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Polyethylenimine-Functionalized Carbon Dots for Delivery of CRISPR/Cas9 Complexes.

Authors :
Hashemzadeh I
Hasanzadeh A
Radmanesh F
Khodadadi Chegeni B
Hosseini ES
Kiani J
Shahbazi A
Naseri M
Fatahi Y
Nourizadeh H
Kheiri Yeghaneh Azar B
Aref AR
Liu Y
Hamblin MR
Karimi M
Source :
ACS applied bio materials [ACS Appl Bio Mater] 2021 Nov 15; Vol. 4 (11), pp. 7979-7992. Date of Electronic Publication: 2021 Nov 03.
Publication Year :
2021

Abstract

Carbon dots (CDs) have become the focus of many studies due to their outstanding optical properties and good biocompatibility. We investigated their potential application to produce a smart and highly efficient yet nontoxic nanovector for gene delivery. This was achieved by conjugating PEI <subscript>1.8k</subscript> -functionalized CDs (synthesized by one-step microwave-assisted pyrolysis) with arginine-disulfide linkers to produce CD-PEI <subscript>1.8k</subscript> -Arg nanoparticles. This nanovector could deliver p-CRISPR (9.3 kb) into different types of cell lines with higher efficiency compared to native PEI <subscript>1.8k</subscript> or PEI <subscript>25k</subscript> . CD-PEI <subscript>1.8k</subscript> -Arg also maintained its outstanding transfection efficiency at a high serum concentration and low p-CRISPR dose, compared to PEI <subscript>25k,</subscript> which was ineffective under those conditions. Additionally, CD-PEI <subscript>1.8k</subscript> -Arg could knock out the GFP gene with great efficiency by delivering the required components of CRISPR/Cas9, including a plasmid encoding Cas9, sgRNA targeting GFP, and Cas9/sgRNA ribonucleoproteins (RNPs) into the HEK 293T-GFP cells. Moreover, the nanoparticles showed potential for the local delivery of p-CRISPR into brain tissue. The remarkable properties of CD-PEI <subscript>1.8k</subscript> -Arg could enable the development of a safe, highly efficient gene-delivery nanovector for the treatment of various diseases in the near future.

Details

Language :
English
ISSN :
2576-6422
Volume :
4
Issue :
11
Database :
MEDLINE
Journal :
ACS applied bio materials
Publication Type :
Academic Journal
Accession number :
35006779
Full Text :
https://doi.org/10.1021/acsabm.1c00890