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| Product Name | glucose-LNP@PTX, glucose-modified liposome loaded with paclitaxel |
| Catalog Number | R-ZHIGF12 |
| Alias | Glucose-lipid nanoparticle-paclitaxel complex |
| Appearance | solid or liquid |
| Molecular Formula | N/A |
| Solubility | Soluble in organic solvents |
| Storage | -20°C, protected from light |
| Purity | 95%+ |
| Shelf Life | 1 year |
| Shipping Condition | low temperature transport |
| Application | targeted drug delivery |
| Specification | 10mg:Inquiry 25mg:Inquiry 50mg:Inquiry |
| Description | Glucose-LNP@PTX is a drug delivery system in which glucose-modified lipid nanoparticles are loaded with paclitaxel (PTX). Lipid nanoparticles (LNP) are composed of lipid components such as phospholipids and cholesterol. They have good biocompatibility and degradability. They can simulate the structure of biological membranes, effectively protect the paclitaxel wrapped in them, and prevent the drug from being degraded or metabolized in advance before reaching the lesion. Glucose, as a targeting modification molecule, can specifically bind to the overexpressed glucose transporter on the surface of tumor cells, giving the system tumor targeting ability and enabling drug-loaded nanoparticles to be enriched in tumor tissues. Paclitaxel is a classic anticancer drug that exerts its anticancer effect by inhibiting microtubule depolymerization and disrupting the mitotic process of tumor cells. Glucose-LNP@PTX, which combines the three, can improve the water solubility, stability and targeting of paclitaxel, reduce the side effects of the drug on normal tissues, and shows broad application prospects in the field of tumor treatment. |