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Publication numberUS3080287 A
Publication typeGrant
Publication dateMar 5, 1963
Filing dateAug 5, 1957
Priority dateAug 5, 1957
Publication numberUS 3080287 A, US 3080287A, US-A-3080287, US3080287 A, US3080287A
InventorsLewenstein Mozes Juda
Original AssigneeLewenstein Mozes Juda
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Analgesic compositions
US 3080287 A
Abstract  available in
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Claims  available in
Description  (OCR text may contain errors)

United States Patent 3,080,287 ANALGESIC COMPOSITIONS Mozes Juda Lewenstein, 83-75 116th St, Kew Gardens, N.Y. No Drawing. Filed Aug. 5, 1957, Ser. No. 676,392 2 Claims. (Cl. 167-65) This invention relates to analgesic compositions and it has particular relation to compositions in which analgesic compounds of the type described hereinafter are used in combination with a barbituric acid compound of the type disclosed and under the conditions described hereinafter.

Combinations of analgesics with barbituric acid compounds have been suggested previously. The purpose of such combinations was not only to relieve pain, but also to simultaneously calm down nervous patients by the action of thereapeutic doses of the barbituric acid ingredient in the combinations. The use of such doses renders these compositions less suitable for daytime administration to patients who have to attend their work or other activities, since therapeutic doses of most barbiturates tend to induce sleep and make the patients drowsy. Another disadvantage of such compositions is the cumulative effect of repeated therapeutic doses of ba-rbituric acid compounds when the compositions have to be repeatedly administered during a protracted period of time.

The use of mild analgesics, such as aminopyrine or aspirin, in combination with barbiturates has also been suggested, but the results were not encouraging, because it has been found that little additional analgesia was conferred by barbiturates in combination with such mild analgesics, neither were other advantages obtained.

It has now unexpectedly been discovered that improved analgesic effects can be obtained by compositions in which the mild analgesics and the barbituric acid compounds described hereinafter are combined with each other under the conditions of the present invention.

According to the present invention it has been found that by using a therapeutic dose of (a) aspirin (acetyl salicylic acid) in combination with (b) phenacetin (acetophenetidine), (c) caffeine and (d) with a sub-therapeutic dose of a barbituric acid compound, which is rapid on onset and short in duration of its effect, composiitons are obtained in which the analgesic effect of the active ingredients is accelerated, increased and prolonged in comparison with the added effects of the individual ingredients, as well as in comparison with partial combinations, e.g. (a), (c) and (d) or (b), (c) and (d), and which are practically free from undesired side-effects. In other words, this increase and improvement of the effect requires the co-action of the ingredients (a), (b), (c) and (d) and represents a novel and unexpected synergistic effect of these ingredients.

In the use of compositions embodying this invention drowsiness and hangover and other undesirable side-effects occurring in the use of known compositions, are usually not encountered.

Example 1 A mixture is prepared from the following ingredients:

(a) Aspirin grains 3 /2 (11) Phenacetin do 2% (c) Caffeine do (d) Hexobarbital milligrams 50 The above ingredients are incorporated in conventional manner in each table for oral administration.

Example 2 Mixtures are prepared from the ingredients named in 3,080,287 Patented Mar. 5, 1963 the above Example 1, whereby the individual ingredients are used in the following ranges:

Aspirin grains 2- 6 Phenacetin do 1- 4 Caffeine do A- 1 Hexobarbital milligrams 20-60 The resulting mixtures are formed to tablets in conventional manner.

Example 4 In any of the above Examples 1-3, an equal part by weight of thiamylal sodium or three times in weight doses of thiopental can be substituted for the hexobarbital. A mixture of these barbiturates can also be used. Furthermore, instead of the respective barbituric acid a therapeutically applicable salt thereof, e.g. the sodium salt, can be used and instead of caffeine an equivalent amount of a therapeutically applicable caffeine salt, can be used.

