A perspective on targeted LNPs

IF 12.4 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Journal of Controlled Release Pub Date : 2026-11-10 Epub Date: 2026-09-09 DOI:10.1016/j.jconrel.2026.115344
Jens B. Simonsen, Philipp Nicolas Spahn
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引用次数: 0

Abstract

Actively targeted lipid nanoparticles (tLNPs), in which LNPs are decorated with ligands for targeted delivery, offer a promising strategy to address a major challenge in nanomedicine: achieving efficient uptake in extrahepatic cells while limiting dominant uptake by the liver and unintended uptake by immune cells. tLNPs have now entered early clinical trials, with encouraging results reported for in vivo T-cell reprogramming. In this Perspective, we cover key considerations for the development of tLNP formulations. We discuss physicochemical factors related to ligand-PEG-lipid design and incorporation into LNPs, including ligand density, orientation, and localization, as well as extracellular and intracellular ligand-target engagement and safety considerations. We highlight recent early-stage clinical results in this area and preclinical applications in which tLNPs are currently being explored. Finally, we briefly highlight potential challenges associated with the reproducible and cost-effective manufacture of tLNPs and emphasize the need for additional analytical methods to adequately characterize these complex formulations.
对目标LNPs的看法。
主动靶向脂质纳米颗粒(tLNPs),其中LNPs用配体修饰以靶向递送,为解决纳米医学的主要挑战提供了一个有希望的策略:实现肝外细胞的有效摄取,同时限制肝脏的显性摄取和免疫细胞的意外摄取。tLNPs目前已进入早期临床试验,在体内t细胞重编程方面取得了令人鼓舞的结果。在这个观点中,我们涵盖了tLNP配方开发的关键考虑因素。我们讨论了与配体- peg -脂质设计和融入LNPs相关的物理化学因素,包括配体密度、取向和定位,以及细胞外和细胞内配体-靶标接合和安全性考虑。我们重点介绍了最近在这一领域的早期临床结果以及目前正在探索的tlnp的临床前应用。最后,我们简要地强调了与tlnp的可重复性和成本效益制造相关的潜在挑战,并强调需要额外的分析方法来充分表征这些复杂的配方。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Controlled Release
Journal of Controlled Release 医学-化学综合
CiteScore
18.50
自引率
5.60%
发文量
700
审稿时长
39 days
期刊介绍: The Journal of Controlled Release (JCR) proudly serves as the Official Journal of the Controlled Release Society and the Japan Society of Drug Delivery System. Dedicated to the broad field of delivery science and technology, JCR publishes high-quality research articles covering drug delivery systems and all facets of formulations. This includes the physicochemical and biological properties of drugs, design and characterization of dosage forms, release mechanisms, in vivo testing, and formulation research and development across pharmaceutical, diagnostic, agricultural, environmental, cosmetic, and food industries. Priority is given to manuscripts that contribute to the fundamental understanding of principles or demonstrate the advantages of novel technologies in terms of safety and efficacy over current clinical standards. JCR strives to be a leading platform for advancements in delivery science and technology.
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