EP1171120A1 - Methods for alleviating discomfort of a hot flash and compositions therefor - Google Patents
Methods for alleviating discomfort of a hot flash and compositions thereforInfo
- Publication number
- EP1171120A1 EP1171120A1 EP00905910A EP00905910A EP1171120A1 EP 1171120 A1 EP1171120 A1 EP 1171120A1 EP 00905910 A EP00905910 A EP 00905910A EP 00905910 A EP00905910 A EP 00905910A EP 1171120 A1 EP1171120 A1 EP 1171120A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- cooling
- group
- cooling agent
- menthyl
- composition
- 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.)
- Withdrawn
Links
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/45—Non condensed piperidines, e.g. piperocaine having oxo groups directly attached to the heterocyclic ring, e.g. cycloheximide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4913—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/16—Central respiratory analeptics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/12—Drugs for genital or sexual disorders; Contraceptives for climacteric disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/16—Emollients or protectives, e.g. against radiation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
- A61P5/30—Oestrogens
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/24—Thermal properties
- A61K2800/244—Endothermic; Cooling; Cooling sensation
Definitions
- the present invention relates to a method of alleviating discomfort experienced by a woman during a hot flash.
- the present invention also relates to the method of use of topical compositions that may be used to alleviate such discomfort. More particularly, the present invention relates to a method of alleviating discomfort, especially the feeling of intense heat, experienced by a woman during a hot flash and the topical application of a composition having cooling ingredients in order to alleviate such discomfort.
- a hot flash is marked by an increase in body temperature accompanied by an intense feeling of unbearable heat, particularly internally radiating body heat.
- a hot flash may also be accompanied by an increase in heart rate, dizziness, anxiety, faintness, a sense of unease, tingling sensations, pressure in the head, nausea, perspiration, and feelings of breathlessness.
- the feeling of heat is often concentrated in the area of the face and neck, and sometimes spreads to the area of the upper chest.
- a hot flash may last for as short as a minute, a hot flash usually lasts as long as two to three minutes, and may last as long as an hour. Regardless of the duration of the hot flash, the discomfort due to the intense feeling of heat is extremely uncomfortable and disconcerting to a woman experiencing the hot flash.
- HRT Estrogen Replacement Therapy
- ERT Estrogen Replacement Therapy
- vitamin supplements such as vitamin E and bioflavonoids
- U.S. Patent No. 5,730,957 to Rizk describes the use of a cooling composition having dimethyl ether and water to alleviate the discomfort associated with heat.
- This cooling composition utilizes the latent heat of vaporization to provide its cooling action and also requires that the cooling composition be at a temperature below ambient temperature and higher than the freezing point of water.
- This patent also provides a method of maintaining the cooling composition at such a temperature that requires a pressurized dispensing container.
- the sole embodiment described in the Rizk patent is a water-dimethyl ether composition contained within an aerosol dispenser (col. 3, line 51 et seq.).
- the use of dimethyl ether has known safety issues.
- U.S. Patent No. 5,703,123 to Pelzer et al. describes the use of compositions having asymmetric carbonates, thiocarbonates and/or carbonates to create a physiologic cooling effect on the skin and on mucosae in compositions such as food stuffs (e.g. beverages, jams,), cosmetic agents (e.g. shaving products, skin care products, etc.), household products (e.g. fabric softeners) and pharmaceutical preparations (e.g. antiseptic ointments, cough mixtures).
- food stuffs e.g. beverages, jams,
- cosmetic agents e.g. shaving products, skin care products, etc.
- household products e.g. fabric softeners
- pharmaceutical preparations e.g. antiseptic ointments, cough mixtures.
- ketals such as 1-methone glycerol ketal or 3,3,5- trimethylcyclohexanone glycerol ketal
- ketals such as 1-methone glycerol ketal or 3,3,5- trimethylcyclohexanone glycerol ketal
- U.S. Patent No. 5,688,497 to Lozeau et al. discloses shaving aids that provide a physiological cooling effect.
- U.S. Patent No. 5,595,970 to Garfield et al. describes the use of a nitric oxide substrate and/or nitric acid donor, either alone or in combination with a progestin or estrogen to alleviate climacterium symptoms such as hot flashes.
- a progestin or estrogen to alleviate climacterium symptoms such as hot flashes.
- the compositions disclosed in Garfield et al. require systemic administration.
- the present invention in brief summary, is a method of alleviating the discomfort associated with hot flashes that comprises the step of applying to the body, particularly to the chest, face and neck area and/or to the wrist and arm area, a topical cooling composition having at least one cooling agent.
- Hot flashes are most commonly associated with the discomforting symptom of an intense feeling of heat that begins in the face, neck, or chest regions and then radiates to other parts of the body.
- many women experience a premonition of an impending hot flash that is accompanied by symptoms, such as a feeling of unease or anxiety, a feeling of pressure in the head, or tingling sensations.
- symptoms such as a feeling of unease or anxiety, a feeling of pressure in the head, or tingling sensations.
- heart rate digital blood flow, and vasodilation of blood vessels of the skin.
- women will experience an intense feeling of heat and which may further be accompanied by feelings of dizziness, nausea and breathlessness.
- the first detectable change is an increase in finger blood flow with a concomitant enhancement of skin conductance, as well as a change in temperature of the skin of the face and neck.
- the increase in skin conductance is followed rapidly by a sharp rise (1-7°C) in finger temperature.
- the degree to which finger temperature rises during a hot flash is inversely proportional to the base-line finger temperature before the flash.
- a 0.5°C increase in finger temperature in a woman with a base-line finger temperature of 35°C may be as good a measure of the occurrence of a hot flash as a 5°C increase in finger temperature in a woman with base-line finger temperature of 29°C, because of the non- linear relationship between skin temperature and blood flow.
- a hot flash is the inverse of a fever.
- the control of body temperature resembles a negative feedback system in which a set point temperature serves as reference for the themoregulatory mechanism.
- a fever can be understood as the upward adjustment of this temperature set point.
- the set point In a febrile episode, the set point is first elevated, initiating vasoconstruction, shivering and behavorial modifications, such as the addition of blankets. This results in an elevation of body temperature to a level that is maintained for a period of time.
- a hot flash is a transient downward adjustment of the set point, which results in the sensation of heat. At the end of a hot flash, the set point returns to normal.
- the trigger for a change in set point may be a series of nerve impulses.
- a fever, even with a rapid onset may last for hours, days or even weeks. In contrast, the duration of a hot flash is in the order of minutes.
- the present invention provides a method of alleviating discomfort experienced by a woman during a hot flash that occurs during menopause including alleviating the feeling of intense heat.
