KR102027176B1 - [((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanecarbonyl)-amino]-acetic acid isopropyl ester and related compounds and their use in therapy - Google Patents

Abstract

The present invention relates generally to coolants and medical therapies. More specifically, the present invention relates to certain analgesics, such as [((1R, 2S, 5R) -2-isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester, which is potent and prolonged Acting and having selective cooling properties for non-keratinized epithelial tissues as compared to keratinized epithelial tissues, e.g. for the treatment of uncomfortable feeling of non-keratinized stratified epithelial (NKSE) tissue (e.g., relief of symptoms; amelioration) Useful for; Thus uncomfortable feeling of the inner surface of the eye surface, the eyelids, the periphery of the eyelid, the front part of the eye, the conjunctiva, the tear system, the tear film, or the cornea, the lining of the oral cavity, the inside of the lips, the pharyngeal surface, the esophagus surface, or the anal genital surface; Ocular discomfort caused by examples of extended wearing of contact lenses, eye deformation and / or fatigue, air contaminants, overexposure to sunlight, conjunctivitis, dry eye, and the like; Uncomfortable feeling associated with oral mucositis; Discomfort in the airways (eg larynx, trachea, and / or bronchus) compression, airways (eg larynx, trachea, and / or bronchus), for example, associated with asthma and / or chronic obstructive pulmonary disease (COPD) , Choking, coughing, and / or difficulty breathing.

Description

[((1R, 2S, 5R) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) amino] -acetic acid isopropyl ester and its related compounds and uses in therapies {[((1R, 2S, 5R) -2-isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester and related compounds and their use in therapy}

Related Applications

The present invention relates to US patent application Ser. No. 12 / 928,184 filed December 6, 2010, the contents of which are incorporated herein by reference in their entirety.

Technical field

The present invention generally relates to the field of coolants and medical therapies. More specifically, the present invention relates to certain analgesics, such as [(( 1R , 2S , 5R ) -2-isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester, Strong, long-acting, selective cooling properties for non-keratinized epithelial tissues as compared to keratinized epithelial tissues, e.g. treatment of uncomfortable feeling of, for example, relief of symptoms Useful for improving; Thus uncomfortable sensations of the eye surface, eyelids, periphery of the eye, the front part of the eye, conjunctiva, tear system, tear film, or cornea, lining of the oral cavity, inside the lips, pharyngeal surface, esophagus surface, or anal genital surface; Eye discomfort caused by examples of extended wearing of contact lenses, eye strain and / or fatigue, air contaminants, overexposure to sunlight, conjunctivitis, dry eye, etc .; Uncomfortable sensations associated with oral mucositis; Airway (eg larynx, trachea, and / or bronchus) tightness, discomfort in the airways (eg larynx, trachea, and / or bronchus), for example, associated with asthma and / or chronic obstructive pulmonary disease (COPD) , Choking, coughing, and / or difficulty breathing.

Many publications are cited in the present invention in order to more fully describe and disclose the present invention and the prior art to which the present invention pertains. Each of these references is herein incorporated by reference in its entirety, in the manner in which each individual reference is specifically and individually named and incorporated by reference.

Throughout this specification and the accompanying claims, unless otherwise stated, the words 'comprises' and variations, such as 'comprises' and 'comprising', refer to the integers or steps mentioned, or to integers or steps A group is understood to be inclusive, without excluding any other integer or step, or group of integers or steps.

As used in the specification and the appended claims, it should be noted that the singular forms “a,” “an” and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, the term 'pharmaceutical carrier' includes a mixture of two or more such carriers, and the like.

Ranges in the present invention are frequently expressed as from 'about' one particular value and / or to 'about' another particular value. When such a range is expressed, another embodiment includes values from one particular value, and / or to another particular value. Similarly, when a value is expressed roughly, it is understood that the specific value represents another embodiment using 'about'.

This document contains information that may be useful in understanding the present invention. It is not admitted that any publication provided herein is related to the prior art, related to the present invention, or that any publication referred to specifically or implicitly is prior art.

Nociception

Invasion acceptance can be defined as neural processes that encode and process harmful stimuli. Of particular interest are peripherally acting antiinvasive (antinociceptive) drugs. "Antineociceptive" means that the psychological and physiological recognition of harmful stimuli is inhibited by the drug. By "peripherally" it is meant that the basic site of action of the drug is located outside of the central nervous system, ie outside of the brain and spinal cord.

Anti-invasive drugs that act peripherally and attenuate the transmission of invasive (harmful) signals to the central nervous system can now be broadly divided into two classes. One class is local anesthetics such as procaine and lidocaine, which act on peripheral nerve fibers to inhibit nerve conduction of nociceptive signals directed to the central nervous system. Another class is agents such as aspirin and ibuprofen that inhibit the synthesis of certain prostaglandins. Or these prostaglandins released by tissues during the inflammatory period lower the threshold for firing sensory nerve fibers in response to noxious stimuli. Another class of antiinvasive drugs is narcotic analgesics, which do not inhibit pain through peripheral action, but instead directly act on neuronal components in the brain and spinal cord.

Pain is defined by Charles Serrington as "the mental burden of compulsory protective reflexes" and is activated by increasing the secretion of small diameter anhydrous nerve fibers called polymorphic C fibers. Pain is classified as invasive or neuropathic. Invasive pain is caused by cell damage, and neuropathic pain is caused by damage to nerve fibers that carry pain signals. There are many conditions that produce pain; The most common are, for example, trauma, inflammation, and autoimmune diseases. Feelings that may accompany pain are irritation, pruritus (itch), and feelings of physical distress and dissatisfaction. As used herein, the mental burden of accepting infringement is grouped together as "sensory discomfort."

There are basically four kinds of animal tissue: connective tissue, muscle tissue, neural tissue and epithelial tissue. Epithelial cells cover the cavity and surface of organs inside the body. When the layer is single cell thick, it is called monolayer epithelium. If more than one layer of cells is present, it is called stratified epithelium. Stratified epithelium mostly contains scaly (flat) cells and small amounts of cuboidal cells. In the skin, outer lip, and tongue, the death of the outer layer cells of the stratified epithelium results in a rough, water-impermeable protein called keratin. The stratified squamous epithelium without keratin comprises the eye surface including the periphery of the eyelid, the anterior part of the eye, the conjunctiva, the tear system, the tear film, and the cornea; Oral lining including the inside of the lips; Pharyngeal surface; Esophagus surface; And on the genital surface. Keratinized tissue is more resistant to damage than non-keratinized tissue. The non-keratinized epithelial surface must be moistened by glandular (serum and mucus) secretions to prevent it from drying out.

Currently topical antiinvasive (pain-inhibitor) compounds have limited the efficacy on pain arising from non-keratinized stratified epithelium (NKSE). This applies in particular for discomfort from the eye surface.

Local anesthetic compounds, such as lidocaine, are used for pain and discomfort on the surface of the genitals (for example, vulvar pain) and for pain and discomfort (for example, cough and pharyngitis) on the pharynx. It can cause hypersensitivity and have side effects that paralyze the senses of tissues against contact and compression. Although local anesthetics may be used in emergencies for pain occurring at the eye surface, such as corneal pain, this class of drugs inhibits epithelial cell growth and therefore prolonged use is dangerous.

Nonsteroidal anti-inflammatory compounds (NSAIDs) such as, for example, ketorolac can be used for a short time on the eye surface, for example to relieve acute pain in cataract surgery, but cannot be used on the eye for a long time. Topical NSADIs do not work against pain occurring in the anal genital or oral NKSE.

Menthol has limited some anesthesia in ointments for hemorrhoid discomfort. In lozenges and sweets, menthol is somewhat effective against sore or tingling throats and coughs. Menthol is quite irritating to the eyes but is used in some eye drops in Japan. For keratinized skin, high concentrations of menthol (eg 2% by weight or more) can be applied without direct irritation to the skin. For example, a topical patch comprising 5% menthol (eg, IcyHot Medicated Patch; Chattem, Inc.) may be applied to the torso skin to relieve myalgia. However, for non-keratinized epithelium, its use is limited due to the stimulating effects of menthol; For example, lozenges containing more than 8 mg per unit cause phobias in taste.

There is a need for a new class of pharmacological agents that can suppress the uncomfortable feeling caused by NKSE without problems of irritation and toxicity.

Many compounds with physiological cooling effects on keratinized epithelium, such as skin and tongue, are described in Watson et al., 1978. The research described herein provides background techniques for finding other compounds with more selective actions on NKSE.

