Patent Application
20130338098
This invention relates to topical analgesia and to methods and compositions, etc. for treating pain or discomfort in a mammal.
Pain occurs frequently and is a common symptom for which patients seek medical assistance. Defined as an unpleasant subjective sensation which results from a noxious stimulus, pain alerts the body to possible or actual danger, such as during disease or physical trauma. The needs of a patient in temporary or chronic pain include comfort, freedom from adverse reactions, the ability to perform the functional activities of daily living, psychological reassurance, and a satisfying quality of life.
The pathological mechanism of pain and its perception by the subject remains an area of considerable research. Despite a lack of comprehensive understanding of the many dimensions of pain, many agents have been developed to be effective in its treatment.
Analgesics are a broad class of agents developed for use in the treatment and management of pain. Major classes of analgesic compounds include analgesic-antipyretic compounds which are compounds that alleviate pain and/or reduce fever, such as salicylates and related compounds, and narcotic analgesics or opiates, which alleviate pain and/or induce sleep. The analgesic potency of a compound generally correlates with its solubility in lipids. It is believed that analgesia occurs when lipid structures in neurosensory cell membranes are disrupted by a dissolved analgesic agent.
Analgesics can be broadly divided into two classes of agents, i.e. systemic analgesics and topical analgesics. Compounds displaying analgesic properties are not necessarily effective as both systemic and topical analgesics. Systemic analgesics, which are typically swallowed or injected, are frequently prescribed for the treatment of pain. The most common treatment for chronic pain is with the use of the salicylate-like agents known as nonsteroidal anti-inflammatory drugs (NSAIDs). Unfortunately, side effects can be associated with the use of these drugs, including gastrointestinal and renal abnormalities.
Unlike systemic agents that are swallowed or injected, topical analgesics, typically available in the form of salves, creams, ointments and rubs, work only on the area they are rubbed into, reducing or eliminating the risk of systemic side effects. Topical analgesics may be appropriate for subjects with muscle ache or mild pain that affects only a few joints. They may also provide relief for subjects whose oral medications alone fail to reduce their pain to manageable levels, such as, for example, from arthritic pain. They may also provide means of prophylaxis of pain. However, topical administration of an analgesic requires that the analgesic be able to reach the sensory receptors implicated in pain. In particular, topical analgesics for use on the skin must first be able to penetrate dense stratum corneum, keratinized comeocytes and the restrictive epidermal cell layer barrier of the skin surface.
Different types of agents have been found to be effective as topical analgesics. Most common topical analgesics include one or more of three commonly used analgesic agents which can be broadly classified as counter-irritants, salicylates, and caspaicin. Counter-irritants stimulate nerve endings distracting the brain's attention from muscoskeletal pain, and encompass such substances as menthol, camphor, etc. Salicylates inhibit prostaglandins which contribute to pain and inflammation. Such compounds are often found to act as systemic analgesics as well. Caspaicin is a naturally occurring drug which works by depleting a neurotransmitter substance that is implicated in sending pain messages to the brain. These active agents are usually applied as components in compositions to an area in need of analgesia. These compositions often include agents that aid in the transcutaneous delivery of the analgesic agent to the sensory receptors. As well, lidocaine, lignocaine, xylocaine, benzocaine, tetracine, prilocaine, bupivacaine, and the like, are used as topical analgesics. However, their toxicities are well established and great care must be taken to ensure that the dosage of these agents is not exceeded to toxic levels. Toxic effects include formation of sulfhemoglobin and methhemoglobin, as well as effects on the central nervous system.
Thus, the development of topical analgesics for the management of pain which provide fast and effective relief or reduction of pain, yet exhibit reduced side effects, is an ongoing need.
The present invention involves alleviation of pain or discomfort of a subject by aliphatic polyamines that produce an analgesic effect in their topical administration to the subject. An analgesic is an agent used in the treatment of pain.
