用于传递CRISPR/Cas9系统的纳米载体
SuJin Hwang1, Hyejun Ko1, Hee-Young Lee2,3
1School of Integrative Engineering, Chung-Ang University, Seoul, Republic of Korea.
Nanomedicine (London, England)
|December 23, 2025
概括
克里斯普尔/卡斯9系统能够精确的基因组编辑,但面临着交付挑战. 本综述探讨了基于纳米载体的传递方法,以实现生物技术和医学中高效的CRISPR/Cas9应用.
科学领域:
- 生物技术是生物技术.
- 分子生物学分子生物学
- 遗传学 是一个遗传学.
背景情况:
- 集群定期间隔的短巴林德罗姆重复/关联蛋白9 (CRISPR/Cas9) 系统是精确的DNA操纵和基因组编辑的强大工具.
- 克里斯普尔/Cas9技术对生物医学应用具有重大前景,包括疾病治疗和遗传查.
研究的目的:
- 审查和讨论CRISPR/Cas9系统的各种交付方法.
- 专注于基于纳米载体的技术,以实现高效和选择性的CRISPR/Cas9传递.
- 分析CRISPR/Cas9传递系统的挑战,未来方向和潜力.
主要方法:
- 使用科学网,Scopus,PubMed和谷歌学者进行全面的文献搜索.
- 对2015年至2024年间发表的文章进行分析.
- 专注于使用纳米载体的传递技术.
主要成果:
- 对CRISPR/Cas9系统的交付仍然是其广泛应用的关键障碍.
- 纳米载体是克服CRISPR/Cas9传递挑战的有希望的策略.
- 各种纳米载体系统为高效和选择性的CRISPR/Cas9传递提供了潜力.
结论:
- 有效和选择性交付对于释放CRISPR/Cas9技术的全部潜力至关重要.
- 纳米载体介导的传递系统是推动CRISPR/Cas9在生物技术和医学中的应用的关键.
- 对优化纳米载体传递的进一步研究对未来的治疗和研究进步具有重大前景.
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