Methods and compositions for stabilizing dried biological materials
View Patent ↗The present invention relates to methods for producing dried formulations of biopharmaceutical agents that aim to minimize the loss of activity of the agents upon drying and to provide dried formulations with an extended shelf life. The method comprises the step of drying an aqueous solution comprising, in addition to the biopharmaceutical agent, at least an amino acid, a polyol and a metal salt. Preferably the amino acid is glutamate, the polyol is sorbitol and optionally also mannitol and the metal salt is a magnesium salt. The solution is dried by vacuum drying or by lyophilization. The methods are particularly useful for preparing dried formulations of viruses such as poliovirus or respiratory syncytial virus to be used for vaccination. The invention also relates to dried formulations prepared in accordance with the methods of the invention and to their use as medicaments, e.g. as vaccines.
1. A method for producing a formulation of a biopharmaceutical agent, comprising drying a solution comprising:
(a) a biopharmaceutical agent comprising poliovirus,
(b) an amino acid selected from the group consisting of glutamate, arginine, histidine, glycine and mixtures thereof,
(c) a polyol comprising sorbitol and/or mannitol, and
(d) at least 0.2% (w/v) of a metal salt and water, wherein the metal salt is Mg 2+ , Ca 2+ , Li + or a mixture thereof.
2. The method according to claim 1 , wherein the solution consists essentially of 1 pg-10 g per ml of the biopharmaceutical agent, 0.01-20% (w/v) of the amino acid, 0.5-20% (w/v) of the polyol, 0.2-10% (w/v) of the metal salt and water.
3. The method according to claim 1 , wherein the glutamate is dissolved in the solution in the form of monosodium glutamate, and/or wherein the arginine is in the form of poly-L-arginine.
4. The method according to claim 3 , wherein the solution consists essentially of 1 pg-10 g per ml of the biopharmaceutical agent, 5-20% (w/v) sorbitol, 5-20% (w/v) monosodium glutamate, 2-10% (w/v) of a magnesium salt, and optionally 5-20% (w/v) mannitol.
5. The method according to claim 1 , wherein the solution comprises a pharmaceutically acceptable buffer and is buffered at a neutral pH.
6. The method according to claim 1 , wherein the drying is by air drying, vacuum drying, spray drying or by lyophilization.
7. The method according to claim 1 , wherein the poliovirus is one or more of poliovirus serotypes 1, 2 or 3.
8. The method according to claim 1 , wherein the poliovirus is inactivated.
9. The method according to claim 1 , wherein the formulation, upon reconstitution in a liquid, retains at least 50% of the activity of the biopharmaceutical agent present in the solution prior to drying.
10. The method according to claim 9 , wherein the formulation comprises at least two different poliovirus serotypes, and wherein the difference in loss of activities for the different agents is less than 50%, whereby the retained activity of the agent with the most loss in activity is expressed as percent of the retained activity of the agent with the least loss, which is set at 100%.
11. The method according to claim 1 , wherein the formulation upon reconstitution after storage for at least one week at 45° C., retains at least 50% of the activity of the biopharmaceutical agent present in the solution prior to drying.
12. The method according to claim 11 , wherein the formulation comprises at least two different poliovirus serotypes, and wherein the difference in loss of activities for the different agents is less than 50%, whereby the retained activity of the agent with the most loss in activity is expressed as percent of the retained activity of the agent with the least loss, which is set at 100%.
13. The method according to claim 4 , wherein the magnesium salt is MgCl 2 and/or MgSO 4 .
14. A method for producing a formulation of a biopharmaceutical agent, comprising drying a solution comprising poliovirus, glutamate, sorbitol, and at least 0.2% (w/v) of Mg 2+ metal salt and water.
15. The method according to claim 14 , wherein the drying is by lyophilisation.
16. The method according to claim 15 , wherein the drying is by vacuum drying.