Prunella vulgaris homogeneous polysaccharide as well as preparation method and application thereof
A technology of Prunella vulgaris and polysaccharides, which is applied in the direction of pharmaceutical formulas, medical preparations containing active ingredients, and plant raw materials, etc. It can solve problems that do not involve polysaccharide molecular weight, purity, and structural analysis, and achieve strong anti-herpes virus activity and high purity , the effect of high polysaccharide content
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0038] Preparation and analysis of embodiment 1 Prunella vulgaris homogeneous polysaccharide PSP-2B
[0039] 1. Preparation
[0040] 【Experimental Materials】
[0041] Prunella vulgaris, heating mantle, condenser tube, round bottom flask, MilliporeLabscale TFF ultrafiltration system, Lambda35 UV spectrophotometer, PerkinElmer SpectrumOne Fourier transform infrared spectrometer, AKTApurifier100 series protein purification instrument, Agilent1100 series high performance gel permeation chromatography, PolarimeterModel341 polarimeter, WatersHClass ultra-high performance liquid chromatography, phenol, carbazole, barium sulfate, gelatin, sulfuric acid, 1-phenyl-3-methyl-5-pyrazolone, etc.
[0042] 【experimental method】
[0043]Decoct 500g of Prunella vulgaris fruit ears for 3 times, add 20 times of water each time, 0.5h each time, pass the water extract through a 0.45μm water membrane microfiltration, collect the filtrate, concentrate the filtrate under reduced pressure at 50°C, an...
Embodiment 2
[0095] Preparation and analysis of embodiment 2 Prunella vulgaris homogeneous polysaccharide B
[0096] Decoct 500g of Prunella vulgaris fruit ears for 3 times, add 20 times of water each time, 0.5h each time, pass the water extract through a 0.45μm water membrane microfiltration, collect the filtrate, concentrate the filtrate under reduced pressure at 50°C, and dilute the concentrated filtrate in turn Pass through ultrafiltration membranes with a molecular weight cut-off of 30KDa and 100KDa, collect the ultrafiltrate with a molecular weight cut-off greater than 30KDa and less than 100KDa, use the Sevag method to remove free protein 7 times, concentrate to saturation, and take the saturated solution and load it on SephadexG-200 dextran Gel column (1.6×100cm), 1.5ml of each sample loaded, the mobile phase is deionized water, the flow rate is 0.4ml / min, collected in separate tubes, 5ml in each tube, the collected solution is detected by the sulfuric acid-phenol method for polysac...
Embodiment 3
[0100] Preparation and analysis of embodiment 3 Prunella vulgaris homogeneous polysaccharide C
[0101] Decoct 500g of Prunella vulgaris fruit ears for 3 times, add 20 times of water each time, 0.5h each time, pass the water extract through a 0.45μm water membrane microfiltration, collect the filtrate, concentrate the filtrate under reduced pressure at 50°C, and dilute the concentrated filtrate in turn Pass through ultrafiltration membranes with a molecular weight cut-off of 30KDa and 100KDa, collect the ultrafiltrate with a molecular weight cut-off greater than 30KDa and less than 100KDa, use the Sevag method to remove free protein 7 times, concentrate to saturation, and take the saturated solution and load it on SephadexG-200 dextran Gel column (1.6×100cm), 2ml of sample loading each time, the mobile phase is deionized water, the flow rate is 0.4ml / min, collected in separate tubes, 5ml in each tube, the collected solution is detected by the sulfuric acid-phenol method for pol...
PUM
| Property | Measurement | Unit |
|---|---|---|
| molecular weight | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 