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EXP001738

Paper

Polyarginine-Mediated siRNA Delivery: A Mechanistic Study of Intracellular Trafficking of PCL-R15/siRNA Nanoplexes (2020)

Peptide

PCL-R15 (PCL3000-b-R15 amphiphilic block polymer)

Sequence: Not a single peptide sequence; block copolymer PCL3000-b-R15 (poly(ε-caprolactone) ~3 kDa conjugated to polyarginine R15).

RNA

siRNA

All experiment fields

Experiment Id EXP001738
Paper Polyarginine-Mediated siRNA Delivery: A Mechanistic Study of Intracellular Trafficking of PCL-R15/si
Peptide PCL-R15 (PCL3000-b-R15 amphiphilic block polymer)
Delivery Success Class no
In Vivo Flag no
Uptake Confirmed yes
Label Confidence high
In Vitro Functional Effect yes
Endosomal Escape Evidence no
Peptide Concentration
Rna Concentration 100 nM siRNA (most in vitro assays; 4 h transfection).
Mixing Ratio N/P = 40 (used for most cellular studies).
Formulation Format PCL-R15 micelles + siRNA nanoplexes (electrostatic adsorption on micelle surface)
Formulation Components PCL-R15 nanoparticles made by thin-film hydration (methanol film → hydrate with 5% glucose; 70 °C sonication). Nanoplexes formed by mixing equal volumes of PCL-R15 NP solution and siRNA in 5% glucose; vortex; stand 10 min.
Size Nm 15.00
Zeta Mv 15.00
Model Scope in_vitro
Model Type in vitro
Cell Lines Or Primary Cells HeLa (human cervical cancer)
Animal Model
Administration Route
Output Type in vitro gene silencing (protein)
Output Value VEGF secretion downregulated vs untreated starting 24 h post-transfection; maximal suppression at ~72 h; effect persists up to 96 h. Sequence-specific (siNC shows no downregulation).
Output Units
Output Notes HeLa cells exposed to Opti-MEM containing PCL-R15/siVEGF (N/P 40; 100 nM) for 4 h, then changed to complete medium; VEGF measured by ELISA at time points.
Toxicity Notes SRB assay: at 100 nM siRNA, PCL-R15/siRNA showed acceptable viability similar to R15/siRNA; higher siRNA concentrations increased PCL-R15 cytotoxicity.
Curation Notes