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脂质纳米颗粒介导的脑部递药。

Lipid nanoparticle-mediated drug delivery to the brain.

机构信息

Graduate School of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, United States.

Department of Chemistry and Biochemistry, The University of Mississippi, MS, United States.

出版信息

Adv Drug Deliv Rev. 2023 Jun;197:114861. doi: 10.1016/j.addr.2023.114861. Epub 2023 May 6.

Abstract

Lipid nanoparticles (LNPs) have revolutionized the field of drug delivery through their applications in siRNA delivery to the liver (Onpattro) and their use in the Pfizer-BioNTech and Moderna COVID-19 mRNA vaccines. While LNPs have been extensively studied for the delivery of RNA drugs to muscle and liver targets, their potential to deliver drugs to challenging tissue targets such as the brain remains underexplored. Multiple brain disorders currently lack safe and effective therapies and therefore repurposing LNPs could potentially be a game changer for improving drug delivery to cellular targets both at and across the blood-brain barrier (BBB). In this review, we will discuss (1) the rationale and factors involved in optimizing LNPs for brain delivery, (2) ionic liquid-coated LNPs as a potential approach for increasing LNP accumulation in the brain tissue and (3) considerations, open questions and potential opportunities in the development of LNPs for delivery to the brain.

摘要

脂质纳米粒(LNPs)在将 siRNA 递送至肝脏(Onpattro)的应用以及在辉瑞-生物技术公司和 Moderna COVID-19 mRNA 疫苗中的应用,彻底改变了药物输送领域。虽然 LNPs 已被广泛研究用于将 RNA 药物递送至肌肉和肝脏靶标,但它们将药物递送至具有挑战性的组织靶标(如大脑)的潜力仍未得到充分探索。目前,多种脑部疾病缺乏安全有效的治疗方法,因此,重新利用 LNPs 可能会成为改善药物递送至血脑屏障(BBB)内外细胞靶标的游戏规则改变者。在这篇综述中,我们将讨论(1)优化 LNPs 用于脑部递药的原理和因素,(2)离子液体包被的 LNPs 作为增加 LNPs 在脑组织中积累的潜在方法,以及(3)开发用于脑部递药的 LNPs 的考虑因素、未解决的问题和潜在机会。

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