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c(RGD)fk-mediated doxorubicin-dihydroartemisinin nanoparticle liposomes

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Cat. No.: X26-05-ZQ2896

c(RGD)fk-mediated doxorubicin-dihydroartemisinin nanoparticle liposomes

Name: c(RGD)fk-mediated doxorubicin-dihydroartemisinin nanoparticle liposomes
SKU: X26-05-ZQ2896

Inquiry

Synonym: c(RGD)fk doxorubicin-dihydroartemisinin NP LPs; c(RGD)fk-mediated DOX-DHA nanoparticle liposomes; c(RGD)fk DOX-dihydroartemisinin nanoliposomes

Product Size

100 mg; 250 mg; 500 mg; 1 g; 5 g

Price

Datasheet

Datasheet

MSDS

MSDS

Properties

Description

This highly advanced multi-functional targeted formulation features c(RGD)fk peptide functionalized liposomes co-loaded with doxorubicin and dihydroartemisinin nanoparticles. The complex structural framework encapsulates pre-formulated dihydroartemisinin core nanoparticles alongside the hydrophilic anthracycline doxorubicin within its aqueous core matrices, while its exterior lipid bilayer shell is surface-modified with specific cyclic arginylglycylaspartic acid-d-phenylalanyl-lysine (c(RGD)fk) targeting peptides linked via covalent polymer-lipid anchors. This precise modification coordinates a dense target-mimetic ligand array with a dual-phase multi-cargo core, altering overall membrane bending elasticity to completely prevent physical particle aggregation and suppress cargo crystallization across variable laboratory media backgrounds.

Source

Custom synthesis

Functional Group

c(RGD)fk cyclic peptide; Doxorubicin; Dihydroartemisinin

Form

Solid or powder

Purity

≥95%

Impurities

No visible impurities to the naked eye.

Identity

HPLC/MS/NMR

Publications

Publications (0)

Publications

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Publications

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