Method for stabilizing Tumor Necrosis Factor and a stable aqueous solution or powder containing the same

Claim 3

A method according to claim 1, wherein said stabilizing agent is a nonionic surfactant.

Claim 4

A method according to claim 2, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 5

A method according to claim 2, wherein said nonionic surfactant is added in an amount of about 1 μg to 1 mg per ml of the aqueous solution containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml.

Claim 6

A method according to claim 4, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 7

A method according to claim 4, wherein the amount of said nonionic surfactant is about 5 μg to 100 μg per ml.

Claim 8

A method according to claim 6, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 9

A method according to claim 2, wherein said nonionic surfactant has an HLB value of 9 to 20.

Claim 10

A method according to claim 8, wherein said nonionic surfactant is added in an amount of about 1 μg to 1 mg per ml of the aqueous solution containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml.

Claim 11

A method according to claim 9, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 12

A method according to claim 9, wherein the amount of said nonionic surfactant is about 5 μg to 100 μg per ml.

Claim 13

A method according to claim 11, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 14

A method according to claim 2, wherein said nonionic surfactant has an HLB value of 13 to 18.

Claim 15

A method according to claim 13, wherein said nonionic surfactant is added in an amount of about 1 μg to 1 mg per ml of the aqueous solution containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml.

Claim 16

A method according to claim 14, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 17

A method according to claim 14, wherein the amount of said nonionic surfactant is about 5 μg to 100 μg per ml.

Claim 18

A method according to claim 16, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 19

A method according to claim 2, wherein said nonionic surfactant is selected from a polyoxyethylene fatty acid ester, a polyoxyethylene alkyl ether, a polyoxyethylene alkylphenyl ether, a polyoxyethylene sorbitan fatty acid ester, a polyoxyethylene glycerin fatty acid ester, a polyoxyethylene hydrogenated castor oil, a polyoxyethylene castor oil, a polyoxyethylene polyoxypropylene alkyl ether, a polyoxyethylene polyoxypropylene block polymer, a sorbitan fatty acid ester, a sucrose fatty acid ester, a glycerin fatty acid ester and mixtures thereof.

Claim 20

A method according to claim 18, wherein said nonionic surfactant is added in an amount of about 1 μg to 1 mg per ml of the aqueous solution containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml.

Claim 21

A method according to claim 19, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 22

A method according to claim 19, wherein the amount of said nonionic surfactant is about 5 μg to 100 μg per ml.

Claim 23

A method according to claim 21, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 24

A method according to claim 2, wherein said nonionic surfactant is selected from a polyoxyethylene fatty acid ester having a saturated or unsaturated fatty acid residue with 8 to 20 carbon atoms in which the number of moles of added ethylene oxide is about 4 to 50, a polyoxyethylene alkyl ether having a saturated or unsaturated alkyl group with 8 to 20 carbon atoms in which the number of moles of added ethylene oxide is about 5 to 55, a polyoxyethylene alkylphenyl ether having a saturated or unsaturated alkyl group with 5 to 10 carbon atoms in which the number of moles of added ethylene oxide is about 5 to 55, a polyoxyethylene sorbitan fatty acid ester having a saturated or unsaturated fatty acid residue with 8 to 20 carbon atoms in which the number of moles of added ethylene oxide is about 5 to 50, a polyoxyethylene glycerin fatty acid ester having a saturated or unsaturated fatty acid residue with 8 to 20 carbon atoms in which the number of moles of added ethylene oxide is about 5 to 50, a polyoxyethylene hydrogenated castor oil or polyoxyethylene castor oil in which the number of moles of added ethylene oxide is about 20 to 150, a polyoxyethylene polyoxypropylene alkyl ether having a saturated or unsaturated alkyl group with 12 to 18 carbon atoms and having an ethylene oxide content of about 65 to 85% by weight, a polyoxyethylene polyoxypropylene block polymer having a number average molecular weight of about 3,000 to 15,000 and having an ethylene oxide content of about 65 to 85% by weight, a sorbitan fatty acid ester which is a mono- or sesqui-acid ester of sorbitan with a saturated or unsaturated fatty acid having 8 to 20 carbon atoms, a sucrose fatty acid ester or glycerin fatty acid ester which is mono-acid ester of sucrose or glycerin with a saturated or unsaturated fatty acid having 8 to 20 carbon atoms, and mixtures thereof.

Claim 25

A method according to claim 23, wherein said nonionic surfactant is added in an amount of about 1 μg to 1 mg per ml of the aqueous solution containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml.

