US 5,137,923 AGrant
Lipophilic Quaternary Ammonium Salicylates, Their Use in Cosmetics and in Dermopharmacy
Issue Date:1992-08-11
•12 Claims
Abstract
Lipophilic quaternary ammonium salicylate, characterized in that it corresponds to the formula: ##STR1## in which: (i) R.sub.1, R.sub.2, R.sub.3 and R.sub.4, which may be identical or different, denote an alkyl or alkylcycloalkyl radical, optionally substituted or interrupted; in which: 0.ltoreq.n.ltoreq.4 and p denotes 0 or 1; R.sub.8 denotes H or an alkyl, alkenyl, alkylcycloalkyl or alkylaryl radical; (ii) R.sub.3 and/or R.sub.4 denote(s) a group: (iii) R.sub.4 denotes an alkylphenyl radical; (iv), (v) R.sub.1 and R.sub.2 can form a saturated or unsaturated aromatic or non-aromatic heterocycle; (vi) R.sub.1, R.sub.2 and R.sub.3 form polycyclic derivatives with the nitrogen atoms; R.sub.5 denotes a group corresponding to the formula: ##STR2## in which n is an integer varying between 0 and 10.
Metadata
Assignee
- L'Oreal
Inventors
- Michel Philippe
- Henri Sebag
- Michel Hocquaux
- Bernard Jacquet
- Jean P. Laugier
Application Information
Application Number:US 5417716
Filing Date:1990-06-21
Priority Date:1986-12-01
Art Unit:121
Classifications
IPC:
A61K 3144A61K 31435C07D21126C07D21170
Field of Search:
546514246;247;248;329;331;334;335;336;337;339;340;341;342;344;346;347315;357;358;396;399;859;852;887
Patent Drawings
This patent does not have any drawings.
Description
The present invention relates to new lipophilic salicylates containing at least one quaternary ammonium group, the process for preparing them and the pharmaceutical and cosmetic compositions containing them.
The use of various hexadecyltrimethylammonium salts, including the salicylate, as a germicidal agent has been described in the prior art. See in particular SHELTON et al., J.A.C.S. (1946), 68, 753 as well as GAUTIER et al., Bull. Soc. Chim. France (1955), 634 and Broh-Kahn, Intern. Rec. Med. (1960), 173, 219.
The Applicant has just discovered, and this forms the subject of the invention, new lipophilic quaternary ammonium salicylates.
It has found, in particular, that these compounds were especially active as bactericidal and keratolytic agents in the treatment of infectious or non-infectious dermatoses which are possibly of bacterial or fungal origin and/or linked to the implantation of certain yeasts having a pathogenic nature. In particular, these new compounds have the advantage of being able to be used in the treatment of acne, comedones and psoriasis, and of preventing skin infections whose onset is a phenomenon secondary to a cutaneous stress of some kind, such as cuts, burns, solar erythema or various kinds of inflammation. In addition, they have good antidandruff and deodorant properties.
The Applicant has also discovered that certain compounds possess good properties of absorption of light and UV radiation.
In addition, these compounds can be used advantageously in ophthalmology and for the treatment of buccal infections and inflammations of the nasal mucosae, and more generally for the treatment of viral conditions. These compounds possess, moreover, spermicidal properties.
These compounds possess, moreover, good preservative properties. Some of these compounds can be used on account of their surfactant and foam-stabilizing properties.
The Applicant has discovered, in particular, that these new compounds possessed special value in the treatment of acne.
As is well known, acne is a polymorphic skin disorder occurring at puberty and regressing spontaneously in the large majority of cases at about 20 to 25 years of age. In the individuals concerned, acne affects all the areas rich in sebaceous glands (the forehead, the face, wings of the nose, trunk, back) with the exception of the scalp.
Although poorly defined, the etiopathogenesis of acne owes its origin to the formation of a characteristic lesion, the comedo. The latter results from the obstruction of the pilosebaceous duct as a consequence of a dyskeratinization of the region of the infundibilum of the duct.