- the present invention further provides a method of alleviating symptoms of physical discomfort resulting from increased heart rate and digital blood flow associated with hot flashes.
- the method of the present invention includes the step of applying topically to the woman a cooling composition having at least one cooling agent.
- a woman experiencing a hot flash may apply the topical cooling composition to any part of her body that feels overheated, it is preferred that the cooling composition is applied topically to the head and/or neck areas. It is more preferred that the cooling composition is applied topically to the face and neck areas. It is most preferred that the cooling composition is applied topically to the temples.
- the cooling composition which is considered a topical composition
- the topical cooling composition may be any form that may be quickly and easily applied to the head and neck areas.
- the topical composition must have at least one cooling agent.
- the cooling agent must be suitable for topical application.
- U.S. Patent No. 5,730,957 to Rizk discloses a cooling mixture of water and dimethyl ether.
- the cooling agents of the present invention are not a mixture of dimethyl ether and water.
- the cooling mixture of the Rizk patent must be delivered at a temperature less than ambient temperature and higher than the freezing point of water.
- the cooling agents suitable and contemplated for use in the present invention do not have any such temperature requirements.
- the cooling mixtures of the Rizk patent achieve their cooling effect through the latent heat of transformation, or evaporation, of both the dimethyl ether and the water components.
- the cooling agents of the present invention in contrast, stimulate the cold receptors of the nervous system, and, thus, achieve a cooling effect that is not dependent upon the temperature of the cooling agent relative to ambient temperature.
- Cooling agents that may be used in the present invention include menthol, and the alkyl-substituted methanols disclosed in U.S. Patent No. 4,069,345 to Gascoyne et al.
- the cooling agent may also be acyclic sulphones or acyclic sulphoxides, phoshine oxides, alkyl-substituted alicyclic carboxylic acids, esters and amides, cyclohexan-amides, cyclic and acyclic amides, substituted ureas and sulphonamides. Examples of the foregoing are disclosed in U.S. Patent Nos. 4,318,900; 4,296,093;
- the cooling agent may also be N-hetero substituted-p-menthane-3-carboxamides as disclosed in U.S. Patent No. 4,190,643 to Watson et al.
- the cooling agent may be monomenthyl succinates, alkali metal salts of monomenthyl succinate, alkaline earth metal salts of monomenthyl succinate, and mixtures thereof. Examples of the foregoing are disclosed in U.S. Patent Nos. 5,725,865 and 5,843,466 to Mane et al.
- the cooling agent can be an asymmetric carbonate, thiocarbonate or urethate as disclosed in U.S. Patent No. 5,703,123 to Pelzer et al.
- the cooling agent can also be a 2-(2-alkoxy-1-methylethyl)-5-methyl cyclohexanol derivative as disclosed in U.S. Patent No. 5,756,857 to Kuribayashi et al.
- Each patent cited in this paragraph is incorporated herein by reference.
- the cooling agent is a ketal, such as menthone glycerin acetal and the ketals disclosed in U.S. Patent No. 5,266,692 to Grub et al., which is incorporated herein by reference, the onset and duration of the effect of the cooling agent may be affected by manipulating the substituents on the ketal.
- the topical cooling composition preferably comprises an alkali metal carbonate and/or bicarbonate and/or alkaline earth metal carbonate as set forth in U.S. Patent No. 5,783,725 to Kuhn et al., which is also incorporated herein by reference, to improve stability of the topical cooling composition.
- cooling composition comprises two or more of the cooling agents, the cooling effect achieved by the cooling composition is enhanced.
- U.S. Patent No. 5,451 ,404 to Furman discloses cooling compositions that are suitable for use in practicing the present invention.
- One example of a topical cooling composition of the Furman '404 patent comprises an effective amount of a first cooling component that is a ketal of the formula
- R 1 represents a C 2 -C 6 -alkylene radical having at least 1 , but not more than 3, hydroxyl group(s) and either R 2 and R 3 independently of one another represent C ⁇ -C ⁇ 0 -alkyl which is optionally substituted by 1 to 3 radicals selected from the group comprising hydroxyl, amino and halogen, or Cs-Cy-cycloalkyl, or C 6 -C ⁇ 2 -aryl, with the proviso that the total of the C atoms of R 2 and R 3 is not less than 3, or R 2 and R 3 together represent an alkylene radical which, together with the carbon atom which carries the radicals R 2 and R 3 , forms a 5-7-membered ring, and a second coolant component selected from the group consisting of menthol, carboxamides and mixtures thereof.
- the preferred cooling agents for the present invention include menthol, menthone glycerin acetal (a non-limiting example of the foregoing is available from Haarmann & Reimer GmbH under the trademark FRESCOLAT ® MGA), menthyl lactate (a non-limiting example of the foregoing is available from Haarmann & Reimer GmbH under the trademark FRESCOLAT ® ML), menthyl pyrrolidane carboxylic acid (PCA) (a non-limiting example of the foregoing is available from Quest International under the tradename QUESTICE L), N-2,3,-Trimethyl-2- isopropyl butanamide (a non-limiting example of the foregoing is available from ChiRex, Inc.
- menthol menthone glycerin acetal
- menthyl lactate a non-limiting example of the foregoing is available from Haarmann & Reimer GmbH under the trademark FRESCOLAT ® ML
- PCA menthyl pyrrolidane carboxylic
- the cooling composition of the present invention comprises from about 0.01 wt% to about 10 wt% of the cooling agent, preferably from about 0.01 wt% to about 5 wt%, more preferably from about 0.1 wt% to about 2 wt%, even more preferably from about 0.1 wt% to about 1 wt%, and most preferably from about 0.2 wt% to about 0.8 wt%.
- the cooling composition is preferably a stick, spray or towelette. It is preferred that the cooling composition is a water-based system. In addition, it is preferred that the when the cooling composition is a water-based composition, the cooling composition further comprises an alcohol, such as ethanol, isopropyl alcohol and propanol. Alcohols act as a solvent and also exert a cooling effect that enhances the benefits of the present invention. When the cooling composition is a water-based system, it is preferred that the cooling composition comprises from about 5 wt% to about 15 wt% of an alcohol. The remainder of the cooling composition may be water. When a water-based system is used, it is preferred that the cooling composition comprises from about 0.01 wt% to about 5 wt% of the cooling agent.
- the cooling composition may also be an anhydrous system.
- an anhydrous system comprising alcohol, such as ethanol, isopropyl alcohol or propanol
- the alcohol comprises the majority of the cooling composition other than the cooling agent.
- an anhydrous, alcohol-free system such as a cosmetic stick
- the composition is comprised of esters, waxes and/or oils in place of the water and alcohol.
- the cooling composition may comprise up to 10 wt% of the cooling agent. It is more preferred that the cooling composition comprises from about 0.1 wt% to about 1 wt% of the cooling agent.