One embodiment of the invention is a method for producing local analgesia in a subject having a site of local discomfort. The method includes topically administering an effective amount of an aliphatic polyamine to the site.
In another embodiment, the invention is a method for producing relief in a subject having a site subject of nociceptive stimulation. The method includes topically administering an effective amount of an aliphatic polyamine to the site.
The polyamine can be in the form of a free base or it can be a pharmaceutically acceptable salt of a polyamine, or it can be a mixture of the two. Of course, the form selected would be compatible with the use to which the polyamine is to be put. For application to human skin, the free base or salt(s) would be compatible for use with human skin. Salts that produce deleterious effects would generally be avoided.
In particular embodiments, the polyamine has up to fifteen carbon atoms. Certain preferred polyamines are limited to four amino groups, while certain embodiments have three amino groups and some have only two amino groups. In certain embodiments, the polyamine(s) is saturated. In certain embodiments, the polyamine is non-cyclic. In certain embodiments, the polyamine has only ten carbon atoms, but it may have more, or less, particularly, nine, or eight, or seven, or six or five carbon atoms. Particular polyamines of the invention are putrescine, cadaverine, spermine and/or spermidine. Spermidine is the “doublet” of putrescine and spermine is the “triplet.” Preferably, the polyamine has at least four carbon atoms.
In compositions of the invention, the polyamine can make up between 0.1 and 10 weight percent of the composition that is to be administered to the site. In other embodiments, between 0.2 and 9 percent, or between 0.3 and 8 percent, or between 0.4 and 7 percent, or between 0.5 and 6 percent, or between 0.6 and 5 percent, or between 0.7 and 5 percent, or between 0.8 and 5 percent, or between 1 and 4 percent or between 1 and 3 percent, or between 1 and 2 percent. The polyamine can thus constitute about 0.1, 0.2, 0.3, 0.4, 0.5, 0.8, 1.0, 1.3, 1.5, 1.8, 2.0, 2.3, 2.5, 2.8, 3.0, 3.5, 4.0, 4.5, 5.0, 5.5, 6, 7, 8, 9 or 10 weight percent of the composition that is to be administered to the site.
The site of topical application would usually be the epidermis, the outer skin layer of the subject. The subject is usually human, but could be another mammal, such as a horse or dog, for example.
A composition of the invention preferably includes a chaotropic agent, or penetration agent, which enhances delivery of the analgesic component into lower layers of the skin aiding its delivery to the site of action. The agent can be urea, or it can be oleic acid, for example, or it can be a combination of such agents.
Urea has been found to be particularly useful in this regard. Preferred embodiment compositions include urea in a concentration of at least 10 percent, more preferably in a concentration of at least 15 percent by weight of the composition. Usually, the concentration of urea would be no more than 40 percent. The concentration of urea could be about 10, or about 15 or about 20, or about 25 or about 30 or about 35 or about 40 percent by weight of the total weight of the composition.
In certain embodiments of the invention, the composition is a cream, or a spray, or an ointment, or a gel or a lotion, for application to a subject's skin.
A preferred mode of administration is with the use of a patch. A patch can be mounted to the site to be treated. The patch has the polyamine incorporate thereinto at the site such that the polyamine is transferred from the patch to the site.
In using such a patch, release of the polyamine from the patch can be controlled to produce the analgesic effect over a period of time. The period of time can be, for example, up to about one week, or between about one hour and one week, or between one hour and six days, or between six hours and five days, or between six hours and four days, or between twenty-four hours and three days, or between one day and two days.
In certain preferred embodiments, the composition can include beta 1,3-D glucan.
In a particularly preferred embodiment, the composition includes lidocaine, a known local anaesthetic.
Topical sites treatable through the present invention include those where discomfort is the result of a sports injury, a physical assault, arthritis, rheumatism, headache, shingles, surgical pain, or a combination of any of the foregoing.
The source of discomfort can be one of non-pathological etiology.
The invention can be used in a subject suffering from fibromyalgia.
