Application of chitosan oligosaccharide in preparation of medicaments for preventing and/or treating neurodegenerative diseases
A neurodegenerative and chitosan oligosaccharide technology, applied in the fields of nervous system diseases, neuromuscular system diseases, antipyretics, etc., can solve the problems such as the anti-neurodegenerative disease effect of chitosan oligosaccharide, inflammatory reaction damage, etc. To achieve the effect of improving immunity, lowering blood sugar, and good biocompatibility
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Embodiment 1
[0032] Oligochitosan is administered in the form of an aqueous preparation, and the specific operation of the liquid preparation is as follows: (1) accurately take by weighing 10.0 mg oligochitosan, be dissolved in 10 ml of IMDM medium (V / V) containing 10% fetal bovine serum, The formation of oligochitosan with a final concentration of 1 mg / ml; (2) filter the aforementioned medicinal liquid with a needle filter with a pore size of 0.22 μm to obtain a sterile oligochitosan stock solution; (3) divide the above-mentioned stock solution into After loading, they were stored at -80°C and used in the following examples.
Embodiment 2
[0034] Analysis of iNOS transcriptional repression by oligochitosan on LPS-induced N9 microglia. The main operations are as follows: (1) The experiment is divided into 5 groups, which are normal cell control group (Control), lipopolysaccharide model group (LPS), chitooligosaccharide pre-protection treatment group 1 (50 μg / ml), chitooligosaccharide pre-protection group 1 Protection treatment group 2 (100 μg / ml), chitooligosaccharide pre-protection treatment group 3 (200 μg / ml). (2) The cultured N9 microglial cells were digested with trypsin (0.125%), and then 5×10 4 Inoculate in a 6-well plate at a density of / ml, add 3ml of IMDM culture solution to each well, and store at 37°C, 5% CO 2 cultured in an incubator for 24 h. (3) Take out the 6-well plate, discard the supernatant, add 3ml of fresh IMDM medium to the control and LPS groups, respectively, and add 50, 100 and 200 μg / ml chitosan oligosaccharides to the IMDM culture in the chitosan oligosaccharide pre-protection group ...
Embodiment 3
[0037] Analysis of protein expression inhibition of iNOS by oligochitosan in N9 microglial cells. The main operations are as follows: (1) The experiment is divided into 5 groups, which are normal cell control group (Control), lipopolysaccharide model group (LPS), chitooligosaccharide pre-protection treatment group 1 (50 μg / ml), chitooligosaccharide pre-protection group 1 Protection treatment group 2 (100 μg / ml), chitooligosaccharide pre-protection treatment group 3 (200 μg / ml). (2) The cultured N9 microglial cells were digested with trypsin (0.125%), and then 5×10 4 Inoculate in a 6-well plate at a density of / ml, add 3ml of IMDM culture solution to each well, and store at 37°C, 5% CO 2 cultured in an incubator for 24 h. (3) Take out the 6-well plate, discard the supernatant, add 3ml of fresh IMDM medium to the control and LPS groups, respectively, and add 50, 100 and 200 μg / ml chitosan oligosaccharides to the IMDM culture in the chitosan oligosaccharide pre-protection group...
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