Claim 26

A method according to claim 24, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 27

A method according to claim 24, wherein the amount of said nonionic surfactant is about 5 μg to 100 μg per ml.

Claim 28

A method according to claim 26, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 29

A method according to claim 23, wherein said nonionic surfactant is selected from a polyoxyethylene sorbitan fatty acid having a saturated or unsaturated fatty acid residue with 8 to 20 carbon atoms in which the number of moles of added ethylene oxide is about 5 to 50, a polyoxyethylene hydrogenated castor oil in which the number of moles of added ethylene oxide is about 20 to 150, a polyoxyethylene castor oil in which the number of moles of added ethylene oxide is about 20 to 150, a polyoxyethylene polyoxypropylene block a average molecular weight of about 3,000 to 15,000 and having an ethylene oxide content of about 65 to 85% by weight, and mixtures thereof.

Claim 30

A method according to claim 28, wherein said nonionic surfactant is added in an amount of about 1 μg to 1 mg per ml of the aqueous solution containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml.

Claim 31

A method according to claim 29, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 32

A method according to claim 29, wherein the amoung of said nonionic surfactant is about 5 μg to 100 μg per ml.

Claim 33

A method according to claim 31, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 34

A method according to claim 28, wherein said nonionic surfactant is selected from polyoxyethylene (20) sorbitan monooleate, polyoxyethylene (60) hydrogenated castor oil, polyoxyethylene polyoxypropylene block polymer having a number average melecular weight of about 8,350 and having an ethylene oxide content of 80% by weight, and mixtures thereof.

Claim 35

A method according to claim 33, wherein said nonionic surfactant is added in an amount of about 1 μg to 1 mg per ml of the aqueous solution containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml.

Claim 36

A method according to claim 34, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 37

A method according to claim 34, wherein the amount of said nonionic surfactant is about 5 μg to 100 μg per ml.

Claim 38

A method according to claim 36, which further comprises subjecting to lyophilization the aqueous solution having said nonionic surfactant added thereto.

Claim 39

A method according to claim 1, wherein said stabilizing agent is at least one substance selected from the group consisting of D-glucose, D-galactose, D-xylose, D-glucuronic acid, a salt of D-glucuronic acid, trehalose, a dextran and a hydroxyethyl starch.

Claim 40

A method according to claim 38, which further comprises subjecting to lyophilization the aqueous solution having said substance added thereto.

Claim 41

A method according to claim 38, wherein said substance is added in an amount of about 10 mg to 500 mg per ml of the aqueous solution containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml.

Claim 42

A method according to claim 40, which further comprises subjecting to lyophilization the aqueous solution having said substance added thereto.

Claim 43

A method according to claim 40, wherein the amount of said substance is about 100 mg to 500 mg per ml.

Claim 44

A method according to claim 42, which further comprises subjecting to lyophilization the aqueous solution having said substance added thereto.

Claim 45

A method according to claim 38, wherein said substance is trehalose.

Claim 46

A method according to claim 44, wherein said substance is added in an amount of about 10 mg to 500 mg per ml of the aqueous solution containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml.

Claim 47

A method according to claim 45, which further comprises subjecting to lyophilization the aqueous solution having said substance added thereto.

Claim 48

A method according to claim 45, wherein the amount of said substance is about 100 mg to 500 mg per ml.

Claim 49

A method according to claim 47, which further comprises subjecting to lyophilization the aqueous solution having said substance added thereto.

Claim 50

A stable aqueous solution or powder which contains Tumor Necrosis Factor and an effective amount of a stabilizing agent selected from a nonionic surfactant, at least one substance selected from the group consisting of D-glucose, D-galactose, D-xylose, D-glucuronic acid, a salt of D-glucuronic acid, trehalose, a dextran and a hydroxyethyl starch, and mixtures thereof.

Claim 51

A stable aqueous solution or powder which contains Tumor Necrosis Factor and an effective amount of a stabilizing agent selected from a nonionic surfactant, at least one substance selected from the group consisting of D-glucose, D-galactose, D-xylose, D-glucuronic acid, a salt of D-glucuronic acid, trehalose, a dextran and a hydroxyethyl starch, and mixtures thereof.

Claim 52

A stable aqueous solution or powder according to claim 49, wherein said stabilizing agent is a nonionic surfactant.

Claim 53

A stable aqueous solution or powder according to claim 50, wherein said nonionic surfactant is contained in an amount of about 1 μg to 1 mg per ml of the aqueous solution itself containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml, or is contained in an amount of about 1 μg to 1 mg per ml of an aqueous solution having a TNF activity of 10 2 to 10 9 units/ml which solution is one obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 54

A stable aqueous solution or powder according to claim 51, wherein the amount of said nonionic surfactant is about 5 μg to 100 μg per ml of the aqueous solution itself containing Tumor Necrosis Factor or an aqueous solution obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 55

A stable aqueous solution or powder according to claim 50, wherein said nonionic surfactant has an HLB value of 9 to 20.