“N-Substituted Paramentane Carboxamides” of the formula are described in Watson et al., 1979. In these examples, R 'is -H and R''is CH ₂ C (= 0) OCH ₃ , CH ₂ C (= 0) OCH ₂ CH ₃ , or CH ₂ C (= 0) OCH ₂ CH ₂ CH _{There are three} phosphorus compounds. Corresponding compounds where R '' is CH ₂ C (= 0) OCH (CH ₃ ) ₂ are not described.

Summary of the Invention

As disclosed herein, one aspect of the present invention relates to an IPE compound.

As disclosed herein, another aspect of the invention relates to a composition comprising an IPE compound.

As disclosed herein, another aspect of the invention relates to an IPE compound for use in the treatment of a human or animal by therapy.

As disclosed herein, another aspect of the invention relates to an IPE compound for use in the treatment of an uncomfortable feeling in a human.

As disclosed herein, another aspect of the invention relates to a method of treating a discomfort in a human, comprising administering a therapeutically effective amount of an IPE compound.

As disclosed herein, another aspect of the present invention relates to the use of an IPE compound used in the manufacture of a medicament for treating a discomfort in a human.

As will be understood by one skilled in the art, the features and preferred embodiments of one aspect of the present invention may also relate to other aspects of the present invention.

compound

We have found that certain compounds are surprisingly and unexpectedly effective cooling agents for non-keratinized stratified epithelial (NKSE) tissue. These compounds have strong and long lasting efficacy and have a selective cooling effect on non-keratinized epithelial tissues in contrast to keratinized epithelial tissues.

These compounds are collectively referred to herein as "isopropyl ester compounds" or "IPE compounds", as follows:

[(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester ("Gly-O-iPr") and

[(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -methyl-amino] -acetic acid isopropyl ester ("N-Gly-O-iPr");

And pharmaceutically acceptable salts, hydrates, and solvates thereof.

Accordingly, one aspect of the present invention is the following compound:

[((1 R, 2 S , 5 R) -2- iso propyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester ( "Gly-O-iPr" ), or

[(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -methyl-amino] -acetic acid isopropyl ester ("N-Gly-O-iPr");

Or pharmaceutically acceptable salts, hydrates, and solvates thereof.

Compounds Gly-O-iPr and N-Gly-O-iPr are listed in the table below.

Code Name Compound name Compound structure Gly-o-ipr [(( 1R , 2S , 5R ) -2-Isopropyl-
5-Methyl-cyclohexanecarbonyl)-
Amino] -acetic acid isopropyl ester

N -Gly-O-iPr [(( 1R , 2S , 5R ) -2-Isopropyl-
5-Methyl-cyclohexanecarbonyl) -methyl-amino] -acetic acid isopropyl ester

These compounds are structurally related to (-)-menthol and have the same chiral center in the same structure, as found in (-)-menthol.

designation Compound name Compound structure (-)-Mensol ( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanol

In structural terms, the compounds may be described conventionally as isopropyl esters of glycine amide and N-methylglycine amide of the carboxylic acid, respectively corresponding to (-)-menthol. In one embodiment, the compound is [(( 1R , 2S , 5R ) -2-isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester or a pharmaceutically acceptable thereof Salts, hydrates, or solvates.

In one embodiment, the compound is [(( 1R , 2S , 5R ) -2-isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester or a pharmaceutically acceptable thereof Salt.

In one embodiment, the compound is [(( 1R , 2S , 5R ) -2-isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester.

Compound synthesis

In one embodiment, the alkyl ester of the glycine amide of the carboxylic acid corresponding to (-)-mensole is an acid halide (e.g., acid chloride) of the carboxylic acid corresponding to (-)-menthol, e.g. For example, by reaction with a suitable glycine alkyl ester as described below.

Scheme 1

Many glycine alkyl esters (including methyl and ethyl glycine esters) are commercially available, for example, from Sigma-Aldrich. Other glycine alkyl esters can be prepared by one skilled in the art using known and / or conventional methods.

For example, an ethyl ester compound referred to herein as Gly-O-Et (if R is Et) can be prepared as follows: 28 mL of 1.0 g glycine ethyl ester hydrochloride (Sigma-Aldrich) was prepared. It was dissolved in ethyl ether and 1 mL secondary distilled water and then cooled to 0 ° C. A small amount of the catalyst diaminopyrimidine was added. 1.62 mL of p-mentoyl chloride was added dropwise, followed by 2 mL of triethylamine. A white precipitate mass appeared in the mixture, which was stirred overnight at room temperature. A precipitate was obtained, which was dissolved in ethyl acetate, washed with secondary distilled water and dried over sodium sulfate. The organic phase was then evaporated under reduced pressure to give the final product (2 g) which crystallized at room temperature. High performance liquid chromatography (HPLC) showed a single peak, indicating that the material was at least 95%. Mass spectrometry (MS) and nuclear magnetic resonance (NMR) were used to confirm the type of component.

Isopropyl compounds, referred to herein as Gly-O-iPr, where R is iPr, were prepared by Phoenix Pharmaceuticals, Burlingame, California (www.phoenixpeptide.com): Lot No. 427497; C ₁₆ H ₂₉ NO ₃ ; Molecular weight 283.41; Purity ≧ 95% by weight; Appearance: White crystalline powder. Additional compounds were prepared by Diapharm Ltd., St. Petersburg, Russia.

The following compounds were prepared.

# code Compound name Compound structure One Gly-o-me [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid methyl ester

2 Gly-O-Et [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid ethyl ester

3 Gly-O-nPr [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid n-propyl ester

4 Gly-o-ipr [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester

5 Gly-O-nBu [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid n-butyl ester

Physiological evaluation

When tested in human subjects, compounds that produce cool heat sensations have some observable properties. First, the senses themselves; For example, the subject may be asked the following questions: Do you feel slightly cool, cool, or cold? Second, the intensity of the senses; For example, the subject may be asked: Is it refreshing cool, intense cool, strong cold, or hot cold? Third, duration of action; The subject may be asked the following questions: How long does efficacy last? The duration of action is usually measured by the onset and disappearance of feeling, generally on the order of minutes or hours. Fifth, efficacy; The efficacy of certain test compounds used to derive coolness is commonly reported using the concentrations added (eg, weight percent; mg / mL; etc.) or dosages (eg, mg per unit body weight). .

Physiological analysis of keratinized stratified epithelium: human analysis

The weight is a recessed area in the center of the upper boundary of the upper lip. Drug test locations were the skin on the upper lip (above the lip of the lips), in the middle of the lungs, to the side of the nose, and sometimes on the lower nostrils (below the nasal cavity). Such facial parts are known to be densely distributed by the cool / cold receptors, followed by the degree of surface of the eye and anogenitalia. In addition, it is known in the scientific literature that the area around the lips has high density of "cold spots" (see, for example, Dhaka et al., 2008).

, 이것은 41% 페트롤라툼, 및 잔량의 미네랄 오일, 세레신 및 라놀린 알코올이다)에 우선 용해시키고 (5 mg/mL), 플라스틱 막대를 사용하여 인중 피부 표면 상에 단독으로 적용한다 (40 내지 70 mg). 이 위치에서, 피부에서의 시원함 및 차가움 감각을 느끼며, 개시 시간 및 강도에 대해 평가할 수 있다. 주관적인 피부 감각의 강도를 다음과 같이 0, 1, 2 또는 3으로 평가한다: 변화가 없는 경우 0; 약간 시원하거나, 추운 경우 1; 확실히 시원하거나 추운 경우 2; 및 매우 시원하거나 추운 경우 3. 기록하는 간격은 5 내지 10 분이며, 0(제로)를 연속하여 2회 수득할 때까지 수행한다. 약물 작용의 개시시간은 시원함 강도가 2 값에 도달하는 시점에서 취하고, 약물 작용의 종결시간은 이전의 2 값을 지난 후, 시원함 강도가 2 이하로 떨어지는 시점이다. 시원함 작용의 지속시간은 소멸시간에서 개시시간을 뺀 것으로 정의된다. 비활성 화합물은, 적용 후 언제라도 5 분 동안 2 값의 시원함을 넘지 않는 화합물로서 정의된다.To test anti-invasive activity, the test substance is ointment (Aquaphor

This is first dissolved in 41% petrolatum, and the remaining mineral oil, ceresin and lanolin alcohols (5 mg / mL) and applied alone on the surface of the skin in humans using a plastic rod (40-70 mg). . At this location, a feeling of coolness and coolness in the skin can be felt, and the onset time and intensity can be evaluated. Subjective skin sensation intensity is assessed as 0, 1, 2 or 3 as follows: 0 if no change; 1 if it is slightly cool or cold; 2 if it is cool or cold for sure; And very cool or cold. 3. The recording interval is 5 to 10 minutes, and is carried out until two (0) consecutive zeros are obtained. The onset time of drug action is taken when the cool intensity reaches 2 values, and the end time of drug action is a time when cool intensity drops below 2 after the previous 2 values. The duration of the cool action is defined as the decay time minus the onset time. Inactive compounds are defined as compounds which do not exceed 2 values of coolness at any time for 5 minutes after application.

