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Streptavidin-modified daunorubicin/tetrandrine co-loaded liposomes (SA-DNR-TET LPs)
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Cat. No.: X26-05-ZQ2861

Streptavidin-modified daunorubicin/tetrandrine co-loaded liposomes (SA-DNR-TET LPs)

Synonym: SA-DNR-TET LPs; Streptavidin-modified daunorubicin-tetrandrine co-loaded liposomes; SA-functionalized DNR/TET 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 streptavidin functionalized liposomes co-loaded with daunorubicin and tetrandrine (SA-DNR-TET LPs). The complex structural framework encapsulates the hydrophilic anthracycline daunorubicin (DNR) within its central aqueous core while simultaneously incorporating the hydrophobic bisbenzylisoquinoline alkaloid tetrandrine (TET) within the lipophilic tail regions of its bilayer shell, whose exterior boundary is surface-modified with macromolecular streptavidin (SA) proteins linked via covalent lipid anchors. This intricate configuration coordinates an exceptionally versatile biotin-binding protein surface array with a protective dual-phase multi-cargo boundary, completely preventing alkaloid crystallization, anthracycline leakage, and physical vesicle aggregation across variable laboratory media.
Source
Custom synthesis
Functional Group
Streptavidin; Daunorubicin; Tetrandrine
Form
Solid or powder
Purity
≥95%
Impurities
No visible impurities to the naked eye.
Identity
HPLC/MS/NMR
Publications
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