{"title":"A perspective on targeted LNPs","authors":"Jens B. Simonsen, Philipp Nicolas Spahn","doi":"10.1016/j.jconrel.2026.115344","DOIUrl":null,"url":null,"abstract":"<div><div>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.</div></div>","PeriodicalId":15450,"journal":{"name":"Journal of Controlled Release","volume":"399 ","pages":"Article 115344"},"PeriodicalIF":12.4000,"publicationDate":"2026-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Controlled Release","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0168365926007480","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/9 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
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.
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.
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