Claim 56

A stable aqueous solution or powder according to claim 53, wherein said nonionic surfactant is contained in an amount of about 1 μg to 1 mg per ml of the aqueous solution itself containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml, or is contained in an amount of about 1 μg to 1 mg per ml of an aqueous solution having a TNF activity of 10 2 to 10 9 units/ml which solution is one obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 57

A stable aqueous solution or powder according to claim 54, wherein the amount of said nonionic surfactant is about 5 μg to 100 μg per ml of the aqueous solution itself containing Tumor Necrosis Factor or an aqueous solution obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 58

A stable aqueous solution or powder according to claim 50, wherein said nonionic surfactant has an HLB value of 13 to 18.

Claim 59

A stable aqueous solution or powder according to claim 56, wherein said nonionic surfactant is contained in an amount of about 1 μg to 1 mg per ml of the aqueous solution itself containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml, or is contained in an amount of about 1 μg to 1 mg per ml of an aqueous solution having a TNF activity of 10 2 to 10 9 units/ml which solution is one obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 60

A stable aqueous solution or powder according to claim 57, wherein the amount of said nonionic surfactant is about 5 μg to 100 μg per ml of the aqueous solution itself containing Tumor Necrosis Factor or an aqueous solution obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 61

A stable aqueous solution or powder according to claim 50, wherein said nonionic surfactant is selected from a polyoxyethylene fatty acid ester, a polyoxyethylene alkyl ether, a polyoxyethylene alkylphenyl ether, a polyoxyethylene sorbitan fatty acid ester, a polyoxyethylene glycerin fatty acid ester, a polyoxyethylene hydrogenated castor oil, a polyoxyethylene castor oil, a polyoxyethylene polyoxypropylene alkyl ether, a polyoxyethylene polyoxypropylene block polymer, a sorbitan fatty acid ester, a sucrose fatty acid ester, a glycerin fatty acid ester, and mixtures thereof.

Claim 62

A stable aqueous solution or powder according to claim 59, wherein said nonionic surfactant is contained in an amount of about 1 μg to 1 mg per ml of the aqueous solution itself containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml, or is contained in an amount of about 1 μg to 1 mg per ml of an aqueous solution having a TNF activity of 10 2 to 10 9 units/ml which solution is one obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 63

A stable aqueous solution or powder according to claim 60, wherein the amount of said nonionic surfactant is about 5 μg to 100 μg per ml of the aqueous solution itself containing Tumor Necrosis Factor or an aqueous solution obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 64

A stable aqueous solution or powder according to claim 50, wherein said nonionic surfactant is selected from a polyoxyethylene fatty acid ester having a saturated or unsaturated fatty acid residue with 8 to 20 carbon atoms in which the number of moles of added ethylene oxide is about 4 to 50, a polyoxyethylene alkyl ether having a saturated alkyl group with 8 to 20 carbon atoms in which the number of moles of added ethylene oxide is about 5 to 55, a polyoxyethylene alkylphenyl ether having a saturated or unsaturated alkyl group with 5 to 10 carbon atoms in which the number of moles of added ethylene oxide is about 5 to 55, a polyoxyethylene sorbitan fatty acid ester having a saturated or unsaturated fatty acid residue with 8 to 20 carbon atoms in which the number of moles of added ethylene oxide is about 5 to 50, a polyoxyethylene glycerin fatty acid ester having a saturated or unsaturated fatty acid residue with 8 to 20 carbon atoms in which the number of moles of added ethylene oxide is about 5 to 50, a polyoxyethylene hydrogenated castor oil or polyoxyethylene castor oil in which the number of moles of added ethylene oxide is about 20 to 150, a polyoxyethylene polyoxypropylene alkyl ether having a saturated or unsaturated alkyl group with 12 to 18 carbon atoms and having an ethylene oxide content of about 65 to 85% by weight, a polyoxyethylene polyoxypropylene block polymer having a number average molecular weight of about 3,000 to 15,000 and having an ethylene oxide content of about 65 to 85% by weight, a sorbitan fatty acid ester which is a mono- or sesquiacid ester of sorbitan with a saturated or unsaturated fatty acid having 8 to 20 carbon atoms, a sucrose fatty acid ester or glycerin fatty acid ester which is a mono-acid ester of sucrose or glycerin with a saturated or unsaturated fatty acid having 8 to 20 carbon atoms, and mixtures thereof.