Watson et al. Tested the properties of volunteers' N-substituted p-mentancarboxamide by injecting filter paper (1 × 1 cm) infiltrating known compound contents into the back of the subject's tongue. After 30 seconds, the presence or absence of the cooling effect of the subject was recorded. The data was reported as “threshold, μg”, which means the threshold amount of test compound that produces a cool feeling when applied to the tongue of the human volunteer panel. The mean threshold of (-)-mensol for six subjects was 0.25 μg, but there was a 100-fold difference in individual senses. The back of the tongue is keratinized. Keratin is a component of the finger-like processes called papillae and is responsible for the taste. The cool signal detected using the method described in Watson et al., 1979 cannot reflect drug action on NKSE.

Physiological Analysis of Unkeratinized Stratified Epithelium: Eye Surface

, Jarden Corp.)를 사용하여 개별적으로 밀봉하였다. 샘플을 냉각기 또는 냉장고에 저장하고, 사용하기 전에 실온으로 해동하였다. 상기 면 패드로 닦는 것은, 감은 눈꺼풀에 40 내지 45 μL의 액상 성분을 전달한다 (눈 표면 당 ~20 내지 22 μL). 따라서, 상기 테스트 화합물의 농도가 1 mg/mL인 경우, 양쪽 눈에 전달된 투여량은 합계량 ~40 내지 42 μg이거나, 눈 당 ~20 μg이다. 눈 표면에서 느껴진 시원한 느낌의 유무는, 5 내지 10분 간격으로 느껴짐 또는 안느껴짐으로 간략히 기재하였고, 연속적인 2회의 테스트 간격에서 시원함이 느껴지지 않을 때까지 수행하였다. 느껴지는 강도를 정량화시키지 않고, 단지 눈 표면 상에서 시원함이 지속되는 시간만을 기록하였다.For testing on the ocular surface, a disposable towelette containing the test compound was used as the delivery unit. The test compound was first dissolved in anhydrous ethanol and then distilled water was added to form a 1 mg / mL standard solution in a 3-5 wt% ethanol-water solution. 3 mL of the test solution was then added to 0.4 g of square side (50 mm x 60 mm) (CS-being, Daisan Cotton, Japan) and vacuum device (Foodsaver).

, Jarden Corp.) was individually sealed. Samples were stored in a cooler or refrigerator and thawed to room temperature before use. Wiping with the cotton pads delivers 40 to 45 μL of liquid components to the closed eyelid (˜20 to 22 μL per eye surface). Thus, when the concentration of the test compound is 1 mg / mL, the dose delivered to both eyes is a total amount of 40 to 42 μg, or 20 μg per eye. The presence or absence of a cool feeling felt at the eye surface was briefly described as feeling or not feeling at 5 to 10 minute intervals, and performed until no coolness was felt at two consecutive test intervals. Rather than quantify the intensity felt, only the duration of coolness on the eye surface was recorded.

Physiological Analysis of Non-keratinized Stratified Epithelium: Oral Pharyngeal Surface

칠리 페퍼 소스 (YS Gourmet Productions, Inc., PO Box 26189, San Francisco, CA 94126)이며, 딤섬(중국 차 점심)과 함께 사용하기 위한, 잘 알려진 양념이다. 상기 칠리 페퍼 소스와 관련된 느낌은 입의 뒷쪽 벽에 위치하며, 테스트 대상에 의해 분명히 인지되고, 목청을 가다듬기 위한 욕구와 관련된다. 상기 칠리-페퍼 소스에 의해 유발된 느낌은 얼음처럼 차가운 물을 마시거나, 냉각 성분을 포함하는 경구 붕해형 정제(ODT)를 사용함으로써 즉시 제거될 수 있으나, 부형제만을 포함하는 ODT에 의해서는 영향을 받지 않는다.As a measure of pharyngeal sensation, a number of stimuli to induce a feeling of cough were evaluated (see, eg, Morice et al., 2001). Typically, citric acid or capsaicin is delivered to the volunteer via the inhalation route and the number of coughs is counted. The inventors found that the sensation in the lower pharynx associated with the desire to clear the throat can be repeated by applying 0.2 to 0.25 mL of chili pepper sauce to the back of the tongue (using a syringe or plastic rod). It was. The chili pepper sauce is mixed with the saliva, which is then placed behind the oropharyngeal. The chili pepper sauce used was Yank Sing

Chili Pepper Sauce (YS Gourmet Productions, Inc., PO Box 26189, San Francisco, CA 94126) is a well-known condiment for use with dim sum (Chinese tea lunch). The feeling associated with the chili pepper sauce is located on the back wall of the mouth and is clearly recognized by the test subject and relates to the desire to trim the throat. The feeling caused by the chili-pepper sauce can be immediately removed by drinking ice-cold water or by using oral disintegrating tablets (ODTs) containing cooling ingredients, but may be affected by ODTs containing only excipients. Do not receive.

The ODT was formulated by taking one component and dissolving it in anhydrous ethanol, then adding 10 wt% maltitol, 90 wt% mannitol, and the same volume of distilled water. The mixture was stirred with a glass rod and dispensed onto a piece of wax paper with a disposable plastic pipette. Each dry tablet averaged 150 mg and was completely dissolved in saliva on the back of the tongue to coat the pharyngeal surface. On average, the content of the test substance was 2.5 to 3 mg per tablet.

To test anti-invasive activity, ODT containing the test compound was first administered on the back of the tongue; After 45-50 minutes, the chili-pepper sauce test is performed. In this case, the cool sensation induced by the test compound has disappeared and the test will determine if an anticidence effect remains. The results were as follows: score was (0) if there was no alleviation of the stimulus attempted, score was (+) if some suppressed, and score was (++) if stimulus signal was completely eliminated. In the case of ODTs containing an active ingredient exhibiting a (++) score, the stimulus signal disappears completely, but the salty taste used in the sour source of the spice can be immediately revealed and felt.

Research 1

The data obtained in the tests for keratinized stratified epithelium and non-keratinized stratified epithelium (NKSE) are summarized in the table below.

# code
Keratinized stratified epithelium Non-keratinized stratified epithelium (NKSE) Phosphorus Skin (min) ⁽¹⁾ Snow Surface (min) ⁽²⁾ Oral pharyngeal surface ⁽³⁾ One Gly-o-me 10 5 0 2 Gly-O-Et 24 15 0 3 Gly-O-nPr 42 54 0 4 Gly-o-ipr 27 300 ++ 5 Gly-O-nBu 38 35 0

연고 5 mg/mL을 인중 피부에 가함⁽²⁾ 5%-95% v/v 에탄올-증류수 내의 1 mg/mL에서 타월렛을 사용하여 감긴 눈꺼품에 가함. ⁽¹⁾ Aquaphor

Ointment 5 mg / mL added to human skin ⁽²⁾ 5% -95% v / v added to eyelids wound using a towelette at 1 mg / mL in ethanol-distilled water.

⁽³⁾ ODT comprising 2.5 to 3 mg active ingredient, applied on the back, back of tongue; After 45 minutes, chili pepper sauce is added to the tongue surface and the subject's feelings are recorded. When the (++) response was recorded, the stimulus properties of the chili pepper sauce were no longer detected.

Gly-O-iPr has one of the shortest durations in keratinized epithelium, but has the longest duration so far for non-keratinized epithelium. The very long effect of Gly-O-iPr on the eye surface was surprising and unpredictable. The cool effect lasted for an average of 5 hours. Increasing the test concentration of Gly-O-iPr from 1 mg / mL to 1.5 mg / mL further increased the duration on the eye surface to about 6.5 hours. In comparison, when the concentration of Gly-O-Et was increased from 1 mg / mL to 2 mg / mL or even 5 mg / mL, the intensity of the cool feeling increased, but each duration only increased by 15 to 22 minutes. It was. The selective action of Gly-O-iPr on the non-keratinized eye surface reflects the type difference of physiological activity and is not a matter of simple dosage.