- the cooling composition may further include ingredients such as sunscreens, odor masking agents, natural/botanical extracts, alpha-hydoxy acids, polyhydroxy alpha-hydroxy acids, alpha-keto acids, vitamins, anti- mycobacterial agents, analgesics, lipidic compounds, moisturizers or lubricants.
- ingredients such as sunscreens, odor masking agents, natural/botanical extracts, alpha-hydoxy acids, polyhydroxy alpha-hydroxy acids, alpha-keto acids, vitamins, anti- mycobacterial agents, analgesics, lipidic compounds, moisturizers or lubricants.
- the natural/botanical extract comprises a soy extract, a black cohosh extract, or a ginseng extract, or mixtures thereof. More preferably, the natural/botanical extract will be a mixture of all three of the foregoing extracts.
- the cooling composition comprises a fragrant component, which is preferably a natural extract
- the alleviation of the discomfort associated with hot flashes is augmented.
- the aromatherapeutic benefits of the fragrant component will provide a calming effect, and thus synergistically enhance the cooling composition's effect on relieving the discomfort, both emotional as well as physiological, associated with hot flashes.
- the cooling composition may also include emulsifiers, thickeners and preservatives.
- Emulsifiers (solubilizers) that can be used in the cooling compositions of the present invention can be cationic, anionic, non-ionic, amphoteric, zwitterionic, or combinations thereof.
- the emulsifier is a polysorbate emulsifier.
- polysorbate emulsifiers are Polysorbate 20 and Polysorbate 80.
- thickeners that can be used are, xanthan gum, magnesium aluminum silicate (a non-limiting example of the foregoing is available under the tradename Veegum), cellulosic thickeners, and polymeric thickeners, such as CARBOPOL, PEMULENTM copolymers and acrylate copolymers.
- a non-limiting example of an acrylate copolymer that may be used in the present invention is an acrylate/Cio to C30 alkyl acrylate copolymer.
- the cooling composition also includes a neutralizer to adjust pH.
- the preferred neutralizer is sodium hydroxide.
- the pH of the cooling composition should be adjusted according to the cooling agent used. For example, it is preferred that when the cooling agent comprises menthone glycerin acetal that the pH of the cooling composition is greater than 7. In contrast, when the cooling agent comprises menthyl lactate, it is preferred that the pH of the cooling composition is less than 7.
- the cooling composition of the present invention has a preservative.
- Suitable preservatives include disodium EDTA, methyl paraben and benzyl alcohol.
- Other suitable preservatives include EDTA salts, EDTA fatty acid conjugates, alkanols, especially ethanol, isopropyl alcohol, benzyl alcohol, parabens, sorbates, phenoxyethanol, urea derivatives and isothiazolinone.
- the cooling composition of the present invention described above is used to alleviate the physical symptoms experienced by a woman during a hot flash. It is contemplated that when the cooling composition may be applied immediately when the woman either senses a hot flash about to occur or after a hot flash begins. Although a woman may apply the cooling composition to any surface area of her body that requires relief, it is contemplated that the most useful areas for application will be the chest, face and neck areas, particularly the areas around the temple and at the base of the neck adjacent the spine. In addition, it is also believed that topically applying the cooling composition to the wrist and arm areas will be particularly useful in alleviating discomfort associated with a hot flash.
- the method of the present invention will be used most often to alleviate the discomfort of a hot flash on an as needed basis, it is believed that the method of the present invention may be extended to prophylaxis.
- many women have their slumber disturbed by "night time" hot flashes.
- the onset and duration of action of the cooling agent may be manipulated via changes in chemical structure. Accordingly, women who frequently experience such night time hot flashes may apply, just prior to sleep, topical cooling compositions having cooling agents with either delayed onset or prolonged effect.
- cooling spray When the topical cooling composition is a spray (hereinafter "cooling spray"), it is believed that the optimum benefits of the present invention are achieved in the following manner.
- the user will spray the cooling spray onto the palm(s) of the hand(s) or onto the fingertips.
- the user will then transfer the cooling spray onto the skin.
- the cooling composition should never be directly sprayed onto or near the face area.
- non-spray cooling composition(s) When the topical cooling composition is a stick, towelette, lotion, cream or gel, (hereinafter collectively referred to as "non-spray cooling composition(s)"), the consumer may also manually apply the non-spray cooling composition to the area of skin that feels uncomfortably warm or hot due to the hot flash. It is preferred that the non-spray cooling composition is spread over the surface of the skin, but not rubbed deeply into the skin. Extensive rubbing of the skin may intensify the feeling of heat experienced by the consumer, and is preferably to be avoided.
- Sample A comprised 0.65 wt% menthone glycerin acetal in a compatible vehicle made according to Example 1 above.
- the participants applied Sample A to various parts of their body when experiencing a hot flash.
- Those parts of the body to which the participants applied Sample A included the face, chest, neck/throat, shoulders, back, stomach, legs, arms, wrists and hands.
Abstract
The present invention relates to a method of alleviating the discomfort, such as the feeling of intense heat, experienced by a woman during a hot flash. The present invention also relates to compositions that may be used to practice the foregoing method. More particularly, the present invention relates to the topical application of compositions having cooling compounds as a method of alleviating discomfort experienced by a woman during a hot flash.
Description
METHODS FOR ALLEVIATING DISCOMFORT OF A HOT FLASH AND COMPOSITIONS THEREFOR
BACKGROUND OF THE INVENTION The present invention relates to a method of alleviating discomfort experienced by a woman during a hot flash. The present invention also relates to the method of use of topical compositions that may be used to alleviate such discomfort. More particularly, the present invention relates to a method of alleviating discomfort, especially the feeling of intense heat, experienced by a woman during a hot flash and the topical application of a composition having cooling ingredients in order to alleviate such discomfort.
1. Field of the Invention It is believed that a vast majority, perhaps as much as 80 percent, of women experience the discomfort of the "hot flash/flush" associated with menopause. A hot flash is believed to be the result of the hormonal changes, particularly the decline in estrogen levels, that occur during menopause. (Although some sources differentiate between a "hot flash" and "hot flush," both conditions will be referred to herein collectively as "hot flash" or "hot flashes.")
A hot flash is marked by an increase in body temperature accompanied by an intense feeling of unbearable heat, particularly internally radiating body heat. A hot flash may also be accompanied by an increase in heart rate, dizziness, anxiety, faintness, a sense of unease, tingling sensations, pressure in the head, nausea, perspiration, and feelings of breathlessness. The feeling of heat is often concentrated in the area of the face and neck, and sometimes spreads to the area of the upper chest. Although a hot flash may last for as short as a minute, a hot flash usually lasts as long as two to three minutes, and may last as long as an hour. Regardless of the duration of the hot flash, the discomfort due to the
intense feeling of heat is extremely uncomfortable and disconcerting to a woman experiencing the hot flash.
