Stable, aqueous solution of human erythropoietin, not containing serum albumin
The present invention provides an aqueous formulation of human erythropoietin having the storage stability over a long period without serum albumin, in which the formulation comprises a pharmaceutically effective amount of human erythropoietin; non-ionic surfactant, polyhydric alcohol, neutral amino acid and sugar alcohol as stabilizers; isotonic reagent; and buffering reagent.
1. An aqueous formulation of human erythropoietin, comprising:
the human erythropoietin;
a non-ionic surfactant;
0.001 to 0.1% (w/v) of a polyhydric alcohol;
a neutral amino acid;
0.1 to 1.0% (w/v) of mannitol;
a water-soluble inorganic salt; and
a buffering reagent.
2. The aqueous formulation of human erythropoietin according to claim 1 , wherein said human erythropoietin is native or recombinant erythropoietin.
3. The aqueous formulation of human erythropoietin according to claim 1 , wherein said non-ionic surfactant is a polysorbate-based non-ionic surfactant or poloxamer-based non-ionic surfactant or a combination thereof;
said polyhydric alcohol is one or more selected from the group consisting of propylene glycol, polyethylene glycol of a low molecular weight, glycerol and polypropylene glycol of a low molecular weight;
said neutral amino acid is one or more selected from the group consisting of glycine, alanine, leucine and isoleucine;
said water-soluble inorganic salt is one or more selected from the group consisting of sodium chloride, calcium chloride and sodium sulfate; and
said buffering reagent is one or more selected from the group consisting of a phosphate buffer and citrate buffer.
4. The aqueous formulation of human erythropoietin according to claim 3 , wherein said non-ionic surfactant is a polysorbate 20, said polyhydric alcohol is propylene glycol, said neutral amino acid is glycine, said water-soluble inorganic salt is sodium chloride, and said buffering reagent is the phosphate buffer.
5. The aqueous formulation of human erythropoietin according to claim 1 , wherein the content of non-ionic surfactant is in the range of 0.0001 to 0.01% (w/v).
6. The aqueous formulation of human erythropoietin according to claim 1 , wherein the content of neutral amino acid is in the range of 0.001 to 2% (w/v).
7. The aqueous formulation of human erythropoietin according to claim 1 , wherein the content of said water-soluble inorganic salt is in the range of 0.001 to 0.7% (w/v).
8. The aqueous formulation of human erythropoietin according to claim 1 , wherein the concentration of salt in the buffering reagent is in the range of 1 mM to 50 mM, and pH thereof is in the range of 6.0 to 7.5.
9. The aqueous formulation of human erythropoietin according to claim 1 , wherein the content of erythropoietin is in the range of 100 IU/ml to 120,000 IU/ml.