Six subjects agreed to test Gly-O-Et, Gly-O-iPr, and Gly-O-nPr eye wipes in a randomized double-blind irradiation and tried three times per wipe. The results were clear and indicated the activity duration of Gly-O-iPr >> Gly-O-nPr> Gly-O-Et.

For oropharyngeal surfaces, both Gly-O-iPr and Gly-O-Et provided a refreshing and cool feeling. However, Gly-O-iPr provided a long, long-lasting refreshing "feel" in the oral cavity, which was not experienced with Gly-O-Et or Gly-O-nPr, and responds to chili pepper sauce Blocked. Gly-O-Et and Gly-O-nPr were not effective under the same test conditions.

Thus, Gly-O-iPr has surprising and unexpected properties, which are distinguished from Gly-O-Me, Gly-O-Et, Gly-O-nPr, and Gly-O-nBu.

Research 2

The Ames test (named after Prof. B.N.Ames of the University of California at Berkeley) is an assay performed in bacteria that assesses the likelihood of mutation of a test compound. Once a positive reaction is obtained, the test compound reacts with the nucleic acid and thus poses a risk to the genetic material. The Ames test is a standard tool in safety assessment.

In the material safety data sheet of Gly-O-Et under classification of artificial mutations (MSDS Number 2984, 09 November 2005, from SCM Europe SA / NV, 141 Rue St. Lambert Suite 2, B-1200, Brussels, Belgium), Note: "The Ames test showed weak mutation results for [Gly-O-Et] in the TA 1535 strain under these test conditions. The response was small and showed some degree of reproducibility."

Mutant activity was evaluated for Gly-O-iPr in Salmonella typhoid tester strain TA1535 by a contract research organization specializing in safety assessment and testing (Notox, BV, Hambakenwetering, PO Box 34763, Hertogenbosch, the Netherlands). Gly-O-iPr was tested in TA1535 in the presence and absence of S9-mix (rat-to-rat S9-mix induced by a combination of phenobarbital and β-naphthoflavones). Gly-O-iPr is Phoenix Pharmaceuticals, Inc. It was provided as a white crystalline powder (purity of ≧ 95%) synthesized by (Burlingame, California) and dissolved in dimethyl sulfoxide (DMSO).

Gly-O-iPr was tested at eight doses with concentrations ranging from 3 to 5000 μg / plate. Gly-O-iPr did not precipitate on the plate at the maximum dose of 5000 μg / plate. No bacterial background lawn was reduced at any concentration tested, and no biologically relevant decrease in the number of return mutants was observed.

In the presence or absence of S9-metabolic activity, Gly-O-iPr did not induce a dose related significant increase in the number of return mutant (His ⁺ ) colonies in TA1535. In this study, negative and strain-specific positive comparison values (derived by sodium azide or 2-aminoanthracene) are included within the range of laboratory-derived comparative data, which was appropriate for test conditions and appropriate for metabolic activity systems. Means it works. Based on these studies, it was concluded that Gly-O-iPR did not increase the incidence of mutations in Salmonella typhoid tester strain TA1535.

Thus, Gly-O-iPR does not share the zoological properties of Gly-O-Et. This result was surprising and unexpected because the structures of these two compounds were closely related.

Research 3

Laboratory researchers had seasonal allergic conjunctivitis. This disease was severely exacerbated when he began experimenting with laboratory animals (rats and mice) and became sensitive to the related allergens. The conjunctivitis was alleviated with oral or topical eye drops containing antihistamines, and the subject was reluctant to use anti-inflammatory steroid ointments. His research showed that his eyes were red and teared, and he continued to rub the eyelids with his fingers, knowing that they could worsen itching and discomfort. He volunteered to try eye wipes containing 1.0 mg / mL of Gly-O-iPr. Within 5 minutes, itching and discomfort alleviated and lasted for at least 4 hours. He used the towel on an "as-needed basis" for three days, and he was surprised to see a significant reduction in overall itching and redness.

Research 4

The 52-year-old man's daughter left from his neighborhood to go to college, and he took care of two cats. At first everything was fine, but I became sensitive to the dust in my pet toilet when I removed these cats. His throat became dry and stinging by coughing, which was severely exacerbated by seasonal allergies to grass pollen, and as a result he was steadily trimming his throat. Standard antihistamines that had no soothing effect did not relieve their irritated upper airways. After coughing and discomfort lasting about two weeks, he agreed to use Gly-O-iPr, first applying 3 mg of Wrigley's Spearmint Chewing Gum per wafer and then orally at 3 mg per unit dose. Disintegrated tablets were prescribed. Both chewing gum and ODT containing the drug alleviated symptoms within 5 minutes after administration. Discomfort in the neck was diminished, the effect lasted for about 4 hours, and the dose could be repeated with the same efficacy. This person prefers ODT delivery and believes it is more effective than chewing gum. After using Gly-O-iPr-containing ODT "on demand" for 10 days, his cough and tingling throat disappeared and are now doing well.

Research 5

A 60-year-old venturer lives a stressful life and smokes two packs of cigarettes a day. He had a smoker's cough and warned that his doctor was on the lookout for chronic obstructive pulmonary disease (COPD), he said. He used an ODT containing 2.5 mg of Gly-O-iPr and said it improved, but he feared he would smoke more if he used it. Later one evening, he went to a supper of northern Chinese recipes and began to cough when he ate a piece of fish that was heavily seasoned with chili pepper. Everyone at the dinner table was amazed by his very severe cough, which caused his face to bulge. He immediately took two ODT tablets containing Gly-O-iPr, and in amazement everyone stopped coughing in minutes.

Research 6

으로 약물을 투여 받았으며, 또한 항히스타민제를 사용하였고, 가끔씩 스테로이드를 흡입하였다. 그는 기침을 자주 하였으며 흉골 주변 가슴 부분에서 답답함 및 불편함을 호소하였다. 그는 부형제로서 만니톨과 함께 180 mg 정제에 배합된 12 mg의 아이실린(icilin)과 함께 3 mg의 Gly-O-iPr을 함유하는 ODT를 사용하는 것에 동의하였다. Gly-O-iPr/아이실린을 함유하는 첫 ODT를 사용한 후, 그는 처음 15분 동안 매우 좋아짐을 느꼈지만, 반복적인 복용을 통해 목과 기도의 불편함의 완화는 10시간 동안 지속되었다. 그는 더 쉽고 덜 불편하게 이동할 수 있음을 느꼈다. 그는 일주일 동안 Gly-O-iPr/아이실린 함유 ODT를 계속 사용하였고, 기침을 덜 하게 되고, 그의 목청을 덜 자주 가다듬으며, 잠을 더 잘 잘 수 있게 되었음을 느끼게 되었다.A 66-year-old man has suffered adult-onset asthma over the past few decades and is exacerbated by seasonal allergies to tree pollen. He bronchodilator inhaler and Singulair

The drug was administered as well as antihistamines, and inhaled steroids occasionally. He coughed frequently and complained of stuffiness and discomfort in the chest area around the sternum. He agreed to use ODT containing 3 mg of Gly-O-iPr with 12 mg of icilin formulated in 180 mg tablets with mannitol as excipient. After using the first ODT containing Gly-O-iPr / icillin, he felt very good for the first 15 minutes, but repeated doses of relief of neck and airway discomfort lasted 10 hours. He felt he could move easier and less uncomfortable. He continued to use Gly-O-iPr / icillin-containing ODT for a week, feeling less coughing, grooming his throat less often, and getting better sleep.

Composition

As disclosed herein, one aspect of the present invention relates to a composition (eg, a pharmaceutical composition) comprising an IPE compound and a pharmaceutically acceptable carrier, diluent or excipient.

As disclosed herein, another aspect of the present invention relates to a method of preparing a composition (eg, a pharmaceutical composition) comprising an IPE compound and a pharmaceutically acceptable carrier, diluent or excipient.

Specific composition

In one embodiment, the composition is in the form of a liquid (eg, an aqueous liquid).

In one embodiment of the invention, the compound is present in the composition at a concentration of 0.01 to 5% w / v.

In one embodiment, the composition is in the form of an eye drop solution.