In a particular embodiment, the site of treatment is free of extracellular wound scar skin tissue and/or the site is free of a wound undergoing healing of the skin.
The invention includes manufacture of a composition of the invention, and particularly those for use according to any method of the invention, for example, in topically administering the composition to an affected site.
In preferred embodiment compositions, the polyamine of the invention is admixed with a suitable pharmaceutically-acceptable diluent or carrier.
Several properties of putrescine are known that make it suitable for use as a topical analgesic, including that it is a naturally occurring substance which is a normal metabolite in cells, it is a ubiquitous component in foods, and it has been shown to have a very low toxicity when administered via many routes including orally, intravenously, intraperitoneally, and intramuscularly.
In a preferred embodiment, the aliphatic polyamine is putrescine dihydrochloride.
In another aspect, the invention relates to a pharmaceutical composition in dosage unit form suitable for topical administration to a mammal for effecting analgesia in a mammal desiring such analgesia, which comprises an effective amount of an aliphatic polyamine or a pharmaceutically-acceptable salt thereof, in admixture with a suitable pharmaceutically acceptable diluent or carrier.
In another aspect, the invention provides a commercial package containing as an active pharmaceutical ingredient an aliphatic alkyl polyamine or a pharmaceutically-acceptable salt thereof, together with instructions for the use thereof for inducing analgesia in a mammal.
In another aspect, the invention provides a process for preparing an agent for effecting topical analgesia in a mammal, in ready-to-use drug form for the treatment of pain, characterized in that an aliphatic polyamine or a pharmaceutically acceptable salt thereof is used as an active ingredient in the agent.
For purposes of clarity, the following terms and phrases used throughout this specification and the appended claims are defined in the manner set forth directly below.
The term “analgesia” as used herein means the reduction, or absence, of sensibility to pain, designating particularly the relief of pain without consciousness.
The term “malady” generally refers to an illness or disease.
The term “composition” is meant to embrace both a single substance and a mixture of substances.
The term “polyamine” as used herein means one or more than one amino group.
The term “amino” as used herein means —NH2.
The term “aliphatic” means acyclic or cyclic, saturated or unsaturated carbon compounds, excluding aromatic compounds. Saturated carbon compounds include hydrocarbons having from one to twenty carbon atoms, within which includes from four to eleven carbon atoms, and further which includes from four to five carbons, and which can be straight or branched chain. Representatives of such groups are n-butyl, n-pentyl, n-propyl, sec-butyl, isobutyl, etc.
The term “alkyl” as employed herein means a saturated hydrocarbon having from one to twenty carbon atoms, within which includes from four to eleven carbon atoms, and further which includes from four to five carbons, and which can be straight or branched chain. Representatives of such groups are n-butyl, n-pentyl, n-propyl, sec-butyl, isobutyl, etc.
The term “pharmaceutically-acceptable” as employed herein means those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgement, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problems or complication, commensurate with a reasonable benefit/risk ratio.
The term “pharmaceutically-acceptable salts” in this respect refers to the relatively-non-toxic, inorganic and organic addition salts of compounds of the present invention. Representative salts include the hydrochloride, hydrobromide, sulphate, phosphate, nitrate, acetate (see for example, S. M. Berge et al., “Pharmaceutical Salts”, J. Pharm. Sci. 66:1-19 (1977)).
The term “chaotropic agent” as employed herein means an agent that breaks up dense macromolecular and lipid-rich domains. Some examples of materials that can serve as chaotropic agents include urea, substitutes ureas, amides and dimethyl sulphoxide.
