Process for preparing antrodia camphorata polysaccharide and antrodia camphorata triterpene with micro-prorous adsorptive resin and its product
Antrodia camphorata triterpenes and pore adsorption technology, applied in medical preparations containing active ingredients, adsorption purification/separation, pharmaceutical formulations, etc., can solve the problem of limited research work on the separation and purification of physiologically active substances, complicated steps, and lack of data, etc. question
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Embodiment 1
[0017] Example 1: Separation and Preparation of Antrodia Camphorata Polysaccharides and Antrodia Camphorata Triterpenes Using Nonpolar Macroporous Resin D-101
[0018] The chromatographic column is a glass chromatographic column with an internal diameter of 4 cm and a length of 80 cm, with a built-in D-101 filler (produced by Tianjin Haiguang Chemical Co., Ltd.), a height of 50 cm, and a corresponding filler volume of 628 ml. The water extract of the liquid fermentation product of Antrodia camphorata was prepared to be 100 mg / ml for sample loading, the sample volume was 140 ml, and the flow rate of sample loading and elution was maintained at 5 ml / min. After sample loading, elute with 1900ml of distilled water, collect the eluate, concentrate, add ethanol until the final ethanol concentration reaches 75%, leave it at 4°C for 24 hours, collect the white precipitate, and dry it in vacuum to obtain 2.6g of Antrodia camphorata polysaccharide.
[0019] After washing with water, elu...
Embodiment 2
[0020] Example 2: Separation and preparation of Antrodia camphorata polysaccharides and Antrodia camphorata triterpenoids with medium polarity macroporous resin HPD400
[0021] The chromatographic column is a glass chromatographic column with an internal diameter of 4 cm and a length of 80 cm, with HPD400 packing (produced by Hebei Cangzhou Baoen Chemical Co., Ltd.), high 50 cm, and a corresponding packing volume of 628 ml. The water extract of the liquid fermentation product of Antrodia camphorata was prepared to be 100 mg / ml for sample loading, the sample volume was 140 ml, and the flow rate of sample loading and elution was maintained at 5 ml / min. After sample loading, elute with 1900ml of distilled water, collect the eluate, concentrate, add ethanol until the final ethanol concentration reaches 75%, leave it at 4°C for 24 hours, collect the white precipitate, and dry it in vacuum to obtain 2.5g of Antrodia camphorata polysaccharide.
[0022] After washing with water, elute...
Embodiment 3
[0023] Example 3: Determination methods and results of Antrodia camphorata triterpenoids prepared by D-101 and HPD400 for anti-oxidation and inhibition of liver cancer cells
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