Process for preparing micronized polypeptide drugs
AssigneeSRI International
InventorsRobert M. Platz, Anna Ip, Clyde L. Whitham
Life of this patent
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Abstract
Solid particle aerosol formulations of polypeptide drugs are made by lyophilizing solutions of the drugs which contain milling stabilizers that inhibit degradation of the drug during subsequent milling. The lyophilized drug is milled in fluid energy mills that have been fitted with abrasion-resistant materials and which use pure nitrogen that has been filtered to eliminate particles of greater than 0.1 .mu.m to transport the drug. The use of (a) milling stabilizers in the solution and (b) abrasion-resistant fluid energy mills that use pure filtered nitrogen in the milling step reduce insoluble contaminants and inactive fractions in the milled product.
Claims16
In a process for preparing a micronized polypeptide drug comprising lyophilizing a solution of the drug in a solvent and milling the lyophilized drug in a fluid energy mill using a pressurized gas to form a powder, the improvement comprising using a pure inert gas filtered to remove particles greater than about 0.1 .mu.m and the improvement wherein the parts of the mill that are contacted by the pressurized gas in which the polypeptide drug is being carried are not substantially abraded by said drug-carrying gas whereby the insoluble contaminants in the micronized polypeptide drug comprise less than 2% by weight of the polypeptide drug.
The process of claim i wherein the polypeptide drug is labile under the milling conditions and the lyophilized drug contains a milling stabilizer.
In a process for preparing a micronized polypeptide drug comprising lyophilizing a solution of the drug in a solvent and milling the lyophilized drug in a fluid energy mill using a pressurized gas to form a powder, the improvement comprising using a pure inert gas filtered to remove particles greater than about 0.1 .mu.m and the improvement wherein the parts of the mill that are contacted by the pressurized gas in which the polypeptide drug is being carried are not substantially abraded by said drug-carrying gas whereby at least 85% of the polypeptide drug is in active form.
Dependencies are inferred from the claim text.