The major effect of this obstruction is to modify the rheological properties of the sebum and the physicochemical characteristics of the medium, such as pH, oxygen tension, and the like.
This modification permits the hyperproliferation of the resident cutaneous strains, chiefly Propionibacterium acnes, which is an anaerobic or air-tolerant strain.
The consequence of the bacterial hyperproliferation is to release into the medium certain proteases or hyaluronidases of bacterial origin, which cause a lysis of the follicular sac and hence the release of inflammatory compounds within the dermis, and initiate the body's inflammatory type reaction.
While the nature of the inflammatory compounds has not at present been determined, their bacterial origin seems to be in little doubt, accounting for the good therapeutic success of antibacterial compounds, both orally and topically, in inflammatory acne.
For this purpose, antibacterial agents such as antibiotics, for example erythromycin, tetracycline and clindamycin have been recommended very frequently in the treatment of acne. These compounds give excellent results, but their over-zealous use renders the Propionibacterium acnes strains resistant to these same antibiotics, so that repeated treatment may prove to have little effect.
The Applicant has discovered that the new lipophilic quaternary ammonium salicylates had an antibacterial activity in vitro, with respect to Propionibacterium acnes, similar to that of the antibiotics used previously, without, however, inducing phenomena of bacterial resistance.
The new lipophilic quaternary ammonium salicylates are especially more active towards Propionibacterium acnes strains than hexadecyltrimethylammonium salicylate, as well as other quaternary ammonium derivatives having an organic counter-anion that are known in the prior art.
The lipophilic quaternary ammonium salicylates according to the invention also have the advantage of not being very irritant to the skin. These new compounds are, moreover, more capable of penetrating the stratum corneum in the case of a topical application.
The subject of the invention is hence, by way of new compounds, lipophilic quaternary salicylates defined below.
Another subject of the invention consists of therapeutic treatment compositions containing the compounds defined above.
The subject of the invention is also a composition and a process for cosmetic treatment based on these compounds.
Other subjects of the invention will emerge on reading the description and examples which follow.
The lipophilic quaternary ammonium salicylates which constitute the main subject of the invention are compounds essentially corresponding to the formula: ##STR3## in which: (i) R.sub.1, R.sub.2, R.sub.3 and R.sub.4, which may be identical or different, denote a C.sub.1 to C.sub.22 saturated or unsaturated alkyl or alkylcycloalkyl radical which can optionally be interrupted by one or more groups chosen from ether, thioether, sulphoxide, ester, amide, sulphonamide, carbamate or ureido groups and/or which can bear, at the end of the chain or in the chain, one or more hydroxyl or halogen group(s);
(ii) R.sub.3 and/or R.sub.4 denote(s) a group:
in which:
0.ltoreq.n.ltoreq.4 and p denotes 0 or 1.
R.sub.8 denotes H or a C.sub.1 to C.sub.18 alkyl, alkenyl, alkylcycloalkyl or alkylaryl radical, it being possible for the alkyl groups to be linear or branched and for the aliphatic or aromatic rings optionally to bear one or more C.sub.1 to C.sub.4 alkyl or alkoxy substituent(s);
R.sub.7 denotes H, CH.sub.3 or CH.sub.2 OH.
When R.sub.7 denotes CH.sub.2 OH, R.sub.8 is then other than H and p equals 1.
In the other cases, p =0.
