Sulfonic resins having a therapeutical activity, preparation thereof and pharmaceutical compositions containing them

Claim 2

A new orally administrable pharmaceutical compound consenting delayed release of the therapeutically active component, comprising a cation exchange sulfonic type resin, wherein the acid groups of said resin are partly combined in the form of salts of said therapeutically active component selected from cis(±)-3-acetyloxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one, cis (±)-3-hydroxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one and the optically active isomers thereof.

Claim 3

A pharmaceutical compound according to claim 1, comprising from 30 to 60% by weight of said therapeutically active component, based on the weight of the product.

Claim 4

A compound according to claim 1 or 2, wherein said resin is selected from sulfonated styrene-divinylbenzene copolymers and sulfonated divinylbenzene-crosslinked polystyrenes.

Claim 5

A compound according to claim 3 wherein the resin acid groups that have not been converted to salts of the therapeutically active component are in the form of salts of alkali metals such as sodium or potassium or of alkaline earth metals such as calcium.

Claim 6

A compound according to claim 4 characterized in that the therapeutically active component is cis(+)-3-acetyloxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one and the metal is preferably sodium or potassium.

Claim 7

A compound according to claim 4, wherein the therapeutically active component is cis(+)-3-hydroxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one and the metal is preferably sodium or potassium.

Claim 8

A new orally administrable pharmaceutical compound consenting delayed release of the therapeutically active component, comprising a cation exchange sulfonic type resin, wherein the acid groups of said resin are partly combined in the form of salts of said therapeutically active component selected from cis(±)-3-acetyloxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one, cis(±)-3-hydroxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one and the optically active isomers thereof, said compound comprises water that is buffered by means of a buffered solution to a pH of between 5 and 7.

Claim 9

A new orally administrable pharmaceutical compound consenting delayed release of the therapeutically active component, comprising a cation exchange sulfonic type resin, wherein the acid groups of said resin are partly combined in the form of salts of said therapeutically active component selected from cis(±)-3-acetyloxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one, cis(±)-3-hydroxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one and the optically active isomers thereof, said compound comprises water that is buffered by means of a buffered solution to a pH of between 5 and 7.

Claim 10

A compound according to claim 7, wherein said buffer solution comprises a buffered acid selected from acetic, citric and phosphoric acid.

Claim 11

A compound according to claim 8, wherein said buffer solution comprises sodium-buffered citric acid having a pH of between 6 and 7, said buffered solution representing from 7 to 15% by weight of the whole compound.

Claim 12

A process for the preparation of a new orally administrable pharmaceutical compound consenting delayed release of the therapeutically active component, comprising a cation exchange sulfonic type resin, where in the acid groups of said resin are partly combined in the form of salts of said therapeutically active component selected from cis(±)-3-acetyloxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one, cis(±)-3-hydroxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one and the optically active isomers thereof, wherein the process comprises the following steps: (a) said resin is contacted, in its acid form, with an alcohol-water solution of said therapeutically active component in its free base form, adopting such a ratio of resin to active component that from 10 to 50% of the resin cationic groups become bound in the form of a salt at a temperature of between 20° and 25° C., said alcohol-water solution including water and an alcohol selected from methanol, ethanol and isopropanol in the ratio of one part of water to three parts of the alcohol; (b) the remaining resin acid groups are converted to salt through reaction with an alkali or alkaline earth metal cation salt; (c) the obtained resin is washed with said buffer solution.

Claim 13

A process for the preparation of a new orally administrable pharmaceutical compound consenting delayed release of the therapeutically active component, comprising a cation exchange sulfonic type resin, where in the acid groups of said resin are partly combined in the form of salts of said therapeutically active component selected from cis(±)-3-acetyloxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one, cis(±)-3-hydroxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one and the optically active isomers thereof, wherein the process comprises the following steps: (a) said resin is contacted, in its acid form, with an alcohol-water solution of said therapeutically active component in its free base form, adopting such a ratio of resin to active component that from 10 to 50% of the resin cationic groups become bound in the form of a salt at a temperature of between 20° and 25° C., said alcohol-water solution including water and an alcohol selected from methanol, ethanol and isopropanol in the ratio of one part of water to three parts of the alcohol; (b) the remaining resin acid groups are converted to salt through reaction with an alkali or alkaline earth metal cation salt; (c) the obtained resin is washed with said buffer solution.

Claim 14

A process for the preparation of a pharmaceutical compound according to claim 10, wherein said resin (whose acid groups have been previously converted to the alkali or alkaline earth metal salt form) is contacted with a buffered aqueous solution of the therapeutically active component.

Claim 15

A process for the preparation of a pharmaceutical compound according to claim 10, wherein said resin (the acid groups of which have been converted to the form of salts of cis(+)-3-hydroxy-5-[2-(dimethylamino)ethyl]-2,3-dihydro-2-(4-methoxyphenyl)-1,5-benzothiazepin-4(5H)-one and possibly also salts an alkali or alkaline earth metal) is reacted with acetic acid anhydride at a temperature of between room temperature and 80° C., finally washing the resin with said buffer solution.

Claim 16

A pharmaceutical composition comprising a compound according to claim 7, wherein one or more pharmaceutically acceptable carriers are included therein.

Claim 17

The use of a compound according to claim 7, for the prohylaxis and therapy of acute and chronical coronary insufficiency and of arterial hypertension, wherein said compound is administered in a daily dose of between 1 and 30 mg per kg of body weight.