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EXP002474

Paper

Dual Strategies Based on Golgi Apparatus/Endoplasmic Reticulum Targeting and Anchoring for High-Efficiency siRNA Delivery and Tumor RNAi Therapy (2025)

Peptide

KDEL-grafted chondroitin sulfate CPD/siBcl-2/CK

Sequence: KDEL

RNA

siRNA

All experiment fields

Experiment Id EXP002474
Paper Dual Strategies Based on Golgi Apparatus/Endoplasmic Reticulum Targeting and Anchoring for High-Effi
Peptide KDEL-grafted chondroitin sulfate CPD/siBcl-2/CK
Delivery Success Class no
In Vivo Flag no
Uptake Confirmed yes
Label Confidence high
In Vitro Functional Effect yes
Endosomal Escape Evidence yes
Peptide Concentration KDEL grafting ratio on chondroitin sulfate approximately 11%
Rna Concentration In vivo siRNA dose 1 mg/kg where applicable; exact in vitro siRNA concentration not fully specified for luciferase assay
Mixing Ratio CPD/siRNA/CK prepared by CPD/siRNA complexation followed by coating with KDEL-grafted chondroitin sulfate; C/Gu ratios screened, same strategy as CPD/siRNA/CS
Formulation Format polymer/polysaccharide nanocomplex
Formulation Components Cell-penetrating poly(disulfide) (CPD), siRNA, KDEL-grafted chondroitin sulfate (CK); CK provides CD44-associated targeting/Golgi transport and KDEL-mediated ER-directed sorting
Size Nm 167.20
Zeta Mv -13.60
Model Scope in_vitro
Model Type in vitro reporter RNAi assay
Cell Lines Or Primary Cells B16F10-Luc melanoma cells
Animal Model
Administration Route
Output Type in vitro target-gene knockdown
Output Value CPD/siLuc/CK reduced luciferase expression to 32.7 ± 2.0%, lower than CPD/siLuc/CS at 46.9 ± 1.3%
Output Units
Output Notes KDEL-directed sorting increased cellular retention and RNAi efficiency versus CS-coated comparator; uptake and ER/Golgi routing were directly evaluated by fluorescence microscopy/flow cytometry.
Toxicity Notes Good cytocompatibility of nanocomplexes was reported in normal cells/HUVEC in supplementary data.
Curation Notes