药物输送
小干扰RNA
纳米技术
核酸
有效载荷(计算)
核糖核酸
靶向给药
RNA干扰
药物发现
药品
化学
计算生物学
免疫系统
药物开发
毒品携带者
再生医学
纳米载体
细胞生物学
药理学
生物
生物技术
生物相容性材料
小RNA
小RNA
领域
人类使用
作者
Sharat Sarmah,Sourav Baidya,Mrinmoy De
出处
期刊:Small
[Wiley]
日期:2025-09-24
卷期号:21 (43): e06812-e06812
被引量:9
标识
DOI:10.1002/smll.202506812
摘要
In the realm of drug delivery, lipid nanoparticles (LNPs) have become a revolutionary platform asthey provide a flexible and effective pathway for the administration of a variety of therapeutic agents, particularly with respect to the target-specific delivery of physiologically "fragile" materials, such as small interfering RNA (siRNA) and messenger RNA (mRNA). The increased access to sophisticated generations of LNPs and the growing need for noninvasive, precision treatment technology that can bypass physiological barriers and reduce adverse effects have sparked the growth and development of this field. In the current scenario, researchers are directing their efforts to address particular issues, including increasing tissue selectivity, increasing payload capacity, and reducing immune system activation. Here, we provide a comprehensive discussion of LNPs, commencing from their fundamental composition and development to their use in nucleic acid delivery, innovative ionizable lipid synthesis techniques and targeting mechanisms. This review highlights the increasing importance of LNPs in contemporary medicine and their potential to revolutionize drug delivery systems.
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