清脆的
基因组编辑
纳米载体
Cas9
固体脂质纳米粒
遗传增强
计算生物学
生物
纳米技术
药物输送
基因
材料科学
遗传学
作者
Aisha Aziz,Urushi Rehman,Afsana Sheikh,Mohammed A.S. Abourehab,Prashant Kesharwani
标识
DOI:10.1080/09205063.2022.2121592
摘要
CRISPR/Cas mediated gene-editing has opened new avenues for therapies that show great potential for treating or curing cancers, genetic disorders, and microbial infections such as HIV. CRISPR/Cas9 tool is highly efficacious in revolutionizing the advent of genome editing; however, its efficient and safe delivery is a major hurdle due to its cellular impermeability and instability. Nano vectors could be explored to scale up the safe and effective delivery of CRISPR/Cas9. This review highlights the importance of CRISPR/Cas9 genome editing system in cancer treatment along with the effect of lipid-based nanoparticles in its safe delivery to cancer cells. The solid-lipid nanoparticles, nanostructured lipid carrier, lipid nanoparticles and niosomes have shown great effect in the delivery of CRISPR compounds to the cancer cells. The design and genome editing application in cancer therapy has been discussed along with the future concern and prospects of lipid nanoparticle based CRISPR/Cas9 has been focused toward the end.
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