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EXP000588

Paper

Lipid-modified cell-penetrating peptide-based self-assembly micelles for co-delivery of narciclasine and siULK1 in hepatocellular carcinoma therapy (2018)

Peptide

Ac-E(Chol)E(Chol)-HHHHH-YGRKKRRQRRR

Sequence: Tat peptide core with variable His repeats and cholesterol–glutamate lipid (see Fig. 4A for exact composition)

RNA

siRNA

All experiment fields

Experiment Id EXP000588
Paper Lipid-modified cell-penetrating peptide-based self-assembly micelles for co-delivery of narciclasine
Peptide Ac-E(Chol)E(Chol)-HHHHH-YGRKKRRQRRR
Delivery Success Class no
In Vivo Flag no
Uptake Confirmed yes
Label Confidence high
In Vitro Functional Effect no
Endosomal Escape Evidence
Peptide Concentration varied (micelle formulation)
Rna Concentration ~50 nM (in vitro)
Mixing Ratio N/P ≥10:1
Formulation Format Self-assembled lipid-modified CPP micelles
Formulation Components Lipid-modified CPP + siULK1 ± narciclasine
Size Nm 96.00
Zeta Mv 15.00
Model Scope in_vitro
Model Type in vitro
Cell Lines Or Primary Cells HepG2; Huh-7; Bel-7402
Animal Model
Administration Route
Output Type Cellular uptake screening
Output Value Screened; not advanced to in vivo studies
Output Units
Output Notes Screening variant shown in Fig. 4A; not selected for further development
Toxicity Notes
Curation Notes