The group (OC.sub.2 H.sub.3 R.sub.7) can denote either or both of the following arrangements: ##STR4## R.sub.1 and R.sub.2 have the meanings assigned in paragraph (i); (iii) R.sub.4 denotes the group; ##STR5## in which n denotes 0 or 1, in which case R.sub.1, R.sub.2 and R.sub.3 have the meanings stated above, R.sub.6 denotes a hydrogen, a hydroxyl, a halogen, an alkyl or hydroxyalkyl residue or a C.sub.1 to C.sub.18 acyl residue;
(iv) R.sub.1 and R.sub.2 form an aromatic heterocycle (in which case R.sub.3 is non-existent) corresponding to the formula: ##STR6## in which R.sub.4 has the meanings stated above;
(v) R.sub.1 and R.sub.2 form a saturated or unsaturated non-aromatic heterocycle, optionally interrupted by an oxygen atom or a nitrogen atom or a sulphur atom; in which case
R.sub.4 denotes a group defined above and R.sub.3 denotes a group also defined in (i);
(vi) R.sub.1, R.sub.2 and R.sub.3 form, together with one or more nitrogen atoms, polycyclic derivatives such as diazabicyclooctane or hexamethylenetetramine, R.sub.4 in this case denoting a group defined above under (i) and (iii).
Generally speaking, the ammonium groups are such that at most two of the radicals R.sub.1 to R.sub.4 consist of 12 or more than 12 consecutive carbon atoms.
In the different cases mentioned above, R.sub.5 denotes a group: ##STR7## n varying from 0 to 10 inclusive.
The compounds according to the invention are preferably prepared from a salt such as, more especially, the corresponding quaternary ammonium carbonate, solubilized in alcoholic medium and preferably in methanol, to which is added the chosen lipophilic salicylic acid derivative, also solubilized in an alcohol such as ethanol or methanol or alternatively in an ether such as tetrahydrofuran. The reaction starts by itself and is followed by the evolution of carbon dioxide.
Preferred compounds are chosen, in particular, from the following compounds: hexadecyltrimethylammonium 5-octanoylsalicylate, hexadecyltrimethylammonium 5-decanoylsalicylate, hexadecyltrimethylammonium 5-dodecanoylsalicylate, hexadecylpyridinium 5-octanoyl salicylate, hexadecylpyridinium 5-decanoylsalicylate, hexadecylpyridinium 5-dodecanoylsalicylate, benzyldimethylhexadecylammonium 5-octanoylsalicylate, benzyldimethylhexadecylammonium 5-decanoylsalicylate, benzyldimethylhexadecylammonium 5-dodecanoylsalicylate, benzyltrimethylammonium 5-decanoylsalicylate, hexadecyldimethyl(hydroxyethyl)ammonium 5-decanoylsalicylate, tetramethylammonium 5-dodecanoylsalicylate, dodecylethyldimethylammonium 5-decanoylsalicylate, trimethyl-(.beta.-hydroxyethyl)-ammonium 5-decanoylsalicylate, trimethyl-(.beta.-hydroxyethyl)-ammonium 5-dodecanoylsalicylate, N-hexadecyl-N-methyl-imidazolinium 5-dodecanoylsalicylate, N-dodecyl-N-methylmorpholinium 5-decanoylsalicylate, N-methyl-N-octylpiperidinium 5-dodecanoylsalicylate, 1'-azonia-4'-azabicyclo[2.2.2]octylhexadecane 5-dodecanoylsalicylate, benzethonium 5-octanoylsalicylate, benzethonium 5-dodecanoylsalicylate, N-(3-chloroallyl)hexaminium 5-octanoylsalicylate and N-(3-chloroallyl)hexaminium 5-dodecanoylsalicylate.
The pharmaceutical compositions which are the subject of the invention are essentially characterized in that they are topical compositions containing at least one of the compounds corresponding to the formula (I) above in a pharmaceutically acceptable medium that is suitable for topical application.
These compositions are especially suitable for the treatment of various dermatoses such as acne.
The compositions can take the form of an aqueous or anhydrous solution or dispersion, or alternatively the form of an emulsion or suspension, containing at least one compound corresponding to the formula (I) in concentrations between 0.001 and 15% by weight based on the total weight of the composition, and preferably between 0.05 and 5%.
