siRNA drug delivery across the blood-brain barrier in Alzheimer's disease

被引:16
|
作者
Sajid, Muhammad Imran [1 ,2 ]
Sheikh, Fahad Sultan [3 ]
Anis, Faiza [4 ]
Nasim, Nourina [5 ]
Sumbria, Rachita K. [1 ,6 ]
Nauli, Surya M. [1 ]
Tiwari, Rakesh Kumar [1 ]
机构
[1] Chapman Univ, Dept Biomed & Pharmaceut Sci, Harry & Diane Rinker Hlth Sci Campus, Sch Pharm, Irvine, CA 92618 USA
[2] Univ Cent Punjab, Fac Pharm, Lahore 54000, Pakistan
[3] Shifa Tameer Emillat Univ, Shifa Coll Pharmaceut Sci, Islamabad 44000, Pakistan
[4] Fed Urdu Univ Arts Sci & Technol, Fac Pharmaceut Sci, Dept Pharmacol, Karachi, Pakistan
[5] Lahore Univ Management Sci, Syed Baber Ali Sch Sci & Engn, Dept Chem & Chem Engn, Lahore 54792, Pakistan
[6] Univ Calif Irvine, Dept Neurol, Irvine, CA 92868 USA
关键词
Alzheimer's disease; Target genes; RNAi; siRNA therapeutics; Mitigation strategies; Coding genes; Non-coding sequences; Gene Silencing; AD models; AMYLOID-PRECURSOR PROTEIN; GENE DELIVERY; MOUSE MODEL; COGNITIVE IMPAIRMENT; LIPID NANOPARTICLES; RNA INTERFERENCE; TAU OLIGOMERS; HIGH-AFFINITY; CELL-LINE; IN-VITRO;
D O I
10.1016/j.addr.2023.114968
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Alzheimer's disease (AD) is a progressive neurodegenerative disease with a few FDA-approved drugs that provide modest symptomatic benefits and only two FDA-approved disease-modifying treatments for AD. The advancements in understanding the causative genes and non-coding sequences at the molecular level of the pathophysiology of AD have resulted in several exciting research papers that employed small interfering RNA (siRNA)-based therapy. Although siRNA is being sought by academia and biopharma industries, several challenges still need to be addressed. We comprehensively report the latest advances in AD pathophysiology, druggable targets, ongoing clinical trials, and the siRNA-based approaches across the blood-brain barrier for addressing AD. This review describes the latest delivery systems employed to address this barrier. Critical insights and future perspectives on siRNA therapy for AD are also provided.& COPY; 2023 Elsevier B.V. All rights reserved.
引用
收藏
页数:26
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