In one embodiment of the invention, the compound is present in the composition at a concentration of 0.01 to 1% w / v.

In one embodiment, the composition is in the form of an ointment or cream.

In one embodiment of the invention, the compound is present in the composition at a concentration of 0.5 to 5 mg / mL.

In one embodiment, the composition is in the form of a powder, tablet, lozenge, candy tablet, film, paste, chewing gum.

In one embodiment, the composition is in the form of a tablet.

In one embodiment, the composition is in the form of an orally disintegrating tablet (ODT).

In one embodiment, the composition is in the form of a sugar candy (e.g., a sugar and confection made from an aqueous concentrated sugar solution, flavoring and coloring agents are added).

In one embodiment, the composition is in the form of gum.

In one embodiment, the composition is in the form of chewing gum (e.g., conventional sugars and products made from synthetic rubber such as chickle, natural latex products, or polyisobutylene).

In one embodiment of the invention, the compound is present in the composition at a concentration of 0.5 to 5% by weight.

Compositions suitable for topical administration

In one embodiment, the composition is suitable for topical administration to a human.

In one embodiment, the composition is suitable for topical ocular administration to a human.

In one embodiment, the composition is suitable for topical eye administration to the human eyelid, the periphery of the eyelid, the front part of the eye, the conjunctiva, the tear system, the tear film, or the cornea.

In one embodiment, the composition is suitable for topical oral administration to a human.

In one embodiment, the composition is suitable for topical administration to the lining of the oral cavity of a human.

In one embodiment, the composition is suitable for topical administration inside the human lips.

In one embodiment, the composition is suitable for topical pharyngeal administration to a human.

In one embodiment, the composition is suitable for topical administration to the human pharyngeal surface.

In one embodiment, the composition is suitable for topical esophageal administration to a human.

In one embodiment, the composition is suitable for topical administration to the human esophagus surface.

In one embodiment, the composition is suitable for local anal genital administration to a human.

In one embodiment, the composition is suitable for topical administration to the anal genital surface of a human.

Wipes, Pads, and Towels

Another aspect of the invention is a wet wipe, pad, or towelette containing an aqueous composition comprising an IPE compound.

In one embodiment, the aqueous composition is water further comprising the compound.

In one embodiment, the aqueous composition is isotonic saline further comprising the compound.

In one embodiment, the compound is present in the aqueous composition at a concentration of 0.01 to 1% w / v.

In one embodiment, the aqueous composition further comprises an additional eye drop.

In one embodiment, the additional eye drops are a polymer lubricant, hypromellose, polyethylene glycol 400, hyaluronan, or propanediol.

In one embodiment, the wipes, pads or towelettes are suitable for use for topical administration of the compound to humans.

In one embodiment, the wipes, pads or towelettes are suitable for use for topical ocular administration of the compound to humans.

In one embodiment, the wipes, pads, or towelettes are suitable for use for topical eye administration of the compound to the human eyelid, the periphery of the eyelid, the front part of the eye, the conjunctiva, the tear system, the tear film, or the cornea.

For example, an eye wipe comprising a single cooling formulation (eg Gly-O-iPr) as the active pharmaceutical additive (API) may be used as the sole anesthetic wipe. Alternatively, the API can be combined with other agents in the wipe to improve the therapeutic effect. Examples of such additional eye drops are emollients such as polymer “lubricants”, hypromellose, polyethylene glycol 400, hyaluronan, and propanediol (s). The glidants increase the viscoelasticity of the eye fluid (usually this can be achieved with eye drops in the range of 25-50 centipoise), and is particularly useful for dry eye.

Usage

As disclosed herein, the IPE compounds are useful for treating, for example, the discomfort of a human.

Use in therapies

As disclosed herein, another aspect of the invention relates to an IPE compound for use in a method of treating a human or animal by therapy.

Use in the manufacture of drugs

As disclosed herein, another aspect of the invention relates to the use of an IPE compound for use in the manufacture of a therapeutic drug.

In one embodiment, the drug comprises the IPE compound.

How to treat

As disclosed herein, another aspect of the present invention relates to a method of treatment comprising administering to a patient in need thereof a therapeutically effective amount of an IPE compound, preferably in the form of a pharmaceutical composition.

Indications

In one embodiment (eg, one embodiment of the use in a method of treatment, one embodiment of the use in the manufacture of a drug, one embodiment of the therapy), the treatment treats an uncomfortable feeling of non-keratinized multilayer epithelial (NKSE) tissue Or to prevent.

As used herein, the term non-keratinized stratified epithelial (NKSE) tissue is intended to refer to tissue comprising (eg, comprising mainly) non-keratinized stratified epithelial (NKSE) tissue. Examples of NKSE tissues include eye surfaces including the periphery of the eyelid, the front part of the eye, the conjunctiva, the tear system, the tear film, and the cornea; An oral lining including the inside of the lip; a pharyngeal surface; Esophagus surface; And anal genital surface.

In one embodiment (eg, one embodiment of the use in the method of treatment, one embodiment of the use in the manufacture of a drug, one embodiment of the therapy), the treatment is to treat or prevent one or more of the following.

Uncomfortable feeling of the eyelids, the periphery of the eyelids, the front part of the eye, the conjunctiva, the tear system, the tear film, or the cornea;

Uncomfortable feeling of the inner wall of the mouth, the inside of the lips, the pharyngeal surface, or the surface of the esophagus;

Uncomfortable feeling on the surface of the anal genitals;

Feeling of discomfort in the eyes;

Eye discomfort caused by extended wearing of contact lenses, eye discomfort caused by eye strain and / or fatigue, eye discomfort caused by air contaminants, or by overexposure to sunlight Induced eye discomfort;

Eye discomfort caused by conjunctivitis;

Eye discomfort caused by dry eye;

Uncomfortable feeling associated with oral mucositis;

Airway (eg larynx, trachea, and / or bronchus) tightness, discomfort in the airway (eg larynx, trachea, and / or bronchus), choking, coughing, and / or dyspnea;

Airway (eg larynx, trachea, and / or bronchus) tightness and / or discomfort in the airway (eg larynx, trachea, and / or bronchus);

cough

Airway (eg larynx, trachea, and / or bronchial) tightness associated with asthma, discomfort in the airway (eg larynx, trachea, and / or bronchus), choking, coughing, and / or dyspnea;

Airway (eg larynx, trachea, and / or bronchus) tightness, discomfort in the airway (eg larynx, trachea, and / or bronchus), associated with chronic obstructive pulmonary disease (COPD), choking, coughing, and / Or difficulty breathing;

Specific Symptoms: Eye

The eye surface is exposed to the external environment. These anatomical structures-the eyelids, anterior (front) part of the eye, conjunctiva, tear system, tear film and cornea-are damaged by physical, chemical and biological agents. The consequences of damage to the eye surface are uncomfortable symptoms and usually include swelling, itching, irritation, fatigue of vision, dry feeling, burning sensation, and / or pain. The signs of damage in the eye are usually redness, swelling, and / or increased blood flow. Ophthalmic products such as solutions (eg, eye drops), ointments, and inserts are used to address the symptoms and signs of eye damage.

The irritated eye surface is a particularly common symptom of disease known as "dry eye", which is caused by reduced tear formation, for example, exacerbated by dry weather, increased use of contact lenses, excessive gaze of the computer screen, and aging. do. The incidence of dry eye rates assessed in the United States is about 10-30% of the population 40 years of age or older, and about 4.9 million people with severe need special medical care. There is a need for improved therapies.

Other eye diseases that cause eye discomfort include:

General eye discomfort: caused by, for example, extended wearing of contact lenses, eye tightness and / or fatigue, air contaminants, or overexposure to sunlight.

Conjunctivitis: Inflammation of the conjunctiva most commonly caused by allergens, smoke, and / or contaminants, but may also be caused by bacterial and viral infections, or by physical agents such as trauma, wind and sunlight.

Dry eye (dry keratoconjunctivitis): Inadequate wetting of the eye surface caused by rapid evaporation or inadequate tear secretion, for example due to poor tear quality.

Specific symptoms: oral cavity and pharynx

The back of the tongue is covered with keratinized epithelium. The oral and pharyngeal surfaces are covered with non-keratinized multilayered epithelium (NKSE). The pharynx is divided into three areas: naso, mouth and laryngo. The oropharynx is a particularly busy traffic zone for adults to pass an average of 12,000 L of air and 2 kg of food each day, and for survival the traffic flow must be accurate and it is essential that food does not pass into the airways. Swallow and cough reflexes protect the airways against solid particles. The narrowest point of the traffic zone is called the lower retropalatal oropharynx (LRO) and has a cross-sectional area of about 1 cm ² .