These compositions can contain pharmaceutically acceptable vehicles and adjuvants which are well known in the prior art. It is possible, for example, to prepare solutions using one or more organic solvent(s) that is/are acceptable from the physiological standpoint, chosen, in addition to water, from solvents such as acetone, ethanol, isopropyl alcohol, glycol ethers such as the products sold under the name "Dowanol", polyglycols and polyethylene glycols, C.sub.1 -C.sub.4 alkyl esters of short-chain acids, preferably ethyl or isopropyl lactate, fatty acid triglycerides such as the products marketed under the name "Miglyol", isopropyl myristate, animal, mineral and vegetable oils and polysiloxanes.
The compositions according to the invention can also contain thickening agents such as cellulose and/or cellulose derivatives, in the proportion of 0.5 to 20% by weight based on the total weight of the composition. They can also contain gums such as xanthan, guar or carob gum or gum arabic, or alternatively polyethylene glycols, bentones and montmorillonites, and the like.
These compositions according to the invention can also contain, in combination, antiacne agents such as retinoic derivatives, antibacterial agents, antiinflammatories, and steroids having a non-hormonal action, in particular pregnenolone, which is already known for the treatment and care of the skin, whose properties are described in U.S. patent application No. 2,791,534.
It is possible to add, if necessary, an adjuvant chosen from antioxidants, surfactants, other preservatives, film-forming, keratolytic or comedolytic agents, perfumes and colourings.
For example, among antioxidants, t-butylhydroquinone, butylated hydroxyanisole, butylated hydroxytoluene and .alpha.-tocopherol and its derivatives may be mentioned.
The galenical forms chiefly conditioned for topical application take the form of creams, milks, gels, dispersions or microemulsions, lotions thickened to a greater or lesser extent, impregnated pads, ointments or sticks, or alternatively the form of aerosol formulations in spray or foam form or alternatively in the form of a cake of soap.
A subject of the invention resides in the use of the compounds of the formula I for the preparation of such compositions intended for the treatment of dermatoses.
The compositions according to the invention can also be used for the cosmetic treatment of the skin, in particular as comedolytic, keratolytic, antisun or verrulytic agents, or as agents for treating the hair or scalp.
These compositions can assume forms similar to those mentioned above, and can contain adjuvants customarily used in cosmetics in compositions intended for the care and cosmetic treatment of the skin.
The process for cosmetic treatment consists in applying such a composition on the skin.
The antibacterial activity of the compounds according to the invention was studied by the dilution method in order to determine the Minimal Inhibitory Concentration (MIC) according to the method described and employed by G. A. DENYS et al., Antimicrobial Agents and Chemotherapy (1983) 23, 335-337, and J. J. LEYDEN et al., J. Am. Acad. Dermatol. (1983) -8 (1) 41-5, using Propionibacterium acnes strain ATCC 6919 as the strain.
The minimal inhibitory concentrations (MIC), expressed in .mu.g/ml (DMSO), of the lipophilic quaternary ammonium salicylates according to the invention are shown in Table 1.
It emerges from this table that the lipophilic salicylates according to the invention are markedly more active with respect to the Propionibacterium acnes strain than the salicylates previously recommended in the prior art.
The examples which follow are designed to illustrate on the one hand the processes for the preparation of the compounds according to the invention, and on the other hand pharmaceutical and cosmetic compositions employing these compounds.
PREPARATION EXAMPLE 1
Preparation of N-hexadecyl-N,N,N-trimethylammonium 5-octanoylsalicylate: compound no. 4 (Table I).
2 g (7.57 mmol) of 5-octanoylsalicylic acid, dissolved beforehand in 15 ml of methanol, are added to a solution of 2.62 g (4.16 mmol) of hexadecyltrimethylammonium carbonate dissolved in 15 ml of methanol; the mixture is stirred for 1 hour at room temperature and the solvent is then evaporated off, and the white solid residue obtained is recrystallized in an acetone/diethyl ether mixture to give 3.8 g (91.5% yield) of hexadecyltrimethylammonium 5-octanoylsalicylate.
