JP2016040279A - Combination of theobromine with decongestant and its use for treatment of cough - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a novel combination composition containing theobromine useful in treatment of cough.SOLUTION: A pharmaceutical composition contains theobromine, pseudoephedrine, and one or more excipients, and optionally further contains one or more additives selected from sweetening agents, flavoring agents, coloring agents and preservatives. The dose of pseudoephedrine is 0.1 to 30 mg/kg/day.SELECTED DRAWING: Figure 1

Description

  The present invention relates to drug combinations, compositions thereof, and their use, particularly in the treatment of cough.

  Cough is a defensive reflex. Persistent cough can be painful. Non-prescription treatments are available, but their effectiveness is questionable.

  WO 98/42322 discloses the use of theobromine for the treatment of cough given orally.

  Usmeni et al., FASEB J. et al. express article 10.1096 discloses that theobromine inhibits sensory nerve action and cough. Data are provided to show the effect of citrate-induced cough in guinea pigs and in capsaicin cough tests in humans after oral dosing and after bathing of isolated guinea pig vagus nerve preparations.

  The decongestant pseudoephedrine has been shown to have very limited efficacy in a citrate-induced cough model in guinea pigs (Minamizawa et al., J Pharmacol Sci, 2006). However, most of this document fails to prove that pseudoephedrine has an antitussive effect. Many research papers describe the effects on “cough and cold” (which has little meaning in the medical field), but none of them have even investigated whether they describe a direct antitussive effect.

  The present invention is based at least in part on data showing a synergistic antitussive effect for theobromine in combination with the decongestant pseudoephedrine in a citric acid-induced cough model. The data show that when theobromine is combined with pseudoephedrine, the effect is surprisingly strong and exceeds the sum of the individual drugs, indicating that the combination has a substantially improved effect. It is clear. This is particularly surprising considering that pseudoephedrine is totally suspicious of having an antitussive effect.

  As a result, both drug doses can be significantly reduced for the same effect as each individual drug, reducing side effects and drug burden.

  Thus, according to the first aspect of the invention, the medicament comprises theobromine and a decongestant as a combined preparation for simultaneous, sequential or separate use in therapy.

  According to a second aspect, the pharmaceutical composition comprises theobromine and a decongestant.

  This synergistic relationship is believed to be demonstrated by all decongestants. While not wishing to be bound by theory, this may be due to the structural similarity of the members of the decongestants class of drugs.

FIG. 1 shows the effect of theobromine and the combination of theobromine and pseudoephedrine on citric acid-induced cough in guinea pigs.

(Description of the invention)
As used herein, the term “decongestant” is a defined type of drug that is well known to those skilled in the art. The decongestant is preferably an α-adrenergic receptor agonist. Any suitable form of decongestant can be selected. These include salts, prodrugs, and active metabolites.

  As used herein, treatment of cough means any treatment that reduces the number and / or severity of cough. Treatment of cough preferably means a direct antitussive effect that reduces the number of coughs, i.e. reduces the urge to cough the body. Thus, according to a preferred embodiment of the invention, the medicament comprises theobromine and a decongestant for use as a cough medicine composition. The agent of the present invention is useful as an antitussive agent in the management of cough. The medicament of the present invention is preferably used in the management of dry cough.

  The decongestant may be used in an amount already known for its use, but the combination according to the invention means that a reduced dose is effective. The dose of the decongestant administered with theobromine will, of course, depend on the usual factors including its efficacy, but is at least 0.1 mg / kg / day, for example at least 5 mg / kg / day Preferably, it may be up to 50 mg / kg / day. The decongestant is preferably administered in the range of 0.1 to 30 mg / kg / day.

  Any suitable form of theobromine can be selected. These include salts, prodrugs, and active metabolites. Theobromine may also be in the form of cocoa or chocolate. Suitable dosage ranges for theobromine are known in the art and depend on normal factors (such as age), but the synergistic effect of the combination means that the effective dosage can be reduced. ing.

  The combinations according to the invention can be provided in a single formulation or in separate formulations for combined, simultaneous or sequential administration.

  The decongestant is preferably selected from the following drugs: ephedrine, levmethamphetamine, naphazoline, oxymetazoline, phenylephrine, phenylpropanolamine, propylhexedrine, pseudoephedrine, synephrine, and tetrahydrozoline. More preferably, the decongestant is pseudoephedrine.

  The compounds of the present invention can be administered by any available route, such as via the oral, inhalation, intranasal, sublingual, intravenous, rectal and vaginal routes.

