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| Product Name | DSPE-HYD-PEGLNP@DEX, distearoylphosphatidylethanolamine-hydrazone bond-polyethylene glycol lipid nanoparticles encapsulating dexamethasone |
| Catalog Number | R-CW-DP001-2k |
| Alias | Responsive phospholipid-encapsulated drugs |
| Appearance | Dispersion |
| Molecular Formula | N/A |
| Solubility | Stable dispersion in aqueous media such as water and physiological saline |
| Storage | 2-8°C, protected from light |
| Purity | 95%+ |
| Shelf Life | 1 year |
| Shipping Condition | low temperature transport |
| Application | drug delivery system |
| Specification | 10mg:Inquiry 20mg:Inquiry 50mg:Inquiry |
| Description | DSPE-HYD-PEGLNP@DEX is a liposome drug delivery system that integrates targeting, responsiveness and drug sustained release functions. It uses distearoylphosphatidylethanolamine (DSPE) and polyethylene glycol (PEG) as the main lipid materials, connected through hydrazone bonds (-C=N-NH-) to form amphipathic lipid molecules, which can self-assemble to form lipid nanoparticles and encapsulate dexamethasone in them. DSPE has good film-forming properties and biofilm compatibility, and can form the hydrophobic core of lipid nanoparticles; PEG gives the nanoparticles good water solubility and steric hindrance effect, reducing recognition and clearance by the immunity system, and prolonging the time in the body circulation; the hydrazone bond is sensitive to acidic environments, and will be rapidly hydrolyzed and broken in acidic microenvironments (pH 5.0-6.5) such as tumor tissue, prompting the release of dexamethasone. Dexamethasone has a variety of activities. After being encapsulated by the lipid nanoparticles, targeted delivery and controlled release of the drug can be achieved, improving the drug effect and reducing systemic side effects. |