M.p. 130.degree. C. (acetone/diethyl ether)
The .sup.1 H and .sup.13 C NMR spectra confirm the expected structure with the characteristic values for the ammonium cation and the 5-octanoylsalicylate anion.
PREPARATION EXAMPLE 2
Preparation of N-hexadecyl-N,N,N-trimethylammonium 5-decanoylsalicylate: compound no. 5.
2 g (6.85 mmol) of 5-decanoylsalicylic acid, dissolved beforehand in 15 ml of ethanol, are added to a solution of 2.2 g (3.5 mmol) of hexadecyltrimethylammonium carbonate dissolved in 15 ml of methanol; the mixture is stirred for 1 hour at room temperature, the solvents are then evaporated off and the white solid residue obtained is recrystallized in an acetone/d ethyl ether mixture to give 3.8 g (96% yield) of hexadecyltrimethylammonium 5-decanoylsalicylate.
M.p. 130.degree. C. (acetone/diethyl ether)
The .sup.1 H and .sup.13 C NMR spectra confirm the expected structure with the characteristic values for the quaternary ammonium cation and the 5-decanoylsalicylate anion.
PREPARATION EXAMPLE 3
Preparation of N-hexadecyl-N,N,N-trimethylammonium 5-dodecanoylsalicylate: compound no. 6.
2 g (6.25 mmol) of 5-dodecanoylsalicylic acid, dissolved beforehand in 15 ml of ethanol, are added to a solution of 2 g (3.18 mmol) of hexadecyltrimethylammonium carbonate dissolved in 15 ml of methanol; the mixture is stirred for 1 hour at room temperature, the solvents are then evaporated off and the white solid residue obtained is recrystallized in an acetone/diethyl ether mixture to give 3.5 g (93% yield) of hexadecyltrimethylammonium 5-dodecanoylsalicylate.
M.p. 130.degree. C. (acetone/diethyl ether)
The .sup.13 C NMR spectrum confirms the expected structure with the characteristic values for the quaternary ammonium cation and the 5-dodecanoylsalicylate anion.
The UV spectrum (ethanol) shows an absorption .lambda..sub.max =280 nm; the molar extinction coefficient .epsilon.=14080.
PREPARATION EXAMPLE 4
Preparation of N-hexadecylpyridinium 5-octanoylsalicylate monohydrate: compound no. 7.
2 g (7.57 mmol) of 5-octanoylsalicylic acid, dissolved beforehand in 15 ml of methanol, are added to a solution of 2.5 g (3.79 mmol) of hexadecylpyridinium carbonate dissolved in 15 ml of methanol; the mixture is stirred for 1 hour at room temperature, the brown crude residue obtained is then filtered off and the filtrate is evaporated to dryness to give 4.2 g (98% yield) of hexadecylpyridinium 5-octanoylsalicylate.
The .sup.13 C NMR spectrum confirms the expected structure with the characteristic values for the quaternary ammonium cation and the 5-octanoylsalicylate anion.
The UV spectrum (ethanol) shows an absorption .lambda..sub.max =279 nm; the molar extinction coefficient .epsilon.=21450.
PREPARATION EXAMPLE 5
Preparation of N-hexadecylpyridinium 5-decanoylsalicylate sesquihydrate; compound no. 8.
2 g (6.85 mmol) of 5-decanoylsalicylic acid, dissolved beforehand in 15 ml of ethanol, are added to a solution of 2.3 g (3.44 mmol) of hexadecylpyridinium carbonate dissolved in 15 ml of methanol; the mixture is stirred for 1 hour at room temperature, the solvents are then evaporated off and the brown residue obtained is recrystallized in an acetone/diethyl ether mixture to give 3.9 g (96% yield) of hexadecylpyridinium 5-decanoylsalicylate.
M.p. 73.degree. C. (acetone/diethyl ether)
The .sup.13 C NMR spectrum confirms the expected structure with the characteristic values for the aromatic quaternary ammonium cation and 5-decanoylsalicylate.
