Advances in Nanoparticles as Non-Viral Vectors for Efficient Delivery of CRISPR/Cas9

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초록

The clustered regularly interspaced short palindromic repeat (CRISPR)/Cas9 system is a gene-editing technology. Nanoparticle delivery systems have attracted attention because of the limitations of conventional viral vectors. In this review, we assess the efficiency of various nanoparticles, including lipid-based, polymer-based, inorganic, and extracellular vesicle-based systems, as non-viral vectors for CRISPR/Cas9 delivery. We discuss their advantages, limitations, and current challenges. By summarizing recent advancements and highlighting key strategies, this review aims to provide a comprehensive overview of the role of non-viral delivery systems in advancing CRISPR/Cas9 technology for clinical applications and gene therapy.

키워드

CRISPR/Cas9; delivery; nanoparticle; non-viral vector; viral vector; BIOMEDICAL APPLICATIONS; GOLD NANOPARTICLES; BETA-THALASSEMIA; GENOME; CAS9; CRISPR-CAS9; RNA; RIBONUCLEOPROTEIN; SYSTEM; HEMOGLOBIN
제목
Advances in Nanoparticles as Non-Viral Vectors for Efficient Delivery of CRISPR/Cas9
저자
Kim, Minse; Hwang, Youngwoo; Lim, Seongyu; Jang, Hyeon-Ki; Kim, Hyun-Ouk
DOI
10.3390/pharmaceutics16091197
발행일
2024-09
유형
Review
저널명
Pharmaceutics
권
16
호
9