METHODS FOR PREPARING PURIFIED LIPOTIDES
First Claim
1. A crystalline or crystal-like lipopeptide or a salt thereof, wherein the lipopeptide is selected from the group consisting of daptomycin, A54145 and a daptomycin-related lipopeptide.
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Abstract
The present invention relates to crystalline and crystal-like forms of lipopeptides, including daptomycin, a lipopeptide antibiotic with potent bactericidal activity against gram-positive bacteria, including strains that are resistant to conventional antibiotics. The present invention relates to methods of purifying lipopeptides, including daptomycin, a lipopeptide antibiotic with potent bactericidal activity against gram-positive bacteria, including strains that are resistant to conventional antibiotics. The present invention also relates to pharmaceutical compositions comprising the purified form of the lipopeptide and methods of using these compositions.
74 Citations
78 Claims
- 1. A crystalline or crystal-like lipopeptide or a salt thereof, wherein the lipopeptide is selected from the group consisting of daptomycin, A54145 and a daptomycin-related lipopeptide.
- 21. A pharmaceutical composition comprising a crystalline or crystal-like lipopeptide antibiotic and a pharmaceutically acceptable carrier, wherein the lipopeptide antibiotic is selected from the group consisting of daptomycin, A54145, and a daptomycin-related lipopeptide.
- 29. A formulation comprising a crystalline or crystal-like lipopeptide antibiotic and a pharmaceutically acceptable carrier, wherein the lipopeptide antibiotic is selected from the group consisting of daptomycin, A54145 and a daptomycin-related lipopeptide.
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35-56. -56. (canceled)
- 57. A method for administering a crystalline or crystal-like lipopeptide, a pharmaceutically acceptable salt thereof or a pharmaceutical composition thereof, wherein the lipopeptide is selected from the group consisting of daptomycin, A54145 and a daptomycin-related lipopeptide, comprising the step of administering to a patient in need thereof a therapeutically effective amount of the crystalline or crystal-like lipopeptide, the pharmaceutically acceptable salt thereof or the pharmaceutical composition thereof.
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66. A method for storing a lipopeptide, wherein the lipopeptide is selected from the group consisting of daptomycin, A54145 and a daptomycin-related lipopeptide, comprising the steps of
a) providing a dissolved solution of a lipopeptide; -
b) crystallizing or precipitating the lipopeptide; c) collecting and drying the lipopeptide; and d) storing the lipopeptide; wherein the crystalline or crystal-like lipopeptide is more stable than an amorphous form of the lipopeptide. - View Dependent Claims (68, 69, 75, 76, 77, 78)
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67. A method for manufacturing a crystalline or crystal-like lipopeptide, wherein the lipopeptide is selected from the group consisting of daptomycin, A54145 and a daptomycin-related lipopeptide, comprising the steps of
a) providing an amorphous form of a lipopeptide; -
b) crystallizing or precipitating the lipopeptide; and c) collecting the crystalline or crystal-like lipopeptide. - View Dependent Claims (70, 71, 72, 73, 74)
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Specification