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EXP000587

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)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 EXP000587
Paper Lipid-modified cell-penetrating peptide-based self-assembly micelles for co-delivery of narciclasine
Peptide Ac-E(Chol)E(Chol)E(Chol)-HHHHH-YGRKKRRQRRR
Delivery Success Class yes
In Vivo Flag yes
Uptake Confirmed yes
Label Confidence high
In Vitro Functional Effect yes
Endosomal Escape Evidence yes
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_vivo
Model Type in vitro / in vivo
Cell Lines Or Primary Cells HepG2; Huh-7; Bel-7402
Animal Model HepG2 xenograft nude mice
Administration Route Intravenous
Output Type ULK1 knockdown; uptake; tumor growth inhibition
Output Value Robust ULK1 knockdown and tumor suppression
Output Units
Output Notes Selected lead formulation for all subsequent functional and in vivo studies
Toxicity Notes Good safety profile
Curation Notes