Reducing, Refining and Replacing the Use of Animals in Toxicity Testing (eBook)

eBook Download: PDF
2013
362 Seiten
Royal Society of Chemistry (Verlag)
978-1-84973-792-0 (ISBN)

Lese- und Medienproben

Reducing, Refining and Replacing the Use of Animals in Toxicity Testing -
Systemvoraussetzungen
214,99 inkl. MwSt
  • Download sofort lieferbar
  • Zahlungsarten anzeigen
This thought-provoking book describes the ever-expanding "toolbox" of methods now available to reduce, refine, or replace animal usage in toxicity testing.
Toxicity testing is used to assess the safety or hazards presented by substances such as industrial chemicals, consumer products, and pharmaceuticals. At present, many methods involve laboratory animals. Alternative procedures, some involving human cell-based technologies, are now being developed which reduce, refine, or replace animal usage and minimize the pain and distress caused. These new tests must protect public health and the environment at least as well as currently accepted methods. This book describes the ever-expanding "toolbox" of methods available to assess toxicity. Such techniques often result from our growing understanding of the biochemical and cellular pathways that mediate toxicity mechanisms. This permits evaluations of information generated from several sources to generate a "weight of evidence". By combining in silico, in vitro, and ex vivo methods with technologies that rely on biochemical- and cell-based in vitro assays, toxicologists are developing mechanistically based alternatives to live animal experimentation. This text also explores the complexities associated with adequate validation, and the assessment of test reliability and relevance. It provides an essential reference source for postgraduates, academics and industrialists working in this rapidly changing area.

David G. Allen has over 10 years experience in molecular and cellular biology. This includes the evaluation of toxicological and pharmacological data for the Food and Drug Administration (FDA), and the identification and validation of alternative toxicological assays that reduce or replace animal usage in regulatory safety testing. He received is BSc and PhD from North Carolina State University in Raleigh, and his MSc from the University of North Carolina in Wilmington. Dr Allen is currently Director of the Environmental and Regulatory Sciences Division of Integrated Laboratory Systems in North Carolina. This involves responsibility for the evaluation of alternative toxicological methods and comprehensive environmental services for the Environmental Protection Agency and the State of Georgia. The role includes all aspects of divisional management such as staffing, budget projections, and business development.

Introduction;The 3R's in Toxicity Testing - From Russell and Birch to 21st Century Toxicology; Regulatory Safety Testing - National and International Requirements; Efforts Towards International Harmonization of Acceptable Alternatives; Refinement Alternatives - Minimizing Pain and Distress in In Vivo Toxicity Testing; In Vitro Toxicity Testing - The Basics; Using Stem Cells in Toxicity Testing; Using Computers Instead of Cells - In Silico Approaches to Toxicity Testing; Acute Safety Testing; Acute Systemic Toxicity - Oral, Dermal, and Inhalation Exposures;Dermal Corrosivity and Irritation Testing; Ocular Corrosivity and Irritation Testing; Skin Sensitization Testing; Integrated Approaches to Acute Safety Testing; Endocrine Disruptors; In Vitro Receptor Binding Assays; In Vitro Receptor Transactivation Assays; Non-mamalian Approaches to Identifying Endocrine Active Substances; Subchronic and Chronic Toxicity Testing; Carcinogenicity - Genetic Toxicity Testing and Beyond; Reproductive and Developmental Toxicity Testing; Immunotoxicity Testing; Application of New Technologies; High Throughput Approaches to Toxicity Testing; Nanotechnology - New Challenges in Toxicity Testing

Erscheint lt. Verlag 31.10.2013
Reihe/Serie ISSN
Verlagsort Cambridge
Sprache englisch
Themenwelt Naturwissenschaften Biologie Biochemie
Schlagworte animals • reducing • Refining • replacing • Testing • Toxicity
ISBN-10 1-84973-792-4 / 1849737924
ISBN-13 978-1-84973-792-0 / 9781849737920
Haben Sie eine Frage zum Produkt?
PDFPDF (Adobe DRM)

Kopierschutz: Adobe-DRM
Adobe-DRM ist ein Kopierschutz, der das eBook vor Mißbrauch schützen soll. Dabei wird das eBook bereits beim Download auf Ihre persönliche Adobe-ID autorisiert. Lesen können Sie das eBook dann nur auf den Geräten, welche ebenfalls auf Ihre Adobe-ID registriert sind.
Details zum Adobe-DRM

Dateiformat: PDF (Portable Document Format)
Mit einem festen Seiten­layout eignet sich die PDF besonders für Fach­bücher mit Spalten, Tabellen und Abbild­ungen. Eine PDF kann auf fast allen Geräten ange­zeigt werden, ist aber für kleine Displays (Smart­phone, eReader) nur einge­schränkt geeignet.

Systemvoraussetzungen:
PC/Mac: Mit einem PC oder Mac können Sie dieses eBook lesen. Sie benötigen eine Adobe-ID und die Software Adobe Digital Editions (kostenlos). Von der Benutzung der OverDrive Media Console raten wir Ihnen ab. Erfahrungsgemäß treten hier gehäuft Probleme mit dem Adobe DRM auf.
eReader: Dieses eBook kann mit (fast) allen eBook-Readern gelesen werden. Mit dem amazon-Kindle ist es aber nicht kompatibel.
Smartphone/Tablet: Egal ob Apple oder Android, dieses eBook können Sie lesen. Sie benötigen eine Adobe-ID sowie eine kostenlose App.
Geräteliste und zusätzliche Hinweise

Buying eBooks from abroad
For tax law reasons we can sell eBooks just within Germany and Switzerland. Regrettably we cannot fulfill eBook-orders from other countries.

Mehr entdecken
aus dem Bereich

von Donald Voet; Judith G. Voet; Charlotte W. Pratt

eBook Download (2019)
Wiley-VCH Verlag GmbH & Co. KGaA
73,99

von Donald Voet; Judith G. Voet; Charlotte W. Pratt

eBook Download (2019)
Wiley-VCH Verlag GmbH & Co. KGaA
73,99