药物输送
寡核苷酸
计算生物学
药品
计算机科学
风险分析(工程)
纳米技术
生物
医学
药理学
遗传学
材料科学
DNA
出处
期刊:Journal of medical pharmaceutical and allied sciences
[Society of Pharmaceutical Tecnocrats]
日期:2025-02-28
卷期号:14 (1): 6945-6950
标识
DOI:10.55522/jmpas.v14i1.6732
摘要
Antisense oligonucleotides (ASOs) are small synthetic nucleic acids designed to bind RNA and modulate gene expression. They have significant therapeutic potential for treating genetic and acquired diseases, especially in cancer and hereditary disorders. Their primary mechanisms include RNA cleavage, mediated by RNase H1 or RNA interference (RNAi), and RNA blockage via steric hindrance or splice modulation. First-generation modifications, such as phosphorothioate linkage, and more advanced forms like locked nucleic acids (LNA) and peptide nucleic acids (PNA) have improved their pharmacokinetics and binding affinity. ASOs have achieved success in treating diseases like spinal muscular atrophy and Duchenne muscular dystrophy, with several FDA-approved drugs.
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