Chiral Graphene Quantum Dots Enhanced Drug Loading into Small Extracellular Vesicles
- PMID: 37127891
- DOI: 10.1021/acsnano.3c00305
Chiral Graphene Quantum Dots Enhanced Drug Loading into Small Extracellular Vesicles
Abstract
As nanoscale extracellular vesicles secreted by cells, small extracellular vesicles (sEVs) have enormous potential as safe and effective vehicles to deliver drugs into lesion locations. Despite promising advances with sEV-based drug delivery systems, there are still challenges to drug loading into sEVs, which hinder the clinical applications of sEVs. Herein, we report an exogenous drug-agnostic chiral graphene quantum dots (GQDs) sEV-loading platform, based on chirality matching with the sEV lipid bilayer. Both hydrophobic and hydrophilic chemical and biological drugs can be functionalized or adsorbed onto GQDs by π-π stacking and van der Waals interactions. By tuning the ligands and GQD size to optimize its chirality, we demonstrate drug loading efficiency of 66.3% and 64.1% for doxorubicin and siRNA, which is significantly higher than other reported sEV loading techniques.
Keywords: chemotherapy; chirality; drug delivery; extracellular vesicles; graphene quantum dots; siRNA.
Update of
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Chiral Graphene Quantum Dots Enhanced Drug Loading into Exosomes.bioRxiv [Preprint]. 2023 Jan 20:2023.01.20.523510. doi: 10.1101/2023.01.20.523510. bioRxiv. 2023. Update in: ACS Nano. 2023 Jun 13;17(11):10191-10205. doi: 10.1021/acsnano.3c00305. PMID: 36711460 Free PMC article. Updated. Preprint.
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