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EXP002476

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 EXP002476
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 therapeutic gene-silencing assay
Cell Lines Or Primary Cells B16F10 melanoma cells
Animal Model
Administration Route
Output Type in vitro target-gene knockdown and apoptosis
Output Value CPD/siBcl-2/CK showed strong Bcl-2 silencing, increased apoptosis, and inhibited B16F10 proliferation; Western blot band ratio approximately 0.29 for CPD/siBcl-2/CK.
Output Units
Output Notes KDEL-directed sorting produced stronger RNAi and pro-apoptotic activity than CPD/siBcl-2/CS. This is in vitro functional RNA activity, not in vivo delivery success.
Toxicity Notes Good cytocompatibility of nanocomplexes reported in normal cells/HUVEC in supplementary data.
Curation Notes