影响治疗性反义寡核苷酸ADME性质的因素:理化特性及其超越。

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Rongrong Jiang, Shirin Hooshfar, Marsha Rebecca Eno, Cassandra Yun, Estevan Sonego Zimmermann, Raku Shinkyo
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引用次数: 0

摘要

治疗性反义寡核苷酸(ASOs)代表了一系列化学修饰的单链脱氧核糖核苷酸,它们互补地影响其mRNA靶点。它们与传统的小分子有很大不同。这些新开发的治疗性ASO具有独特的吸收、分布、代谢和排泄(ADME)过程,这些过程最终决定了它们的药代动力学、疗效和安全性。ASO的ADME特性和相关的关键因素尚未得到充分研究。因此,对其ADME特性的彻底表征和深入研究对于支持安全有效的治疗性ASO的药物发现和开发过程至关重要。在这篇综述中,我们讨论了影响这些小说ADME特征的主要因素和不断发展的治疗方法。ASO骨架和糖化学、偶联方法、给药位点和途径等的主要变化是ADME和PK图谱的主要决定因素,从而影响其疗效和安全性。此外,物种差异和DDI因素在理解ADME图谱和PK可翻译性方面很重要,但对ASOs的研究较少。因此,我们在现有知识的基础上总结了这些方面,并在本次审查中进行了讨论。我们还概述了目前可用于研究影响ASO药物ADME的关键因素的工具、技术和方法,并提供了未来的前景和知识差距分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors Influencing ADME Properties of Therapeutic Antisense Oligonucleotides: Physicochemical Characteristics and Beyond.

Therapeutic antisense oligonucleotides (ASOs) represent a diverse array of chemically modified singlestranded deoxyribonucleotides that work complementarily to affect their mRNA targets. They vastly differ from conventional small molecules. These newly developed therapeutic ASOs possess unique absorption, distribution, metabolism, and excretion (ADME) processes that ultimately determine their pharmacokinetic, efficacy and safety profiles. The ADME properties of ASOs and associated key factors have not been fully investigated. Therefore, thorough characterization and in-depth study of their ADME properties are critical to support drug discovery and development processes for safe and effective therapeutic ASOs. In this review, we discussed the main factors affecting the ADME characteristics of these novels and evolving therapies. The major changes to ASO backbone and sugar chemistry, conjugation approaches, sites and routes of administration, etc., are the principal determinants of ADME and PK profiles that consequentially impact their efficacy and safety profiles. In addition, species difference and DDI considerations are important in understanding ADME profile and PK translatability but are less studied for ASOs. We, therefore, have summarized these aspects based on current knowledge and provided discussions in this review. We also give an overview of the current tools, technologies, and approaches available to investigate key factors that influence the ADME of ASO drugs and provide future perspectives and knowledge gap analysis.

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来源期刊
Current drug metabolism
Current drug metabolism 医学-生化与分子生物学
CiteScore
4.30
自引率
4.30%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Current Drug Metabolism aims to cover all the latest and outstanding developments in drug metabolism, pharmacokinetics, and drug disposition. The journal serves as an international forum for the publication of full-length/mini review, research articles and guest edited issues in drug metabolism. Current Drug Metabolism is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the most important developments. The journal covers the following general topic areas: pharmaceutics, pharmacokinetics, toxicology, and most importantly drug metabolism. More specifically, in vitro and in vivo drug metabolism of phase I and phase II enzymes or metabolic pathways; drug-drug interactions and enzyme kinetics; pharmacokinetics, pharmacokinetic-pharmacodynamic modeling, and toxicokinetics; interspecies differences in metabolism or pharmacokinetics, species scaling and extrapolations; drug transporters; target organ toxicity and interindividual variability in drug exposure-response; extrahepatic metabolism; bioactivation, reactive metabolites, and developments for the identification of drug metabolites. Preclinical and clinical reviews describing the drug metabolism and pharmacokinetics of marketed drugs or drug classes.
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