The sensations that cause discomfort on the oral and pharyngeal surfaces are multifactorial and include short-term diseases such as infections, allergies, chemotherapy of cancer, infections caused by contaminants, and chronic diseases such as pharyngitis, laryngitis, Asthma, chronic obstructive pulmonary disease (COPD), gastroesophageal reflux, lung cancer, pneumonia, pulmonary edema, and congestive heart failure.

The sensitivity of oral and pharyngeal surfaces to injury and pain is described by a disease known as oral mucositis (frequency of 20-40% occurrence) caused by cancer therapies such as radiation and chemotherapy for head and neck cancer. Mucositis originates from the lining of the oral cavity / pharyngeal and usually results from toxic damage to epithelial stem cells that failed to restore and replace the cells of the upper layer lost by desquamation. Oral mucositis feels dry: pain, especially when eating and chewing; Difficulty swallowing; And deterioration of life. The disease progresses over several weeks and threatens life and hinders treatment in the form of ulceration and infection. Pain (main symptom) usually occurs due to loss of epithelial cells down the inflammatory mediator and basement membrane, and then exposes sensory nerve endings of connective tissue stroma. Pain relief is attempted with mouthwashes including local anesthetics, morphine, antihistamines, or sedatives such as honey. These agents have a limited effect duration and unwanted side effects; Local anesthesia, for example, can interfere with proper chewing of food.

Sensory nerve endings in the oral / pharyngeal NKSE are on the local or overall surface of the tissue and are therefore accessible for localized drug delivery.

cure

The term "treatment" used in the context of the treatment of a disease generally refers to some predetermined therapeutic effect, for example, inhibiting the progress of the disease, reducing the rate of progression, stopping the progression rate, alleviating the symptoms of the disease, And to treatment and therapy in humans, including amelioration and treatment of disease. Treatment as a prophylactic measure (ie, prophylaxis) is also included. For example, use in a patient who has not yet developed a disease but is at risk of developing the disease is included in the term "treatment".

For example, treatment includes preventing eye discomfort, reducing the frequency of occurrence of eye discomfort, alleviating symptoms of eye discomfort, and the like.

As used herein, the term “therapeutically effective amount” refers to the amount of a compound that is effective to produce a given therapeutic effect, or the amount of a compound, composition, or formulation that contains the compound, when the amount of the compound is effective according to the desired therapeutic regimen / Related to the risk ratio.

Combination therapy

The term "treatment" includes a combination of treatment and therapy, wherein two or more treatments or therapies are combined, for example, sequentially or simultaneously. For example, the compounds described herein can also be used in combination with combination therapies, eg, with other agents.

One aspect of the invention relates to a compound disclosed herein in combination with one or more (eg, 1, 2, 3, 4, etc.) additional therapeutic agents.

Certain combinations use common general knowledge of the physician and will be at the discretion of the physician selecting the dosage according to the regimen known to the skilled artisan.

The agents (ie, the compounds described herein, addition of one or more other agents) may be administered simultaneously or sequentially, and may be administered via a dosage schedule and a different route that varies from person to person. For example, when administered sequentially, the formulations may be well spaced apart (eg over a period of 5-10 minutes) or longer intervals (eg 1, 2, 3, 4 hours or longer). Intervals, or longer time intervals as required), and the correct dosage is matched to the nature of the therapeutic agent.

The formulations (ie, compounds described herein, addition of one or more other formulations) may be prescribed together in a single dosage form, or the individual formulations may be formulated separately and provided together in the form of a kit (with instructions for use if necessary). Can be.

Pharynx and esophagus fields

Local delivery of TRP-M8 antagonists to the pharynx and esophagus sites may be beneficial in relieving symptoms of airway stuffiness, choking, coughing and dyspnea in diseases such as asthma and / or chronic obstructive pulmonary disease (COPD). This mechanism of action is indirect and is based on the fusion of sensory input from the upper body of the gastrointestinal tract (pharynx and esophagus), and the upper airway in the brain stem (larynx, trachea and bronchus). These sensory inputs come from two types of cranial nerves, the Yeti nerve (9th nerve) and the vagus nerve (10th). Thus, delivery of the TRP-M8 antagonist onto the oropharyngeal and esophagus surfaces allows for transmission of signals through the Yeti / Vagus nerve to the brain stem that indirectly “gates” to the invasive signals generated from the vagus. The result is a therapeutic goal that reduces coughing and airway irritation.

The inventors have found that Gly-O-iPr prescribed with icillin (known TRP-M8 antagonist) has a slight cool feeling in the chest where it extends below the larvae, presumably because of its action on pharyngeal and esophageal receptors. Evaluated. Gly-O-iPr alone is less effective because of its local action in the oropharyngeal. Cool feeling in the chest resulting from the Gly-O-iPr / Icyrin combination can alleviate uncomfortable symptoms in the airways (larynx, trachea and bronchus) in diseases such as asthma and COPD.

Thus, in one embodiment, the additional therapeutic agent is icillin. For example, in one embodiment, the invention relates to a compound in combination with icillin, as described herein.

Kit

One aspect of the invention provides an IPE compound described herein, or an IPE compound-containing composition described herein, preferably (a) preferably provided in the form of, for example, a suitable container and / or suitable packaging, and (b) an example. It relates to a kit comprising instructions for use, for example written instructions on how to administer the compound or composition.

The written instructions may also include a list of symptoms in which the active ingredient is an appropriate therapeutic agent.

Route of administration

The IPE compound or a pharmaceutical composition comprising the IPE compound is administered locally to the subject (ie, at the desired site of action).

In one embodiment, the administration is topical administration to a human.

In one embodiment, the administration is local ocular administration to a human.

In one embodiment, the administration is topical eye administration to the human eyelid, the periphery of the eyelid, the anterior portion of the eye, the conjunctiva, the tear system, the tear film, or the cornea.

In one embodiment, the administration is topical oral administration to a human.

In one embodiment, the administration is topical administration to the lining of the oral cavity of a human.

In one embodiment, the administration is topical administration to the inside of the human lips.

In one embodiment, the administration is topical pharyngeal administration to a human.

In one embodiment, the administration is topical administration to the human pharyngeal surface.

In one embodiment, the administration is local esophageal administration to a human.

In one embodiment, the administration is topical administration to the esophageal surface of a human.

In one embodiment, the administration is local anal genital administration to a human.

In one embodiment, the administration is topical administration to the anal genital surface of a human.

Subject / Patient

In one embodiment, the subject / patient is a human.

Formulation

While the IPE compounds may be administered alone, pharmaceutically acceptable carriers, diluents, excipients, preservatives, fillers, buffers, adjuvants, antioxidants, glidants, stabilizers, solubilizers, emulsifiers (eg, wetting agents) ), At least one IPE compound as described herein, with one or more other pharmaceutically acceptable additives well known to those skilled in the art, including, but not limited to, masking agents, colorants, flavoring agents, and sweetening agents. It is preferred to be present as a pharmaceutical combination (eg, composition, formulation, drug). The combination may further comprise other active agents, for example other therapeutic or prophylactic agents.

Accordingly, the present invention provides a pharmaceutical composition as described above; And mixing at least one IPE compound as described herein with one or more other pharmaceutically acceptable additives well known to those skilled in the art, such as, for example, carriers, diluents, excipients, and the like. It further provides a manufacturing method. When formulated into individual units (eg tablets, etc.), each unit contains a predetermined amount (dose) of the compound.

As used herein, the term “pharmaceutically acceptable” refers to a compound, additive, substance, composition, dosage form, etc., which, within the scope of serious medical judgment, is excessively toxic, irritant, allergic, or otherwise. It has a reasonable benefit / risk ratio and is suitable for use in contact with unknown tissues without problems or complications. Each carrier, diluent, excipient, etc. must also be "acceptable" in the sense of compatibility with the other ingredients of the combination.

Suitable carriers, diluents, excipients and the like are described in general pharmaceutical textbooks such as Remington's Pharmaceutical Sciences , 18th edition, Mack Publishing Company, Easton, Pa., 1990; And Handbook of Pharmaceutical Excipients , 5th edition, 2005.

