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| Product Name | DOX-SAA@LNP-PTP-DTPA, doxorubicin-self-assembled micelles loaded on lipid nanoparticles and coupled with PTP peptide and diethylenetriaminepentaacetic acid |
| Catalog Number | R-LNP2-0323 |
| Alias | DOX-SAA@LNP-PTP peptide-DTPA |
| Appearance | Dispersion |
| Molecular Formula | N/A |
| Solubility | Can be stably dispersed in aqueous solution to form a colloidal system |
| 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 | DOX-SAA@LNP-PTP peptide-DTPA is a multifunctional nanodrug delivery system integrating drug loading, targeted delivery, and imaging functions. Doxorubicin (DOX), as the core anti-tumor drug, can effectively inhibit tumor cell proliferation; the composite carrier formed by self-assembled micelles (SAA) and lipid nanoparticles (LNP) has good biocompatibility and high drug-loading capacity. It can encapsulate doxorubicin, prolong the time the drug circulates in the body, and reduce the early release of the drug and the side effects on normal tissues. As a targeting molecule, PTP peptide can specifically recognize receptors on the surface of tumor cells to achieve accurate drug delivery; diethylenetriaminepentaacetic acid (DTPA) is a metal chelating agent that can chelate radionuclides or magnetic resonance imaging contrast agents, giving the system molecular imaging functions to facilitate real-time monitoring of drug distribution and treatment effects in the body. |