Targeting Neuroinflammation in Central Nervous System Diseases by Oral Delivery of Lipid Nanoparticles.

IF 5.5 3区 医学 Q1 PHARMACOLOGY & PHARMACY Pharmaceutics Pub Date : 2025-03-18 DOI:10.3390/pharmaceutics17030388
Yuan Zou, Jing Zhang, Longmin Chen, Qianqian Xu, Sheng Yao, Hong Chen
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Abstract

Neuroinflammation within the central nervous system (CNS) is a primary characteristic of CNS diseases, such as Parkinson's disease, Alzheimer's disease (AD), amyotrophic lateral sclerosis, and mental disorders. The excessive activation of immune cells results in the massive release of pro-inflammatory cytokines, which subsequently induce neuronal death and accelerate the progression of neurodegeneration. Therefore, mitigating excessive neuroinflammation has emerged as a promising strategy for the treatment of CNS diseases. Despite advancements in drug discovery and the development of novel therapeutics, the effective delivery of these agents to the CNS remains a serious challenge due to the restrictive nature of the blood-brain barrier (BBB). This underscores the need to develop a novel drug delivery system. Recent studies have identified oral lipid nanoparticles (LNPs) as a promising approach to efficiently deliver drugs across the BBB and treat neurological diseases. This review aims to comprehensively summarize the recent advancements in the development of LNPs designed for the controlled delivery and therapeutic modulation of CNS diseases through oral administration. Furthermore, this review addresses the mechanisms by which these LNPs overcome biological barriers and evaluate their clinical implications and therapeutic efficacy in the context of oral drug delivery systems. Specifically, it focuses on LNP formulations that facilitate oral administration, exploring their potential to enhance bioavailability, improve targeting precision, and alleviate or manage the symptoms associated with a range of CNS diseases.

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口服脂质纳米颗粒靶向中枢神经系统疾病的神经炎症。
中枢神经系统(CNS)内的神经炎症是中枢神经系统疾病(如帕金森病、阿尔茨海默病(AD)、肌萎缩侧索硬化症和精神障碍)的主要特征。免疫细胞的过度激活导致促炎细胞因子的大量释放,进而诱导神经元死亡,加速神经退行性变的进展。因此,减轻过度的神经炎症已成为治疗中枢神经系统疾病的一种有希望的策略。尽管药物发现和新疗法的发展取得了进展,但由于血脑屏障(BBB)的限制性,这些药物有效递送到中枢神经系统仍然是一个严峻的挑战。这强调了开发一种新的给药系统的必要性。最近的研究已经确定口服脂质纳米颗粒(LNPs)是一种很有前途的方法,可以有效地通过血脑屏障传递药物并治疗神经系统疾病。本文综述了近年来通过口服给药控制给药和治疗中枢神经系统疾病的LNPs的研究进展。此外,本文综述了这些LNPs克服生物屏障的机制,并评估了它们在口服给药系统中的临床意义和治疗效果。具体而言,它侧重于LNP配方,方便口服给药,探索其潜力,以提高生物利用度,提高靶向精度,缓解或管理与一系列中枢神经系统疾病相关的症状。
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
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
期刊最新文献
RETRACTED: Khan et al. Norfloxacin Loaded Lipid Polymer Hybrid Nanoparticles for Oral Administration: Fabrication, Characterization, In Silico Modelling and Toxicity Evaluation. Pharmaceutics 2021, 13, 1632. Selection of Solubility Enhancement Technologies for S-892216, a Novel COVID-19 Drug Candidate. Silymarin and Silybin: Rejuvenating Traditional Remedies with Modern Delivery Strategies. Correction: Ortiz-Islas et al. Evolution of Alzheimer's Disease Therapeutics: From Conventional Drugs to Medicinal Plants, Immunotherapy, Microbiotherapy and Nanotherapy. Pharmaceutics 2025, 17, 128. Transcriptome-Guided Drug Repurposing Identifies Homoharringtonine (HHT) as a Candidate for Radiation-Induced Pulmonary Fibrosis.
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