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Plasmid Biopharmaceuticals – Basics, Applications and Manufacturing

Software / Digital Media
576 Seiten
2011
Wiley-Blackwell (Hersteller)
978-0-470-93991-8 (ISBN)
CHF 204,95 inkl. MwSt
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A plasmid is a DNA molecule separate from chromosomal DNA and capable of autonomous replication. Plasmid Biopharmaceuticals helps pharmaceutical scientists and engineers understand the basic characteristics of therapeutic DNA plasmids, their potential utilization in drug development, and the issues and solutions for large-scale GMP production.
The book addresses the basics, applications, and manufacturing of plasmid biopharmaceuticals. The survey of the most relevant characteristics of plasmids provides the basics for designing plasmid products (applications) and processes (manufacturing). Key features that the authors include in the book are: i) consistency and clear line of direction, ii) an extensive use of cross-referencing between the individual chapters, iii) a rational integration of chapters, iv) appellative figures, tables and schemes, and v) an updated, but selected choice of references, with a focus on key papers.

Duarte Miguel F. Prazeres, PhD, DSc, is Associate Professor at the Instituto Superior Tecnico (IST) and Senior Researcher at the Instituto de Biotecnologia e Bioengenharia, both within the Universidade Tecnica de Lisboa. Dr. Prazeres has published 140 peer-reviewed articles and fifteen book chapters on such topics as biocatalysis, downstream processing, and nanobiotechnology.

Preface. Acknowledgment. Abbreviations. Part I Basics. 1 Historical Perspective. 2 Gene Transfer with Plasmid Biopharmaceuticals. 3 Product and Process Development. 4 Structure. 5 Analytical Characterization. 6 Delivery. Part II Applications. 7 Ethical and Safety Issues. 8 Human and Veterinary Markets. 9 Human Case Studies: Pandemic Infl uenza and Critical Limb Ischemia. 10 Veterinary Case Studies: West Nile, Infectious Hematopoietic Necrosis, and Melanoma. Part III Manufacturing. 11 Good Manufacturing Practice and Validation. 12 Product Specifi cations and Quality Control. 13 Cell Culture. 14 An Overview of Downstream Processing. 15 Primary Isolation. 16 Intermediate Recovery. 17 Final Purifi cation. 18 Process Synthesis. Part IV Concluding Remarks and Outlook. 19 Concluding Remarks and Outlook. Index.

Erscheint lt. Verlag 19.7.2011
Verlagsort Hoboken
Sprache englisch
Maße 150 x 250 mm
Gewicht 666 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Pharmakologie / Pharmakotherapie
Naturwissenschaften Chemie Technische Chemie
Technik Umwelttechnik / Biotechnologie
ISBN-10 0-470-93991-5 / 0470939915
ISBN-13 978-0-470-93991-8 / 9780470939918
Zustand Neuware
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