitamins, trace elements)
	sodium salt of DNA	2-5%
	preserving system (glucose/glucose	0.9-1.1%
	oxidase/lactoperoxidase)
	PHASE B:
	mucopolysaccharides	20-30%
	superoxide dismutase	0.5-1%
	citric acid	0.2-0.5%
	trisodium citrate	0.5-2%



PRODUCT 2: Refreshing and soothing spray

	PHASE A:
	nutrient composition (amino acids,	qs 100
	vitamins, trace elements)
	preserving system (glucose/glucose	0.9-1.1%
	oxidase/lactoperoxidase)
	PHASE B:
	citric acid	0.2-0.5%
	trisodium citrate	0.5-2%
	PHASE C:
	rhamnose	0.01-5%



PRODUCT 3: Radical-scavenging cream (1) for greasy skin

	PHASE A:
	tocopheryl acetate	0.2-2%
	stearic acid	3-5%
	squalene	2-7%
	triglycerides	2-7%
	PHASE B:
	water	qs 100
	L-arginine	1-2%
	glycerol	1-2%
	citric acid	0.2-0.5%
	trisodium citrate	0.5-2%
	PHASE C:
	nutrient composition (amino acids,	45-55%
	vitamins, trace elements)
	preserving system (glucose/glucose	0.9-1.1%
	oxidase/lactoperoxidase)
	superoxide dismutase	0.5-1%



PRODUCT 4: Moisturizing cream (2) for dry skin

	PHASE A:
	oleic acid	0.2-0.3%
	palmitic acid	0.2-0.3%
	behenic acid	0.2-0.3%
	stearic acid	0.1-0.2%
	linoleic acid	0.1-0.2%
	arachidic acid	0.05-0.1%
	triglycerides	0.1-0.2%
	cholesterol	0.9-1%
	cholesterol ester	0.02-0.04%
	phospholipids	1.5-2.5%
	squalene	3-7%
	PHASE B:
	water	qs 100
	L-arginine	1-2%
	citric acid	0.2-0.5%
	trisodium citrate	0.5-2%
	PHASE C:
	nutrient composition (amino acids,	45-55%
	vitamins, trace elements)
	preserving system (glucose/glucose	0.9-1.1%
	oxidase/lactoperoxidase)
	PHASE D:
	mucopolysaccharides	1-3%



PRODUCT 5: Desensitizing make-up-removing milk

	PHASE A:
	stearic acid	2-5%
	squalene	2-7%
	triglycerides	2-7%
	PHASE B:
	water	qs 100
	L-arginine	1-2%
	citric acid	0.2-0.5%
	trisodium citrate	0.5-2%
	PHASE C:
	nutrient composition (amino acids,	45-55%
	vitamins, trace elements)
	superoxide dismutase	0.5-1%
	preserving system	0.9-1.1%
	fucose	0.0005-1%



PRODUCT 6: Moisturizing lotion

	PHASE A:
	water	qs 100
	L-serine	1-3%
	glycerol	1-2%
	urea	1-3%
	citric acid	0.2-0.5%
	trisodium citrate	0.5-2%
	PHASE B:
	preserving system (glucose/glucose	0.9-1.1%
	oxidase/lactoperoxidase)

PRODUCT 7: Dry oil

	PHASE A:
	squalene	30-70%
	triglycerides	30-70%

PRODUCT 8: Bioprotective suncream

	PHASE A:
	tocopheryl acetate	0.2-2%
	stearic acid	3-5%
	squalene	2-7%
	triglycerides	2-7%
	titanium oxides	1-20%
	PHASE B:
	water	qs 100
	L-arginine	1-2%
	glycerol	1-2%
	citric acid	0.2-0.5%
	trisodium citrate	0.5-2%
	PHASE C:
	preserving system (glucose/glucose	0.9-1.1%
	oxidase/lactoperoxidase)

PRODUCT 9: Anti-sensitizing and regulating cleansing milk

	PHASE A:
	stearic acid	2-5%
	squalene	2-7%
	triglycerides	2-7%
	PHASE B:
	water	qs 100
	L-arginine	1-2%
	glycerol	1-2%
	citric acid	0.2-0.5%
	trisodium citrate	0.5-2%
	PHASE C:
	preserving system (glucose/glucose	0.9-1.1%
	oxidase/lactoperoxidase)
	phospholipids	2-10%
	PHASE D:
	rhamnose	0.1-5%
	fucose	0.0005-1%

The products according to the invention are, for example, in the form of a lotion, milk, cream, soap, etc., depending on their prescription or use. They are in a stable, single-phase, two-phase or three-phase topical form, for example. [0066]

Claims

What is claimed is:

1. A cosmetic or corporal hygiene composition comprising:

98-100% by weight biodermal constituents including at least two different biodermal constituents, each biodermal constituent being cytocompatible with skin; and

0-2% by weight of at least one non-biodermal constituent that is compatible with skin.

2. The composition according to claim 1, wherein at least one of the biodermal constituents are biomimetic with a component of skin.

3. The composition according to claim 1, wherein each of said biodermal constituents are biomimetic with a component of skin.

4. The composition according to claim 1, wherein each of said biodermal constituents are contained in said composition in a weight content that is different from the weight content of that constituent in skin.

5. The composition according to claim 1, wherein a major portion of said composition is a constitutive component of skin and a minor portion of said composition is a skin nutrient.

6. The composition according to claim 1, wherein each biodermal constituent is selected from the group consisting of biological, mineral, organic or biochemical species or entities of which the epidermis or the dermis is composed.

7. The composition according to claim 1, wherein at least one of said biodermal constituents is a skin nutrient.

8. The composition according to claim 1, wherein said composition comprises at least one non-biodermal constituent that is cytocompatible with skin.

9. The composition according to claim 1, wherein said composition is in a two-phase form.

10. The composition according to claim 9, wherein said composition is a water-in-oil dispersion.

11. The composition according to claim 9, wherein said composition is an oil-in-water dispersion.

12. The composition according to claim 1, consisting of biodermal constituents that are cytocompatible with skin.

13. The composition according to claim 1, wherein said biodermal constituents include water.

14. The composition according to claim 1, wherein said composition is not a complex of natural products, without any excipient or vehicle.

15. The composition according to claim 1, wherein said composition does not comprise any excipient or vehicle including water.

16. The composition according to claim 1, wherein each constituent is selected from the group consisting of:

(a) substantially cytocompatible and/or bioassimilable components present in constitutional form in the skin;

(b) macromolecular components identical or similar, respectively, to constituents of the skin;

(c) components assimilable by the skin; and

(d) inert components with respect to skin.

17. A cosmetic method, comprising:

(a) starting from the living epidermis as an ecological medium;

(b) choosing biodermal constituents that are each cytocompatible and biomimetic with a component of the skin;

(c) choosing non-biodermal constituents that are biocompatible with the skin;

(d) formulating a composition for topically use, which comprises 98-100% by weight of said biodermal constituents, including at least one component in a major amount and at least one component in a minor amount, and 0-2% by weight of said non-biodermal constituents, so that said composition is stable and exhibits at least one non-systemic topical beneficial activity; and

(e) applying said composition on a superficial part of the human body so as to maintain the functional biological equilibria of the living epidermis ecological medium.

18. A cosmetic method, comprising topically applying a composition according to claim 1 to skin of a human.

19. The method according to claim 18, wherein at least one of the biodermal constituents of said composition are biomimetic with a component of said skin.

20. The method according to claim 18, wherein a major portion of said composition is a constitutive component of skin and a minor portion of said composition is a skin nutrient.