Molded, storage stable suppository base composition of specified amounts of polyethylene glycol, fatty acid triglyceride and alkylene oxide derivative

Abstract

A suppository base composition comprising 5-80% by weight of polyethylene glycol, 5-80% by weight of triglyceride of fatty acid having 6-22 carbon atoms and 5-80% by weight of a specifically limited alkylene oxide derivative has a melting point of 30.degree.-60.degree. C., a compatibility with both of a polar drug component and a non-polar drug component, and can provide suppositories having excellent moldability and storage stability.

Description

BACKGROUND OF THE INVENTION

(1) Field of the Invention

The present invention relates to a suppository base composition.

(2) Description of the Prior Art

Suppository is smaller than medicine for internal use in the amount of drug component to be decomposed by the action of acid, alkali, digestive enzyme and the like in the digestive fluid, and further does not cause gastroenteric trouble. Particularly, suppository has a merit that can be easily dosed to children. Moreover, when a systemic dosage of a medicine by injection causes serious ill effect, the ill effect can be decreased by a local dosage of a suppository only to the diseased portion, and further the human body can be free from the pain at the injection.

There are mainly used two kinds of suppository bases of polyethylene glycol (hereinafter, abbreviated as PEG) and trigryceride (hereinafter, abbreviated as TG) of fatty acid at present.

Both PEG and TG are excellent suppository bases, but when a suppository is produced by the use of highly hydrophilic PEG, only a highly polar drug component, which dissolves in PEG or disperses uniformly therein, can be used. While, when a suppository is produced by the use of TG, TG is highly lipophilic, and therefore only a non-polar drug component, which dissolves in TG or disperses uniformly therein, can be used. Moreover, PEG and TG have no compatibility with each other, and therefore they cannot be used in admixture, and it is difficult to use a polar drug component in combination with a non-polar drug component.

Further, in the suppository using TG, the suppository is melted by the body temperature to absorb the drug component into the human body. Therefore, the melting point of the suppository is set to a temperature near the body temperature, and the suppository is poor in the strength at high temperature. Therefore, it is necessary to storage the suppository in a cold and dark place in order to prevent the deformation of the shape, and the suppository has a risk of melting during its transportation.

The inventors have made various investigations in order to produce suppository bases free from these drawbacks, and found out that specifically limited alkylene oxide derivative is excellent as a suppository base and is able to mix PEG and TG, and invented a novel suppository base containing these three components.

SUMMARY OF THE INVENTION

The feature of the present invention is to provide a suppository base composition comprising 5-80% by weight of PEG having an average molecular weight of 200-20,000, 5-80% by weight of TG of fatty acid having 6-22 carbon atoms and 5-80% by weight of a compound having the following general formula (1), whose hydroxyl groups may be partly or wholly esterified,

B[(AO).sub.a (C.sub.2 H.sub.4 O).sub.b H].sub.n ( 1) wherein B represents a residue of a compound having 1-8 active hydrogen atoms, A represents C.sub.3 H.sub.6 or C.sub.4 H.sub.8 alone or in admixture, a represents an integer of 15-50, b represents an integer of 20-200, n represents an integer of 1-8, and having an average molecular weight of at least 2,500 per one functional group.

DESCRIPTION OF THE PREFERRED EMBODIMENT

PEGs to be used in the present invention are ones having an average molecular weight of 200-20,000.

TGs of fatty acid having 6-22 carbon atoms to be used in the present invention are TGs of caproic acid, caprilic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, arachic acid, behenic acid and the like. These TGs are used alone or in admixture.

The compounds having the above described general formula (1) are compounds obtained by adding a given amount of alkylene oxide to a compound having 1-8 active hydrogen atoms.

The compounds having 1-8 active hydrogen atoms include methyl alcohol, ethyl alcohol, butyl alcohol, octyl alcohol, lauryl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, oleyl alcohol, isostearyl alcohol, dimeric alcohols formed by a Guerbet process, ethylene glycol, propylene glycol, butylene glycol, hexylene glycol, dodecane diol, hexadecane diol, octadecane diol, glycerine, trimethylolethane, trimethylolpropane, 1,3,5-pentane triol, erythritol, pentaerythritol, diglycerine, triglycerine, dipentaerythritol, sorbitol, sorbitan, sorbide, glucose, fructose, mannose, xylose, methyl glucoside, trehalose, sucrose, ethylenediamine and the like.

