Secure CheckoutPersonal information is secured with SSL technology.
Free ShippingFree global shipping
No minimum order.
Surfactants in Biopharmaceutical Development addresses the progress, challenges and opportunities for surfactant research specific to pharmaceutical development, providing a broad range of important surfactant-related topics as they relate directly to the biopharmaceutical process. Chapters address fundamental topics, like mechanisms of protein stabilization by surfactants, the latest, state-of-the-art technology and methods to illustrate the practical application to biopharmaceutical development, forward-looking chapters on control strategies and novel surfactants, with a special focus on current regulatory aspects of paramount importance for biopharmaceutical companies and regulators.
It has been widely recognized that surfactants provide protection to therapeutic proteins against interfacial stresses. Despite the fact that the very mechanism of protein stabilization by surfactants has not been completely understood, surfactants are universally regarded as critical functional excipients by the industry and by regulators.
- Describes the current state of research on surfactants, drawing upon contributions from international experts across industry and academia
- Addresses the opportunities and challenges associated with surfactants in drug development and delivery
- Provides a defining resource for practitioners in the biopharmaceutical industry, regulators and academics
- Summarizes the latest knowledge of surfactants in biopharmaceutical development in one comprehensive volume
Biopharmaceutical industry professionals working in drug development and pharmaceutical analysis, industry regulators and academics
2. Surfactants used in biopharmaceutics today: An overview (including in vivo fate and a toxicology perspective)
3. Surfactants (polysorbate and poloxamer) synthesis and degradation: Overview and relevance
4. Mechanisms of stabilization of proteins by surfactants
5. Behaviour of surfactant during processing (UF/DF, filter adsorption)
6. Analytical methods for surfactant characterization in Drug Product
7. Oxidative degradation of surfactants: Mechanisms
8. Oxidative surfactant degradation and impact on protein stabilization
9. Hydrolytic degradation of surfactants and impact on protein stabilization
10. Regulatory Perspective on Surfactant Monitoring and Control
11. Control strategies to address surfactant degradation: a quality perspective
12. Surfactants in biotechnnology: A look to the future
- No. of pages:
- © Academic Press 2021
- 1st July 2021
- Academic Press
- Paperback ISBN:
Atanas V. Koulov is the Head of Analytical Development and Quality Control, Drug Product Services at Lonza in Switzerland. His scientific career has focused on surfactants as protective excipients and includes eight years of work in the biopharmaceutical industry. Dr. Koulov’s research is primarily concerned with understanding and preventing aggregation, as well as measuring and characterizing undesired byproducts of surfactant degradation. Dr. Koulov has co-organized and participated in symposia and conference sessions dedicated to surfactants. He has published extensively in the field of protein aggregation and particles and is the immediate past chair of the American Association of Pharmaceutical Scientists Protein Aggregation & Biological Consequences Focus Group.
Head of Analytical Development and Quality Control, Drug Product Services, Lonza AG, Switzerland
Satish Singh has more than 25 years of experience in biopharmaceutical product development. His expertise includes process development, scale-up and technology transfer and ranges from discovery support to development, manufacture and final drug product commercialization.Prior to joining Lonza, Satish was a Research Fellow and Group Leader in Pfizer's Biotherapeutics Pharmaceutical Sciences R&D Unit. Satish has also lead technical teams that focused on particulates, drug substance storage, antibody drug conjugate structure/property relationship, immunogenicity risk evaluation, and the development and application of computational tools in the chemistry, manufacturing and controls (CMC) aspects of biotherapeutics. Satish holds a Ph.D. and MS in Chemical Engineering from Kansas State University and a B.Tech. in Chemical Engineering from the Indian Institute of Technology, New Delhi, India. He has published more than 70 scientific publications on various topics related to the field and is also an Adjunct Professor in the Department of Physical Pharmaceutical Chemistry, BMC, Uppsala University, Sweden. In 2017, Satish was elected an American Association of Pharmaceutical Scientists(AAPS) Fellow in recognition of his contributions to AAPS and drug product development.
Head, Drug Product Process Development, Drug Product Services, Lonza AG, Switzerland
Elsevier.com visitor survey
We are always looking for ways to improve customer experience on Elsevier.com.
We would like to ask you for a moment of your time to fill in a short questionnaire, at the end of your visit.
If you decide to participate, a new browser tab will open so you can complete the survey after you have completed your visit to this website.
Thanks in advance for your time.