Such formulations may be prepared by methods well known in the art of pharmacy. The preparation includes the step of bringing into association the compound with a carrier which constitutes one or more additional ingredients. In general, the formulation is prepared by homogeneously and tightly binding the compound to a carrier (eg, a liquid carrier, a finely divided solid carrier, etc.), and shaping the product if necessary.

Suitable formulations include liquids, solutions (e.g. aqueous, non-aqueous), suspensions (e.g. aqueous, non-aqueous), emulsions (e.g. oil-in-water, water-in-oil), elixirs, syrups, electuaries ), Mouthwashes, drops, tablets (including coated tablets), granules, powders, lozenges, candy tablets, capsules (including hard and soft gelatin capsules), chchets , Pills, gels, pastes, ointments, creams, lotions, oils, foams, sprays, mists, or aerosols.

Formulations suitable for topical oral administration include liquids, solutions (e.g. aqueous, non-aqueous), suspensions (e.g. aqueous, non-aqueous), emulsions (e.g. oil-in-water, water-in-oil), elixirs, syrups, soft, Tablets, granules, powders, capsules, cachets, and pills.

Formulations suitable for topical oral (oral) administration include patches, bandages, depots, and reservoirs in addition to mouthwashes, lozenges, candy tablets. Lozenges typically contain these compounds in a flavored base material, usually sucrose, and acacia or tragacanth. Candy tablets usually contain such compounds in an inert matrix such as gelatin and glycerin, or sucrose and acacia. Mouthwashes usually comprise the compound in a suitable liquid carrier.

Formulations suitable for topical oral (sublingual) administration include tablets, lozenges, candy tablets, capsules and pills.

Formulations suitable for topical oral (mucosal penetration) administration include liquids, solutions (e.g. aqueous, non-aqueous), suspensions (e.g. aqueous, non-aqueous), emulsions (e.g. water-in-oil, oil-in-water), mouthwashes, In addition to lozenges, candy tablets, patches, plasters, depots and reservoirs.

Formulations suitable for topical (parenteral mucosal penetration) administration include liquids, solutions (eg aqueous, non-aqueous), suspensions (eg aqueous, non-aqueous), emulsions (eg water-in-oil, oil-in-water), gels, In addition to pastes, ointments, creams, lotions, oils, patches, plasters, depots and reservoirs.

Formulations suitable for topical (transdermal) administration include patches, bandages, bandages, dressings, depots, and reservoirs in addition to gels, pastes, ointments, creams, lotions, and oils.

Tablets may be prepared by conventional means, for example by compression or molding, and optionally comprise one or more additional ingredients. Compressed tablets may be prepared by compressing the compound in a free flowing form, such as powder or granules, in a suitable device, optionally with one or more binders (e.g. povidone, gelatin, acacia, sorbitol, tregakens, hydride) Oxypropylmethyl cellulose); Fillers or diluents (eg, lactose, microcrystalline cellulose, calcium hydrogen phosphate); Lubricants (eg magnesium stearate, talc, silica); Disintegrants (eg, sodium starch glycolate, crosslinked povidone, crosslinked sodium carboxymethyl cellulose); Surfactants or dispersants or wetting agents (eg, sodium lauryl sulfate); Preservatives (eg, methyl p-hydroxybenzoate, propyl p-hydroxybenzoate, sorbic acid); Mixed with flavors, flavor enhancers, and sweeteners. Molded tablets may be prepared by molding a mixture of a compound moistened with a powdered compound with an inert liquid diluent in a suitable mechanical device.

Ointments are usually prepared from these compounds and paraffinic or water-miscible ointment bases.

Creams are usually prepared from these compounds and oil-in-water cream bases. If necessary, the aqueous phase of the cream is for example at least about 30% w / w of a polyhydric alcohol, ie propylene glycol, butane-1,3-diol, mannitol, sorbitol, glycerol and polyethylene glycol and Alcohols having two or more hydroxy groups, such as mixtures thereof.

Emulsions are usually prepared from the compound and the oil phase and may simply comprise a mulching agent (also known as an emulsion), or may comprise a mixture of at least one emulsifier with fat or oil or both fat and oil. Can be. Preferably, hydrophilic emulsification is included together with lipophilic emulsification which acts as a stabilizer. It is also desirable to include both oils and fats. In addition, the emulsifier (s) with or without stabilizing agent (s) constitute so-called emulsifying wax, and the wax with oil and / or fat together is the so-called emulsifying ointment which forms the oil dispersed phase of the cream formulation. Construct the base.

Suitable emulsions and emulsion stabilizers include Tween 60, Span 80, cetostearyl alcohol, myristyl alcohol, glyceryl monostearate and sodium lauryl sulfate. The selection of suitable oils or fats for such formulations is the basis for achieving the desired cosmetic properties since the solubility of the compounds can be very low in most oils susceptible to use in pharmaceutical emulsion formulations. Thus, preferably, the cream should be non-sticky, non-dyeable and water washable as a product having a suitable concentration so as not to leak out of the tube or other container. Straight or branched chain, mono- or dibasic alkyl esters, for example diisoadiate, isocetyl stearate, propylene glycol diesters of coconut fatty acids, isopropyl myristate, decyl oleate, isopropyl palmitate, butyl Blends of branched chain esters known as stearate, 2-ethylhexyl palmitate, or Crodamol CAP can be used, the latter three being the preferred esters. These can be used individually or in combination according to a required property. Alternatively, high melting point lipids such as white soft paraffin and / or liquid paraffin or other mineral oils can be used.

Formulations suitable for topical (intranasal) administration include, for example, aerosol administration by nasal sprays, nasal drops, or nebulisers when the carrier is liquid, and are aqueous or oily solutions of the compounds. It includes.

Formulations suitable for topical (intranasal) administration may be administered, for example, if the carrier is a solid, for example, by nasal passages, ie by rapid inhalation via the nasal route from a powder container held close to the nose. For example provided in the form of a coarse powder having a particle size in the range of about 20 to about 500 microns.

Formulations suitable for topical (lung) administration (eg, by inhalation or inhalant therapy) are suitable such as dichlorodifluoromethane, trichlorofluoromethane, dichloro-tetrafluoroethane, carbon dioxide, or other suitable gas. Using propellants, those provided as aerosol sprays formed from pressurized packs.

Formulations suitable for topical (eye) administration include eye drops and the compound is dissolved or suspended in a suitable carrier, especially an aqueous solvent for the compound.

Formulations suitable for oral cavity and oropharyngeal include compositions such as, for example, liquids, powders, tablets, films or pastes. As contemplated herein, oral disintegrating tablets (ODT) are pharmaceutical dosage forms that degrade in saliva within 30 seconds upon topical application to the surface of the tongue. Common ODTs mainly include inert vehicles, diluents or carriers. Agents (eg Gly-O-iPr) are interspersed in such carriers. The ODT can dissolve when placed on the back of the tongue to release the medicament and contact the lower oropharyngeal (LRO) tissue. Conventional diluents, carriers or vehicles may be “polyhydric alcohols” that are interpreted when describing the following materials: xylitol, mannitol, sorbitol, maltitol, isomaltitol, maltotriitol, lactitol and β-linked-glucopyranassi Glucopyranasido-sorbitol. Seasonings such as sweeteners, aspartame, sucralose or alitam can be added to mask any taste. Typically, the mixture is granulated into a homogeneously dispersed blend; Dispersants, anti-caking agents and lubricants may be added; The mixture is then compressed to form ODT.

In one formulation (used in the biological evaluation studies described herein), oral disintegrating tablets (ODTs) are prepared using an 80:20 weight mixture of mannitol-maltitol (Pearlitol ^™ and Sweetpearl ^™ ; Roquette Freres, France) It was. Such carriers have the advantage of completely masking the bitter taste that may be present in some of the test compounds. The mixture is first mixed with the mannitol-maltitol using mortar and pestle and then suspended in an equal volume of 10:90 v / v ethanol-distilled water. Next, the liquid mixture was added onto one piece of wax paper using a disposable pipette and dried at room temperature. The dried tablets were then weighed and sorted. It has been found by experiment that an 80 mg tablet comprising 2-3 mg of the test compound dissolves in 15 seconds when placed on the back of the tongue to provide a good test dose.

Reference

Many publications are cited above in order to describe and disclose in detail the present invention and prior art to which the present invention pertains. The full name for these references is provided below. Each reference is incorporated herein by reference in its entirety, in the manner in which each individual reference is specifically and individually named and incorporated by reference.

Dhaka et al ., 2008, "Visualizing cold spots: TRP-M8-expressing sensory neurons and their projections", J. Neuroscience , Vol. 28, pp. 566-575.

