文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
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
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
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 @ 2025

基于聚合物和脂质的 siRNA 纳米颗粒的表面设计选择:使用抗体。

Surface Design Options in Polymer- and Lipid-Based siRNA Nanoparticles Using Antibodies.

机构信息

Medical Clinic I, Research Campus, University Hospital of Erlangen, Hartmannstraße 14, 91052 Erlangen, Germany.

Medical Immunology Campus Erlangen, Medical Clinic 1, Friedrich-Alexander University Erlangen-Nürnberg, 91054 Erlangen, Germany.

出版信息

Int J Mol Sci. 2022 Nov 11;23(22):13929. doi: 10.3390/ijms232213929.


DOI:10.3390/ijms232213929
PMID:36430411
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9692731/
Abstract

The mechanism of RNA interference (RNAi) could represent a breakthrough in the therapy of all diseases that arise from a gene defect or require the inhibition of a specific gene expression. In particular, small interfering RNA (siRNA) offers an attractive opportunity to achieve a new milestone in the therapy of human diseases. The limitations of siRNA, such as poor stability, inefficient cell uptake, and undesired immune activation, as well as the inability to specifically reach the target tissue in the body, can be overcome by further developments in the field of nanoparticulate drug delivery. Therefore, types of surface modified siRNA nanoparticles are presented and illustrate how a more efficient and safer distribution of siRNA at the target site is possible by modifying the surface properties of nanoparticles with antibodies. However, the development of such efficient and safe delivery strategies is currently still a major challenge. In consideration of that, this review article aims to demonstrate the function and targeted delivery of siRNA nanoparticles, focusing on the surface modification via antibodies, various lipid- and polymer-components, and the therapeutic effects of these delivery systems.

摘要

RNA 干扰 (RNAi) 的作用机制可能代表着从基因缺陷引起的所有疾病治疗或特定基因表达抑制治疗的一个突破。特别是小干扰 RNA (siRNA) 为实现人类疾病治疗的新里程碑提供了一个有吸引力的机会。siRNA 的局限性,如稳定性差、细胞摄取效率低、不期望的免疫激活以及无法在体内特异性到达靶组织,可以通过纳米颗粒药物递送领域的进一步发展来克服。因此,本文介绍了各种表面修饰的 siRNA 纳米颗粒,并说明了通过用抗体修饰纳米颗粒的表面特性,如何实现 siRNA 在靶位的更有效和更安全的分布。然而,开发这种高效和安全的递药策略目前仍然是一个重大挑战。有鉴于此,本文旨在展示 siRNA 纳米颗粒的功能和靶向递药,重点介绍通过抗体、各种脂质和聚合物成分进行的表面修饰,以及这些递药系统的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b7a/9692731/f5c6ee44fdff/ijms-23-13929-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b7a/9692731/24eb639bd449/ijms-23-13929-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b7a/9692731/f5c6ee44fdff/ijms-23-13929-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b7a/9692731/24eb639bd449/ijms-23-13929-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b7a/9692731/f5c6ee44fdff/ijms-23-13929-g002.jpg

相似文献

[1]
Surface Design Options in Polymer- and Lipid-Based siRNA Nanoparticles Using Antibodies.

Int J Mol Sci. 2022-11-11

[2]
Lipid and Polymer-Based Nanoparticle siRNA Delivery Systems for Cancer Therapy.

Molecules. 2020-6-10

[3]
SiRNA delivery: challenges and role of carrier systems.

Pharmazie. 2011-5

[4]
The landscape of nanoparticle-based siRNA delivery and therapeutic development.

Mol Ther. 2024-2-7

[5]
Engineering of small interfering RNA-loaded lipidoid-poly(DL-lactic-co-glycolic acid) hybrid nanoparticles for highly efficient and safe gene silencing: A quality by design-based approach.

Eur J Pharm Biopharm. 2017-7-26

[6]
Functional nanostructures for effective delivery of small interfering RNA therapeutics.

Theranostics. 2014-9-19

[7]
Engineering of Solid Dosage Forms of siRNA-Loaded Lipidoid-Polymer Hybrid Nanoparticles Using a Quality-by-Design Approach.

Methods Mol Biol. 2021

[8]
Enhancing siRNA cancer therapy: Multifaceted strategies with lipid and polymer-based carrier systems.

Int J Pharm. 2024-9-30

[9]
Environment-Responsive Lipid/siRNA Nanoparticles for Cancer Therapy.

Adv Healthc Mater. 2021-3

[10]
Advances in the polymeric nanoparticulate delivery systems for RNA therapeutics.

Prog Mol Biol Transl Sci. 2024

引用本文的文献

[1]
Combined Hyaluronic Acid Nanobioconjugates Impair CD44-Signaling for Effective Treatment Against Obesity: A Review of Comparison with Other Actors.

Int J Nanomedicine. 2025-8-21

[2]
Clinical Applications of Combined Immunotherapy Approaches in Gastrointestinal Cancer: A Case-Based Review.

Vaccines (Basel). 2023-9-29

[3]
Advances with Lipid-Based Nanosystems for siRNA Delivery to Breast Cancers.

Pharmaceuticals (Basel). 2023-7-6

本文引用的文献

[1]
Multifunctional nanoparticles co-loaded with Adriamycin and MDR-targeting siRNAs for treatment of chemotherapy-resistant esophageal cancer.

J Nanobiotechnology. 2022-3-28

[2]
Dual pH-Responsive and Tumor-Targeted Nanoparticle-Mediated Anti-Angiogenesis siRNA Delivery for Tumor Treatment.

Int J Nanomedicine. 2022

[3]
Co-Delivery of mRNA and pDNA Using Thermally Stabilized Coacervate-Based Core-Shell Nanosystems.

Pharmaceutics. 2021-11-13

[4]
Simultaneous silencing of the A2aR and PD-1 immune checkpoints by siRNA-loaded nanoparticles enhances the immunotherapeutic potential of dendritic cell vaccine in tumor experimental models.

Life Sci. 2022-1-1

[5]
Modified cyclodextrin-based nanoparticles mediated delivery of siRNA for huntingtin gene silencing across an in vitro BBB model.

Eur J Pharm Biopharm. 2021-12

[6]
Recent Advances and Challenges in Gene Delivery Mediated by Polyester-Based Nanoparticles.

Int J Nanomedicine. 2021

[7]
Delivery of therapeutic oligonucleotides in nanoscale.

Bioact Mater. 2021-6-12

[8]
Lipid nanoparticles for mRNA delivery.

Nat Rev Mater. 2021

[9]
Therapeutic inhibitory RNA in head and neck cancer via functional targeted lipid nanoparticles.

J Control Release. 2021-9-10

[10]
Lipid Nanoparticles─From Liposomes to mRNA Vaccine Delivery, a Landscape of Research Diversity and Advancement.

ACS Nano. 2021-11-23

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索