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Bronchodilator expectorant elixir |
| RE29875 |
Bronchodilator expectorant elixir
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| Patent Drawings: | |
| Inventor: |
Mercer, et al. |
| Date Issued: |
January 2, 1979 |
| Application: |
05/846,873 |
| Filed: |
October 31, 1977 |
| Inventors: |
Bryan; Hugh D. (Evansville, IN)
Mercer; Neil H. (Evansville, IN)
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| Assignee: |
Mead Johnson & Company (Evansville, IN) |
| Primary Examiner: |
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| Assistant Examiner: |
1 |
| Attorney Or Agent: |
Carnahan; Robert E.Uloth; Robert H. |
| U.S. Class: |
514/263.31; 514/263.32; 514/826 |
| Field Of Search: |
424/253 |
| International Class: |
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| U.S Patent Documents: |
RE29359 |
| Foreign Patent Documents: |
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| Other References: |
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| Abstract: |
A bronchodilator expectorant composition containing a sympathomimetic amine bronchodilator, the xanthine bronchodilator theophylline, guaiacol or a water soluble form thereof and a sedative. |
| Claim: |
What is claimed is:
1. A bronchodilator-expectorant composition comprised of a solution containing at least 40% by volume of water and characterized by containing in each 5 milliliters thereof16.6 to 175 mg. of theophylline, 7.5 to 350 mg. of glyceryl guaiacolate or an equivalent solubilizing weight of potassium guaiacol sulfonate or guaiacol, and from 1/6 to a full therapeutic dose of ephedrine, pseudoephedrine, methoxyphenamine, orprotokylol, and from 2 to 35 mg. of cyclopal, aprobarbital, butabarbital, or pentobarbital .[...]. .Iadd.wherein the amount of theophylline dissolved in said solution exceeds the saturated solution amount thereof in the solvents employed in saidsolution, and the theophylline in solution which exceeds said saturated solution amount is solubilized and held in solution by said glyceryl guaiacolate or equivalent solubilizing weight of potassium guaiacol sulfonate or guaiacol. .Iaddend.
2. The composition of claim 1 containing up to 20% by volume of alcohol.
3. The composition of claim 1 containing 4 to 25 mg. of ephedrine hydrochloride or ephedrine sulfate and from 2 to 15 mg. of butabarbital per 5 milliliters of elixir. |
| Description: |
U.S. Pat. 3,109,773, dated Nov. 5, 1963 of Neil H. Mercer and Robert J. Bequette deals with a bronchodilator-expectorant elixir containing theophylline in highly concentrated liquid dosage form made possible through the solubilizing effect of glycerylguaiacolate, or other water-soluble form of guaiacol, on the theophylline. Those compositions have the advantage of providing a therapeutic dose of theophylline and glyceryl guaiacolate or equivalent water soluble form of guaiacol in a relatively smallvolume of elixir which may contain alcohol in sufficient amount to assist in absorption of the theophylline, but in insufficient amount to interfere with patient acceptance. The compositions have solution stability over a wide pH range including acidicconditions. The latter is desirable since considerably more latitude is thereby afforded the flavorist in compounding an acceptably flavored product and because the theophylline remains in solution even under the strongly acid conditions met in thestomach, thus reducing the possiblity of gastric irritation.
The present invention provides the solution to a difficult problem encountered in preparing an elixir of the foregoing type retaining each of the advantages thereof relative to palatability, absorption, tolerance, and acceptability, but includingtherein as additional active ingredients a sympathomimetic amine bronchodilator component, such as ephedrine hydrochloride, and a barbiturate sedative.
Bronchodilator compositions containing both adrenergic and xanthine-type bronchodilator agents to counteract bronchospasm, and a sedative are widely used because of their effectiveness, despite the disadvantages of certain side effects. Thesedative serves the purpose of relieving the anxiety to which patients suffering from bronchial asthma are frequently subject and also counteracting the central nervous system stimulating side effects of the sympathomimetic amines which serves asadrenergic bronchodilator components. Phenobarbital is the most widely used sedative in such compositions, although other barbiturates have been used in tablet or capsule dosage forms.
