Process for encapsulation of medicaments

Claim 2

A process for preparing encapsulated medicines, characterized by dissolving a gastric-soluble, enteric soluble or semipermeable hydrophobic wall material in at least one organic solvent immiscible with water which has a boiling point of not more than 100°C., a vapor pressure higher than that of water and a dielectric constant of not more than 10, dissolving or dispersing in the resulting solution a water-insoluble or slightly water-soluble medicament, dispersing the resulting solution or dispersion to the form of fine drops into a vehicle consisting of a hydrophilic colloid or a surface active agent in water, and then evaporating the organic solvent.

Claim 3

A process according to claim 1, wherein the organic solvent has a boiling point of 40° to 80°C. and a solubility in water of not more than 10% V/V.

Claim 4

A process according to claim 1, wherein the hydrophobic wall material is a mixture of a non-toxic and gastric soluble, enteric soluble or gastric-enteric soluble high molecular weight synthetic polymer with a non-toxic wax or higher fatty acid or an ester thereof which has a melting point of not less than 50°C.

Claim 5

A process according to claim 1, wherein the medicament used as the core substance in an organic solvent-insoluble medicament having a particle size of not more than 5 microns.

Claim 6

A process according to claim 1, wherein the vehicle is a 0.5 to 20% W/V aqueous hydrophilic colloid solution.

Claim 7

A process according to claim 1, wherein the vehicle is a 0.1 to 1% W/V aqueous anionic surface active agent solution having an HLB of not less than 10.

Claim 8

A process according to claim 1, wherein the vehicle is a mixture of 0.5 to 2% W/V aqueous hydrophilic colloid solution with a 0.05 to 0.5% W/V aqueous anionic surface active agent solution having an HLB of not less than 10.

Claim 9

A process according to claim 1, wherein content of the medicament in microcapsule is not more than 66% W/W; the hydrophobic wall material is used at a concentration of 5 to 10% W/V; the medicament is used in not more than 2 times the amount of hydrophobic wall material; and the vehicle is used in 2 to 5 times the amount of the organic solvent containing the medicament and the hydrophobic wall material.

Claim 10

A process according to claim 1, wherein said hydrophobic wall material is dissolved in a mixture of at least two organic solvents.

Claim 11

A process according to claim 9, wherein the difference between boiling points between the organic solvents is not less than 10°C.

Claim 12

A process according to claim 1, wherein the solution of the hydrophobic wall material in the water-immiscible organic solvent further contains a miscible organic solvent miscible with said vehicle and miscible with said water-immiscible organic solvent, said miscible organic solvent having a boiling point of no more than 100°C.

Claim 13

A process according to claim 11, wherein said solution contains no more than 10% V/V of sad miscible organic solvent.

Claim 14

A process according to clailm 1, wherein said medicament is dissolved in said resulting solution.

Claim 15

A process according to clailm 1, wherein said medicament is dissolved in said resulting solution.

Claim 16

A process according to claim 1, wherein said hydrophobic wall material does not react with said medicament.

Claim 17

A process according to claim 1, wherein said vehicle consists essentially of 0.5 to 20% W/V aqueous hydrophilic colloid solution or 0.1 to 1% W/V aqueous anionic surface active agent solution having an HLB of not less than 10.

Claim 18

A process for preparing water repellent encapsulated medicines, which comprises dissolving a mixture of a polymer selected from the group consisting of cellulose acetate dibutylaminohydroxypropyl ether, polyvinyl acetal diethylamino acetate, 2-methyl-5-vinylpyridine methacrylate-methacrylic acid copolymer, hydroxypropyl methyl cellulose phthalate, ethyl cellulose, cellulose acetate, cellulose propionate, cellulose butyrate, cellulose valerate, cellulose acetate propionate, polyvinyl acetate, polyvinyl formal, polyvinyl butyral, ladder polymer of sesquiphenyl siloxane, polymethyl methacrylate, polycarbonate, polystyrene, polyester, cumarone-indene polymer, polybutadiene, ethylene-vinyl acetate copolymer and vinyl chloride-propylene-vinyl acetate copolymer with a non-toxic wax or a higher fatty acid or an ester thereof having a melting point of not less than 50°C in at least one organic solvent immiscible with water which has a boiling point of not more than 100°C, a vapor pressure higher than that of water and a dielectric constant of not more than 10, dissolving or dispersing in the resulting solution a medicament selected from the group consisting of kitasamycin, acetyl-kitasamycin, spiramycin, acetylspiramycin, estradiol, erythromycin, erythromycin ethyl succinate, cortisone acetate, hydrocortisone acetate, predomisolone acetate, diazepam, triacetyl oleandomycin, chloramphenicol palmitate, phenacetin, progesterone, testosterone propionate, hexobarbital, methyl testosteron, ampicillin trihydrate, chloramphenicol, chlorodiazepoxide, cyclobarbital, strychnine nitrate, dexamethazone, tetracycline, nalidixic acid, barbital, hydrocortisone, predonisolone, bromvalerylurea and folic acid, dispersing the resulting solution or dispersion in the form of fine drops into a vehicle consisting of a hydrophilic colloid or a surface active agent in water, and then evaporating the solvent.

Claim 19

A process for preparing water repellent encapsulated medicines, which comprises dissolving a mixture of a polymer selected from the group consisting of cellulose acetate dibutylaminohydroxypropyl ether, polyvinyl acetal diethylamino acetate, 2-methyl-5-vinylpyridine methacrylate-methacrylic acid copolymer, hydroxypropyl methyl cellulose phthalate, ethyl cellulose, cellulose acetate, cellulose propionate, cellulose butyrate, cellulose valerate, cellulose acetate propionate, polyvinyl acetate, polyvinyl formal, polyvinyl butyral, ladder polymer of sesquiphenyl siloxane, polymethyl methacrylate, polycarbonate, polystyrene, polyester, cumarone-indene polymer, polybutadiene, ethylene-vinyl acetate copolymer and vinyl chloride-propylene-vinyl acetate copolymer with a non-toxic wax or a higher fatty acid or an ester thereof having a melting point of not less than 50°C in at least one organic solvent immiscible with water which has a boiling point of not more than 100°C, a vapor pressure higher than that of water and a dielectric constant of not more than 10, dissolving or dispersing in the resulting solution a medicament selected from the group consisting of kitasamycin, acetyl-kitasamycin, spiramycin, acetylspiramycin, estradiol, erythromycin, erythromycin ethyl succinate, cortisone acetate, hydrocortisone acetate, predomisolone acetate, diazepam, triacetyl oleandomycin, chloramphenicol palmitate, phenacetin, progesterone, testosterone propionate, hexobarbital, methyl testosteron, ampicillin trihydrate, chloramphenicol, chlorodiazepoxide, cyclobarbital, strychnine nitrate, dexamethazone, tetracycline, nalidixic acid, barbital, hydrocortisone, predonisolone, bromvalerylurea and folic acid, dispersing the resulting solution or dispersion in the form of fine drops into a vehicle consisting of a hydrophilic colloid or a surface active agent in water, and then evaporating the solvent.