2. Description of the Related Art Perhaps the most common treatment of a hot flash is Hormone
Replacement Therapy (HRT), more specifically Estrogen Replacement Therapy (ERT). Some sources recommend vitamin supplements, such as vitamin E and bioflavonoids, to treat a hot flash. These treatments are systemic methods of treatment that require foresight. In addition in the case of HRT/ERT, one needs a prescription from a medical professional.
U.S. Patent No. 5,730,957 to Rizk describes the use of a cooling composition having dimethyl ether and water to alleviate the discomfort associated with heat. This cooling composition utilizes the latent heat of vaporization to provide its cooling action and also requires that the cooling composition be at a temperature below ambient temperature and higher than the freezing point of water. This patent also provides a method of maintaining the cooling composition at such a temperature that requires a pressurized dispensing container. In addition, the sole embodiment described in the Rizk patent is a water-dimethyl ether composition contained within an aerosol dispenser (col. 3, line 51 et seq.). In addition to the fact that maintaining the composition at a cold temperature is an inconvenient and impractical requirement, the use of dimethyl ether has known safety issues.
Some prior art provides for topical cooling of the skin. For example, U.S. Patent No. 5,703,123 to Pelzer et al. describes the use of compositions having asymmetric carbonates, thiocarbonates and/or carbonates to create a physiologic cooling effect on the skin and on mucosae in compositions such as food stuffs (e.g. beverages, jams,), cosmetic agents (e.g. shaving products, skin care products, etc.), household products (e.g. fabric softeners) and pharmaceutical preparations
(e.g. antiseptic ointments, cough mixtures). U.S. Patent No. 5,266,692 to Grub et al. provides that ketals, such as 1-methone glycerol ketal or 3,3,5- trimethylcyclohexanone glycerol ketal, have a physiological cooling effect when applied to the skin or mucous membranes in preparations, such as dentifrices, mouth washes, perfumes and shaving foams. In addition, U.S. Patent No. 5,688,497 to Lozeau et al. discloses shaving aids that provide a physiological cooling effect.
U.S. Patent No. 5,451 ,404 to Furman, the disclosure of which is incorporated herein by reference, provides coolant compositions that may be administered topically. Also, U.S. Patent No. 4,661 ,476 to Lane et al. describes a method of cooling skin overheated by exposure to heat, sun or wind that is the topical application of an aqueous gel having a starch- polyacrylamide graft copolymer.
U.S. Patent No. 5,595,970 to Garfield et al. describes the use of a nitric oxide substrate and/or nitric acid donor, either alone or in combination with a progestin or estrogen to alleviate climacterium symptoms such as hot flashes. However, the compositions disclosed in Garfield et al. require systemic administration.
Until now, there has not been a method of alleviating the discomfort of hot flashes experienced by women that is non-systemic, easy to use and relatively inexpensive.
SUMMARY OF THE INVENTION
It is an object of the present invention to provide a method of alleviating the discomfort associated with a hot flash.
It is another object of the present invention to provide such a method for alleviating the feeling of intense heat associated with a hot flash.
It is a further object of the present invention to provide such a method that includes the topical application of a composition having a cooling agent.
The present invention, in brief summary, is a method of alleviating the discomfort associated with hot flashes that comprises the step of applying to the body, particularly to the chest, face and neck area and/or to the wrist and arm area, a topical cooling composition having at least one cooling agent.
DETAILED DESCRIPTION OF THE INVENTION
Hot flashes are most commonly associated with the discomforting symptom of an intense feeling of heat that begins in the face, neck, or chest regions and then radiates to other parts of the body. However, prior to the intense feeling of heat, many women experience a premonition of an impending hot flash that is accompanied by symptoms, such as a feeling of unease or anxiety, a feeling of pressure in the head, or tingling sensations. During this time, there is a concurrent increase in heart rate, digital blood flow, and vasodilation of blood vessels of the skin. At this point, women will experience an intense feeling of heat and which may further be accompanied by feelings of dizziness, nausea and breathlessness.
For most women who experience hot flashes, these foregoing symptoms are very unpleasant. Indeed, for some women the extent of these symptoms experienced during a hot flash can be downright unbearable.
The first detectable change is an increase in finger blood flow with a concomitant enhancement of skin conductance, as well as a change in temperature of the skin of the face and neck. The increase in skin conductance is followed rapidly by a sharp rise (1-7°C) in finger temperature. The degree to which finger temperature rises during a hot flash is inversely proportional to the base-line finger temperature before the
flash. Thus, a 0.5°C increase in finger temperature in a woman with a base-line finger temperature of 35°C may be as good a measure of the occurrence of a hot flash as a 5°C increase in finger temperature in a woman with base-line finger temperature of 29°C, because of the non- linear relationship between skin temperature and blood flow.
As vasodilation and sweating ensue, internal body temperature drops. The magnitude of decrease in core temperature ranges from 0.1 °C to 0.9°C. The onset of sweating is rapid and is particularly profuse in the face and scalp. It may occur in five minute bursts accompanying short, discrete hot flashes, or continue in waves for more than thirty minutes during prolonged hot flashes.
A hot flash is the inverse of a fever. In mammals, the control of body temperature resembles a negative feedback system in which a set point temperature serves as reference for the themoregulatory mechanism. A fever can be understood as the upward adjustment of this temperature set point. In a febrile episode, the set point is first elevated, initiating vasoconstruction, shivering and behavorial modifications, such as the addition of blankets. This results in an elevation of body temperature to a level that is maintained for a period of time. A hot flash, on the other hand, is a transient downward adjustment of the set point, which results in the sensation of heat. At the end of a hot flash, the set point returns to normal. The trigger for a change in set point may be a series of nerve impulses. A fever, even with a rapid onset, may last for hours, days or even weeks. In contrast, the duration of a hot flash is in the order of minutes.
The present invention provides a method of alleviating discomfort experienced by a woman during a hot flash that occurs during menopause including alleviating the feeling of intense heat. The present invention further provides a method of alleviating symptoms of physical discomfort resulting from increased heart rate and digital blood flow associated with
hot flashes. The method of the present invention includes the step of applying topically to the woman a cooling composition having at least one cooling agent.
Although to practice the method of the present invention, a woman experiencing a hot flash may apply the topical cooling composition to any part of her body that feels overheated, it is preferred that the cooling composition is applied topically to the head and/or neck areas. It is more preferred that the cooling composition is applied topically to the face and neck areas. It is most preferred that the cooling composition is applied topically to the temples.
