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OverviewFull Product DetailsAuthor: Jose V. Bonilla (Girindus America, Cincinnati, Ohio, USA) , G. Susan Srivatsa (ElixinPharma, Encinitas, California, USA)Publisher: Taylor & Francis Ltd Imprint: CRC Press Weight: 0.920kg ISBN: 9781138198456ISBN 10: 1138198455 Pages: 512 Publication Date: 19 October 2016 Audience: College/higher education , Professional and scholarly , Tertiary & Higher Education , Professional & Vocational Format: Paperback Publisher's Status: Active Availability: In Print ![]() This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us. Table of ContentsReviewsThis is a unique resource for guiding the analysis of oligonucleotide-based drug products. No other single source provides such a comprehensive overview of the necessary analytical techniques that assess the qualitative characteristics of oligonucleotides intended for pharmaceutical use. —Rachel R Chennault, Ph.D.(American College of Clinical Pharmacy), in Doody's Notes This is a unique resource for guiding the analysis of oligonucleotide-based drug products. No other single source provides such a comprehensive overview of the necessary analytical techniques that assess the qualitative characteristics of oligonucleotides intended for pharmaceutical use. -Rachel R Chennault, Ph.D.(American College of Clinical Pharmacy), in Doody's Notes This is a unique resource for guiding the analysis of oligonucleotide-based drug products. No other single source provides such a comprehensive overview of the necessary analytical techniques that assess the qualitative characteristics of oligonucleotides intended for pharmaceutical use. -Rachel R Chennault, Ph.D.(American College of Clinical Pharmacy), in Doody's Notes Author InformationDr. Jose V. Bonilla’s career has been dedicated to the introduction and implementation of cutting-edge analytical technologies such as LC-MS, high-speed gas chromatography, high-speed GPC, online GC, online HPLC, and online near-IR. He has extensive experience in the management of industrial and pharmaceutical analytical laboratories in compliance with regulatory requirements and is the author and coauthor of several peer-reviewed publications. Dr. G. Susan Srivatsa has more than 20 years of experience in the development of small molecules, proteins, peptides, and oligonucleotides as therapeutics. She has contributed to the successful development of more than 35 DNA and RNA oligonucleotide drug candidates through various stages of clinical development and has published widely in the area of oligonucleotide analysis in peer-reviewed journals. Tab Content 6Author Website:Countries AvailableAll regions |