• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于 CRISPR/Cas9 的聚合物纳米颗粒治疗/抑制微生物感染。

A CRISPR/Cas9 based polymeric nanoparticles to treat/inhibit microbial infections.

机构信息

Center for Nanobiotechnology Research, Department of Biological Sciences, Alabama State University, Montgomery, AL, 36104, USA.

Amity Institute of Biotechnology, Amity University, Jaipur, Rajasthan, 303002, India.

出版信息

Semin Cell Dev Biol. 2019 Dec;96:44-52. doi: 10.1016/j.semcdb.2019.04.007. Epub 2019 May 23.

DOI:10.1016/j.semcdb.2019.04.007
PMID:30986568
Abstract

The latest breakthrough towards the adequate and decisive methods of gene editing tools provided by CRISPR/Cas9 (Clustered Regularly Interspaced Short Palindromic Repeat/CRISPR Associated System), has been repurposed into a tool for genetically engineering eukaryotic cells and now considered as the major innovation in gene-related disorders. Nanotechnology has provided an alternate way to overcome the conventional problems where methods to deliver therapeutic agents have failed. The use of nanotechnology has the potential to safe-side the CRISPR/Cas9 components delivery by using customized polymeric nanoparticles for safety and efficacy. The pairing of two (CRISPR/Cas9 and nanotechnology) has the potential for opening new avenues in therapeutic use. In this review, we will discuss the most recent advances in developing nanoparticle-based CRISPR/Cas9 gene editing cargo delivery with a focus on several polymeric nanoparticles including fabrication proposals to combat microbial infections.

摘要

最新的突破是利用 CRISPR/Cas9(成簇规律间隔短回文重复/CRISPR 相关系统)提供的适当且决定性的基因编辑工具方法,已被重新用作基因工程真核细胞的工具,现在被认为是基因相关疾病的主要创新。纳米技术提供了一种替代方法来克服传统问题,其中输送治疗剂的方法已经失败。使用纳米技术有可能通过使用定制的聚合物纳米粒子来安全有效地输送 CRISPR/Cas9 组件。将两者(CRISPR/Cas9 和纳米技术)结合起来,有可能开辟治疗用途的新途径。在这篇综述中,我们将讨论基于纳米粒子的 CRISPR/Cas9 基因编辑货物输送的最新进展,重点介绍几种聚合物纳米粒子,包括制造建议,以对抗微生物感染。

相似文献

1
A CRISPR/Cas9 based polymeric nanoparticles to treat/inhibit microbial infections.基于 CRISPR/Cas9 的聚合物纳米颗粒治疗/抑制微生物感染。
Semin Cell Dev Biol. 2019 Dec;96:44-52. doi: 10.1016/j.semcdb.2019.04.007. Epub 2019 May 23.
2
Delivery of CRISPR/Cas9 for therapeutic genome editing.CRISPR/Cas9 基因编辑治疗的递送。
J Gene Med. 2019 Jul;21(7):e3107. doi: 10.1002/jgm.3107.
3
Therapeutic gene editing in haematological disorders with CRISPR/Cas9.CRISPR/Cas9 基因编辑治疗血液系统疾病。
Br J Haematol. 2019 Jun;185(5):821-835. doi: 10.1111/bjh.15851. Epub 2019 Mar 12.
4
CRISPR/Cas9: an advanced tool for editing plant genomes.CRISPR/Cas9:一种用于编辑植物基因组的先进工具。
Transgenic Res. 2016 Oct;25(5):561-73. doi: 10.1007/s11248-016-9953-5. Epub 2016 Mar 24.
5
Synthetic multi-layer nanoparticles for CRISPR-Cas9 genome editing.用于 CRISPR-Cas9 基因组编辑的合成多层纳米颗粒。
Adv Drug Deliv Rev. 2021 Jan;168:55-78. doi: 10.1016/j.addr.2020.03.001. Epub 2020 Mar 5.
6
Cationic Polymer-Mediated CRISPR/Cas9 Plasmid Delivery for Genome Editing.阳离子聚合物介导的 CRISPR/Cas9 质粒递送用于基因组编辑。
Macromol Rapid Commun. 2019 Mar;40(5):e1800068. doi: 10.1002/marc.201800068. Epub 2018 Apr 30.
7
Use of CRISPR/Cas9 gene-editing tools for developing models in drug discovery.使用 CRISPR/Cas9 基因编辑工具开发药物发现模型。
Drug Discov Today. 2018 Mar;23(3):519-533. doi: 10.1016/j.drudis.2018.01.014. Epub 2018 Jan 8.
8
[Advances in application of clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated 9 system in stem cells research].成簇规律间隔短回文重复序列(CRISPR)/CRISPR相关蛋白9系统在干细胞研究中的应用进展
Zhonghua Shao Shang Za Zhi. 2018 Apr 20;34(4):253-256. doi: 10.3760/cma.j.issn.1009-2587.2018.04.013.
9
Strategies for nonviral nanoparticle-based delivery of CRISPR/Cas9 therapeutics.基于非病毒纳米颗粒的 CRISPR/Cas9 治疗药物的递送策略。
Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2020 May;12(3):e1609. doi: 10.1002/wnan.1609. Epub 2019 Dec 2.
10
In Vivo Delivery of CRISPR/Cas9 for Therapeutic Gene Editing: Progress and Challenges.用于治疗性基因编辑的CRISPR/Cas9体内递送:进展与挑战
Bioconjug Chem. 2017 Apr 19;28(4):880-884. doi: 10.1021/acs.bioconjchem.7b00057. Epub 2017 Mar 17.

