Application of dual-aliphatic-chain substituent phosphatidyl ethanolamine chitosan
A technology based on phosphatidylethanolamine shell and lauroyl phosphatidylethanolamine, which is applied in the field of drug delivery, can solve the problems of leakage and destruction of encapsulated drugs, and achieve high biocompatibility, broad application prospects, and high drug delivery efficiency.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 2
[0038] Weigh 0.16g of formyl chitosan, disperse it into 20mL of methanol solution, add 0.14g of 1,2-dioleoylphosphatidylethanolamine, nitrogen protection, stir and react at 60°C for 42h, add 0.1g of sodium borohydride and continue stirring at room temperature After 24 hours, the ethanol solvent was removed by rotary evaporation, dispersed in water, dialyzed with deionized water, and freeze-dried to obtain 1,2-dioleoylphosphatidylethanolamine chitosan.
[0039] Prepare a 1mg / mL 1,2-dioleoylphosphatidylethanolamine aqueous solution, take 100uL, mix it with 1mL of DOTAP cationic liposome containing SPIO by ultrasound, then let it stand for 1h, and through the post-insertion self-assembly method, the The liposome is modified to obtain the liposome drug carrier with chitosan brushes on the surface.
Embodiment 3
[0041] Weigh 0.16g of formyl chitosan, disperse it into 20mL of methanol solution, add 0.14g of 1,2-dilauroylphosphatidylethanolamine, under nitrogen protection, stir and react at 60°C for 42h, add 0.1g of sodium borohydride and continue stirring at room temperature After 24 hours, the ethanol solvent was removed by rotary evaporation, dispersed in water, dialyzed with deionized water, and freeze-dried to obtain 1,2-dilauroylphosphatidylethanolamine chitosan.
[0042] Prepare a 1mg / mL 1,2-dilauroylphosphatidylethanolamine aqueous solution, take 100uL, mix it with 1mL of DOTAP cationic liposomes containing SPIO by ultrasound, then let it stand for 1h, and pass the post-insertion self-assembly method. The liposome is modified to obtain the liposome drug carrier with chitosan brushes on the surface.
Embodiment 4
[0044] Weigh 0.16g of formyl chitosan, disperse it into 20mL of methanol solution, add 0.14g of 1,2-dimyristoylphosphatidylethanolamine, under nitrogen protection, stir and react at 60°C for 42h, add 0.1g of sodium borohydride and continue at room temperature Stir for 24 hours, remove the ethanol solvent by rotary evaporation, disperse into water, dialyze with deionized water, and freeze-dry to obtain 1,2-dimyristoylphosphatidylethanolamine chitosan.
[0045] Prepare a 1mg / mL aqueous solution of 1,2-dimyristoylphosphatidylethanolamine, take 100uL, mix it with 1mL of DOTAP cationic liposomes containing SPIO by ultrasonication, then let it stand for 1h, and pass the post-insertion self-assembly method, The liposome is modified to obtain the liposome drug carrier with chitosan brushes on the surface.
PUM
| Property | Measurement | Unit |
|---|---|---|
| particle diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 