PREPARATION EXAMPLE 6
Preparation of N-hexadecylpyridinium 5-dodecanoylsalicylate hydrate: compound no. 9.
2 g (6.25 mmol) of 5-dodecanoylsalicylic acid, dissolved beforehand in 15 ml of ethanol, are added to a solution of 2.1 g (3.14 mmol) of hexadecylpyridinium carbonate dissolved in 15 ml of methanol; the mixture is stirred for 1 hour at room temperature, the solvents are then evaporated off and the brown residue obtained is recrystallized in an acetone/diethyl ether mixture to give 3.7 g (95% yield) of hexadecylpyridinium 5-dodecanoylsalicylate.
M.p. 79.degree. C. (acetone/diethyl ether)
The .sup.13 C NMR spectrum confirms the expected structure with the characteristic values for the aromatic quaternary ammonium cation and 5-dodecanoylsalicylate.
The UV spectrum (ethanol) shows an absorption .lambda..sub.max =279 nm; the molar extinction coefficient .epsilon.=18910.
PREPARATION EXAMPLE 7
Preparation of N-benzyl-N,N-dimethyl-N-hexadecylammonium 5-octanoylsalicylate: compound no. 10.
2 g (7.57 mmol) of 5-octanoylsalicylic acid, dissolved beforehand in 15 ml of methanol, are added to a solution of 3 g (3.84 mmol) of benzyldimethylhexadecylammonium carbonate dissolved in 15 ml of methanol; the mixture is stirred for 1 hour at room temperature, the solvent is then evaporated off and the white residue is recrystallized in an acetone/diethyl ether mixture to give 4.5 g (95% yield) of benzyldimethylhexadecylammonium 5-octanoylsalicylate.
M.p. 114.degree. C. (acetone/diethyl ether)
The .sup.13 C NMR spectrum confirms the expected structure with the characteristic signals of the quaternary ammonium cation and 5-octanoylsalicylate.
The compounds of Examples nos. 8 to 21 are prepared in a manner similar to that described in Examples 1 to 7.
PREPARATION EXAMPLE 8
Preparation of N-benzyl-N,N-dimethyl-N-hexadecylammonium 5-decanoylsalicylate: compound no. 11.
M.p. 113.degree. C. (acetone/diethyl ether)
PREPARATION EXAMPLE 9
Preparation of N-benzyl-N,N-dimethyl-N-hexadecylammonium 5-dodecanoylsalicylate: compound no. 12.
M.p. 117.degree. C. (acetone/diethyl ether)
The UV spectrum (ethanol) shows an absorption .lambda..sub.max =281 nm; the molar extinction coefficient .epsilon.=17720.
PREPARATION EXAMPLE 10
Preparation of N-benzyl-N,N,N-trimethylammonium 5-decanoylsalicylate: compound no. 13.
M.p. 135.degree. C. (acetone/diethyl ether)
PREPARATION EXAMPLE 11
Preparation of N-hexadecyl-N,N-dimethyl-N-(.beta.-hydroxyethyl)ammonium 5-decanoylsalicylate: compound no. 14.
PREPARATION EXAMPLE 12
Preparation of N,N,N,N-tetramethylammonium 5-dodecanoylsalicylate: compound no. 15.
M.p. 97.degree. C. (acetone/diethyl ether)
PREPARATION EXAMPLE 13
Preparation of trimethyl-(.beta.-hydroxyethyl)ammonium 5-dodecanoylsalicylate: compound no. 18.
M.p. 67.degree. C. (methanol/diethyl ether)
UV spectrum (ethanol): .lambda..sub.max =280 nm; .epsilon.=16640.
PREPARATION EXAMPLE 14
Preparation of trimethyl-(.beta.-hydroxyethyl)ammonium 5-decanoylsalicylate: compound no. 17.
PREPARATION EXAMPLE 15
Preparation of dimethylethyldodecylammonium 5-decanoylsalicylate: compound no. 16.