To practice the present invention, the cooling composition, which is considered a topical composition, may be a solution, gel, cream, lotion, emulsion, solid stick, towelette or spray. It is preferred that the topical cooling composition is a stick, spray or a towelette. However, the topical cooling composition may be any form that may be quickly and easily applied to the head and neck areas.
To practice the present invention, the topical composition must have at least one cooling agent. The cooling agent must be suitable for topical application. As stated above, U.S. Patent No. 5,730,957 to Rizk discloses a cooling mixture of water and dimethyl ether. The cooling agents of the present invention are not a mixture of dimethyl ether and water. In addition, the cooling mixture of the Rizk patent must be delivered at a temperature less than ambient temperature and higher than the freezing point of water. The cooling agents suitable and contemplated for use in the present invention do not have any such temperature requirements. Also, the cooling mixtures of the Rizk patent achieve their cooling effect through the latent heat of transformation, or evaporation, of both the dimethyl ether and the water components. The cooling agents of the present invention, in contrast, stimulate the cold receptors of the nervous system, and, thus,
achieve a cooling effect that is not dependent upon the temperature of the cooling agent relative to ambient temperature.
Cooling agents that may be used in the present invention include menthol, and the alkyl-substituted methanols disclosed in U.S. Patent No. 4,069,345 to Gascoyne et al. The cooling agent may also be acyclic sulphones or acyclic sulphoxides, phoshine oxides, alkyl-substituted alicyclic carboxylic acids, esters and amides, cyclohexan-amides, cyclic and acyclic amides, substituted ureas and sulphonamides. Examples of the foregoing are disclosed in U.S. Patent Nos. 4,318,900; 4,296,093;
4,136,164; 4,070,496; and 4,070,449 to Rowsell et al. Further, the cooling agent may also be N-hetero substituted-p-menthane-3-carboxamides as disclosed in U.S. Patent No. 4,190,643 to Watson et al. Still further, the cooling agent may be monomenthyl succinates, alkali metal salts of monomenthyl succinate, alkaline earth metal salts of monomenthyl succinate, and mixtures thereof. Examples of the foregoing are disclosed in U.S. Patent Nos. 5,725,865 and 5,843,466 to Mane et al. Yet further, the cooling agent can be an asymmetric carbonate, thiocarbonate or urethate as disclosed in U.S. Patent No. 5,703,123 to Pelzer et al. The cooling agent can also be a 2-(2-alkoxy-1-methylethyl)-5-methyl cyclohexanol derivative as disclosed in U.S. Patent No. 5,756,857 to Kuribayashi et al. Each patent cited in this paragraph is incorporated herein by reference.
When the cooling agent is a ketal, such as menthone glycerin acetal and the ketals disclosed in U.S. Patent No. 5,266,692 to Grub et al., which is incorporated herein by reference, the onset and duration of the effect of the cooling agent may be affected by manipulating the substituents on the ketal.
When the cooling agent is menthol lactate, the topical cooling composition preferably comprises an alkali metal carbonate and/or bicarbonate and/or alkaline earth metal carbonate as set forth in U.S.
Patent No. 5,783,725 to Kuhn et al., which is also incorporated herein by reference, to improve stability of the topical cooling composition.
It is believed that when the cooling composition comprises two or more of the cooling agents, the cooling effect achieved by the cooling composition is enhanced. For example, U.S. Patent No. 5,451 ,404 to Furman discloses cooling compositions that are suitable for use in practicing the present invention. One example of a topical cooling composition of the Furman '404 patent comprises an effective amount of a first cooling component that is a ketal of the formula
in which R1 represents a C2-C6-alkylene radical having at least 1 , but not more than 3, hydroxyl group(s) and either R2 and R3 independently of one another represent Cι-Cι0-alkyl which is optionally substituted by 1 to 3 radicals selected from the group comprising hydroxyl, amino and halogen, or Cs-Cy-cycloalkyl, or C6-Cι2-aryl, with the proviso that the total of the C atoms of R2 and R3 is not less than 3, or R2 and R3 together represent an alkylene radical which, together with the carbon atom which carries the radicals R2 and R3, forms a 5-7-membered ring, and a second coolant component selected from the group consisting of menthol, carboxamides and mixtures thereof.
The preferred cooling agents for the present invention include menthol, menthone glycerin acetal (a non-limiting example of the foregoing is available from Haarmann & Reimer GmbH under the trademark FRESCOLAT® MGA), menthyl lactate (a non-limiting example of the foregoing is available from Haarmann & Reimer GmbH under the trademark FRESCOLAT® ML), menthyl pyrrolidane carboxylic acid (PCA)
(a non-limiting example of the foregoing is available from Quest International under the tradename QUESTICE L), N-2,3,-Trimethyl-2- isopropyl butanamide (a non-limiting example of the foregoing is available from ChiRex, Inc. under the tradename WS-23), N-ethyl-p-menthan-3- carboxamide (a non-limiting example is available from ChiRex, Inc. under the tradename WS-3), 3-1-methoxypropane-1 ,2-diol, (1-(2- hydroxyphenyl)4-(3-nitrophenyl)-1 ,2,3,6-tetrahydropyrimidine-2-one), Ci to C5 derivatives of 2-(2-alkoxy-1-methylethyl)-5-methyl cylcohexanols, 1- menthanyl carbonates and mixtures of the foregoing. Menthone glycerin acetal is the most preferred cooling agent. One reason why menthyl pyrrolidane carboxylic acid is a preferred cooling agent is because it exhibits moisturizing properties as well as coolant properties.
The cooling composition of the present invention comprises from about 0.01 wt% to about 10 wt% of the cooling agent, preferably from about 0.01 wt% to about 5 wt%, more preferably from about 0.1 wt% to about 2 wt%, even more preferably from about 0.1 wt% to about 1 wt%, and most preferably from about 0.2 wt% to about 0.8 wt%.
As stated above, the cooling composition is preferably a stick, spray or towelette. It is preferred that the cooling composition is a water-based system. In addition, it is preferred that the when the cooling composition is a water-based composition, the cooling composition further comprises an alcohol, such as ethanol, isopropyl alcohol and propanol. Alcohols act as a solvent and also exert a cooling effect that enhances the benefits of the present invention. When the cooling composition is a water-based system, it is preferred that the cooling composition comprises from about 5 wt% to about 15 wt% of an alcohol. The remainder of the cooling composition may be water. When a water-based system is used, it is preferred that the cooling composition comprises from about 0.01 wt% to about 5 wt% of the cooling agent.
