Method of preparing gamma globulin suitable for intravenous administration

Claim 1

A method of preparing gamma globulin suitable for intravenous administration, which comprises the steps of: dissolving (a) a gamma globulin composition selected from the group consisting of Cohn Fraction II and Cohn Fraction III, said composition containing aggregates of gamma globulin, in (b) a buffer solution having a pH in the range of 4.0 to 8.0, to obtain a solution; adding to said solution (1) at least 0.1 to 15% of polypropylene glycol having a molecular weight in the range of 2000 to 10,000 and (2) a dispersing agent in an amount effective to disperse said polypropylene glycol in said solution, said dispersing agent being selected from the group consisting of monosaccharides, amino acids, inorganic salts, and mixtures thereof, thereby to obtain a dispersion liquid; and filtering said dispersion liquid to obtain a filtrate containing said gamma globulin suitable for intravenous administration.

Claim 2

A method of preparing gamma globulin suitable for intravenous administration, which comprises the steps of: dissolving (a) a gamma globulin composition selected from the group consisting of Cohn Fraction II and Cohn Fraction III, said composition containing aggregates of gamma globulin, in (b) a buffer solution having a pH in the range of 4.0 to 8.0, to obtain a solution; adding to said solution (1) at least 0.1 to 15% of polypropylene glycol having a molecular weight in the range of 2000 to 10,000 and (2) a dispersing agent in an amount effective to disperse said polypropylene glycol in said solution, said dispersing agent being selected from the group consisting of monosaccharides, amino acids, inorganic salts, and mixtures thereof, thereby to obtain a dispersion liquid; and filtering said dispersion liquid to obtain a filtrate containing said gamma globulin suitable for intravenous administration.

Claim 7

A method of preparing gamma globulin suitable for intravenous administration, which comprises the steps of: dissolving (a) a gamma globulin composition selected from the group consisting of Cohn Fraction II and Cohn Fraction III obtained by Cohn Method 9, and containing aggregates of gamma globulin, in (b) a phosphate buffer solution or an acetate buffer solution having a pH in the range of 4.0 to 8.0, said buffer solution containing 0.1% to 1.0% of a dispersing agent for polypropylene glycol selected from the group consisting of monosaccharides, amino acids, inorganic acids, and mixtures thereof, to thereby obtain a solution; then filtering said solution to obtain a first filtrate containing dissolved gamma globulin; then adding to and mixing in said first filtrate from 0.1 to 15% of polypropylene glycol having molecular weight in the range of 2000 to 10,000 to thereby obtain a dispersion liquid; and then filtering said dispersion liquid to obtain a second filtrate containing said gamma globulin suitable for intravenous administration.

Claim 8

A method of preparing gamma globulin suitable for intravenous administration, which comprises the steps of: dissolving (a) a gamma globulin composition selected from the group consisting of Cohn Fraction II and Cohn Fraction III obtained by Cohn Method 9, and containing aggregates of gamma globulin, in (b) a phosphate buffer solution or an acetate buffer solution having a pH in the range of 4.0 to 8.0, said buffer solution containing 0.1% to 1.0% of a dispersing agent for polypropylene glycol selected from the group consisting of monosaccharides, amino acids, inorganic acids, and mixtures thereof, to thereby obtain a solution; then filtering said solution to obtain a first filtrate containing dissolved gamma globulin; then adding to and mixing in said first filtrate from 0.1 to 15% of polypropylene glycol having molecular weight in the range of 2000 to 10,000 to thereby obtain a dispersion liquid; and then filtering said dispersion liquid to obtain a second filtrate containing said gamma globulin suitable for intravenous administration.