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R8 peptide-modified epirubicin and dihydroartemisinin co-loaded liposomes
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Cat. No.: X26-05-ZQ2912

R8 peptide-modified epirubicin and dihydroartemisinin co-loaded liposomes

Synonym: R8-modified epirubicin/DHA co-loaded LPs; R8 peptide-modified epirubicin-dihydroartemisinin liposomes; R8-functionalized epirubicin/DHA co-delivery liposomes

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Product Size
100 mg; 250 mg; 500 mg; 1 g; 5 g
Price
Datasheet
MSDS
Properties
Description
This highly advanced multi-functional targeted formulation features octa-arginine peptide functionalized liposomes co-loaded with epirubicin and dihydroartemisinin. The complex structural framework encapsulates the hydrophilic anthracycline epirubicin within its central aqueous core via an active remote-loading gradient, while simultaneously incorporating the hydrophobic sesquiterpene lactone compound dihydroartemisinin within the lipophilic tail regions of its bilayer shell, whose exterior boundary is surface-modified with cell-penetrating octa-arginine (R8) peptides linked via covalent polymer anchors. This precise modification coordinates a highly uniform charged cell-penetrating peptide layer with a protective dual-phase multi-cargo boundary, completely preventing drug crystallization, anthracycline leakage, and physical vesicle aggregation across variable laboratory media.
Source
Custom synthesis
Functional Group
R8 peptide; Epirubicin; Dihydroartemisinin
Form
Solid or powder
Purity
≥95%
Impurities
No visible impurities to the naked eye.
Identity
HPLC/MS/NMR
Publications
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