Particles and Nanoparticles in Pharmaceutical Products : Design, Manufacturing, Behavior and Performance
Language: English
Published by Springer, 2018
Series: Book 29 of 38 - AAPS Advances in the Pharmaceutical Sciences
- Softcover
- New
Seller: AHA-BUCH GmbH, Einbeck, GermanyAHA-BUCH GmbH
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- Title
- Particles and Nanoparticles in Pharmaceutical Products : Design, Manufacturing, Behavior and Performance
- Author
- Wim Oostra
- Publisher
- Springer
- Publication year
- 2018
- Condition
- Neu
- Binding
- Taschenbuch
- Language
- English
- ISBN 10
- 3030068099
- ISBN 13
- 9783030068097
- Item weight
- 692 grams
- Dimensions
- 235x155x25 mm
- Series
- Book 29 of 38: AAPS Advances in the Pharmaceutical Sciences
This edited volume brings together the expertise of numerous specialists on the topic of particles – their physical, chemical, pharmacological and toxicological characteristics – when they are a component of pharmaceutical products and formulations. The book discusses in detail properties such as the composition, size, shape, surface properties and porosity of particles with respect to how they impact the formulations and products in which they are used and the effective delivery of pharmaceutical active ingredients. It considers all dosage forms of pharmaceuticals involving particles, from powders to tablets, creams to ointments, and solutions to dry-powder inhalers, also including the latest nanomedicine products. Further, it discusses examples of particle toxicity, as well as the important subject of pharmaceutical industry regulations, guidelines and legislation.
The book is of interest to researchers and practitioners who work on testing and developing pharmaceutical dosageand delivery systems.
"Synopsis" may belong to another edition of this title.
About the Author
Merkus is the Editor of three other Springer books: “Particle Size Measurements” (2009), "Particulate Products" (2014) and “Production, Handling and Characterization of Particulate Materials” (2016), the latter two in collaboration with co-editor Gabriel M.H. Meesters.
Gabriel M. H. Meesters has a BSc and MSc in Chemical Engineering with a major in BioProcessTechnology from the Delft University of Technology. He has a PhD in Particle Technology also from the Delft University of Technology. He worked at biotechnology companies like Gist-Brocades in The Netherlands , as well as for Genencor International and currently at DSM in research and development in The Netherlands. In all these functions he was working on formulation and product development. Since 1996 he holds a part time position at the Delft University of Technology, as assistant professor at the faculty of Applied Sciences, first in the Particle Technology group, later the Nano Structured Materials Group and currently in the Product and Process Engineering group. He supervised over 15 PhD students and more than 50 MSc students. He published over 70 refereed papers, holds around 15 patents and patent applications and is co-author and co-editor of the books ‘Particulate Products – Tailoring Properties for Optimal Performance’ (2014; Springer) and ‘Production, Handling and Characterization of Particulate Materials’ (2016, Springer). He (co-) organized several international conferences in the field of particle technology and was president of the World Congress on Particle Technology in 2010.
Wim Oostra obtained his PhD in chemical engineering from Delft University of Technology. He works in Pharma since 1998. Originally he started his career in formulation development, later moving to process development and upscaling. He currently works for Abbott’s Established Products Division where he is a Sr. Technical Manager in the Manufacturing Science and Technology department. While working previously for Organon, Schering Plough and MSD, Wim was a member of the corresponding quality by design (QbD) and process analytical technology (PAT) teams, and was actively involved in two QbD filings of new products, including the online control of Blend uniformity by near infra‐red spectroscopy (NIR). Wim was a member of the International Society for Pharmaceutical Engineering (ISPE) Product Quality Lifecycle Implementation® (PQLI) initiative and is co‐chair of the European federation for pharmaceutical sciences (EuFEPS) PAT and QbD network.
"About the title" may belong to another edition of this title.
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