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EXP001878

Paper

iRGD-guided Tumor-penetrating Nanocomplexes for Therapeutic siRNA Delivery to Pancreatic Cancer (2018)

Peptide

iRGD TPN (PEGylated vs non-PEG) biodistribution (healthy mice)

Sequence: Palmitoyl-transportan-iRGD (pTP-TAMRA-iRGD): CH3(CH)15-[GWTLNSAGYLLGKINLKALAALAKKIL-GGK(TAMRA)GGCRGDKGPDC] (Cys-Cys bridge) ; Palmitoyl-transportan-PEG(5kDa)-iRGD (pTP-PEG-iRGD): (CH3(CH)15-[GWTLNSAGYLLGKINLKALAALAKKILC]-S-S-PEG(5kDa)-X-[GGGCRGDKGPDC] (Cys-Cys bridge))

RNA

siRNA

All experiment fields

Experiment Id EXP001878
Paper iRGD-guided Tumor-penetrating Nanocomplexes for Therapeutic siRNA Delivery to Pancreatic Cancer
Peptide iRGD TPN (PEGylated vs non-PEG) biodistribution (healthy mice)
Delivery Success Class no
In Vivo Flag yes
Uptake Confirmed yes
Label Confidence medium
In Vitro Functional Effect
Endosomal Escape Evidence
Peptide Concentration TPNs formed by mixing peptide and siRNA solutions; in vitro dosing at 100 nM siRNA (typical); in vivo dose 0.5 mg/kg siRNA for key PDAC studies
Rna Concentration In vitro: 100 nM siRNA (typical transfection); In vivo: 0.5 mg/kg siRNA per dose (therapeutic and knockdown studies)
Mixing Ratio Non-PEG vs 15:10:1 PEGylated iRGD TPNs (reported for biodistribution)
Formulation Format Self-assembled tandem peptide/siRNA nanocomplex (TPN), with optional PEG-peptide component
Formulation Components Tandem peptide core: palmitoyl-transportan-iRGD; PEGylated formulation includes pTP-PEG-iRGD as third component
Size Nm
Zeta Mv
Model Scope in_vivo
Model Type in vivo
Cell Lines Or Primary Cells
Animal Model Swiss Webster mice (healthy, wild-type)
Administration Route Intravenous injection; organs collected at 3 h for near-IR scanning
Output Type In vivo distribution (organ biodistribution by fluorescence intensity)
Output Value PEGylation reduced lung/spleen/liver accumulation vs non-PEG iRGD TPNs
Output Units
Output Notes Distribution-only experiment (no in vivo functional gene knockdown endpoint in healthy animals).
Toxicity Notes
Curation Notes