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Produktbild: Handbook of Pharmaceutical Wet Granulation

Handbook of Pharmaceutical Wet Granulation Theory and Practice in a Quality by Design Paradigm

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Beschreibung

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

17.12.2025

Herausgeber

Ajit S. Narang + weitere

Verlag

Elsevier Science & Technology

Seitenzahl

978

Maße (L/B/H)

23,8/19,9/5,4 cm

Gewicht

2118 g

Auflage

2nd edition

Sprache

Englisch

ISBN

978-0-443-29817-2

Beschreibung

Portrait

Ajit S. Narang works for the Bristol-Myers Squibb, Co. in New Brunswick, New Jersey, in the biopharmaceutical aspects of drug delivery. He has more than eight years of experience in the pharmaceutical industry in the development of oral dosage forms and drug delivery platforms. In addition to the Bristol-Myers Squibb, Co., he has worked for Ranbaxy Research Labs (currently a subsidiary of Daiichi Sankyo, Japan) in Gurgaon, India, and Morton Grove Pharmaceuticals (currently a subsidiary of Wockhardt USA LLC, Parsippany, New Jersey) in Vernon Hills, Illinois. He has more than 35 publications and three pending patent applications and has contributed to the development of several marketed drug products.

Sherif Badawy, Ph.D., is a Research Fellow in the Drug product Science and Technology of the Bristol-Myers Squibb Company. He received his B.S. in Pharmacy and M.S. in Pharmaceutics from Cairo University, and his Ph.D. in Pharmaceutics from Duquesne University. He has more than 20 years of industrial experience in drug product development. His current responsibilities at Bristol-Myers Squibb include formulation and process development and scale-up of commercial oral solid and liquid dosage forms. His areas of research interest include high shear wet granulation, tablet compaction, stability of solid dosage forms and bioavailability enhancement of poorly water-soluble compounds. He authored more than 40 manuscripts and numerous abstracts and presentations in those areas.

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

17.12.2025

Herausgeber

Verlag

Elsevier Science & Technology

Seitenzahl

978

Maße (L/B/H)

23,8/19,9/5,4 cm

Gewicht

2118 g

Auflage

2nd edition

Sprache

Englisch

ISBN

978-0-443-29817-2

EU-Ansprechpartner

Elsevier B.V.
Radarweg 29
1043 NX Amsterdam
NL
productsafety@elsevier.com

Herstelleradresse

Elsevier Science & Technology
London Wall 125
EC2Y 5AS London
GB
tradeorders@elsevier.com

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  • Produktbild: Handbook of Pharmaceutical Wet Granulation
  • Section 1: Process Design and Product Quality Attributes
    1. Physicochemical Principles Governing Agglomeration and Growth Kinetics
    2. Microstructure and Mechanical Properties of Granules Formed in High Shear Wet Granulation
    3. Mechanistic Basis for the Effects of Process Parameters on Quality Attributes in High Shear Wet Granulation
    4. Structures and Properties of Granules Prepared By High Shear Wet Granulation
    5. Wet Granulation and Chemical Stability of Drug Products
    6. Material Physical Modifications Induced by Wet Granulation (Current chapter 6)
    7. Current Practices in Wet Granulation-Based Generic Product Development
    Section 2: Excipients and Input Material Attributes
    8. Material Attributes and Their Impact on Wet Granulation Process Performance
    9. Binders in Wet Granulation
    10. Effect of Binder Attributes on Granule Growth and Densification
    11. Role of Drug Substance Material Properties in the Processibility and Performance of Wet Granulated Products
    12. Critical Material Attributes in Wet Granulation
    13. Critical material attributes during continuous twin-screw wet granulation
    Section 3: PAT, Scale-up, Control Strategy
    14. Inline Focused Beam Reflectance Measurement During Wet Granulation
    15. Principles and Applications of Drag Force Flow Sensor
    16. An Introduction to Powder Characterization
    17. A Quality By Design Approach to Scale-Up of High Shear Wet Granulation Process
    18. Integrated Application of Quality-by-Design Principles to Drug Product and Its Control Strategy Development
    19. Implementation of Pharmaceutical Quality by Design in Wet Granulation
    Section 4: Process Modeling and Emerging Trends
    20. Numerical Modeling for Wet Granulation Processes
    21. Application of the Discrete Element Method to Scale-Up of High-Shear Granulation
    22. Advances in Computational Modelling and Simulation of Wet Granulation Processes
    23. Twin Screw Continuous Wet Granulation
    24. Melt granulation: Granulation mechanisms, Formulation and process design for batch and twin-screw systems
    25. The application of the state-of-art material library/material database approach to the process understanding and process modeling of wet granulation
    26. Emerging Paradigms in Pharmaceutical Wet Granulation