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探索适体在靶向神经炎症和神经退行性疾病中的潜力:机遇与挑战。

Exploring the Potential of Aptamers in Targeting Neuroinflammation and Neurodegenerative Disorders: Opportunities and Challenges.

机构信息

Teaching and Research Division, School of Chinese Medicine, Hong Kong Baptist University, Hong Kong SAR, China.

Law Sau Fai Institute for Advancing Translational Medicine in Bone & Joint Diseases, School of Chinese Medicine, Hong Kong Baptist University, Hong Kong SAR, China.

出版信息

Int J Mol Sci. 2023 Jul 22;24(14):11780. doi: 10.3390/ijms241411780.

DOI:10.3390/ijms241411780
PMID:37511539
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10380291/
Abstract

Neuroinflammation is the precursor for several neurodegenerative diseases (NDDs), such as Alzheimer's disease (AD), Parkinson's disease (PD), and multiple sclerosis (MS). Targeting neuroinflammation has emerged as a promising strategy to address a wide range of CNS pathologies. These NDDs still present significant challenges in terms of limited and ineffective diagnosis and treatment options, driving the need to explore innovative and novel therapeutic alternatives. Aptamers are single-stranded nucleic acids that offer the potential for addressing these challenges through diagnostic and therapeutic applications. In this review, we summarize diagnostic and therapeutic aptamers for inflammatory biomolecules, as well as the inflammatory cells in NDDs. We also discussed the potential of short nucleotides for Aptamer-Based Targeted Brain Delivery through their unique features and modifications, as well as their ability to penetrate the blood-brain barrier. Moreover, the unprecedented opportunities and substantial challenges of using aptamers as therapeutic agents, such as drug efficacy, safety considerations, and pharmacokinetics, are also discussed. Taken together, this review assesses the potential of aptamers as a pioneering approach for target delivery to the CNS and the treatment of neuroinflammation and NDDs.

摘要

神经炎症是几种神经退行性疾病(NDDs)的前兆,如阿尔茨海默病(AD)、帕金森病(PD)和多发性硬化症(MS)。针对神经炎症已成为一种有前途的策略,可以解决广泛的中枢神经系统疾病。这些 NDDs 在诊断和治疗选择有限且效果不佳方面仍然存在重大挑战,这促使人们需要探索创新和新颖的治疗替代方案。适体是单链核酸,通过诊断和治疗应用提供了解决这些挑战的潜力。在这篇综述中,我们总结了针对炎症生物分子和 NDDs 中炎症细胞的诊断和治疗适体。我们还讨论了短核苷酸通过其独特的特性和修饰以及穿透血脑屏障的能力,作为基于适体的靶向脑递药的潜在应用。此外,还讨论了适体作为治疗剂的前所未有的机会和重大挑战,例如药物疗效、安全性考虑因素和药代动力学。综上所述,本综述评估了适体作为一种开创性的方法,用于将药物靶向递送至中枢神经系统,并治疗神经炎症和 NDDs。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38f0/10380291/d086abb5f8ec/ijms-24-11780-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38f0/10380291/9f8f025f124f/ijms-24-11780-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38f0/10380291/51a7056bf08e/ijms-24-11780-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38f0/10380291/d086abb5f8ec/ijms-24-11780-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38f0/10380291/9f8f025f124f/ijms-24-11780-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38f0/10380291/fd2845b44bc3/ijms-24-11780-g002.jpg
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