Nanometering method for improving intestinal absorption of hericium erinaceus polysaccharide
A technology of Hericium erinaceus polysaccharide and intestinal absorption, applied in the field of medicine, can solve the problems of reducing the encapsulation rate, being unfavorable to the formation of small nanoparticles, complex substances in the Hericium erinaceus extract, and achieving the effect of improving the efficacy of the medicine
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Embodiment 1
[0016] A nanometerization method for improving intestinal absorption of Hericium erinaceus polysaccharides, said method comprising the following steps:
[0017] (1) Make a 5wt.% solution of purified Hericium erinaceus polysaccharide and put it in a beaker, then add 5wt.% PEG solution according to the volume ratio of Hericium erinaceus polysaccharide solution: PEG solution is 1:40, magnetic stirrer Stir at 2000 rpm for 10 minutes, let it stand until the bubbles on the surface disappear, and then pre-freeze in a refrigerator at -20°C for 12 hours;
[0018] (2) Freeze the frozen sample in a vacuum freeze dryer for 24 h; wash the freeze-dried powder with dichloromethane, vortex to dissolve the PEG fully, then centrifuge at 12000 rpm for 5 min, remove the supernatant, and add New dichloromethane, repeated 3 times, put into a vacuum oven overnight to obtain dry polysaccharide nanoparticles;
[0019] (3) Dissolve polysaccharide nanoparticles and PLGA in a mixture of dichloromethane ...
Embodiment 2
[0022] 1. Preparation of Chicken Intestinal Epithelial Primary Cells
[0023] Aseptically take intestinal tissue from chicken embryos, wash repeatedly with PBS, remove mesentery, and cut into smaller than 1 mm 3 The tissue blocks were digested with type Ⅰ dispase and type Ⅺ collagenase, and stirred in a 37°C water bath at 80 r / min for 30 min. After the digestion was completed, centrifuge at 1000 r / min for 10 min, add a small amount of DMEM medium to the cell pellet to suspend the cells, centrifuge and wash 3 times, and wash the collected cells with 10% FBS-containing cell culture medium DMEM 12 g / L + 20 μg / L epidermal growth factor+100 mg / L heparin sodium+110mg / L sodium pyruvate+2.5 mg / L insulin+200 mmol / L glutamate+100 U / L penicillin+100 μg / L streptomycin suspension, Planted into glass cell flasks.
[0024] 2. Establishment of Chicken Small Intestinal Epithelial Cell Monolayer Model
[0025] Cells in the logarithmic growth phase were divided into 1 × 10 5 / cm 2 Culture...
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