The cooling composition may also be an anhydrous system. In an anhydrous system comprising alcohol, such as ethanol, isopropyl alcohol or propanol, it is preferred that the alcohol comprises the majority of the cooling composition other than the cooling agent. In an anhydrous, alcohol-free system, such as a cosmetic stick, the composition is comprised of esters, waxes and/or oils in place of the water and alcohol. When the cooling composition is an anhydrous system, the cooling composition may comprise up to 10 wt% of the cooling agent. It is more preferred that the cooling composition comprises from about 0.1 wt% to about 1 wt% of the cooling agent.
The cooling composition, whether a water-based system or an anhydrous system, may further include ingredients such as sunscreens, odor masking agents, natural/botanical extracts, alpha-hydoxy acids, polyhydroxy alpha-hydroxy acids, alpha-keto acids, vitamins, anti- mycobacterial agents, analgesics, lipidic compounds, moisturizers or lubricants.
When the cooling composition contains a natural/botanical extract, it is preferred that the natural/botanical extract comprises a soy extract, a black cohosh extract, or a ginseng extract, or mixtures thereof. More preferably, the natural/botanical extract will be a mixture of all three of the foregoing extracts.
Since many women experience feelings of anxiety during hot flashes, it is believed that when the cooling composition comprises a fragrant component, which is preferably a natural extract, the alleviation of the discomfort associated with hot flashes is augmented. It is believed that the aromatherapeutic benefits of the fragrant component will provide a calming effect, and thus synergistically enhance the cooling composition's effect on relieving the discomfort, both emotional as well as physiological, associated with hot flashes.
The cooling composition may also include emulsifiers, thickeners and preservatives. Emulsifiers (solubilizers) that can be used in the cooling compositions of the present invention can be cationic, anionic, non-ionic, amphoteric, zwitterionic, or combinations thereof. However, it is preferred that the emulsifier is a polysorbate emulsifier. Non-limiting examples of polysorbate emulsifiers are Polysorbate 20 and Polysorbate 80. Examples of thickeners that can be used are, xanthan gum, magnesium aluminum silicate (a non-limiting example of the foregoing is available under the tradename Veegum), cellulosic thickeners, and polymeric thickeners, such as CARBOPOL, PEMULEN™ copolymers and acrylate copolymers. A non-limiting example of an acrylate copolymer that may be used in the present invention is an acrylate/Cio to C30 alkyl acrylate copolymer.
It is preferred that the cooling composition also includes a neutralizer to adjust pH. The preferred neutralizer is sodium hydroxide. The pH of the cooling composition should be adjusted according to the cooling agent used. For example, it is preferred that when the cooling agent comprises menthone glycerin acetal that the pH of the cooling composition is greater than 7. In contrast, when the cooling agent comprises menthyl lactate, it is preferred that the pH of the cooling composition is less than 7.
It is preferred that the cooling composition of the present invention has a preservative. Suitable preservatives include disodium EDTA, methyl paraben and benzyl alcohol. Other suitable preservatives include EDTA salts, EDTA fatty acid conjugates, alkanols, especially ethanol, isopropyl alcohol, benzyl alcohol, parabens, sorbates, phenoxyethanol, urea derivatives and isothiazolinone.
An example of a contemplated composition that would be suitable for practicing the present invention is as follows:
EXAMPLE 1
INGREDIENT Wt Percent of Total Composition
Menthone glycerin acetal 0.01 to 5 Vehicle
Polysorbates 0.01 to 5
Methylparaben 0.01 to 5
Acrylates copolymer 0.01 to 4
Sodium Hydroxide 0.01 to 2 Alcohol 5 to 15
Disodium EDTA 0.01 to 0.8
Water QS
The cooling composition of the present invention described above is used to alleviate the physical symptoms experienced by a woman during a hot flash. It is contemplated that when the cooling composition may be applied immediately when the woman either senses a hot flash about to occur or after a hot flash begins. Although a woman may apply the cooling composition to any surface area of her body that requires relief, it is contemplated that the most useful areas for application will be the chest, face and neck areas, particularly the areas around the temple and at the base of the neck adjacent the spine. In addition, it is also believed that topically applying the cooling composition to the wrist and arm areas will be particularly useful in alleviating discomfort associated with a hot flash.
Although it is contemplated that the method of the present invention will be used most often to alleviate the discomfort of a hot flash on an as needed basis, it is believed that the method of the present invention may be extended to prophylaxis. For example, many women have their slumber disturbed by "night time" hot flashes. As stated above, the onset and duration of action of the cooling agent may be manipulated via changes in chemical structure. Accordingly, women who frequently experience such
night time hot flashes may apply, just prior to sleep, topical cooling compositions having cooling agents with either delayed onset or prolonged effect.
When the topical cooling composition is a spray (hereinafter "cooling spray"), it is believed that the optimum benefits of the present invention are achieved in the following manner. The user will spray the cooling spray onto the palm(s) of the hand(s) or onto the fingertips. The user will then transfer the cooling spray onto the skin. In order to avoid inhalation of the cooling composition and to avoid contact of the cooling composition with the eyes, it is recommended that the cooling composition should never be directly sprayed onto or near the face area. When the topical cooling composition is a stick, towelette, lotion, cream or gel, (hereinafter collectively referred to as "non-spray cooling composition(s)"), the consumer may also manually apply the non-spray cooling composition to the area of skin that feels uncomfortably warm or hot due to the hot flash. It is preferred that the non-spray cooling composition is spread over the surface of the skin, but not rubbed deeply into the skin. Extensive rubbing of the skin may intensify the feeling of heat experienced by the consumer, and is preferably to be avoided.
EXAMPLE 2
A study was conducted to test the effectiveness of the present invention in alleviating discomfort and symptoms experienced by women during a hot flash.
Forty-five women between 40 and 60 years of age participated in the study. The participants experienced at least three to four hot flashes per day. Some participants experienced as many as ten hot flashes per day. In addition to hot flashes, the participants also reported experiencing
headaches, sleeplessness, mood changes, night sweats and/or erratic or stopped menstrual periods.
The participants were given spray bottles containing Sample A. Sample A comprised 0.65 wt% menthone glycerin acetal in a compatible vehicle made according to Example 1 above. During a two-week period, the participants applied Sample A to various parts of their body when experiencing a hot flash. Those parts of the body to which the participants applied Sample A included the face, chest, neck/throat, shoulders, back, stomach, legs, arms, wrists and hands.
Over sixty percent of the participants expressed that Sample A was effective in alleviating discomfort experienced during hot flash episodes. In addition, over sixty percent of the participants expressed that Sample A either met or exceeded their expectations of performance.
Various modifications and alterations to the present invention may be appreciated based on a review of this disclosure. These changes and additions are intended to be within the scope and spirit of the present invention as defined by the following claims.