The addition amount of alkylene oxides to the above described compound having 1-8 active hydrogen atoms is such that propylene oxide, buthylene oxide or tetrahydrofuran or mixtures thereof is added to the compound in an amount of 15-50 moles per one functional group of the compound and ethylene oxide is added to the compound in an amount of 20-200 moles per one functional group of the compound. Moreover, it is necessary that the resulting addition product having the above described general formula (1) has an average molecular weight of at least 2,500 per one functional group. When the addition amount of the alkylene oxides is smaller than the above described amount, the resulting addition product having the above described general formula (1) can not be able to mix homogeneously PEG and TG. While, when the addition amount exceeds the above described amount, the addition product has excessively high melting point and viscosity and is difficult to be handled in the formulation of a small size suppository. The compound having the general formula (1) has such an excellent property that the compound can solve or disperse more easily than PEG and TG, and that the compound can mix PEG and TG in an optional mixing ratio. The compound having the general formula (1) has a melting point of 10.degree.-70.degree. C., and when PEG and TG to be compounded with the compound are properly selected, suppository base compositions having an optional melting point can be produced.

The suppository base composition of the present invention is a homogeneous mixture consisting of 5-80% by weight, respectively, of the above described three components of PEG, TG and the compound having the general formula (1). When the amount of any one of the above described three components exceeds 80% by weight, the drawbacks of the respective three components appear. While, when the amount of any one of the three components is smaller than 5% by weight, the mixing effect of the three components does not appear. Particularly, when the amount of the compound having the general formula (1) is smaller than 5% by weight, PEG can not be homogeneously mixed with TG, and separates from TG. It is preferable that the ethylene oxide chain of the compound having the general formula (1) occupy 40-90% of the total molecular weight of that compound; and that the compound of general formula (1) have an average molecular weight of 3,000-9,000 per functional group. It is also preferable that the residue B be a residue of alcohol or glycol having 1-22 carbon atoms.

The suppository base composition of the present invention contains both of hydrophilic component and lipophilic component, and therefore the composition can be used as a base for both of polar drug component and non-polar drug component, and suppository base compositions having an optional melting point of 30.degree.-60.degree. C. can be produced. Therefore, the suppository base composition can be widely used, and the resulting suppository is very excellent in the moldability and storage stability.

The suppository base composition of the present invention may contain water, propylene glycol, glycerine, propylene glycol fatty acid ester, sucrose fatty acid ester, sorbitan fatty acid ester, polyoxyethylene alkyl ether, polyoxyethylene polyhydric alcohol fatty acid ester and oil-soluble polyoxyalkylene glycol derivative in order to lower its viscosity at the production, to adjust its melting point, to improve its lubricating property at the insertion of the suppository into the human body and to promote the liberation of drug component.

The following examples are given for the purpose of illustration of this invention and are not intended as limitations thereof. In the examples, "%" means % by weight.

EXAMPLE 1

Suppository base compositions shown in the following Table 2 were prepared by the use of PEG, TG and a compound having the general formula (1) shown in the following Table 1, and a compatibility test of the compositions was carried out.

Test method and evaluation method

Into a beaker of 300 ml capacity is charged 100 g of a sample composition, and stirred at 60.degree. C. until the composition becomes homogeneous. When the composition has become homogeneous, the stirring is stopped, and the beaker is cooled to 20.degree. C. to solidify the composition.

The composition is evaluated according to the following standard.

o . . . homogeneously solidified composition x . . . two or more separated layers or inhomogeneously solidified composition.

The tested compositions and the test results are shown in Table 2.

It can be seen from Table 2 that all the suppository base compositions of the present invention, which are prepared by the use of the compound having the general formula (1), have homogeneously solidified, and has a good compatibility.