M.p. 65.degree. C. (acetone/diethyl ether)
PREPARATION EXAMPLE 16
Preparation of N-hexadecyl-N-methylimidazolinium 5-dodecanoylsalicylate: compound no. 20.
M.p. 82.degree. C. (acetone/diethyl ether)
UV spectrum (ethanol): .lambda..sub.max =281 nm; .epsilon.=15385
PREPARATION EXAMPLE 17
Preparation of 1'-azonia-4'-azabicyclo[2.2.2]octylhexadecane 5-dodecanoylsalicylate: compound no. 23.
M.p. 96.degree. C. (acetone/diethyl ether)
PREPARATION EXAMPLE 18
Preparation of N-methyl-N-octylpiperidinium 5-dodecanoylsalicylate: compound no. 22.
M.p. 45.degree. C. (acetone/diethyl ether)
PREPARATION EXAMPLE 19
Preparation of N-dodecyl-N-methylmorpholinium 5-decanoylsalicylate: compound no. 21.
M.p. 78.degree. C. (acetone/diethyl ether)
PREPARATION EXAMPLE 20
Preparation of benzethonium 5-octanoylsalicylate.
2.2 g (8.4 mmol) of 5-octanoylsalicylic acid, dissolved beforehand in 100 ml of methanol, are added to a solution of 3.7 g (4.2 mmol) of benzethonium carbonate dissolved in 100 ml of methanol; the mixture is stirred for 1 hour at room temperature, the solution is then filtered and the filtrate is evaporated to dryness to give 5.5 g (98% yield) of benzethonium 5-octanoylsalicylate.
The .sup.13 C NMR spectrum confirms the expected structure with the characteristic values for the quaternary ammonium cation and the octanoylsalicylate anion.
PREPARATION EXAMPLE 21
Preparation of benzethonium 5-dodecanoylsalicylate.
2 g (6.4 mmol) of 5-dodecanoylsalicylic acid, dissolved beforehand in 100 ml of ethanol, are added to a solution of 2.82 g (3.2 mmol) of benzethonium carbonate dissolved in 100 ml of methanol; the mixture is stirred for 1 hour at room temperature, the solution is then filtered and the filtrate is evaporated to dryness to give 4.5 g (97% yield) of benzethonium 5-dodecanoylsalicylate.
The .sup.13 C NMR spectrum confirms the expected structure with the characteristic values for the quaternary ammonium cation and the 5-dodecanoylsalicylate anion.
The term benzethonium denotes:
N,N-dimethyl-N-[2-{2-[4-(1,1,3,3-tetramethylbutyl)phenoxy]-ethoxy}ethyl]ben zenemethaminium, or
benzyldimethyl-[2-{2-[p-(1,1,3,3,-tetramethylbutyl)phenoxy]-ethoxy}ethyl]am monium.
The examples which follow are designed to illustrate more especially pharmaceutical or cosmetic compositions employing the compounds according to the invention.
Pharmaceutical and cosmetic compositions
EXAMPLE 1
The following composition is prepared:
EXAMPLE 2
The following composition is prepared:
EXAMPLE 3
The following composition is prepared:
EXAMPLE 4
The following composition is prepared:
The compositions of Examples 1 to 4 take the form of a gel, and are intended especially for the topical treatment of acne.
EXAMPLE 5
The following composition is prepared:
EXAMPLE 6
The following composition is prepared:
EXAMPLE 7
The following composition is prepared:
EXAMPLE 8
The following composition is prepared:
These compositions of Examples 5, 6, 7 and 8 take the form of a lotion which is particularly effective in the treatment of acne.
EXAMPLE 9
The following composition is prepared:
This composition takes the form of a stick which is suitable for the treatment of acne.
EXAMPLE 10
This composition takes the form of a stick which is suitable for protecting the lips against solar radiation.