Phenobarbital is generally preferred for such compositions because of its relatively long duration of action providing a continuous calming effect during dosage for chronic conditions. Unfortunately a physical incompatibility betweenphenobarbital and theophylline is operant which results in their precipitation from solution when it is attempted to incorporate phenobarbital in sedative effective amounts into a theophylline-glyceryl guaiacolate elixir of the type described in U.S. 3,109,773. Apparently the phenobarbital interferes with the solubilizing action of the glyceryl guaiacolate on the theophylline, resulting in precipitation thereof. Furthermore, the phenobarbital is itself rendered insoluble. It is thus impossible toformulate a clear solution free from insoluble suspended ingredients. Solutions are preferred in accordance with the object of providing rapid and uniform absorption without gastric irritation and for convenience and accuracy of administration. Theuncertainty of uniform resuspension of insoluble ingredients is an ever-present problem in the administration of drugs as liquid suspensions.
We have found that certain barbiturates form clear solutions when employed in combination with theophylline, ephedrine hydrochloride, and glyceryl guaiacolate. The reason for the specific compatibility which we have discovered is not known sincethe operability of certain barbiturates does not appear to be a function of their water or alcohol solubilities.
There is provided according to the present invention a bronchodilator expectorant composition containing a sympathomimetic amine bronchodilator such as ephedrine, pseudophedrine, methoxyphenamine, or protokylol or an acid addition salt thereof;the xanthine bronchodilator theophylline; glyceryl guaiacolate, or a water soluble form thereof such as guaiacol itself, or potassium guaiacol sulfonate; and a sedative component, cyclopal, aprobarbital, butabarbital, or pentobarbital. These ingredientsare contained in an aqueous alcoholic vehicle to provide final composition which contains at least 40% by volume of water and up to 20% by volume of ethanol, which shares the advantage of pH stability, palatability, freedom from gastric irritation, andeffective absorption with the compositions of U.S. 3,109,773.
The compositions are designed to contain a therapeutically effective dosage of each active ingredient in a dosage volume of up to 2 tablespoons (30 ml.) of elixir. Each 5 ml. unit contains from about 1/6 up to a full therapeutic dose of eachingredient, or more particularly from 16.6 to 175 mg. of theophylline; from 7.5 to 350 mg. of glyceryl guaiacolate, or an equivalent solubilizing weight of potassium guaiacol sulfonate or guaiacol; from 4 to 25 mg. of ephedrine hydrochloride,ephedrine sulfate, or a pharmacologically equivalent amount of one of the previously mentioned sympathomimetic bronchodilators; from 2 to 35 mg. of one of the barbiturates listed above, preferably butabarbital. For the latter, concentrations in therange of 2 to 15 mg./5 ml. are employed. A soluble form of ephedrine, pseudoephedrine, methoxyphenamine, or protokylol is, of course, used. Ephedrine sulfate and ephedrine hydrochloride may be used interchangeably in the amount specified. Theconcentrations of other adrenergic bronchodilators for use in the present elixirs are adjusted in accordance with accepted dosage practice for each drug.
In its broadest concept, the present bronchodilator expectorant compositions are clear aqueous or aqueous-alcoholic solutions containing at least 40% by volume of water and up to 20% by volume of alcohol, and having dissolved therein 0.83 g. to4.37 g. of theophylline per 100 ml. of water in the composition, sufficient guaiacol or pharmaceutically acceptable water soluble form thereof to serve as solubilizer for the theophylline, a pharmacologically effective dose of a sympathomimeticbronchodilator, and a sedative dose of a barbiturate selected from 5-allyl-5-cyclopentenylbarbituric acid (cyclopal), 5-allyl-5-isopropylbarbituric acid (aprobarbital), 5-ethyl-5-(2-butyl)barbituric acid (butabarbital), and 5-ethyl-5-(2-pentyl)barbituricacid (pentobarbital).
The foregoing concentration range of theophylline exceeds that of a saturated solution thereof in the solvents selected as vehicles in this invention. It is solubilized in accordance with the invention set forth in U.S. 3,109,773. Theaforementioned barbiturates in the concentrations given, in company with the sympathomimetic amine ingredient, are soluble in the composition and surprisingly do not themselves precipitate nor cause precipitation of the theophylline. In order toillustrate the specificity required of the barbiturate for use in the present compositions, the following experiment is described.
EXAMPLE
Stock solutions as follows were prepared.