TABLE 1______________________________________Compound used in the test______________________________________1. PEG*.sup.5 average molecular weight PEG #300 300 PEG #400 400 PEG #1540 1500 PEG #4000 3000 PEG #6000 90002. TG composition of alkyl groups TG - A C.sub.8 : 85%, C.sub.10 : 15% TG - B C.sub.12 : 50%, C.sub.14 : 23%, C.sub.16 : 14%, C.sub.18 : 13% TG - C C.sub.12 : 42%, C.sub.14 : 18%, C.sub.16 : 17%, C.sub.18 : 23% TG - D C.sub.12 : 68%, C.sub.14 : 10%, C.sub.16 : 11%, C.sub.18 : 11%3. Compound having the general formula (1) C - 1 C.sub.16 H.sub.33 O(C.sub.3 H.sub.6 O).sub.30 (C.sub.2 H.sub.4 O).sub.25 H C - 2 C.sub.18 H.sub.37 O(C.sub.3 H.sub.6 O).sub.30 (C.sub.2 H.sub.4 O).sub.40 H C - 3 C.sub.24 H.sub.49 O(C.sub.3 H.sub.6 O).sub.25 (C.sub.2 H.sub.4 O).sub.50 H C - 4*.sup.1 P[(C.sub.3 H.sub.6 O).sub.17 (C.sub.2 H.sub.4 O).sub.50 H].sub.2 C - 5 P[(C.sub.3 H.sub.6 O).sub.25 (C.sub.2 H.sub.4 O).sub.70 H].sub.2 C - 6 P[(C.sub.3 H.sub.6 O).sub.35 (C.sub.2 H.sub.4 O).sub.100 H].sub.2 C - 7 P[(C.sub.4 H.sub.8 O).sub.2 (C.sub.3 H.sub.6 O).sub.30 (C.sub.2 H.sub.4 O).sub.60 COC.sub.11 H.sub.28 ].sub.2 C - 8*.sup.2 D[(C.sub.3 H.sub.6 O).sub.40 (C.sub.2 H.sub.4 O).sub.120 H].sub.2 C - 9*.sup.3 G[(C.sub.3 H.sub.6 O).sub.30 (C.sub.2 H.sub.40 O).sub.70 H].sub.3 C - 10*.sup.4 S[(C.sub.3 H.sub.6 O).sub.30 (C.sub.2 H.sub.4 O).sub.80 H].sub.64. Other compound D - 1 C.sub.16 H.sub.33 O(C.sub.2 H.sub.4 O).sub.25 H D - 2 C.sub.15 H.sub.37 O(C.sub.3 H.sub.6 O).sub.30 (C.sub.2 H.sub.4 O).sub.3 H D - 3*.sup.1 P[(C.sub.3 H.sub. 6 O).sub.10 (C.sub.2 H.sub.4 O).sub.15 H].sub.2 D - 4 polyoxyethylene(20)-sorbitan monooleate D - 5 polyoxyethylene(70)-pentaerythritol tristearate D - 6 glycerine monostearate D - 7 propylene glycol D - 8 water______________________________________ Note *1: P means propyleneglycol residue *2: means dodecanediol residue *3: means glycerine residue *4: means sorbitol residue *5: PEGs #300, #400, #1540, #4000 and #6000 are Trademarks of PEGs sold b Nippon Oil and Fats Company Ltd. TABLE 2__________________________________________________________________________Results of compatibility test Suppository base composition Compound having the Other Melting Test PEG TG general formula (1) compound point No. Compound % Compound % Compound % Compound % Evaluation (.degree.C.)__________________________________________________________________________Composition 1 #6000 30 TG-B 30 C-1 40 -- -- o 48according to 2 " 30 " 30 C-2 40 -- -- o 52the present 3 " 35 " 35 C-3 30 -- -- o 50invention 4 " 30 " 20 C-4 50 -- -- o 46 5 " 30 " 20 C-5 50 -- -- o 50 6 " 40 " 40 C-6 20 -- -- o 55 7 " 40 " 30 C-7 30 -- -- o 50 8 " 30 " 30 C-8 40 -- -- o 54 9 " 30 " 30 C-9 40 -- -- o 52 10 " 30 " 30 C-10 40 -- -- o 52 11 #400 35 TG-C 35 C-6 30 -- -- o 46 12 #400 35 TG-D 35 C-6 30 -- -- o 46 13 #6000 25 TG-D 5 C-2 70 -- -- o 52 14 #6000 5 TG-D 25 C-5 70 -- -- o 50 #300 20 C-3 29 15 TG-C 30 -- -- o 50 #1540 20 C-6 10 C-2 20 16 #400 30 TG-A 30 -- -- o 43 C-6 20 #400 20 C-2 20 17 TG-D 40 -- -- o 45 #4000 10 C-8 10 #400 20 C-2 20 18 TG-C 35 D-1 5 o 45 #4000 10 C-6 10 #400 30 C-6 20 19 TG-B 7 D-2 8 o 47 #4000 30 C-10 5 #400 5 C-2 5 20 TG-C 68 D-3 2 o 45 #4000 5 C-6 15 21 #1540 35 TG-D 40 C-6 20 D-4 5 o 55 #4000 30 TG-C 25 C-2 20 D-5 10 22 C-6 15 23 #4000 30 TG-C 30 C-6 35 D-6 5 o 52 24 " 30 " 30 " 35 D-7 5 o 48 25 " 30 " 30 " 35 D-8 5 o 46Comparative 26 #6000 25 TG-B 25 -- -- D-1 50 x --composition 27 " " " " -- -- 2 " x -- 28 " " " " -- -- 3 " x -- 29 " " " " -- -- 4 " x -- 30 " " " " -- -- 5 " x -- 31 #6000 15 TG-B 15 -- -- D-1 70 x -- 32 " " " " -- -- 2 " x -- 33 " " " " -- -- 3 " x -- 34 " " " " -- -- 4 " x -- 35 " " " " -- -- 5 " x --__________________________________________________________________________