Claim 65

A stable aqueous solution or powder according to claim 62, wherein said nonionic surfactant is contained in an amount of about 1 μg to 1 mg per ml of the aqueous solution itself containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml, or is contained in an amount of about 1 μg to 1 mg per ml of an aqueous solution having a TNF activity of 10 2 to 10 9 units/ml which solution is one obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 66

A stable aqueous solution or powder according to claim 63, wherein the amount of said nonionic surfactant is about 5 μg to 100 μg per ml of the aqueous solution itself containing Tumor Necrosis Factor or an aqueous solution obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 67

A stable aqueous solution or powder according to claim 62, wherein said nonionic surfactant is selected from a polyoxyethylene sorbitan fatty acid ester having a saturated or unsaturated fatty acid residue with 8 to 20 carbon atoms in which the number of moles of added ethylene oxide is about 5 to 50, a polyoxyethylene hydrogenated castor oil in which the number of moles of added ethylene oxide is about 20 to 150, a polyoxyethylene castor oil in which the number of moles of added ethylene oxide is about 20 to 150, a polyoxyethylene polyoxypropylene block polymer having a number average molecular weight of about 3,000 to 15,000 and having an ethylene oxide content of about 65 to 85% by weight, and mixtures thereof.

Claim 68

A stable aqueous solution or powder according to claim 65, wherein said nonionic surfactant is contained in an amount of about 1 μg to 1 mg per ml of the aqueous solution itself containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml, or is contained in an amount of about 1 μg to 1 mg per ml of an aqueous solution having a TNF activity of 10 2 to 10 9 units/ml which solution is one obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 69

A stable aqueous solution or powder according to claim 66, wherein the amount of said nonionic surfactant is about 5 μg to 100 μg per ml of the aqueous solution itself containing Tumor Necrosis Factor or an aqueous solution obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 70

A stable aqueous solution or powder according to claim 65, wherein said nonionic surfactant is selected from polyoxyethylene (20) sorbitan monooleate, polyoxyethylene (60) hydrogenated castor oil, polyoxyethylene polyoxypropylene block polymer having a number average molecular weight of about 8,350 and having an ethylene oxide content of 80% by weight, and mixtures thereof.

Claim 71

A stable aqueous solution or powder according to claim 68, wherein said nonionic surfactant is contained in an amount of about 1 μg to 1 mg per ml of the aqueous solution itself containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml, or is contained in an amount of about 1 μg to 1 mg per ml of an aqueous solution having a TNF activity of 10 2 to 10 9 units/ml which solution is one obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 72

A stable aqueous solution or powder according to claim 69, wherein the amount of said nonionic surfactant is about 5 μg to 100 μg per ml of the aqueous solution itself containing Tumor Necrosis Factor or an aqueous solution obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 73

A stable aqueous solution or powder according to claim 49, wherein said stabilizing agent is at least one substance selected from the group consisting of D-glucose, D-galactose, D-xylose, D-glucuronic acid, a salt of D-glucuronic acid, trehalose, a dextran and a hydroxyethyl starch.

Claim 74

A stable aqueous solution or powder according to claim 71, wherein said substance is contained in an amount of about 10 mg to 500 mg per ml of the aqueous solution itself containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml, or is contained in an amount of about 10 mg to 500 mg per ml of an aqueous solution having a TNF activity of 10 2 to 10 9 units/ml which solution is one obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 75

A stable aqueous solution or powder according to claim 72, wherein the amount of said substance is about 100 mg to 500 mg per ml of the aqueous solution itself containing Tumor Necrosis Factor or an aqueous solution obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 76

A stable aqueous solution or powder according to claim 71, wherein said substance is trehalose.

Claim 77

A stable aqueous solution or powder according to claim 74, wherein said substance is contained in an amount of about 10 mg to 500 mg per ml of the aqueous solution itself containing Tumor Necrosis Factor, said aqueous solution having a TNF activity of 10 2 to 10 9 units/ml, or is contained in an amount of about 10 mg to 500 mg per ml of an aqueous solution having a TNF activity of 10 2 to 10 9 units/ml which solution is one obtained by dissolving the powder containing Tumor Necrosis Factor.

Claim 78

A stable aqueous solution or powder according to claim 75, wherein the amount of said substance is about 100 mg to 500 mg per ml of the aqueous solution itself containing Tumor Necrosis Factor or an aqueous solution obtained by dissolving the powder containing Tumor Necrosis Factor.