A liposome-based method for controlled release of active small molecules and its application
A technology of liposomes and plastids, which is applied in liposome delivery, prostheses, pharmaceutical formulations, etc., can solve problems such as less research, and achieve the effects of simple raw materials, good induction of differentiation, and prolonged action time
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0097] The preparation of embodiment 1 Aspirin liposome (Asp@Lipo)
[0098] 1.1 Preparation of Aspirin liposomes (Asp@Lipo)
[0099] The liposome-loaded aspirin was prepared by film dispersion method.
[0100] Take a round-bottomed flask, dissolve aspirin and lipids in a mixture of methanol and chloroform (1:1, v / v), predetermine the proportion of aspirin in the mixture of methanol and chloroform, and then mix it in different volumes Proportionally add aspirin. Next, methanol and chloroform were removed using a rotary vacuum evaporator, followed by hydration of the lipid film with phosphate buffered saline (PBS). The aspirin-loaded liposomes can be obtained after ultrasonication in a water bath for 5 minutes (T=47° C.). It was sequentially passed through porous polycarbonate membranes (Millipore, USA) with pore diameters of 450 nm, 220 nm and 100 nm, each extruded 5 times to ensure the uniformity of the finally obtained liposome size. Then, the aspirin-loaded liposomes...
Embodiment 2
[0177] Example 2 Construction of Aspirin / BFP-1 two-factor composite PS system
[0178] Preparation and characterization of different ratios of Aspirin / BFP-1 modified culture plate surface (PS-Asp@Lipo / BFP-1)
[0179] First, prepare Asp@Lipo according to the experimental method of 1.1 in Example 1.
[0180] Using dopamine technology, we grafted Asp@Lipo and BFP-1 polypeptides on PS culture plates according to the preset ratio Asp@Lipo:BFP-1=7:3, 5:5, 3:7.
[0181] The main experimental steps are as follows: firstly, 2 mL of dopamine solution (pH=8.5, 2 mg / mL) was added to each well of the culture plate, and then incubated on a constant temperature shaker (37° C., 70 rpm) for 24 hours. After washing twice with PBS, add 2 mL of activation solution (5 mM NHS, 2 mM EDC dissolved in 0.1 M MES buffer) to each well at room temperature to pretreat the polydopamine (PDA)-modified surface, activate for 40 min, discard the activation solution, and Asp@Lipo and BFP-1 polypeptides wer...
Embodiment 3
[0220] The preparation of the PS surface of embodiment 3 Dex / Mino liposome modification
[0221] 3.1.1 Dex / Mino liposome preparation
[0222] Prepared by thin film dispersion method; accurately weigh appropriate amount of dipalmitoylphosphatidylcholine (DPPC), cholesterol (Chol), distearoyl Put phosphatidylethanolamine-polyethylene glycol-amino (DSPE-PEG2000-NH2) and Dex in an eggplant-shaped flask, add a mixed solvent of methanol and chloroform (1:1, v / v), shake to dissolve the solute; use rotary evaporation Drying machine (75rpm) in a constant temperature water bath (47°C) reduced pressure and dried thoroughly to remove the organic solvent, and a uniform lipid film was formed on the inner wall of the bottle; take an appropriate amount of hydration solution (a mixture of 120mM anhydrous sodium acetate and anhydrous calcium chloride) solution, pH=7.9) into an eggplant-shaped bottle, and ultrasonically hydrate in a constant temperature water bath (47°C) until the lipid mem...
PUM
Property | Measurement | Unit |
---|---|---|
particle diameter | aaaaa | aaaaa |
particle diameter | aaaaa | aaaaa |
particle diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com