According to the present invention the above named in gredients, i.e. aspirin, phenacetin, caffeine are used in the usual therapeutic doses, while a barbituric acid compound which is rapid on onset and short in duration, is used in sub-therapeutic doses. In the above described proportions, due to co-action of these ingredients a substantially increased synergistic analgesic effect results, which cannot be obtained in the absence of ingredients and proportions called for by the present invention. Thus, for example the composition according to the above Example 1 yields a considerably increased analgesic effect in comparison with a similar composition, in which the phenacetin is omitted or substituted by aspirin, or in which the aspirin is omitted or substituted by phenacetin, or in which the conditions called for by the present invention are not observed in other respects.

The term rapid on onset and short in duration is used in the present application to denote barbituric acid compounds, the therapeutic action of which is analogous to that of the compounds described in the above Examples.

The parts mentioned above are parts by weight if not otherwise stated.

What is claimed is:

1. Analgesic compositions containing as active ingredients (a) -390 parts of acetyl salicylic acid; (b) 65-260 parts of acetophenetidine; (0) 16-65 parts of a compound selected from the group consisting of caffeine and therapeutically applicable salts thereof; and at least one compound selected from the group consisting of hexobarbital, thioamylal, thiopental, analogous barbituric acid compounds rapid on onset and short in duration, and therapeutically applicable salts of these compounds, the hexobarbital being used in an amount of 20-60 parts and thioamylal, thiopental and said analogous barbituric acid 3 compounds, being used in amounts equivalent to 20-60 parts of hexobarbital.

2. Analgesic compositions containing as active ingredients (a) aspirin, (b) acetophenetidine, (c) caffeine and (d) hexobarbital, in the proportions of (a) 3 /2 grains (1)) 2% grains (0) /2 grain and (d) 50 milligrams.

References Cited in the file of this patent Goodman et 211.: Pharmacological Basis of Therapeutics, 2nd ed., (1955), Macmillan Co., N.Y., pp 125, 127, 138 and 141.

Friedman et al.: J.A.M.A., vol. 163, No. 13, Mar. 30, 1957, pp. 11114117.

Orkin et al.: Survey of Anesthesiology, October 1957, pp. 460-464.

Batterman: I.A.M.A., vol. 155, No. 11, July 10, 1954, pp. 965-968.

Beecher: J.A.M.A., vol. 158, No. 5, June 4, 1955, pp. 399-401.

J.A.M.A., vol. 165, N0. 9, Nov. 2, 1957, pp. 1172- 1173.

Non-Patent Citations
Reference
1 *None
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3218233 *Jan 24, 1963Nov 16, 1965Lewenstein Mozes JudaAnalgesic compositions
US3274203 *May 31, 1963Sep 20, 1966Du Pont1-carbamyl and thiocarbamyl-3-amino-4-nonsubstituted and substituted pyrazoles
US3277100 *May 31, 1963Oct 4, 1966Du PontNovel substituted pyrazoles
US3320262 *Sep 22, 1964May 16, 1967Lewenstein14 hydroxy morphine and codeine carboxymethyloximes
US3331828 *Sep 30, 1964Jul 18, 1967Merck & Co IncIsolation of gamma-l-glutamyl dipeptides from glutamic acid fermentation broths by ion exchange
US4505862 *Sep 13, 1982Mar 19, 1985Bristol-Myers CompanyDiphenydramine dihydrogencitrate
US4880791 *Jul 14, 1988Nov 14, 1989Hoechst AktiengesellschaftBlood disorders
US5055460 *Apr 26, 1990Oct 8, 1991Mitchell FriedlanderMethod for weight loss
US5972916 *Feb 10, 1998Oct 26, 1999Bristol-Myers Squibb CompanyTreating migraine pain and the cluster of symptoms characteristic of migraine attack, such as nausea, photophobia, phonophobia and functional disabilities
US6642243Jun 14, 2000Nov 4, 2003Ashkan ImanzahraiPseudoephedrine, acetaminophen, and caffeine to alleviate the pain and cluster of symptoms characteristic of migraine attacks such as nausea, photophobia, phonophobia,
Classifications
U.S. Classification514/161, 514/165, 514/164
Cooperative ClassificationA61K31/60
European ClassificationA61K31/60