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Titlebook: Drug-Induced Liver Toxicity; Minjun Chen,Yvonne Will Book 2018 Springer Science+Business Media, LLC, part of Springer Nature 2018 Acute li

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发表于 2025-3-21 19:04:40 | 显示全部楼层 |阅读模式
书目名称Drug-Induced Liver Toxicity
编辑Minjun Chen,Yvonne Will
视频video
概述Includes cutting-edge techniques for the study of DILI.Contains key implementation advice from the experts.Features detail essential for labs, from basic research through to clinical action
丛书名称Methods in Pharmacology and Toxicology
图书封面Titlebook: Drug-Induced Liver Toxicity;  Minjun Chen,Yvonne Will Book 2018 Springer Science+Business Media, LLC, part of Springer Nature 2018 Acute li
描述This book provides a comprehensive view of the methodologies used for the study of liver toxicity encountered throughout the whole life cycle of a drug, from drug discovery, to clinical trial, post-marketing, and even clinical practice. Organized into six sections, the first section introduces the mechanisms contributing to drug-induced liver toxicity.  The second and third section explore in silico and in vitro approaches used to help mitigate hepatotoxicity liability at the early stages of drug development. The fourth section describes methodologies applied in regulatory processes, including preclinical studies, clinical trials, and post-marketing surveillance. The fifth section discusses clinical hepatotoxicity. Emerging technologies are examined in the final section. As a volume in the Methods in Pharmacology and Toxicology series, chapters include the kind of expert advice that will lead to optimal results. .Authoritative and practical, .Drug-InducedLiver Toxicity. serves all those who aim to improve assessment and understanding of hepatotoxic potentials of new medications and marketed drugs..Chapter 30 is open access under a CC BY 4.0 license via link.springer.com. .
出版日期Book 2018
关键词Acute liver failure; Drug development; Regulatory processes; Preclinical and clinical studies; Hepatotox
版次1
doihttps://doi.org/10.1007/978-1-4939-7677-5
isbn_softcover978-1-4939-9256-0
isbn_ebook978-1-4939-7677-5Series ISSN 1557-2153 Series E-ISSN 1940-6053
issn_series 1557-2153
copyrightSpringer Science+Business Media, LLC, part of Springer Nature 2018
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发表于 2025-3-21 23:13:36 | 显示全部楼层
Detection, Elimination, Mitigation, and Prediction of Drug-Induced Liver Injury in Drug Discovery major hurdle and is recognized to be a major cause of drug attrition and market withdrawal. DILI impacts many different sectors of society including patients, public health systems, health insurers and the pharmaceutical industry. Animal models are very efficient at detecting direct, dose-dependent
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Physicochemical Properties and Structural Alertsm the market. Significant efforts are being made to utilize existing knowledge of chemical and biological mechanisms that have been linked with causing DILI. These mechanisms are often varied and can include overt chemical reactivity or bioactivation to reactive metabolites; unintended interactions
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Prediction of Human Liver Toxicity Using In Vitro Assays: Limitations and Opportunitiess. Simple single cell-type in vitro cytotoxicity assays may fail to predict complex in vivo interconnected mechanism-based toxicities. Additionally, the lack of standardization of in vitro assays complicates data interpretation and makes assay comparison difficult. The selection of a given assay may
发表于 2025-3-22 21:39:28 | 显示全部楼层
Use of Liver-Derived Cell Lines for the Study of Drug-Induced Liver Injurycytes. Multiple hepatocyte derived cellular carcinoma cell lines, such as HepG2, Huh7, and HepaRG cells, have been established over the years, and they display distinct characteristics regarding the expression and activity levels of drug-metabolizing enzymes and other hepatocyte-specific factors. Th
发表于 2025-3-23 01:36:51 | 显示全部楼层
Evaluation of Drug-Induced Liver Injuries (DILI) with Human Hepatocytes: Scientific Rationale and Ex. Here the Human Cell Paradigm, namely, that human-specific drug properties can be obtained with in vitro human-based experimental systems is proposed. The success of the Human Cell Paradigm depends on the physiological relevance of the in vitro system, namely, the retention of human-specific and or
发表于 2025-3-23 07:08:41 | 显示全部楼层
Status and Use of Induced Pluripotent Stem Cells (iPSCs) in Toxicity Testingon reasons given for drug attrition or withdrawal; this occurs for a multitude of reasons among which is certainly the lack of adequate models able to recapitulate hepatotoxicity in vitro. The loss of compounds in late-stage testing or after marketing is a major financial burden for the pharmaceutic
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