Morice et al ., 2001, "Cough Challenge in the Assessment of Cough Reflex", Brit. J. Clin. Pharmacol. , Vol. 52, pp. 365-375.

Watson et al ., 1978, "Compounds with the Menthol Cooling Effect", J. Soc. Cosmet. Chem. , Vol. 29, pp. 185-200.

Watson et al ., 1979, " N -Substituted paramenthane carboxamides", US Patent No 4,178,459 granted 11 December 1979.

Claims (72)

[(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound, and a pharmaceutically acceptable carrier, diluent, or excipient A pharmaceutical composition for topical ocular administration to a human, comprising. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound, and a pharmaceutically acceptable carrier, diluent, or excipient A pharmaceutical composition for topical oral administration to a human, comprising. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound, and a pharmaceutically acceptable carrier, diluent, or excipient A pharmaceutical composition for topical administration to an oral lining of a human, comprising. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound, and a pharmaceutically acceptable carrier, diluent, or excipient A pharmaceutical composition for topical administration to a human pharyngeal surface, comprising. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound, and a pharmaceutically acceptable carrier, diluent, or excipient A pharmaceutical composition for topical administration to a human esophagus surface, comprising. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound, and a pharmaceutically acceptable carrier, diluent, or excipient A pharmaceutical composition comprising in liquid form. The pharmaceutical composition of claim 6, wherein the compound is present in the composition at a concentration of 0.01 to 5% w / v. A pharmaceutical composition according to claim 7 for topical administration to humans. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound, and a pharmaceutically acceptable carrier, diluent, or excipient A pharmaceutical composition in the form of an eye drop comprising. The pharmaceutical composition of claim 9, wherein the compound is present in the composition at a concentration of 0.01 to 1% w / v. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound, and a pharmaceutically acceptable carrier, diluent, or excipient A pharmaceutical composition comprising, in the form of an ointment or cream. The pharmaceutical composition of claim 11, wherein the compound is present in the composition at a concentration of 0.5 to 5 mg / mL. The pharmaceutical composition of claim 12 for topical ocular administration to a human. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound, and a pharmaceutically acceptable carrier, diluent, or excipient A pharmaceutical composition comprising, in the form of a powder, lozenge, candy pill, film or paste. The pharmaceutical composition of claim 14, wherein the compound is present in the composition at a concentration of 0.5 to 5 wt%. The pharmaceutical composition of claim 15 for topical oral administration to humans. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound, and a pharmaceutically acceptable carrier, diluent, or excipient A pharmaceutical composition in the form of a tablet, comprising. The pharmaceutical composition of claim 17, wherein the compound is present in the composition at a concentration of 0.5 to 5% by weight. The pharmaceutical composition of claim 18 for topical oral administration to humans. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound, and a pharmaceutically acceptable carrier, diluent, or excipient A pharmaceutical composition in the form of an oral disintegrating tablet (ODT), comprising. The pharmaceutical composition of claim 20, wherein the compound is present in the composition at a concentration of 0.5 to 5 wt%. The pharmaceutical composition of claim 21 for topical oral administration to humans. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound, and a pharmaceutically acceptable carrier, diluent, or excipient A pharmaceutical composition in the form of a sugar candy, comprising. The pharmaceutical composition of claim 23, wherein the compound is present in the composition at a concentration of 0.5 to 5 wt%. The pharmaceutical composition of claim 24 for topical oral administration to humans. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound, and a pharmaceutically acceptable carrier, diluent, or excipient A pharmaceutical composition in the form of chewing gum, comprising. The pharmaceutical composition of claim 26, wherein the compound is present in the composition at a concentration of 0.5 to 5% by weight. The pharmaceutical composition of claim 27 for topical oral administration to humans. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound, and a pharmaceutically acceptable carrier, diluent, or excipient A pharmaceutical composition in the form of an aerosol, comprising. For the treatment of human non-keratinization of the pain-layer epithelium, [((1 R, 2 S, 5 R) -2- iso propyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester Pharmaceutical compositions for topical administration comprising a. For the treatment of human non-stratified epithelium keratinization itching, [((1 R, 2 S, 5 R) -2- iso propyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester Pharmaceutical compositions for topical administration comprising a. Topical administration comprising [(( 1R , 2S , 5R ) -2-isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound for treating eye pain Pharmaceutical composition for. [((1 R , 2 S , 5 R ) -2-isopropyl-5-methyl for treating pain in the human eyelid, the periphery of the eyelid, the anterior part of the eye, the conjunctiva, the tear system, the tear film or the cornea. A pharmaceutical composition for topical administration comprising -cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound. Eye pain caused by prolonged wearing of contact lenses; Eye pain caused by eye strain, eye fatigue, or both; Pain in the eyes caused by air contaminants; Or [(( 1R , 2S , 5R ) -2-isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -isoacetic acid for treating eye pain caused by overexposure to sunlight A pharmaceutical composition for topical administration comprising a propyl ester compound. For the treatment of pain in the eye caused by conjunctivitis, acetic acid isopropyl ester - [((1 R, 2 S, 5 R) -2- iso propyl-5-methyl-cyclohexanecarbonyl) -amino] Pharmaceutical compositions for topical administration comprising. For the treatment of pain in the eye caused by the dry eye syndrome, [((1 R, 2 S, 5 R) -2- iso propyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester Pharmaceutical compositions for topical administration comprising a. For the treatment of pain in the inner wall of the human oral cavity, the inside of the lips, the iron surface, esophagus, or the surface, [((1 R, 2 S, 5 R) -2- iso propyl-5-methyl-cyclohexanecarbonyl) A pharmaceutical composition for topical administration comprising -amino] -acetic acid isopropyl ester compound. For the treatment of pain associated with a human oral mucositis, [((1 R, 2 S, 5 R) -2- iso propyl-5-methyl-cyclohexanecarbonyl) -amino] - acetic acid isopropyl ester A pharmaceutical composition for topical administration. Topical administration comprising [(( 1R , 2S , 5R ) -2-isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound for treating human airway pain Pharmaceutical composition for. Contains [(( 1R , 2S , 5R ) -2-isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compounds for treating airway pain associated with human asthma A pharmaceutical composition for topical administration. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid for treating airway pain associated with chronic obstructive pulmonary disease (COPD) in humans A pharmaceutical composition for topical administration comprising an isopropyl ester compound. For the treatment of any of the pain is selected from the group consisting of a human larynx, trachea and bronchus, [((1 R, 2 S, 5 R) -2- iso propyl-5-methyl-cyclohexanecarbonyl) - A pharmaceutical composition for topical administration comprising an amino] -acetic acid isopropyl ester compound. For the treatment of any of the pain it is selected from the group consisting of larynx, trachea and bronchus associated with human asthma, [((1 R, 2 S, 5 R) -2- iso propyl-5-methyl-cyclohexanecarboxylic A pharmaceutical composition for topical administration comprising a carbonyl) -amino] -acetic acid isopropyl ester compound. [((1 R , 2 S , 5 R ) -2-isopropyl-5 for treating any one pain selected from the group consisting of larynx, trachea and bronchus associated with chronic obstructive pulmonary disease (COPD) in humans A pharmaceutical composition for topical administration comprising -methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound. Topical administration comprising [(( 1R , 2S , 5R ) -2-isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound for treating a human cough Pharmaceutical composition for. Comprising [(( 1R , 2S , 5R ) -2-isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound for treating cough associated with human asthma Pharmaceutical compositions for topical administration. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -isoacetic acid for treating cough associated with chronic obstructive pulmonary disease (COPD) in humans A pharmaceutical composition for topical administration comprising a propyl ester compound. Topical administration comprising [(( 1R , 2S , 5R ) -2-isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound to treat human respiratory distress Pharmaceutical composition for. Contains [(( 1R , 2S , 5R ) -2-isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid isopropyl ester compound for treating dyspnea associated with human asthma A pharmaceutical composition for topical administration. [(( 1R , 2S , 5R ) -2-Isopropyl-5-methyl-cyclohexanecarbonyl) -amino] -acetic acid for treating dyspnea associated with chronic obstructive pulmonary disease (COPD) in humans A pharmaceutical composition for topical administration comprising an isopropyl ester compound. delete delete delete delete delete delete delete delete delete delete delete delete delete delete delete delete delete delete delete delete delete delete