Claims
1. A method of treating a hot flash, the method comprising the step of: applying topically a cooling composition having an effective amount of a cooling agent, wherein the cooling agent is substantially at ambient temperature when applied.
2. The method of claim 1 , wherein the cooling agent is selected from the group consisting of menthol, menthyl lactate, menthyl pyrrolidane carboxylic acid, N,2,3-trimethyl-2-isopropyl butanamide, N-ethyl-p- menthan-3-carboxamide, 3-1-menthoxy propane-1 ,2-diol, 1-(2- hydroxyphenyl)-4-(3-nitrophenyl)-1 ,2,3,6-tetrahydropyriidine-2-one, 2-(2- alkoxy-1-methylethyl)-5-methyl cyclohexanols, 1-menthanyl carbonates, a formula (I) ketal, and mixtures thereof, wherein the formula (I) ketal is as follows:
in which R1 represents a C2-C6-alkyiene radical having at least 1 , but not more than 3, hydroxyl group(s) and either R2 and R3 independently of one another represent Cι-Cι0-alkyl which is optionally substituted by 1 to 3 radicals selected from the group comprising hydroxyl, amino and halogen, or C5-C7-cycloalkyl, or C6-C12-aryl, with the proviso that the total of the C atoms of R2 and R3 is not less than 3, or R2 and R3 together represent an alkylene radical which, together with the carbon atom which carries the radicals R2 and R3, forms a 5-7-membered ring.
3. The method of claim 1 , wherein the cooling agent is selected from the group consisting of menthyl pyrrolidane carboxylic acid, menthone glycerin acetal, menthyl lactate, and mixtures thereof.
4. The method of claim 1 , wherein the cooling agent comprises menthone glycerin acetal.
5. The method of claim 1 , wherein the cooling agent comprises menthyl pyrrolidane carboxylic acid.
6. The method of claim 1 , wherein the cooling agent comprises from about 0.01 wt% to about 5 wt% of menthone glycerin acetal.
7. The method of claim 3, wherein the cooling agent comprises menthyl pyrrolidane carboxylic acid and menthone glycerin acetal.
8. The method of claim 1 , wherein the cooling agent comprises: an effective amount of a first cooling component that is a ketal of the formula
in which R1 represents a C2-C6-alkylene radical having at least 1, but not more than 3, hydroxyl group(s) and either R2 and R3 independently of one another represent Cι-Cιo-alkyl which is optionally substituted by 1 to 3 radicals selected from the group comprising hydroxyl, amino and halogen, or C5-C7-cycloalkyl, or C6-Cι2-aryl, with the proviso that the total of the C atoms of R2 and R3 is not less than 3, or R2 and R3 together represent an alkylene radical which, together with the carbon atom which carries the radicals R2 and R3, forms a 5-7-membered ring, and
a second cooling component selected from the group consisting of menthol, carboxamides, and mixtures thereof.
9. The method of claim 8, wherein the first cooling component is menthone glycerin acetal, and wherein said carboxamides is selected from the group consisting of N,2,3-trimethyl-2-isopropyl butanamide, N-ethyl-p- menthan-3-carboxamide, and a mixture thereof.
10. The method of claim 1 , wherein the cooling composition is applied to a part of the body selected from the group consisting of the face, neck, chest, wrist, arm, and combinations thereof.
11. The method of claim 10, wherein the cooling composition is applied to a temple area of the face.
12. The method of claim 5, further comprising moisturizing skin.
13. A method of providing prolonged cooling relief from the feeling of heat associated with a hot flash, comprising applying topically a cooling composition having an effective amount of a cooling agent selected from the group consisting of menthol, menthyl lactate, menthyl pyrrolidane carboxylic acid, N,2,3-trimethyl-2-isopropyl butanamide, N-ethyl-p- menthan-3-carboxamide, 3-1-menthoxy propane-1 ,2-diol, 1-(2- hydroxyphenyl)-4-(3-nitrophenyl)-1 ,2,3,6-tetrahydropyriidine-2-one, 2-(2- alkoxy-1-methylethyl)-5-methyl cyclohexanols, 1-menthanyl carbonates, a formula (I) ketal, and mixtures thereof, wherein the formula (I) ketal is as follows:
in which R1 represents a C2-C6-alkylene radical having at least 1 , but not more than 3, hydroxyl group(s) and either R2 and R3 independently of one another represent Ci-Cio-alkyl which is optionally substituted by 1 to 3 radicals selected from the group comprising hydroxyl, amino and halogen, or C5-C7-cycloalkyl, or C6-Cι2-aryl, with the proviso that the total of the C atoms of R2 and R3 is not less than 3, or R2 and R3 together represent an alkylene radical which, together with the carbon atom which carries the radicals R2 and R3, forms a 5-7-membered ring.
14. A method of alleviating one or more physical symptoms experienced in connection with a hot flash, comprising applying topically a composition having an effective amount of a cooling agent, wherein the cooling agent is substantially at ambient temperature when applied.
15. The method of claim 14, wherein said cooling agent is selected from the group consisting of menthol, menthyl lactate, menthyl pyrrolidane carboxylic acid, N,2,3-trimethyl-2-isopropyl butanamide, N- ethyl-p-menthan-3-carboxamide, 3-1-menthoxy propane-1 ,2-diol, 1-(2- hydroxyphenyl)-4-(3-nitrophenyl)-1 ,2,3,6-tetrahydropyriidine-2-one, 2-(2- alkoxy-1-methylethyl)-5-methyl cyclohexanols, 1-menthanyl carbonates, a formula (I) ketal, and mixtures thereof, wherein the formula (I) ketal is as follows:
in which R1 represents a C2-C6-alkylene radical having at least 1 , but not more than 3, hydroxyl group(s) and either R2 and R3 independently of one another represent CrCio-alkyl which is optionally substituted by 1 to 3 radicals selected from the group comprising hydroxyl, amino and halogen, or C5-C -cycloalkyl, or C6-Cι2-aryl, with the proviso that the total of the C atoms of R2 and R3 is not less than 3, or R2 and R3 together represent an alkylene radical which, together with the carbon atom which carries the radicals R2 and R3, forms a 5-7-membered ring.
16. The method of claim 14, wherein said physical symptom is selected from the group consisting of anxiety, a sense of unease, pressure in the hand, tingling sensations, sweating, faintness, dizziness, nausea, breathlessness, sensations of body heat, and combinations thereof.
17. The method of claim 15, wherein said physical symptom is selected from the group consisting of sweating, anxiety, a sense of unease, sensations of internal body heat, dizziness and combination thereof.
18. The method of claim 14, wherein said cooling agent is selected from the group consisting of menthyl pyrrolidane carboxylic acid, menthone glycerin acetal, menthyl lactate, and mixtures thereof.