The phrase “pharmaceutically-acceptable carrier” as employed herein means a pharmaceutically-acceptable material, composition or vehicle, as defined directly above, such as a liquid or solid filler, diluent, excipient, solvent, involved in carrying or transporting a chemical compound or pharmaceutical agent from one portion of the body to another portion of the body. Some examples of materials that can serve as carriers include: sugars, such as lactose and glucose; starches, such as corn starch; cellulose, and its derivatives, such as sodium carboxymethyl cellulose and cellulose acetate; malt; gelatin; talc; oils, such as olive oil; glycols, such as propylene glycol; polyols, such as glycerin, polyethylene glycol; esters, such as ethyl oleate; agar; buffering agents, such as magnesium hydroxide; water; ethyl alcohol; and other non-toxic compatible substances employed in pharmaceutical formulations.
The present invention includes a use of an aliphatic polyamine as a topical analgesic and topical analgesic compositions containing an aliphatic alkyl polyamine.
A number of the aliphatic alkyl polyamine compounds useful in the composition and methods of the present invention are known in the chemical art. The amine group contained by the aliphatic polyamines may be either primary or secondary and may be located either in a terminal position, within the alkane chain, or both. In a preferred embodiment, the preferred aliphatic polyamines useful in the compositions and methods of the present invention are spermidine (4,4′-iminobis butylamine), spermine (N,N′-Bis(3-aminopropyl)-1,4-butane-diamine), cadaverine (1,5-pentanediamine) and putrescine (1,4-diaminobutane). Details of the synthetic preparation of a number of the aliphatic polyamines utilizable in the compositions and methods of the present invention may be found in Beilsteins Handbuch Der Organischen Chemie. The Merck Index, 11th edition, also references many of the preferred compounds of this invention.
The free base form of the aliphatic polyamines utilized in the present invention may be conveniently converted to the corresponding acid addition salt by contacting a solution of the free base with the appropriate acid. Particularly preferred salts are the acid addition salts formed with hydrochloric and sulfuric acids, e.g., hydrochloride and sulfate.
The compositions of the present invention comprise one or more of the above-mentioned aliphatic polyamines in a sufficient quantity together with a suitable pharmaceutical carrier to induce topical analgesia. The aliphatic polyamines act as analgesic agents. A sufficient quantity is defined as the amount of compound necessary to induce analgesia. In the usual course of therapy, the aliphatic polyamine is incorporated into an acceptable vehicle to form a composition for topical administration to the area sensing pain and, thus, requiring analgesia.
The dosage levels of the aliphatic polyamine in the pharmaceutical compositions of this invention may be varied so as to obtain an amount of the active ingredient that is effective to achieve the desired therapeutic response for a particular use, or composition without being toxic to the subject. In a preferred embodiment, the amount is 1.0 weight percent. In another embodiment, the amount is 0.8 weight percent. In yet another preferred embodiment, the amount is 2.0 weight percent. In other embodiments, the percentage may be higher or lower. In a preferred embodiment, a concentration of putrescine at 0.8 percent weight per volume of the composition in a eutectic base is used for inducing analgesia to an area of the skin of a human. A topical composition containing 0.8 percent weight per volume of putrescine in a eutectic base for the treatment of scar tissue is described in U.S. Pat. No. 5,885,982. In general, such compositions are envisioned to contain the active ingredient in from about 0.005% to about 5% volume by weight of the total composition. The use of putrescine as a non-topical, systemic analgesic by intraperitoneal and intracerebroventricular injection into rats at 200 to 400 mg/kg of body weight is known. See, Genedani et al., Life Sciences, 34, 2407-2412 (1984).
While it is might be possible for an aliphatic alkyl polyamine of the present invention to be administered in pure form, it is preferable to administer the compound as a topical pharmaceutical composition to facilitate spreading over the area in need of analgesia. Compositions for topical application may be exemplified by ointments, creams, lotions, solutions, suspensions, aerosols, gels, dusting powder, and impregnated bandages and dressings. Such compositions would normally be based upon standard carriers such as pharmaceutically acceptable vegetable oils and gelatins, gums and petrolatum. Other ingredients of the composition of the invention may be preservatives, coloring, thickening, suspending, disbursing, emulsifying, swelling, stabilizing and buffering agents, fats, oils, waxes, paraffins, starch, polyethylene glycols, silicones, bentonites, talc, zinc oxide, etc., as required by the specific formulation. In a preferred embodiment, the pharmaceutical carrier is a eutectic base (Glaxo Canada Ltd., Toronto, Ont.).
