Alpha-Hed-CS-CD147 nanoparticles as well as preparation method, application and preparation thereof
A technology of -hed-cs-cd147, -hed-cs-np, applied in the field of pharmaceutical preparations, can solve the problems of poor water solubility of α-hedera saponin, affecting application and research, and low bioavailability, so as to increase selectivity , Improve the relative bioavailability in the body, and enhance the therapeutic effect
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Embodiment 1
[0060] Preparation of Example 1α-Hed-CS-CD147 Nanoparticles
[0061] Accurately weighed 80mg F68 and 50mg CS, dissolved in 20mL of 0.2% acetic acid aqueous solution as the aqueous phase; accurately weighed 20mgα-Hed and 80mg phospholipids, dissolved in 4mL ethanol / acetone (1:1) mixed solvent as the organic phase, in Under the condition of magnetic stirring at 30°C, quickly inject the organic phase into the water phase, keep stirring for 5 minutes, then dilute to 70mL with distilled water, and cut it with a high-speed shearer at 20000rpm for 5min, and then homogenize it with a high-pressure homogenizer at 1000bar. After massaging for 5 minutes, filter through a 0.45 μm microporous membrane to obtain α-Hed-CS-NP (α-hedera-CS nanoparticles) colloidal solution.
[0062] The α-Hed-CS-NP colloidal solution prepared above was concentrated to 1 / 10 of the original volume, and the residual organic solvent was removed by ultracentrifugation. The precipitate was washed twice and then resu...
Embodiment 2
[0063] Preparation of Example 2α-Hed-CS-CD147 Nanoparticles
[0064] Accurately weighed 80mg F68 and 50mg CS, dissolved in 20mL of 0.2% acetic acid aqueous solution as the aqueous phase; accurately weighed 20mgα-Hed and 80mg phospholipids dissolved in 4mL ethanol as the organic phase, under the condition of magnetic stirring at 30°C, the organic Inject the phase into the water phase quickly, keep stirring for 10min, then dilute to 70mL with distilled water, and cut it with a high-speed shearer at 20000rpm for 5min, then homogenize it at 1000bar for 5min with a high-pressure homogenizer, and pass through a 0.45μm microporous filter Membrane filtration to obtain α-Hed-CS-NP (α-hedera-CS nanoparticles) colloidal solution.
[0065] The α-Hed-CS-NP colloidal solution prepared above was concentrated to 1 / 10 of the original volume, and the residual organic solvent was removed by ultracentrifugation. The precipitate was washed twice and then resuspended with 0.2% acetic acid solution....
Embodiment 3
[0066] Preparation of Example 3α-Hed-CS-CD147 Nanoparticles
[0067] Accurately weighed 80mg F68 and 50mg CS, dissolved in 20mL of 0.2% acetic acid aqueous solution as the aqueous phase; accurately weighed 20mgα-Hed and 80mg phospholipids dissolved in 2mL acetone as the organic phase, under the condition of magnetic stirring at 30°C, the organic Inject the phase into the water phase quickly, keep stirring for 5min, and then dilute to 70mL with distilled water, while shearing with a high-speed shearer at 20000rpm for 5min, then homogenize for 5min at 1000bar with a high-pressure homogenizer, and pass through a 0.45μm microporous filter Membrane filtration to obtain α-Hed-CS-NP (α-hedera-CS nanoparticles) colloidal solution.
[0068] The α-Hed-CS-NP colloidal solution prepared above was concentrated to 1 / 10 of the original volume, and the residual organic solvent was removed by ultracentrifugation. The precipitate was washed twice and then resuspended with 0.2% acetic acid solut...
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