Claims
We claim:
1. A lipophilic quaternary ammonium salicylate that has either formula (1) or formula (2): ##STR21## wherein: R.sub.5 has the formula: ##STR22## in which n is an integer between 0 and 10 inclusive; R.sub.3 and R.sub.4 are: (i) identical or different and are a C.sub.1 to C.sub.22 alkyl or alkylcycloalkyl radical, which is unsubstituted, or which is interrupted by one or more groups selected from the group consisting of ether, thioether, sulphoxide, ester, amide, sulphonamide, carbamate and ureido moieties in the chain or bears at least one hydroxyl or halogen group at the end of the chain or in the chain; or (ii) the group: in which the group, (OC.sub.2 H.sub.3 R.sub.7), denotes either or both of the following formulas: ##STR23## and 0.ltoreq.n.ltoreq.4 and p is 0 or 1; or (iii) R.sub.3 has the meanings set forth in paragraph (i) and R.sub.4 is the group; ##STR24## in which n is o or 1; R.sub.6 is hydrogen, hydroxyl, halogen, alkyl, hydroxyalkyl or a C.sub.1 to C.sub.18 acyl radical; R.sub.8 is hydrogen or a C.sub.1 to C.sub.18 alkyl, alkenyl, alkylcycloalkyl or alkylaryl radical, in which the alkyl groups are linear or branched and the aliphatic or aromatic rings are unsubstituted or substituted with one or more C.sub.1 to C.sub.4 alkyl or alkoxy substituents; and R.sub.7 is H, CH.sub.3 or CH.sub.2 OH; when R.sub.7 is CH.sub.2 OH, then R.sub.8 is not hydrogen and p equals 1, when R.sub.7 is H or CH.sub.3, then p=0.
2. A compound of claim 1 wherein each of R.sub.3 and R.sub.4 is, independently, a C.sub.1 to C.sub.22 alkyl or alkylcycloalkyl radical, which is optionally subsitituted and wherein the alkyl chain is optionally interrupted by a member selected from the group consisting of an ether, thioether, sulphoxide, ester, amide, sulphonamide, carbamate and ureido moiety, any substituent being a chain substituent and being hydroxyl or halo.
3. The compound of claim 1, wherein R.sub.4 is a benzyl group.
4. A lipophilic quaternary ammonium salicylate compound of claim 1, selected from the group consisting of hexadecylpyridinium 5-octanoylsalicylate, hexadecylpyridinium 5-decanoylsalicylate, hexadecylpyridinium 5-dodecanoylsalicylate and N-methyl-N-octylpiperidinium 5-dodecanoylsalicylate.
5. A composition for topical application for the treatment of dermatoses or skin disorders, comprising an effective amount of at least one compound of claim 1 in a pharmaceutically or cosmetically acceptable vehicle.
6. The composition of claim 5, further comprising at least one other anti-acne agent selected from the group consisting of pregnenolone, retinoic derivatives, antibiotics and anti-inflammatories.
7. The composition of claim 5 which is formulated as a solution, an anhydrous dispersion, an emulsion or a suspension and in which the concentration of the lipophilic quaternary ammonium salicylate is between 0.001 and 15% by weight based on the total weight of the composition.
8. A method of treating acne, comprising applying an effective amount of a composition containing at least one compound of claim 1 and a pharmaceutically acceptable carrier to the affected area of skin.
9. A method of treating dandruff, comprising applying an effective amount of a composition comprising at least one compound of claim 1 and a pharmaceutically acceptable carrier to the scalp.
10. A method of treating warts, comprising applying to the wart a composition comprising an effective amount of at least one compound of claim 1 and a pharmaceutically acceptable carrier.
11. A method of treating solar erythema, comprising applying to the affected area of skin a composition comprising an effective amount of at least one compound of claim 1 and a pharmaceutically acceptable carrier.
12. A method of treating inflammations of the skin, comprising applying to the affected area of skin a composition comprising an effective amount of at least one compound of claim 1 and a pharmaceutically acceptable carrier.
Patent Citations (1)
| Patent | Date | Inventor | Cited By |
|---|---|---|---|
| EPX124905 | 1984-11-01 |