寡核苷酸临床前开发化学考虑因素指南》。

IF 4 2区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Nucleic acid therapeutics Pub Date : 2024-08-07 DOI:10.1089/nat.2024.0031
Daniel O'Reilly, Willeke van Roon-Mom, Annemieke Aartsma-Rus
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引用次数: 0

摘要

寡核苷酸疗法是现代药物的一个先锋类别,在利用先天机制调节基因表达方面处于领先地位。目前有 18 种基于寡核苷酸的药物获得了美国食品及药物管理局(FDA)的批准,可用于治疗各种临床疾病,这一领域展示出的创新潜力尚待充分挖掘。纯度、配方和内毒素水平等因素对这些疗法的疗效和安全性有着深刻的影响。因此,透彻了解生产用于临床前研究的高质量寡核苷酸所必需的化学因素,对于开发这些药物以进一步应用于临床至关重要。本文简要介绍了这些化学因素,旨在启发研究人员,使他们掌握必要的知识,在这一激动人心的创新领域取得进展。
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A Guide to Chemical Considerations for the Pre-Clinical Development of Oligonucleotides.

Oligonucleotide therapeutics, a pioneering category of modern medicinal drugs, are at the forefront of utilizing innate mechanisms to modulate gene expression. With 18 oligonucleotide-based FDA-approved medicines currently available for treating various clinical conditions, this field showcases an innovative potential yet to be fully explored. Factors such as purity, formulation, and endotoxin levels profoundly influence the efficacy and safety of these therapeutics. Therefore, a thorough understanding of the chemical factors essential for producing high-quality oligonucleotides for preclinical studies is crucial in their development for further clinical application. This paper serves as a concise guide to these chemical considerations, aiming to inspire and equip researchers with the necessary knowledge to advance in this exciting and innovative field.

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来源期刊
Nucleic acid therapeutics
Nucleic acid therapeutics BIOCHEMISTRY & MOLECULAR BIOLOGY-CHEMISTRY, MEDICINAL
CiteScore
7.60
自引率
7.50%
发文量
47
审稿时长
>12 weeks
期刊介绍: Nucleic Acid Therapeutics is the leading journal in its field focusing on cutting-edge basic research, therapeutic applications, and drug development using nucleic acids or related compounds to alter gene expression. The Journal examines many new approaches for using nucleic acids as therapeutic agents or in modifying nucleic acids for therapeutic purposes including: oligonucleotides, gene modification, aptamers, RNA nanoparticles, and ribozymes.
期刊最新文献
It is Time to Revisit miRNA Therapeutics. Characterization of the TLR9-Activating Potential of LNA-Modified Antisense Oligonucleotides. Peptide Nucleic Acid-Mediated Regulation of CRISPR-Cas9 Specificity. Levels of Exon-Skipping Are Not Artificially Overestimated Because of the Increased Affinity of Tricyclo-DNA-Modified Antisense Oligonucleotides to the Target DMD Exon. Near Sequence Homology Does Not Guarantee siRNA Cross-Species Efficacy.
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