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Genotoxic Impurities – Strategies for Identification and Control

Andrew Teasdale (Herausgeber)

Software / Digital Media
444 Seiten
2011
Wiley-Blackwell (Hersteller)
978-0-470-92937-7 (ISBN)
CHF 179,95 inkl. MwSt
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This book provides a primary reference point for anyone addressing the issue of genotoxic impurities, providing not only a definitive narrative of regulatory guidelines but also practical solutions to effectively manage the issue. Specific sections examine this from both a toxicological and analytical perspective.
This book examines genotoxic impurities and their impact on the pharmaceutical industry.Specific sections examine this from both a toxicological and analytical perspective. Within these sections, the book defines appropriate strategies to both assess and ultimately control genotoxic impurities, thus aiding the reader to develop effective control measures. An opening section covers the development of guidelines and the threshold of toxicological concern (TTC) and is followed byasection on safety aspects, including safety tests in vivo and vitro, and data interpretation.The second section addresses the risk posed by genotoxic impurities fromoutside sources and from mutagenswithin DNA.In the final section, the book deals with the quality perspective of genotoxic impurities focused on two critical aspects, the first being the analysis and the second how to practically evaluate the impurities.

ANDREW TEASDALE , PhD, is a senior QA executive with AstraZeneca and chairs the company's internal genotoxic impurities advisory group. With over fifteen years of experience in analytical chemistry and quality assurance, Dr. Teasdale has published a number of papers relating to GIs and has been a speaker on genotoxic impurities at a number of conferences. Dr. Teasdale has also led two expert groups working in the field of genotoxic impurities, including an analytical group in the UK and a Project Quality Research Institute (PQRI) working group, which focused on the critical area of sulfonate ester formation and control.

Foreword. Preface. Section I: Development of GI Guidelines and the TTC Concept. Chapter 1. Historical Overview of the Development of Genotoxic Impurities Guidelines and their Impact (R. Ogilvie and A. Teasdale). Chapter 2. Development of the Threshold of Toxicological Concern Concept (TTC) and its Relationship to Duration of Exposure (A. Brigo and L. Muller). Section 2: Evaluation of Genotoxic Risk from a Pre-clinical Perspective. Chapter 3. Genetic Toxicity Testing to Qualify Alerting Impurities (M. O'Donovan). Chapter 4. Use of Structure Activity Relationship (SAR) Evaluation as a Critical Tool in the Evaluation of the Genotoxic Potential of Impurities (S. Glowienke and C. Hasselgren). Chapter 5. Compound-Specific Risk Assessments for Genotoxic Impurities: Examples and Issues (A. Teasdale and C. Humfrey). Chapter 6. Human Genotoxic Metabolites: Identification and Risk (K. Dobo, D. Walker and A. Teasdale). Section 3. Perspective on Risk Posed by Genotoxic Impurities . Chapter 7. Genotoxic Thresholds (G. Jenkins, G. Johnson, J. Parry and S. Doak). Chapter 8. Genotoxic Impurities a Risk in Perspective? (D. Elder). Section 4. Assessment of Genotoxic Risk: Quality Perspective. Chapter 9. Strategies for the Evaluation of Genotoxic Impurity Risk (A. Teasdale, S. Fenner and D. Elder). Chapter 10. Analysis of Genotoxic Impurities: Review of Approaches (D. Elder). Chapter 11. Development of a Strategy for Analysis of Genotoxic Impurities (Andrew Baker). Chapter 12. Strategic Approaches to the Chromatograpic Analysis of Genotoxic Impurities (Frank David, Karine Jacq, Gerd Canhoenacker and Pat Sandra). Chapter 13. Analysis of Genotoxic Impurities by Nuclear Resonance (NMR) Spectroscopy (Andrew Philips). Chapter 14. Mechanism and Processing Parameters Affecting the Formation of Sulfonate Esters: Summary of the PQRI Studies - PQRI Working Group (Andrew Teasdale). Chapter 15. Aspects to Consider when Devising a Strategy to Understand if Low Level API/DP Degradants have the Potential for Genotoxicity (Alan P. McKeown and Andrew Teasdale).

Erscheint lt. Verlag 4.1.2011
Verlagsort Hoboken
Sprache englisch
Maße 150 x 250 mm
Gewicht 666 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Pharmakologie / Pharmakotherapie
Studium 2. Studienabschnitt (Klinik) Humangenetik
Naturwissenschaften Chemie
ISBN-10 0-470-92937-5 / 0470929375
ISBN-13 978-0-470-92937-7 / 9780470929377
Zustand Neuware
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