______________________________________ Solution No. 1-Syrup base Ingredient: Amount/500 ml. of solution ______________________________________ Theophylline g 5.1 Glyceryl guaiacolate g 3.0 Sucrose g 250.0 Sodium saccharin g 0.5 Sodiumcyclamate g 3.0 70% sorbitol solution ml 25.0 Citric acid g 2.0 Sodium Citrate g 1.5 Distilled water, q.s. ml 400 Solution No.2.-Alcohol solution Methylparaben g 0.6 Propylbaraben g 0.15 Ethyl vanillin g 0.10 Menthol (4% in ethanol) ml 0.08 Grenadine flavor ml 0.04 Ethyl alcohol ml 78.95 Solution No.3.-Ephedrine hydrochloride solution Ephedrine hydrochloride g 0.8 Distilled water q.s. ml 10.0 ______________________________________
The amounts of barbiturates specified in the following list were then weighed and dissolved in a 79 ml. portion of the alcohol solution (Solution No. 2). This was then mixed with 400 ml. of Solution No. 1 and 10 ml. of Solution No. 3 wasadded thereto. The mixture was then diluted to 500 ml. with distilled water. In some instances the ingredients did not dissolve and stability studies were
______________________________________ Con- A- centra- mount tion used per per 15 ml. Barbituric acid 500 ml. elixir derivative (g.) (mg.) Stability result ______________________________________ 5,5-diethyl- 9.9 300 1 (barbital). 5-allyl-5-(2-pentyl)- 3.3 100 1 (secobarbital 5-ethyl-5-isoamyl- 1.65 50 Precipitation occurred (amobarbital). within 1 wk. 5-ethyl-5-n-butyl- 3.3 100 1 (butothal) 5-ethyl-methyl-5- 1.98 60 1 phenyl (mephobarbital). 5-ethyl-5-(2-butyl)- 0.99 30 Solution clear after 4 wks. (butabarbital). storage at room temp. crystallization occurred at 0.degree. C. after 4 wks. 5,5-diallyl 0.99 30 Solution remained clear for 1 wk. but slight crystallization occurred both at room temp. and at0.degree. C. after 4 wks. 5-allyl-5-cyclopent- 3.3 100 Solution remained clear 1-onyl(cyclopal). at room temp. for 4 wks., but light crystalli- zation occurred at 0.degree. C. 5-allyl-5-isobutyl- 6.6 200 1 (itobarbital) 5-allyl-5-isopropyl- 1.98 60 Solution remained clear (aprobarbital). at room temp. for 4 wks. but slight crystalliza- tion occurred at 0.degree. C. after 4 wks., but not after 1 wk. 5-allyl-5-phenyl- 0.6 200 1 (alphenyl). ______________________________________ 1clear solution failed to form on mixing the ingredients, and no stability studies were therefore initiated. not then initiated with suc sample. The solutions which formed satisfactorily were filtered to remove any foreign material, and put aside andstored in paired lots at 0.degree. C. and at room temperature. They were examined after 4 weeks for crystallization.
In the preceding table there are identified the various barbiturates tested, the amounts used, and the dose thereof contained in 15 ml. of the final composition, to which the amount employed corresponds. In each instance this dose is a sedativedose of the barbiturate as specified in either the Merck Index. U.S.P. XVI, NF X or NF XI.
It is apparent from the foregoing that the results obtained with cyclopal, aprobarbital, and butabarbital are truly unexpected in view of the similarity of the chemical structures properties of these substances to closely related barbiturateswhich were found to be unsatisfactory. Refer, for instance, to itobarital, diallylbarbituric acid, secobarbital, barbital, butethal, and the 5-phenyl barbiturates. Pentobarbital at a concentration of 10 mg./15 ml. provided a clear solution of thecomposition given in the foregoing example. This concentration of pentobarbital is slightly less than a sedative dose (the recommended dose is 30-500 mg.) Stable clear solutions having a sedative dose of 15 mg. of pentobarbital per 15 ml. of elixircan, however, be formulated as outlined above.
Attempts were made to formulate elixirs as described in the foregoing example using various concentrations of the barbiturates listed below. They proved to be unsatisfactory for failure to form clear solutions containing effective sedativeamounts in volumes of 5-30 ml. of the elixir.
5-allyl-5-ethylbarbituric acid
5-methyl-5-phenylbarbituric acid
5-cyclohex-1-enyl-1,5-dimethylbarbituric acid (hexobarbital)
5-cyclohex-1-enyl-5-ethylbarbituric acid (cyclobarbital)
5-ethyl-5-phenylbarbituric acid (phenobarbital)
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