A polyamine of the invention can also be incorporated into patches or so-called transdermal therapeutic systems (TTS). From these the active substance components act on the skin over a defined area of the body surface in occlusive manner at a controlled release rate and are appropriately brought to transdermal absorption.
It is well known that the rate of transport of some substances through the skin depends on the polar-nonpolar nature of the substance, size of the substance, hydration of the skin, blood supply, and modification of the stratum corneum by chemicals. Thus, in a preferred embodiment, a chaotropic agent is present in the composition. In a preferred embodiment, the chaotropic agent is urea. In yet another preferred embodiment, urea is present at about fifteen weight percent of the composition. In yet another preferred embodiment, urea is present from between about one and twenty weight percent of the composition. Such chaotropic agents can facilitate penetration of the analgesic agent into the skin as they break up dense macromolecular domains of fibrous and globular proteins.
In another preferred embodiment, a beta-1,3-glucan can be added to promote healing in the area of the subject requiring analgesia should the area also require healing. In another embodiment, a beta-1,3-glucan is present at about six to eight percent by weight of the total composition. Beta-1,3-glucans may be derived from, among other things, purified yeast cell walls, and are well known to stimulate the immunosystem.
Repeated use of the analgesic compositions of the present invention is envisaged, the length of time of use being dependent upon the length of time that is required until analgesia is effected. As well, the dosage size and frequency of administration can vary depending upon the nature and intensity of the pain. The exact dosage to be administered and length of time of use with a subject will, of course, be dependent upon, among other factors, the particular compositions employed, and the disease or injury being treated.
A variety of uses have been tried for the analgesic compositions of the present invention, for example: headache, frontal headache, arthritis, anti-nociception, rheumatism, shingles, post-herpetic neuralgia, joint pain (in the arm, leg, shoulder, toe, ankle, etc. for example), post surgical pain, tenderness in breasts, burns, tense muscles, chest pain, injuries, sports injuries (for example, shin splints, pulled muscles, sprain, etc.), repetitive stress injuries including tennis elbow, fibromyalgia, rotator cuff pain, muscoskeletal pain. In a preferred embodiment, the composition of the invention is applied to an area of a shoulder requiring analgesia due to pain originating from the rotator cuff and includes putrescine at about 2 percent by weight of the composition.
The following examples describe in detail compositions illustrative of the present invention and methods for their utilization. It will be apparent to those skilled in the art that many modifications, both of materials and methods may be practiced without departing from the purpose and intent of the disclosure. For example, although references are made to “lotion”, “cream” and “balm”, it will be understood that a given form of the respective composition may converted to another by altering the non-medicinal components in methods known to persons skilled in the art. For example, a topical cream composition can also be provided in a topical lotion or balm form. All components are commercially available.
A topical cream composition according to an aspect of the present invention was prepared from the following components:
A topical balm composition according to an aspect of the present invention was prepared from the following components:
A topical lotion composition according to an aspect of the present invention was prepared from the following components:
A topical lotion composition according to an aspect of the present invention was prepared from the following components:
A topical composition according to an aspect of the present invention with lidocaine and putrescine present was prepared from the following components:
A topical massage cream composition according to an aspect of the present invention was prepared from the following components:
A topical cream composition according to an aspect of the present invention was prepared from the following components:
The putrescine is dissolved in deionized water in a one to one ratio before adding to the Glaxo base.
A composition for topical application, according to an aspect of the present invention, was prepared from the components listed below. The composition was prepared in the form of a lotion but can also be adapted to a cream or balm form as will be known in the art.
The above individual phases were prepared individually, as would be known to persons skilled in the art, and subsequently mixed together to form the composition.
