Back to browse

EXP001725

Paper

Self-Assisted Membrane-Penetrating Helical Polypeptides Mediate Anti-Inflammatory RNAi against Myocardial Ischemic Reperfusion (IR) Injury (2019)

Peptide

P-Homo

Sequence: Not specified as a single sequence (composition-based guanidinated α-helical polypeptide; DP≈113; no aromatic).

RNA

siRNA

All experiment fields

Experiment Id EXP001725
Paper Self-Assisted Membrane-Penetrating Helical Polypeptides Mediate Anti-Inflammatory RNAi against Myoca
Peptide P-Homo
Delivery Success Class yes
In Vivo Flag yes
Uptake Confirmed yes
Label Confidence high
In Vitro Functional Effect
Endosomal Escape Evidence
Peptide Concentration
Rna Concentration
Mixing Ratio P-Homo/siRAGE w/w=20 for intracardial injections (150 µg siRNA/kg); imaging used w/w=15
Formulation Format Helical polypeptide/siRNA polyplexes by simple mixing and incubation
Formulation Components Intramyocardial injection polyplex: P-Homo/siRAGE (w/w=20) at 150 µg siRNA/kg.
Size Nm
Zeta Mv
Model Scope in_vivo
Model Type in vivo
Cell Lines Or Primary Cells
Animal Model Male Sprague–Dawley rats (myocardial IR injury, LAD ligation)
Administration Route Intramyocardial injection 10 min after reperfusion
Output Type in vivo gene knockdown (less effective than P-Ben)
Output Value ~55% RAGE mRNA knockdown at 24 h; higher infarct size (~35.7%) and fibrosis/apoptosis vs P-Ben group.
Output Units
Output Notes Rat myocardial IR model (LAD ligation 40 min + reperfusion). Intramyocardial injection 10 min post reperfusion: polyplexes at 150 µg siRNA/kg (50 µL/rat).
Toxicity Notes
Curation Notes