药物安全评价中的“计算机”毒理学方法

Q4 Pharmacology, Toxicology and Pharmaceutics Arhiv za Farmaciju Pub Date : 2021-01-01 DOI:10.5937/arhfarm71-32966
Danijela Đukić-Ćosić, K. Baralić, D. Jorgovanović, K. Živančević, D. Javorac, N. Stojilković, B. Radović, Đ. Marić, M. Ćurčić, Aleksandra Buha-Đorđević, Z. Bulat, Evica Antonijević-Miljaković, B. Antonijević
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引用次数: 0

摘要

虽然实验动物研究历来是评估药物安全性的最传统方法,目前被认为是确定药物毒性的主要方法,但这些研究受到成本、时间和伦理批准的限制。在过去的20年里,计算科学和计算机数据处理取得了重大进展,而替代技术及其应用的知识已经发展成为毒理学中的一项宝贵技能。因此,计算机方法在药品安全性评价中的应用不断增加。它们非常复杂,并以毒理学、生物信息学、生物化学、统计学、数学以及分子生物学积累的知识为基础。本综述将总结目前关于在毒性试验中使用计算机方法的最新科学数据,考虑到它们的缺点,并强调应该提供一致结果的策略,同时涵盖计算机方法在临床前试验和药物杂质毒性试验中的应用。
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'In silico' toxicology methods in drug safety assessment
While experimental animal investigation has historically been the most conventional approach conducted to assess drug safety and is currently considered the main method for determining drug toxicity, these studies are constricted by cost, time, and ethical approvals. Over the last 20 years, there have been significant advances in computational sciences and computer data processing, while knowledge of alternative techniques and their application has developed into a valuable skill in toxicology. Thus, the application of in silico methods in drug safety assessment is constantly increasing. They are very complex and are grounded on accumulated knowledge from toxicology, bioinformatics, biochemistry, statistics, mathematics, as well as molecular biology. This review will summarize current state-of-the-art scientific data on the use of in silico methods in toxicity testing, taking into account their shortcomings, and highlighting the strategies that should deliver consistent results, while covering the applications of in silico methods in preclinical trials and drug impurities toxicity testing.
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来源期刊
Arhiv za Farmaciju
Arhiv za Farmaciju Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
自引率
0.00%
发文量
19
审稿时长
12 weeks
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