High-yield separation and purification method of prostaglandin E2
A prostaglandin, separation and purification technology, applied in the field of high-yield separation and purification of prostaglandin E2, can solve the problems of failing to meet qualified standards, low sample purity, etc., and achieve the effects of short purification cycle and no pollution cost
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Embodiment 1
[0026] A sample was taken, and the crude prostaglandin E2 was dissolved in an acidic solution with a content of 2 mg / mL. After the solution was clarified, it was filtered through a filter membrane with a pore size of 0.45 μm, and the filtrate was collected for later use. A chromatographic column of 4.6×250 mm was used, and UniSil C18 or C8 microspheres (manufactured by Suzhou Nawei Technology Co., Ltd.) were used as the packing material of the chromatographic column, and the packing volume was 4.2 ml. Pre-column pretreatment was performed on the chromatographic column, and 0.2% acetic acid aqueous solution (phase A) and acetonitrile (phase B) were used as mobile phases for gradient elution, and the flow rate was controlled at 0.7ml / min. The isocratic elution process is as follows: wash with 30% phase B for 72 minutes, collect the solution of the target peak in sections, summarize the components that meet the requirements, and analyze by high performance liquid chromatography. ...
Embodiment 2
[0029] Take a sample, and the crude prostaglandin E2 is dissolved in an acidic aqueous solution with a content of 2 mg / mL. After the solution was clarified, it was filtered with a filter membrane with a pore size of 0.45 μm, and the filtrate was collected for later use. A chromatographic column of DAC50×250mm was used, and UniSilC18 or C8 microspheres (produced by Suzhou Nawei Technology Co., Ltd.) were used as the chromatographic column filler, and the column volume was 490.6ml. Pre-column pretreatment was performed on the chromatographic column, and 0.2% acetic acid aqueous solution (phase A) and acetonitrile (phase B) were used as mobile phases for gradient elution, and the flow rate was controlled at 50 ml / min. The isocratic elution process is as follows: wash with phase B with a content of 30% for 80 minutes, collect the solution of the target peak in sections, summarize the components that meet the requirements, and analyze by high performance liquid chromatography. The ...
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