Purification method of carbetocin
A carbetocin and purification method technology, which is applied in the field of carbetocin purification, can solve the problems of low product purity, single purification method, and low product yield, and achieve the effect of simple operation and obvious cost advantage
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Embodiment 1
[0020] 1. Pretreatment: prepare carbetocin to be purified into water with a concentration of 200-300mg / ml
[0021] The solution was filtered through a microporous membrane with a pore size of 0.45um, and the filtrate was collected.
[0022] Reversed-phase column pretreatment: wash the column with 60% acetonitrile aqueous solution for 6 minutes, and then wash with 5% acetonitrile aqueous solution for 6 minutes.
[0023] Ion-exchange chromatography column pretreatment: Regenerate with NaOH aqueous solution with a concentration of 2mol / L for 6 minutes, then wash with pure water until neutral.
[0024] 2. Separation and purification: Take the filtrate, inject it into the treated chromatographic column for separation and purification, and elute the target
[0025] The peak of the liquid is divided into three sections: front, qualified product, and post-peak. The purity of the pre-peak part is 90%-99.5%, the purity of the qualified product part is greater than 99.5%, and the purity...
Embodiment 2
[0030] 1. Pretreatment: prepare carbetocin to be purified into water with a concentration of 200-300mg / ml
[0031] The solution was filtered through a microporous membrane with a pore size of 0.45um, and the filtrate was collected.
[0032] Reversed-phase column pretreatment: wash the column with 60% acetonitrile aqueous solution for 6 minutes, and then wash with 5% acetonitrile aqueous solution for 6 minutes.
[0033] Ion-exchange chromatography column pretreatment: Regenerate with NaOH aqueous solution with a concentration of 2mol / L for 6 minutes, then wash with pure water until neutral.
[0034] 2. Separation and purification: Take the filtrate, inject it into the treated chromatographic column for separation and purification, and elute the target
[0035] The peak of the liquid is divided into three sections: front, qualified product, and post-peak. The purity of the pre-peak part is 90%-99.5%, the purity of the qualified product part is greater than 99.5%, and the purity...
Embodiment 3
[0040] 1. Pretreatment: prepare carbetocin to be purified into water with a concentration of 200-300mg / ml
[0041] The solution was filtered through a microporous membrane with a pore size of 0.45um, and the filtrate was collected.
[0042] Reversed-phase column pretreatment: wash the column with 60% acetonitrile aqueous solution for 6 minutes, and then wash with 5% acetonitrile aqueous solution for 6 minutes.
[0043] Ion-exchange chromatography column pretreatment: Regenerate with NaOH aqueous solution with a concentration of 2mol / L for 6 minutes, then wash with pure water until neutral.
[0044] 2. Separation and purification: Take the filtrate, inject it into the treated chromatographic column for separation and purification, and elute the target
[0045] The peak of the liquid is divided into three sections: front, qualified product, and post-peak. The purity of the pre-peak part is 90%-99.5%, the purity of the qualified product part is greater than 99.5%, and the purity o...
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