  The compound of the present invention is preferably administered as a combination orally, for example, as a tablet, troche, lozenge, aqueous or oily suspension, dispersible powder or granule. Preferred pharmaceutical compositions of the present invention are tablets and capsules. Liquid dispersions for oral administration may be syrups, emulsions and suspensions. More preferably, the combined pharmaceutical composition is a compressed tablet or capsule using conventional excipients, examples of which are described below.

  Compositions intended for oral use can be prepared according to any method known in the art for producing pharmaceutical compositions, such compositions are pharmaceutically refined and One or more agents selected from the group consisting of sweeteners, flavoring agents, coloring agents, and preservatives can be included to provide a palatable preparation. Tablets contain the active ingredient in admixture with non-toxic pharmaceutically acceptable excipients that are suitable for the manufacture of tablets. These excipients include, for example, inert diluents such as calcium carbonate, sodium carbonate, lactose, calcium phosphate, or sodium phosphate; granulating and disintegrating agents such as corn starch or alginic acid; binders such as starch And gelatin, gum arabic, microcrystalline cellulose, or polyvinylpyrrolidone; and lubricants such as magnesium stearate, stearic acid, or talc. The tablets may be uncoated or they may be coated by known techniques to delay disintegration and absorption in the gastrointestinal tract and thereby provide a sustained action over a longer period. . For example, a time delay material such as glyceryl monostearate or glyceryl distearate can be employed.

  Aqueous suspensions contain the active materials in admixture with excipients suitable for the manufacture of aqueous suspensions. Such excipients include suspending agents such as sodium carboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose, sodium alginate, polyvinylpyrrolidone, gum tragacanth, and gum arabic; naturally occurring phospholipids such as lecithin, or alkylene A product derived from a condensation product of an oxide with a fatty acid (eg, polyoxyethylene stearate), or a condensation product of an ethylene oxide with a long-chain aliphatic alcohol (eg, heptadecaethyleneoxycetanol), or a portion derived from an ethylene oxide fatty acid A dispersing or wetting agent that may be a condensation product with an ester (eg, polyoxyethylene sorbitan monooleate). Aqueous suspensions also contain one or more preservatives, such as ethyl or n-propyl p-hydroxybenzoate, one or more colorants, one or more flavoring agents, and one such as sucrose or saccharin. One or more sweeteners can also be included.

  Oily suspensions may be vegetable oils such as peanut oil, olive oil, sesame oil, or coconut oil, polyoxyethylene hydrogenated castor oil, fatty acids such as oleic acid, or mineral oils such as liquid paraffin, or other surfactants or It can be formulated by suspending the active ingredient in a cleaning agent. The oily suspensions can contain a thickening agent, for example beeswax, hard paraffin, or cetyl alcohol. Sweetening agents such as those set forth above, and flavoring agents can be added to provide a palatable oral preparation. These compositions can be preserved by the addition of an anti-oxidant such as ascorbic acid.

  Dispersible powders and granules suitable for preparation of an aqueous suspension by the addition of water are combined in a mixture with a dispersing or wetting agent, suspending agent, and one or more preservatives. Active ingredient. Appropriate sweetening, flavoring, and coloring agents can also be present.

  The combined pharmaceutical composition of the present invention may be in the form of an oil-in-water emulsion. The oily phase may be a vegetable oil, for example olive oil or arachis oil, or a mineral oil, for example liquid paraffin or mixtures of these. Suitable emulsifiers include naturally occurring gums such as gum arabic or tragacanth, naturally occurring phospholipids such as soy lecithin, and esters or partial esters derived from fatty acids and hexitol anhydrides such as monooleic acid. It may be sorbitan and the condensation product of the above partial ester with ethylene oxide, for example, polyoxyethylene sorbitan monooleate. Emulsions can also contain sweetening and flavoring agents.

  Syrups and elixirs may be formulated with sweetening agents, for example glycerol, propylene glycol, sorbitol or sucrose. Such formulations may also contain a demulcent, a preservative, flavoring and coloring agents.

  Suspensions and emulsions can contain carriers such as natural rubber, agar, sodium alginate, pectin, methylcellulose, carboxymethylcellulose, or polyvinyl alcohol.

  A combination composition according to the present invention can be produced using conventional formulation techniques. In particular, spray drying methods can be used to produce microparticles containing active agents dispersed or suspended in a material that provides controlled release properties.

  Milling methods, such as jet milling methods, can also be used to formulate therapeutic compositions. This is especially true for particles intended for administration by inhalation. Production of fine particles by milling can be accomplished using conventional techniques. The term “milling” is used herein to refer to any mechanical process that applies sufficient force to the particles of active material to break or break the particles into fine particles. A variety of milling equipment and conditions are suitable for use in making the compositions of the present invention.

