Development of nucleic acid medicines based on chemical technology

被引:18
|
作者
Kawamoto, Yusuke [1 ]
Wu, You [1 ]
Takahashi, Yuki [1 ]
Takakura, Yoshinobu [1 ]
机构
[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Dept Biopharmaceut & Drug Metab, Sakyo, Kyoto 6068501, Japan
关键词
Therapeutic oligonucleotides; mRNA vaccines; Chemical modifications; Bioconjugations; Nanoparticles; Cellular uptake; Tissue-selective delivery; IN-VIVO DELIVERY; SOLID-PHASE SYNTHESIS; ALPHA-L-LNA; CONJUGATED ANTISENSE OLIGONUCLEOTIDES; RESTRICTED CONFORMATIONAL FLEXIBILITY; SPLICE-SWITCHING OLIGONUCLEOTIDES; CELL-PENETRATING PEPTIDES; SHAPED NANOCIRCULAR RNAS; GENE-SILENCING ACTIVITY; SMALL INTERFERING RNAS;
D O I
10.1016/j.addr.2023.114872
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Oligonucleotide-based therapeutics have attracted attention as an emerging modality that includes the modulation of genes and their binding proteins related to diseases, allowing us to take action on previously undruggable targets. Since the late 2010s, the number of oligonucleotide medicines approved for clinical uses has dramatically increased. Various chemistry-based technologies have been developed to improve the therapeutic properties of oligonucleotides, such as chemical modification, conjugation, and nanoparticle formation, which can increase nuclease resistance, enhance affinity and selectivity to target sites, suppress off-target effects, and improve pharmacokinetic properties. Similar strategies employing modified nucleobases and lipid nanoparticles have been used for developing coronavirus disease 2019 mRNA vaccines. In this review, we provide an overview of the development of chemistry-based technologies aimed at using nucleic acids for developing therapeutics over the past several decades, with a specific emphasis on the structural design and functionality of chemical modification strategies.& COPY; 2023 Elsevier B.V. All rights reserved.
引用
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页数:50
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