EXAMPLE 2

A mixture of 5 g of a drug component and 75 g of a suppository base composition shown in the following Table 3 was melted at 70.degree. C. The melted mixture, after fully stirred, was filled in a container pack of 2.5 g capacity for suppository. The storage stability of the resulting suppositories was measured after the suppositories were kept at 5.degree. C., 20.degree. C. or 35.degree. C. for 2 weeks; or kept at 5.degree. C. and at 40.degree. C. on alternate days for two weeks, and was evaluated according to the following standard.

o . . . Original homogeneous state was maintained. x . . . Crystals of drug component grew, and the suppository became inhomogeneous. xx . . . Almost all the drug component was separated.

The following Table 3 shows the results of the test.

It can be seen from Table 3 that the suppository of the present invention maintains always homogeneous state within the temperature range of 5.degree.-70.degree. C. and has a good storage stability.

TABLE 3__________________________________________________________________________Storage stability test for suppository 70.degree. C. (at the 5.degree. C. and 40.degree. C. onDrug component Base composition formulation) 5.degree. C. 20.degree. C. 35.degree. C. alternate days__________________________________________________________________________Indomethacin * No. 11 composition homogeneous o o o o in Table 2 transparent liquid * No. 18 composition homogeneous o o o o in Table 2 transparent liquid PEG #1540 75% homogeneous x x x x PEG #4000 25% transparent liquid TG-B 50% substantially o o x xx TG-C 50% homogeneous dispersionAcetylsalicylic * No. 12 composition homogeneous o o o oacid in Table 2 transparent liquid * No. 20 composition homogeneous o o o o in Table 2 transparent liquid PEG #400 10% homogeneous x o o o PEG #4000 90% transparent liquid TG-B 40% substantially o o o xx TG-D 60% homogeneous dispersionErgosterol * No. 6 composition homogeneous o o o o in Table 2 transparent liquid * No. 16 composition homogeneous o o o o in Table 2 transparent liquid REG #1540 80% substantially x x o o REG #6000 20% homogeneous transparent liquid TG-C 50% substantially o o x xx TG-D 50% homogeneous dispersion__________________________________________________________________________ Note: Among the base compositions, indicated by the mark * are those according to the present invention, and base compositions having no mark are comparative compositions.

Claims

1. A molded, storage-stable suppository, stable in a temperature range of from 5.degree. C. to 70.degree. C., comprising a composition which is:

about 40% by weight of a polyethylene glycol having an average molecular weight of about 9000;

about 40% by weight of triglycerides of fatty acids comprising alkyl groups which are about 50% by weight of C12, 23 by weight of C14, 14% by weight of C16 and 13% by weight of C18 alkyl groups; and

about 20% by weight of Y((C.sub.3 H.sub.6 O).sub.35 (C.sub.2 H.sub.4 O).sub.100 H).sub.2 wherein Y is propylene glycol residue.

