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EXP002455

Paper

Systemic delivery of microRNA-21 antisense oligonucleotides to the brain using T7-peptide decorated exosomes (2020)

Peptide

T7 peptide-decorated exosome

Sequence: HAIYPRH

RNA

anti-miRNA

All experiment fields

Experiment Id EXP002455
Paper Systemic delivery of microRNA-21 antisense oligonucleotides to the brain using T7-peptide decorated
Peptide T7 peptide-decorated exosome
Delivery Success Class no
In Vivo Flag no
Uptake Confirmed yes
Label Confidence high
In Vitro Functional Effect yes
Endosomal Escape Evidence
Peptide Concentration not reported as peptide concentration; T7 is displayed on exosome surface via T7-Lamp2b expression
Rna Concentration In vitro: FAM-AMO-21 amount fixed at 1 ug/well for uptake assay; loading used 20 ug AMO-21 with 20 ug exosome protein. In vivo: 60 ug AMO-21 electroporated with exosomes per rat before purification; 200 ug exosomes used for fluorescence imaging.
Mixing Ratio AMO-21 loaded into exosomes by electroporation; 20 ug exosome protein mixed with 20 ug AMO-21 in 400 uL PBS for loading assay.
Formulation Format T7 peptide-decorated exosome loaded with AMO-21 by electroporation
Formulation Components T7-Lamp2b-displaying exosomes, AMO-21 anti-miR oligonucleotide
Size Nm 15.00
Zeta Mv -10.00
Model Scope in_vitro
Model Type in vitro
Cell Lines Or Primary Cells C6 rat glioblastoma cells
Animal Model
Administration Route cell culture exposure to AMO-21-loaded T7-exosomes
Output Type cellular uptake and miR-21 inhibition
Output Value T7-exo showed the highest DiI exosome and FAM-AMO-21 signals in C6 cells; flow cytometry showed higher AMO-21 delivery than unmodified and RVG exosomes; T7-exo/AMO-21 reduced miR-21 levels dose-dependently.
Output Units
Output Notes Functional in vitro anti-miR effect was demonstrated, but in vitro activity does not qualify as in vivo delivery success.
Toxicity Notes Exosomes showed lower cytotoxicity than PEI25k in C6 cells and no remarkable hemolysis/aggregation in rat red blood cell compatibility assay.
Curation Notes