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Liposome-encapsulated mesoporous polydopamine co-loaded with doxorubicin and allicin

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Cat. No.: X26-05-ZQ2902

Liposome-encapsulated mesoporous polydopamine co-loaded with doxorubicin and allicin

Name: Liposome-encapsulated mesoporous polydopamine co-loaded with doxorubicin and allicin
SKU: X26-05-ZQ2902

Inquiry

Synonym: Liposome-encapsulated MPDA@DOX/allicin; Liposomal mesoporous polydopamine co-loaded with doxorubicin and allicin; Liposome-MPDA doxorubicin/allicin nanocomposites

Product Size

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

Price

Datasheet

Datasheet

MSDS

MSDS

Properties

Description

This highly advanced core-shell hybrid material features mesoporous polydopamine nanoparticles co-loaded with doxorubicin and allicin encapsulated within a liposomal vesicle template. The complex structural framework encapsulates porous mesoporous polydopamine (MPDA) nanoparticles co-loaded with the hydrophilic anthracycline doxorubicin and the volatile organosulfur compound allicin entirely within the central aqueous core of a high-purity phospholipid bilayer shell. This hybrid configuration couples the immense surface area, photothermal conversion properties, and rigid mass transfer resistance of a polydopamine core with the flexible fluid dynamics of a lipid envelope, establishing a robust structural network that completely prevents cargo volatilization or core aggregation across variable laboratory media.

Source

Custom synthesis

Functional Group

Mesoporous polydopamine core; Doxorubicin; Allicin

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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