引用本文的文献

1
CRISPR/Cas9 systems: Delivery technologies and biomedical applications.CRISPR/Cas9系统:递送技术与生物医学应用
Asian J Pharm Sci. 2023 Nov;18(6):100854. doi: 10.1016/j.ajps.2023.100854. Epub 2023 Oct 21.
2
Inherent and Composite Hydrogels as Promising Materials to Limit Antimicrobial Resistance.天然和复合水凝胶作为限制抗生素耐药性的有前景材料。
Gels. 2022 Jan 20;8(2):70. doi: 10.3390/gels8020070.
3
Exploring nano-enabled CRISPR-Cas-powered strategies for efficient diagnostics and treatment of infectious diseases.探索基于纳米技术的CRISPR-Cas驱动策略用于传染病的高效诊断与治疗。
J Nanostructure Chem. 2022;12(5):833-864. doi: 10.1007/s40097-022-00472-7. Epub 2022 Feb 14.
4
Current Potential Therapeutic Approaches against SARS-CoV-2: A Review.当前针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的潜在治疗方法:综述
Biomedicines. 2021 Nov 4;9(11):1620. doi: 10.3390/biomedicines9111620.
5
TNBC: Potential Targeting of Multiple Receptors for a Therapeutic Breakthrough, Nanomedicine, and Immunotherapy.三阴性乳腺癌:针对多种受体实现治疗突破、纳米医学及免疫疗法的潜在靶点
Biomedicines. 2021 Jul 23;9(8):876. doi: 10.3390/biomedicines9080876.
6
Harnessing lipid nanoparticles for efficient CRISPR delivery.利用脂质纳米颗粒实现高效 CRISPR 递送。
Biomater Sci. 2021 Sep 14;9(18):6001-6011. doi: 10.1039/d1bm00537e.
7
CRISPR/Cas9 based genome editing for targeted transcriptional control in triple-negative breast cancer.基于CRISPR/Cas9的基因组编辑用于三阴性乳腺癌的靶向转录调控
Comput Struct Biotechnol J. 2021 Apr 18;19:2384-2397. doi: 10.1016/j.csbj.2021.04.036. eCollection 2021.
8
Novel Strategy to Combat Antibiotic Resistance: A Sight into the Combination of CRISPR/Cas9 and Nanoparticles.对抗抗生素耐药性的新策略:深入了解CRISPR/Cas9与纳米颗粒的结合
Pharmaceutics. 2021 Mar 8;13(3):352. doi: 10.3390/pharmaceutics13030352.
9
Recent Advances in Pathophysiology, Drug Development and Future Perspectives of SARS-CoV-2.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病理生理学、药物研发的最新进展及未来展望
Front Cell Dev Biol. 2020 Nov 6;8:580202. doi: 10.3389/fcell.2020.580202. eCollection 2020.