CPC C08B 37/0003 (2013.01) [A61K 31/715 (2013.01); A61K 31/716 (2013.01); A61K 36/488 (2013.01); A61P 3/06 (2018.01); C08B 37/0006 (2013.01); C08B 37/0009 (2013.01)] | 2 Claims |
1. A method of using Radix Puerariae polysaccharide QL to promote lipid-lowering activity in a subject, comprising:
preparing a therapeutically effective dosage of a Radix Puerariae polysaccharide QL;
wherein, the Radix Puerariae polysaccharide QL is a homopolysaccharide composed of one monosaccharide glucose, and has a molecular weight of 10 KDa to 60 KDa, a protein content of 0.64%, no glycuronic acid, and a sugar content of 98.7%;
wherein, an infrared spectrum (IR) of the Radix Puerariae polysaccharide QL shows typical polysaccharide absorption peaks comprising a hydroxyl absorption peak around 3,300 cm−1, and a glycosyl absorption peak around 957 cm−1, but shows no carbonyl absorption peak at 1,700 cm−1, the IR of the Radix Puerariae polysaccharide QL is consistent with a measured glycuronic acid content;
wherein, gas chromatography-mass spectrometry (GC-MS) analysis confirms that the Radix Puerariae polysaccharide QL is composed of glucose, wherein most glucose units are linked through α-1,3-Glu and a small number of glucose units are linked through terminal-Glu; and wherein, an atomic force microscopy (AFM) test shows that a spatial structure of the Radix Puerariae polysaccharide QL has a spherical characteristic; administering the therapeutically effective dosage of a Radix Puerariae polysaccharide QL in vivo to the subject at a dosage between 25 mg/kg and 100 mg/kg.
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