  The selection of appropriate milling conditions, such as milling strength and time, to provide the required degree of force will be within the ability of one skilled in the art. Ball milling is a preferred method. As an alternative, a high pressure homogenizer can be used that forces the fluid containing the particles through the valve at high pressure, creating high shear and turbulent conditions. Cavitation due to shear forces on the particles, impacts between the particles and the machine surface or other particles, and fluid acceleration can all contribute to particle crushing.

  Suitable homogenizers include EmulsiFlex high pressure homogenizers, Niro Soavi high pressure homogenizers, and Microfluidics Microfluidizer. A milling method can be used to provide microparticles with mass median aerodynamic diameter as defined above. If hygroscopic, the active agent can be milled with a hydrophobic material, as described above.

  If required, the microparticles produced by the milling process can then be formulated with additional excipients. This formulation can be achieved by spray drying methods, for example, co-spray drying methods. In this embodiment, the particles are suspended in a solvent and co-spray dried with a solution or suspension of additional excipients. Preferred additional excipients include polysaccharides. Additional pharmaceutically effective excipients can also be used.

  A combination composition intended for inhalation, topical, intranasal, sublingual, intravenous, rectal, and vaginal use is any method known in the art for producing pharmaceutical compositions. Can be prepared according to

  Treatment according to the present invention can be performed in a generally known manner depending on various factors such as the patient's sex, age, or health status, and the presence or absence of one or more combination treatments. The patient population may be important.

  The present invention is based at least in part on the following tests.

(test)
A study was designed to examine the antitussive activity of theobromine in combination with two different doses of pseudoephedrine against citrate-induced cough in awake guinea pigs.

Test dose 1-vehicle control 2-theobromine (10 mg / kg po)
3-theobromine (10 mg / kg, po) + pseudoephedrine (10 mg / kg, po)
4-theobromine (10 mg / kg, po) + pseudoephedrine (30 mg / kg, po)

Methods Male Dunkin Hartley guinea pigs (400-500 g, supplied by Harlan UK Ltd) were used throughout the study.

  Thirty guinea pigs were randomly assigned to one of four treatment groups according to the blinding code. The blinding code was not revealed to researchers until coughs from all animals were counted.

  Guinea pigs were dosed with theobromine dosed 2 hours prior to citric acid exposure via an oral gastric tube (dosing volume 2 mL / kg). Pseudoephedrine was dosed 30 minutes prior to citric acid exposure, and vehicle control animals were dosed both 2 and 30 minutes prior to citric acid exposure.

  Individual guinea pigs were placed in the exposure chamber with a flow of 2 L / min t = 10 minutes prior to citric acid exposure to acclimatize. At t = 0 min, cough response was elicited by exposure to citrate aerosol (1M) generated by an ultrasonic nebulizer at a spray rate of 0.6 mL / min for 10 min.

  Cough was counted during 10 minutes of citric acid exposure and for an additional 5 minutes after exposure.

Results The results show that prior treatment with theobromine (10 mg / kg, po) increased the number of citric acid-induced cough (13 ± 3) (see FIG. 1), as well as the onset time to the first cough (156 ± 15 s ) (Data omitted). In combination with pseudoephedrine (10 mg / kg and 30 mg / kg), the inhibitory response of theobromine to citrate-induced cough activity is the total number of cough (9 ± 2 cf 13 ± 3) (FIG. 1) and up to the first cough With respect to both onset time (170 ± 15 s cf156 ± 15 s) (data not shown), it was enhanced at the highest dose.

Claims (6)

  A medicament comprising theobromine and a decongestant as a combined preparation for simultaneous, sequential or separate use in therapy.   The medicament according to claim 1, wherein the treatment is treatment of cough.   A pharmaceutical composition comprising theobromine and a decongestant.   The agent according to claim 1 or 2, wherein the decongestant is selected from ephedrine, levmethamphetamine, naphazoline, oxymetazoline, phenylephrine, phenylpropanolamine, propylhexedrine, pseudoephedrine, synephrine, and tetrahydrozoline. Item 4. The composition according to Item 3.   The drug or composition according to claim 4, wherein the decongestant is pseudoephedrine.   The medicament according to any one of claims 1, 2, 4, and 5, or any one of claims 3 to 5, wherein the decongestant is administered at a dose of 0.1 to 30 mg / kg / day. The composition according to claim 1.

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