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<title>Asian Journal of Pharmaceutical Sciences Volume 18, Issue 6 2023</title>
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<place><placeTerm type="text">China</placeTerm></place>
<publisher>China Medical University</publisher>
<dateIssued>2023</dateIssued>
<issuance>monographic</issuance>
<edition>Volume 18, Issue 6 2023</edition>
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<languageTerm type="text">Indonesia</languageTerm>
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<note>a b s t r a c t
The emergence of the clustered regularly interspaced short palindromic repeats
(CRISPR)/CRISPR-associated protein 9 (Cas9) genome-editing system has brought about
a significant revolution in the realm of managing human diseases, establishing animal
models, and so on. To fully harness the potential of this potent gene-editing tool, ensuring
efficient and secure delivery to the target site is paramount. Consequently, developing
effective delivery methods for the CRISPR/Cas9 system has become a critical area of
research. In this review, we present a comprehensive outline of delivery strategies and

discuss their biomedical applications in the CRISPR/Cas9 system. We also provide an in-
depth analysis of physical, viral vector, and non-viral vector delivery strategies, including

plasmid-, mRNA- and protein-based approach. In addition, we illustrate the biomedical
applications of the CRISPR/Cas9 system. This review highlights the key factors affecting
the delivery process and the current challenges facing the CRISPR/Cas9 system, while also
delineating future directions and prospects that could inspire innovative delivery strategies. This review aims to provide new insights and ideas for advancing CRISPR/Cas9-based
delivery strategies and to facilitate breakthroughs in biomedical research and therapeutic applications.</note>
<subject authority=""><topic>Physical delivery</topic></subject>
<subject authority=""><topic>Viral vector</topic></subject>
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