Application of brown algae oligosaccharide
A fucoid oligosaccharide and fucoidobiose technology, which is applied in the field of biomedicine, can solve the problems of unsuitable treatment of AKI, complicated pathogenesis, etc., and achieve the effects of preventing the transformation of chronic kidney disease, maintaining kidney function, and reducing expression.
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Embodiment 1
[0079] Example 1 Preparation and Structure Identification of Fucobiose with Uniform Polymerization Degree
[0080] Dissolve 100 g of purchased alginate (purchased from Qingdao Mingyue Seaweed Group Co., Ltd.) in water, add fucose lyase (obtained from Ocean University of China) at a certain temperature, and centrifuge in a high-speed centrifuge after a certain period of lysis. Take the supernatant. The supernatant was purified with a gel column to remove a small amount of impurity oligosaccharides, polysaccharides and non-sugar impurities to obtain 60 g of fucobiose sodium salt with a purity of more than 95%. Gained fucobiose sodium salt is detected by high performance liquid chromatography (HPLC, 230nm), and is detected by proton nuclear magnetic spectrum ( 1 HNMR) and high-resolution mass spectrometry (HRMS-ESI) for structure identification.
[0081] HPLC: purity 99.06%, RT=13.6min (see the relevant spectrogram figure 1 );
[0082] 1 HNMR spectrum see figure 2 ;
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Embodiment 2
[0085] Example 2 Preparation and structure identification of fucoidan with uniform polymerization degree
[0086] Dissolve 100 g of purchased alginate in water, add fucose lyase (obtained from Ocean University of China) at a certain temperature, centrifuge in a high-speed centrifuge after a certain period of time, and take the supernatant. The supernatant was purified with a gel column to remove a small amount of impurity oligosaccharides, polysaccharides and non-sugar impurities to obtain 70 g of fucotriose sodium salt with a purity of more than 95%. Gained fucotriose sodium salt is detected by high performance liquid chromatography (HPLC, 230nm), and is detected by proton nuclear magnetic spectrum ( 1 HNMR) and high-resolution mass spectrometry (HRMS-ESI) for structure identification.
[0087] HPLC: 100% purity, RT=17.43min (see the relevant spectrum Figure 4 );
[0088] 1 HNMR spectrum see Figure 5 ;
[0089] HRMS(ESI)m / z:C 18 h 23 o 18 {(M-H) -}, the calculat...
Embodiment 3
[0091] Example 3 Preparation and Structure Identification of Fucotetraose with Uniform Polymerization Degree
[0092] Dissolve 100 g of purchased alginate in water, add fucose lyase (obtained from Ocean University of China) at a certain temperature, centrifuge in a high-speed centrifuge after a certain period of time, and take the supernatant. The supernatant was purified with a gel column to remove a small amount of impurity oligosaccharides, polysaccharides and non-sugar impurities to obtain 55 g of fucotetraose sodium salt with a purity of more than 95%. Gained fucotetraose sodium salt is detected by high performance liquid chromatography (HPLC, 230nm), and is detected by proton nuclear magnetic spectrum ( 1 HNMR) and high-resolution mass spectrometry (HRMS-ESI) for structure identification.
[0093] HPLC: purity 99.71%, RT=18.71min (see the relevant spectrogram Figure 7 );
[0094] 1 HNMR spectrum see Figure 8 ;
[0095] HRMS (ESI) m / z: C 24 h 31 o 24 {(M-H) ...
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