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Cell-penetrating peptide (TAT)-modified paclitaxel/tamoxifen co-loaded liposomes

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Cat. No.: X26-05-ZQ2901

Cell-penetrating peptide (TAT)-modified paclitaxel/tamoxifen co-loaded liposomes

Name: Cell-penetrating peptide (TAT)-modified paclitaxel/tamoxifen co-loaded liposomes
SKU: X26-05-ZQ2901

Inquiry

Synonym: TAT-modified PTX/tamoxifen co-loaded LPs; TAT-modified paclitaxel-tamoxifen co-loaded liposomes; TAT-functionalized PTX/tamoxifen co-delivery liposomes

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 transactivator of transcription peptide functionalized liposomes co-loaded with paclitaxel and tamoxifen. The structural matrix co-incorporates the highly hydrophobic diterpenoid paclitaxel and the triphenylethylene derivative tamoxifen directly within the lipophilic hydrocarbon tail domains of its bilayer shell, whose exterior boundary is surface-modified with transactivator of transcription (TAT) cell-penetrating peptides linked via polymer anchors. This complex layout coordinates a highly uniform charged cell-penetrating peptide layer with an optimized dual-phase hydrophobic core, completely preventing physical vesicle aggregation while completely suppressing paclitaxel or tamoxifen crystallization in open laboratory testing media.

Source

Custom synthesis

Functional Group

TAT peptide; Paclitaxel; Tamoxifen

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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