A reversible self-assembled surface with blood purification function and its preparation method
A technology of blood purification and self-assembly, which is applied in chemical instruments and methods, and other chemical processes, can solve the problems of high production cost of bilirubin adsorption columns, non-recyclable materials, and application restrictions, so as to reduce material costs and improve Utilization, the effect of optimizing performance
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Embodiment 1
[0040] The preparation method of the reversible self-assembled surface with blood purification function in this example, the synthesis route is shown in Figure 1 (a) to (c), including the following steps:
[0041] (1) Add 79.04mg Ad-NH to 2mL dichloromethane 3 Cl, 42.5 mg triethylamine, 10 mg HS-PEG-NHS (n=3), Ad-NH 3 The molar ratio of Cl, triethylamine and HS-PEG-NHS is 15:15:1, react at 25°C for 2 hours, remove the solvent in a vacuum, add a small amount of deionized water to dissolve, centrifuge, collect the solution, and freeze-dry to obtain HS- PEG-Ad. Its NMR spectrum is shown in figure 2 .
[0042] (2) Dissolve 1.135g of β-cyclodextrin and 1.82mg of IBX in 12mL of DMSO, the molar ratio of β-cyclodextrin and IBX is 1:5, stir and dissolve, react at 30°C for 24h, and use Precipitate in 180mL of acetone, centrifuge, vacuum dry, dissolve with a certain amount of deionized water, filter, and freeze-dry to obtain β-cyclodextrin monoaldehyde; weigh 1.904g of β-cyclodextrin...
Embodiment 2
[0065] The preparation method of the reversible self-assembled surface with blood purification function in this embodiment includes the following steps:
[0066] (1) Add 3.75mg Ad-NH to 2mL dichloromethane 3 Cl, 6.08 mg triethylamine, 100 mg HS-PEG-NHS (n=120), Ad-NH 3 The molar ratio of Cl, triethylamine and HS-PEG-NHS is 1:3:1, react at 20°C for 2 hours, remove the solvent in a vacuum, add deionized water to dissolve, centrifuge, collect the solution, freeze-dry to obtain HS-PEG -Ad. Its NMR spectrum is shown in Figure 7 .
[0067] (2) Dissolve 1.135g of β-cyclodextrin and 364mg of IBX in 12mL of DMSO, the molar ratio of β-cyclodextrin and IBX is 1:1, stir and dissolve, react at 20°C for 18h, precipitate with 180mL of acetone, centrifuge , vacuum-dried, dissolved with a certain amount of deionized water, filtered, and freeze-dried to obtain β-cyclodextrin monoaldehyde; weigh 476mg β-cyclodextrin monoaldehyde and 124mg α, ω-diaminoalkane (m 1 =40) was dissolved in 20mL ...
Embodiment 3
[0071] The preparation method of the reversible self-assembled surface with blood purification function in this embodiment includes the following steps:
[0072] (1) Add 3.752mg Ad-NH to 2mL dichloromethane 3 Cl, 2.02 mg triethylamine, 10 mg HS-PEG-NHS with a molecular weight of 5000, Ad-NH 3 The molar ratio of Cl to HS-PEG-NHS was 10:10:1, reacted at 25°C for 1 h, vacuumed off the solvent, dissolved in deionized water, centrifuged, collected the solution, and lyophilized to obtain HS-PEG-Ad. Its infrared spectrum is shown in Figure 9 .
[0073] (2) Dissolve 1.135g of β-cyclodextrin and 1.092g of IBX in 12mL of DMSO, the molar ratio of β-cyclodextrin and IBX is 1:3, stir and dissolve, react at 25°C for 24h, precipitate with 180mL of acetone, centrifuge , vacuum-dried, dissolved with a certain amount of deionized water, filtered, and freeze-dried to obtain β-cyclodextrin monoaldehyde; weigh 1.190 mg β-cyclodextrin monoaldehyde and 40 mg α, ω-diaminopolyethylene glycol (NH ...
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