In a variation of the above formulation, Phase C (i.e. menthol and camphor) may be omitted and the water content adjusted accordingly.
In another variation of the above formulation, 0.1% eucalyptus oil may be used instead of 0.2% zinc, with the water content adjusted accordingly.
In the formulation of the present example, copper is included. Preferably, copper is included in the form of copper peptide, which is known the art, particularly for skin care compositions. The inventors postulate that the presence of copper serves to keep putrescine accumulated under the skin, thereby improving the efficacy thereof. This is based on a previously published finding that copper putrescine accumulates under a copper wire in a willow tree branch. Thus, although copper peptide is included in the above formulation, other suitable (i.e. cosmetically or dermatologically suitable) copper containing components may also be used instead of or together with copper peptide. It will be understood that the invention is not to be limited to any particular theory concerning how copper may affect the effectiveness of the formulation.
The above formulation was made with concentrations of copper peptide from about 0.1% to 0.2% w/w. These formulations have been used in treating tertiary pain on patients, in some cases resulting in patients being able to reduce dependence on opioid drugs.
In order to assess the analgesic effects of the method of use of the compounds of the invention and the compositions of the present invention, studies have been conducted. In the following study, the effect of the composition on a group of subjects in pain was evaluated.
Sixteen subjects experiencing pain were given a sample of the composition of Example 1 (the “Example 1” composition) and a sample of the composition of Example 1 that does not include the active ingredient, putrescine (the “placebo” composition). The subjects were advised to topically administer the compositions at different periods of pain and to then rate the effectiveness of the two compositions. Pain was estimated by a ranking system from 0 to 5, wherein 0 was no effect, while 5 represented maximum perceived relief of pain. The data are presented in Table 1 and show that the perceived pain decreased with application of the composition containing putrescine. As well, 15 out of 16 subjects did not perceive a decrease in pain after application of the placebo composition.
Similarly, subjects experiencing pain were given a sample of the composition of Example 1 (the “Example 1” composition) and a sample of the composition of Example 1 that does not include the active ingredient, putrescine (the “placebo” composition). The subjects were advised to administer the compositions at different periods of pain and to then rate the effectiveness of the two compositions. Pain was estimated by a ranking system from 0 to 5, wherein 0 was no effect, while 5 represented maximum perceived relief of pain. The data are presented in Table 2 and show that the perceived pain decreased with application of the composition containing putrescine.
Tests were also conducted on twelve subjects suffering from arthritis. Half of the subjects were given a placebo for topical administration and the others were given the following composition:
This composition contains 2% putrescine. The results are summarized in Table 3. Three people who were given the placebo dropped out prior to completion of the study.
Tests were also conducted on people suffering from fibromyalgia to compare relief obtained with a topical composition containing 20 percent triethanolamine salicylate (Bayer Myoflex) to the above-indicated 2 percent putrescine composition. The test was double blind. The results obtained are summarized in Table 4.
A useful embodiment of the invention is one in which lidocaine is incorporated into a topical composition:
While in this specification the invention has been described in detail through an example of some of the preferred embodiments thereof, it will be obvious to a person skilled in the art that many variations and modifications could be made without departing from the scope and spirit of the present invention. Therefore, the present invention should be considered as limited only by the scope of the appended claims.
All patents and publications referenced to throughout the specification are hereby incorporated in their entirety as though the contents thereof had been reproduced herein, without admission that such is prior art.
This application is a Continuation in Part of U.S. application Ser. No. 10/380,675, filed on Aug. 28, 2003, which is a National Entry under 35 USC §371 of PCT Application number PCT/CA01/01337, filed Sep. 19, 2001, which claims priority under the Paris Convention to U.S. Application No. 60/233,488, filed Sep. 19, 2000. The entire contents of the aforementioned prior applications are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| 60233488 | Sep 2000 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10380675 | Aug 2003 | US |
| Child | 13801381 | US |
