G6 lectin extracted from traditional Chinese medicines and applications thereof in detoxification, pressure stabilization, blood vessel softening and complication resistance
A technology of lectin and traditional Chinese medicine, which is applied to cardiovascular system diseases, medical preparations containing active ingredients, drug combinations, etc., can solve problems such as prone to complications, toxic and side effects cannot be ruled out, achieve high permeability, and improve adjuvant therapy effect, easy absorption effect
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Embodiment 1
[0040] Example 1: Preparation of G6 lectin
[0041] Weigh 50 grams each of Panax notoginseng, Eucommia, Pueraria root, Rehmannia glutinosa, Salvia miltiorrhiza, and kelp dry medicine, grind into 50-mesh fine powder, add 5 times the volume of Tris buffer (50mmol / L Tris-HCl, 1mmol / L MgCl 2 , 1mmol / L CaCl 2 , pH8.0), homogenate, and soak for 12 hours at 4°C. Centrifuge at 3000rpm for 15min at 4°C, and take the supernatant.
[0042] Filter the obtained supernatant by hypertonic agglutination method to filter out protein, starch, pectin, tannin and other macromolecular substances and microorganisms, take the filtrate, and use 50 times the volume of 0.5mol / L PBS with pH 7.4 at 4°C Dialyzed for 24 hours, concentrated and dried to obtain G6 lectin. The obtained protein was quantitatively analyzed, and the result was that 250 mg of G6 lectin protein was obtained from 300 g of Chinese patent medicine powder.
Embodiment 2
[0043] Example 2: Preparation of G6 lectin
[0044] Weigh 100 grams each of Panax notoginseng, Eucommia, Pueraria root, Rehmannia glutinosa, Salvia miltiorrhiza, and kelp dry medicine, grind into 100 mesh fine powder, add 5 times the volume of Tris buffer (50mmol / L Tris-HCl, 1mmol / LMgCl 2 , 1mmol / L CaCl 2 , pH8.0), homogenate, and soak for 12 hours at 4°C. Centrifuge at 3000rpm for 15min at 4°C, and take the supernatant.
[0045] Filter the obtained supernatant by hypertonic agglutination method to filter out protein, starch, pectin, tannin and other macromolecular substances and microorganisms, take the filtrate, and use 50 times the volume of 0.5mol / L PBS with pH 7.4 at 4°C Dialyzed for 24 hours, concentrated and dried to obtain G6 lectin. The obtained protein was quantitatively analyzed, and the result was that 550 mg of G6 lectin protein was obtained from 600 g of Chinese patent medicine powder.
Embodiment 3
[0046] Example 3: Preparation of G6 lectin
[0047] Weigh 70 grams each of Panax notoginseng, Eucommia, Pueraria root, Rehmannia glutinosa, Salvia miltiorrhiza, and kelp dry medicine, grind into 80-mesh fine powder, add 5 times the volume of Tris buffer (50mmol / L Tris-HCl, 1mmol / LMgCl 2 , 1mmol / L CaCl 2 , pH8.0), homogenate, and soak for 12 hours at 4°C. Centrifuge at 3000rpm for 15min at 4°C, and take the supernatant.
[0048] Filter the obtained supernatant by hypertonic agglutination method to filter out protein, starch, pectin, tannin and other macromolecular substances and microorganisms, take the filtrate, and use 50 times the volume of 0.5mol / L PBS with pH 7.4 at 4°C Dialyzed for 24 hours, concentrated and dried to obtain G6 lectin. Quantitative analysis of the obtained protein showed that 370 mg of G6 lectin protein was obtained from 420 g of Chinese patent medicine powder.
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