19. The method of claim 14, wherein the cooling composition is applied to a part of the body selected from the group consisting of the face, neck, chest, wrist, arm, and combinations thereof.
20. The method of claim 14, wherein the cooling composition is applied to a temple area of the face.
21. A method of providing relief from internal body heat associated with a hot flash, the method comprising applying topically a cooling composition having an effective amount of a cooling agent, wherein the cooling agent is substantially at ambient temperature when applied.
22. The method of claim 21 , wherein perspiration accompanies the internal body heat.
23. The method of claim 21 , wherein said cooling agent is selected from the group consisting of menthol, menthyl lactate, menthyl pyrrolidane carboxylic acid, N,2,3-trimethyl-2-isopropyl butanamide, N- ethyl-p-menthan-3-carboxamide, 3-1-menthoxy propane-1 ,2-diol, 1-(2- hydroxyphenyl)-4-(3-nitrophenyl)-1 ,2,3,6-tetrahydropyriidine-2-one, 2-(2- alkoxy-1-methylethyl)-5-methyl cyclohexanols, 1-menthanyl carbonates, a formula (I) ketal, and mixtures thereof, wherein the formula (I) ketal is as follows:
in which R1 represents a C2-C6-alkylene radical having at least 1 , but not more than 3, hydroxyl group(s) and either R2 and R3 independently of one another represent Cι-Cι0-alkyl which is optionally substituted by 1 to 3 radicals selected from the group comprising hydroxyl, amino and halogen, or C5-C -cycloalkyl, or C6-C12-aryl, with the proviso that the total of the C atoms of R2 and R3 is not less than 3, or R2 and R3 together represent an alkylene radical which, together with the carbon atom which carries the radicals R2 and R3, forms a 5-7-membered ring.
24. The method of claim 23, wherein said cooling agent is selected from the group consisting of menthyl pyrrolidane carboxylic acid, menthone glycerin acetal, menthyl lactate, and mixtures thereof.
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PCT/US2000/002638 WO2000045815A1 (en) | 1999-02-02 | 2000-02-02 | Methods for alleviating discomfort of a hot flash and compositions therefor |
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JP4018032B2 (en) * | 2003-06-17 | 2007-12-05 | 高砂香料工業株式会社 | Hair and body cleaning composition |
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US7141686B2 (en) | 2003-07-10 | 2006-11-28 | International Flavors & Fragrances Inc. | E2, E4, Z8-undecatrienoic acid and ester and carboxamide derivatives thereof, organoleptic uses thereof and processes for preparing same |
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US7541055B2 (en) | 2004-09-10 | 2009-06-02 | International Flavors & Fragrances Inc. | Saturated and unsaturated N-alkamides exhibiting taste and flavor enhancement effect in flavor compositions |
US7427421B2 (en) | 2004-09-10 | 2008-09-23 | International Flavors & Fragrances Inc. | Saturated and unsaturated N-alkamides exhibiting taste and flavor enhancement effect in flavor compositions |
DE102004048987B3 (en) * | 2004-10-04 | 2005-12-15 | Coty Deutschland Gmbh | Cooling cosmetic composition and its use |
MX2007008154A (en) * | 2005-01-04 | 2007-07-24 | Teikoku Pharma Usa Inc | Cooling topical patch preparation. |
US8425583B2 (en) | 2006-04-20 | 2013-04-23 | University of Pittsburgh—of the Commonwealth System of Higher Education | Methods, devices and systems for treating insomnia by inducing frontal cerebral hypothermia |
US11684510B2 (en) | 2006-04-20 | 2023-06-27 | University of Pittsburgh—of the Commonwealth System of Higher Education | Noninvasive, regional brain thermal stimuli for the treatment of neurological disorders |
US9480633B2 (en) * | 2011-04-28 | 2016-11-01 | Kimberly-Clark Worldwide, Inc. | Temperature management composition |
EP2858639B1 (en) | 2012-06-08 | 2018-09-12 | The Ohio State University | Treating scar injury using tocotrienol |
EP2941292B1 (en) | 2013-01-02 | 2021-02-24 | EBB Therapeutics, Inc. | Systems for enhancing sleep |
AU2016211528A1 (en) * | 2015-01-27 | 2017-05-18 | Ebb Therapeutics, Inc. | Method and apparatuses for modulating sleep by chemical activation of temperature receptors |
WO2021207478A1 (en) * | 2020-04-10 | 2021-10-14 | The Procter & Gamble Company | Compositions and methods for treating hot flashes |
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US4193936A (en) * | 1971-02-04 | 1980-03-18 | Wilkinson Sword Limited | N-substituted paramenthane carboxamides |
US5266592A (en) * | 1991-04-05 | 1993-11-30 | Haarmann & Reimer Gmbh | Compositions which have a physiological cooling effect, and active compounds suitable for these compositions |
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GB1421743A (en) * | 1972-04-18 | 1976-01-21 | Wilkinson Sword Ltd | Ingestible topical and other compositions |
GB1436329A (en) * | 1972-08-07 | 1976-05-19 | Unilever Ltd | Esters of menthol and a heterocyclic carboxylic acid and their use in cosmetic preparations |
WO1993023005A1 (en) * | 1992-05-18 | 1993-11-25 | The Procter & Gamble Company | Coolant compositions |
GB2273299A (en) * | 1992-12-08 | 1994-06-15 | Nelly Kamel Rizk | Mixture that produces cooling |
-
2000
- 2000-02-02 WO PCT/US2000/002638 patent/WO2000045815A1/en not_active Application Discontinuation
- 2000-02-02 AU AU27510/00A patent/AU2751000A/en not_active Abandoned
- 2000-02-02 CA CA002361046A patent/CA2361046A1/en not_active Abandoned
- 2000-02-02 EP EP00905910A patent/EP1171120A4/en not_active Withdrawn
- 2000-02-02 JP JP2000596935A patent/JP2002536069A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4193936A (en) * | 1971-02-04 | 1980-03-18 | Wilkinson Sword Limited | N-substituted paramenthane carboxamides |
US5266592A (en) * | 1991-04-05 | 1993-11-30 | Haarmann & Reimer Gmbh | Compositions which have a physiological cooling effect, and active compounds suitable for these compositions |
Non-Patent Citations (1)
Title |
---|
See also references of WO0045815A1 * |
Also Published As
Publication number | Publication date |
---|---|
JP2002536069A (en) | 2002-10-29 |
CA2361046A1 (en) | 2000-08-10 |
WO2000045815A1 (en) | 2000-08-10 |
AU2751000A (en) | 2000-08-25 |
EP1171120A4 (en) | 2004-11-17 |
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