2. A molded, storage-stable suppository, stable in a temperature range of from 5.degree. C. to 70.degree. C., comprising a composition which is:

about 35% by weight of a polyethylene glycol having an average molecular weight of about 4000;

about 35% by weight of triglycerides of fatty acids comprising alkyl groups which are about 42% by weight of C12, 18% by weight of C14, 17% by weight of C16 and 23% by weight of C18 alkyl groups; and

about 30% by weight of Y(C.sub.3 H.sub.6 O).sub.36 (C.sub.2 H.sub.4).sub.100 H).sub.2 wherein Y is propylene glycol residue.

3. A molded, storage-stable suppository, stable in a temperature range of from 5.degree. C. to 70.degree. C., comprising a composition which is:

about 35% by weight of a polyethylene glycol having an average molecular weight of about 4000;

about 35% by weight of triglycerides of fatty acids comprising alkyl groups which are about 68% by weight of C12, 10% by weight of C14, 11% by weight of C16 and 11% by weight of C18 alkyl groups; and

about 30% by weight of Y ((C.sub.3 H.sub.6 O).sub.35 (C.sub.2 H.sub.4 O).sub.100 H).sub.2 wherein Y is propylene glycol residue.

4. A molded, storage-stable suppository, stable in a temperature range of from 5.degree. C. to 70.degree. C., comprising a composition which is:

about 30% by weight of a polyethylene glycol having an average molecular weight of about 400;

about 30% by weight of triglycerides of fatty acids comprising of alkyl groups which are about 85% by weight of C8 and 15% by weight of C10 alkyl groups;

about 20% by weight of C.sub.18 H.sub.37 O (C.sub.3 H.sub.6 O).sub.30 (C.sub.2 H.sub.4 O).sub.40 ; and

about 20% by weight of Y ((C.sub.3 H.sub.6 O).sub.35 (C.sub.2 H.sub.4 O).sub.100 H).sub.2 wherein Y is propylene glycol residue.

5. A molded, storage-stable suppository, stable in a temperature range of from 5.degree. C. to 70.degree. C., comprising a composition which is:

about 20% by weight of a polyethylene glycol having an average molecular weight of about 400;

about 10.degree. C. by weight of a polyethylene glycol having an average molecular weight of 3000;

about 35% by weight of triglycerides of fatty acids comprising alkyl groups which are about 42% by weight of C12, 18% by weight of C14, 17% by weight of C16 and 23% by weight of C18 alkyl groups;

about 20% by weight of C.sub.18 H.sub.37 O (C.sub.3 H.sub.6 O).sub.30 (C.sub.2 H.sub.4 O).sub.40 H;

about 10% by weight of Y ((C.sub.3 H.sub.6 O).sub.35 (C.sub.2 H.sub.4 O).sub.100 H).sub.2 wherein Y is propylene glycol residue and

about 5% by weight of C.sub.16 H.sub.3 O (C.sub.2 H.sub.4 O).sub.25 H.

6. A molded, storage-stable suppository, stable in a temperature range of from 5.degree. C. to 70.degree. C., comprising a composition which is:

about 5% by weight of a polyethylene glycol having an average molecular weight of about 400;

about 5% by weight of a polyethylene glocol having an average molecular weight of about 3000;

about 68% by weight of tryglycerides of fatty acids comprising alkyl groups which are about 42% by weight of C12, 18% by weight of C14, 17% by weight of C16 and 23% by weight of C18 alkyl groups;

about 5% by weight of C.sub.18 H.sub.37 O (C.sub.3 H.sub.6 O).sub.30 (C.sub.2 H.sub.4 O).sub.40 H;

about 15% by weight of Y ((C.sub.3 H.sub.6 O).sub.35 (C.sub.2 H.sub.4 O).sub.100 H).sub.2 wherein Y is propylene glycol residue; and

about 2% by weight of Y ((C.sub.3 H.sub.6 O).sub.10 (C.sub.2 H.sub.4 O).sub.15 H).sub.2, wherein Y is propylene glycol residue.