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Titlebook: Alternatives for Dermal Toxicity Testing; Chantra Eskes,Erwin van Vliet,Howard I. Maibach Book 2017 Springer International Publishing AG 2

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發(fā)表于 2025-3-21 18:13:06 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
期刊全稱Alternatives for Dermal Toxicity Testing
影響因子2023Chantra Eskes,Erwin van Vliet,Howard I. Maibach
視頻videohttp://file.papertrans.cn/155/154155/154155.mp4
發(fā)行地址Provides in-depth information on the alternatives to animal testing.Identifies the most suitable test method(s) for specific uses and endpoints.Describes the regulatory acceptance, protocols, performa
圖書封面Titlebook: Alternatives for Dermal Toxicity Testing;  Chantra Eskes,Erwin van Vliet,Howard I. Maibach Book 2017 Springer International Publishing AG 2
影響因子This book provides comprehensive information on the alternative (non-animal) dermal toxicity test methods currently available for industrial, regulatory, and academic use and also explores potential future developments. It encompasses all areas of dermal toxicity, including skin irritation, skin corrosion, skin sensitization, UV-induced effects, and skin genotoxicity. An individual chapter is devoted to each test method, with coverage of the scientific basis, validation status and regulatory acceptance, applications and limitations, available protocols, and potential role within testing strategies. In addition, perspectives from the test developer are presented, for example regarding critical steps in the protocol. The closing section addresses areas that may be of relevance for the future of dermal toxicity safety testing, including the validation and regulatory acceptance of integrated testing strategies, novel complex skin models, and high-throughput screening techniques.
Pindex Book 2017
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https://doi.org/10.1007/978-3-8349-9707-4on centers and regulators, several in vitro test methods have been developed, validated and regulatory adopted as potential replacements of the rabbit skin irritation test..This chapter describes in details the skin irritation test (SIT) based on the use of the in vitro reconstructed human epidermis
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https://doi.org/10.1007/978-3-8349-9707-4consists of normal human epidermal keratinocytes whose biological origin is neonatal foreskin. The several validation studies of the . skin irritation test method using LabCyte EPI-MODEL24 (LabCyte EPI-MODEL24 SIT) were conducted at three laboratories to assess both intra- and interlaboratory reprod
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https://doi.org/10.1007/978-3-8349-9707-4duction, these cells differentiate in a multilayered epidermis that serves as a model for human . epidermis. For the epiCS. SIT method, the tissues are exposed to test substances for 20 min followed by a 42 h post-incubation period. Subsequently, the relative viability of the tissues is determined b
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https://doi.org/10.1007/978-3-8349-9707-4ve been validated and adopted in the regulation as early as 2000 in the European Union and in 2004 at the OECD level. Current internationally agreed approaches recommend the use of Integrated Approach for Testing and Assessment (IATA) that allow to replace or minimize to the extent possible the use
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https://doi.org/10.1007/978-3-8349-9707-4od has been shown to be robust, transferable, and reproducible in validation studies organised with three laboratories. The overall accuracy of the EpiSkin? test method in distinguishing between corrosive and non-corrosive chemicals was 92.4% with a large set of 113 chemicals through a systematic .
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