Description

Book Synopsis

A guide to the important chemical engineering concepts for the development of new drugs, revised second edition

The revised and updated second edition of Chemical Engineering in the Pharmaceutical Industry offers a guide to the experimental and computational methods related to drug product design and development. The second edition has been greatly expanded and covers a range of topics related to formulation design and process development of drug products. The authors review basic analytics for quantitation of drug product quality attributes, such as potency, purity, content uniformity, and dissolution, that are addressed with consideration of the applied statistics, process analytical technology, and process control. The 2nd Edition is divided into two separate books: 1) Active Pharmaceutical Ingredients (API's) and 2) Drug Product Design, Development and Modeling.

The contributors explore technology transfer and scale-up of batch processes th

Table of Contents

List of Contributors ix

Preface xv

Unit Conversions xvii

Part I Introduction 1

1 Chemical Engineering in the Pharmaceutical Industry: An Introduction 3
David J. am Ende and Mary T. am Ende

Part II Drug Product Design, Development, and Modeling 19

2 Design of Solid Dosage Formulations 21
Kevin J. Bittorf, Tapan Sanghvi, and Jeffrey P. Katstra

3 Powder Process Challenges and Solutions 53
Thomas Baxter and James Prescott

4 Design and Scale-up of Dry Granulation Processes 81
Howard J. Stamato and Omar L. Sprockel

5 Model-based Development of Roller Compaction Processes 119
Gavin Reynolds

6 Wet Granulation Processes 147
Karen P. Hapgood and James D. Litster

7 Toward a Generic Model for Twin-screw Wet Granulation 173
Daan Van Hauwermeiren, Maxim Verstraeten, Michaël Ghijs, Kai Lee, Neil Turnbull, Mary T. am Ende, Pankaj Doshi, David Wilsdon, Thomas De Beer, and Ingmar Nopens

8 Modeling a Dosator Capsule Filling Process for Hard-shell Capsules 187
Peter Loidolt, Eva Faulhammer, and Johannes G. Khinast

9 Powder Compaction: Process Design and Understanding 203
David Wilson, Ron Roberts, and John Blyth

10 Punch Sticking: Factors and Solutions 227
Daryl M. Simmons

11 Spray Atomization Modeling for Tablet Film Coating Processes 245
Alfred Berchielli, Pankaj Doshi, Alberto Aliseda, and Juan C. Lasheras

12 Spray Drying and Amorphous Dispersions 267
Kristin J.M. Ploeger, Pavithra Sundararajan, Pedro C. Valente, Kenneth J. Rosenberg, João G. Henriques, and Paige Adack

13 The Freeze Drying Process: The Use of Mathematical Modeling in Process Design, Understanding, and Scale-up 293
Venkat Koganti, Sumit Luthra, and Michael J. Pikal

14 Sterilization Processes in the Pharmaceutical Industry 311
Piero M. Armenante and Otute Akiti

15 Controlled Release Technology and Design of Oral Controlled Release Dosage Forms 381
Avinash G. Thombre, Xiao Yu (Shirley) Wu, and Mary T. am Ende

16 Process Design and Development for Novel Pharmaceutical Dosage Forms 409
Leah Appel, Joshua Shockey, Matthew Shaffer, and Jennifer Chu

17 Multiscale Modeling of a Pharmaceutical Fluid Bed Coating Process Using CFD/DEM and Population Balance Models to Predict Coating Uniformity 419
Avik Sarkar, Dalibor Jajcevic, Peter Böhling, Peter Toson, Matej Zadravec, Brian Shoemaker, Pankaj Doshi, Johannes Khinast, and Mary T. am Ende

18 Process Design of Topical Semisolids: Application of Fundamental Concepts in Pharmaceutical Engineering to PEG Ointment Development 451
Amanda Samuel, Thean Yeoh, Rolf Larsen, and Avik Sarkar

19 Achieving a Hot Melt Extrusion Design Space for the Production of Solid Solutions 469
Luke Schenck, Gregory M. Troup, Mike Lowinger, Li Li, and Craig Mckelvey

20 Drug Product Process Modeling 489
Mary T. am Ende, William Ketterhagen, Andrew Prpich, Pankaj Doshi, Salvador García-Muñoz, and Rahul Bharadwajh

Part III Continuous Manufacturing 527

21 Continuous Manufacturing in Secondary Production 529
Martin Warman

22 Continuous Direct Compression Using Portable Continuous Miniature Modular & Manufacturing (PCM&M) 547
Daniel O. Blackwood, Alexandre Bonnassieux, and Giuseppe Cogoni

23 Process Control Levels for Continuous Pharmaceutical Tablet Manufacturing 561
Niels Nicolaï, Ingmar Nopens, Maxim Verstraeten, and Thomas De Beer

Part IV Applied Statistics and Regulatory Environment 585

24 Multivariate Analysis for Pharmaceutical and Medical Device Development 587
Frederick H. Long

25 Pharmaceutical Manufacturing: The Role of Multivariate Analysis in Design Space, Control Strategy, Process Understanding, Troubleshooting, and Optimization 601
Theodora Kourti

26 Quality by Design: Pilot to Reality-The Honeymoon Phase to the Stormy Years 631
Mary T. am Ende and Christine B. Seymour

Index 645

Chemical Engineering in the Pharmaceutical

    Product form

    £192.80

    Includes FREE delivery

    RRP £202.95 – you save £10.15 (5%)

    Order before 4pm today for delivery by Mon 13 Jul 2026.

    A Hardback by Mary T. am Ende, David J. am Ende

    10 in stock

      Trusted by thousands of customers. See 2,385+ Customer Reviews

      View other formats and editions of Chemical Engineering in the Pharmaceutical by Mary T. am Ende

      Publisher: John Wiley & Sons Inc
      Publication Date: 21/06/2019
      ISBN13: 9781119285496, 978-1119285496
      ISBN10: 1119285496
      Also in:
      Chemistry

      Description

      Book Synopsis

      A guide to the important chemical engineering concepts for the development of new drugs, revised second edition

      The revised and updated second edition of Chemical Engineering in the Pharmaceutical Industry offers a guide to the experimental and computational methods related to drug product design and development. The second edition has been greatly expanded and covers a range of topics related to formulation design and process development of drug products. The authors review basic analytics for quantitation of drug product quality attributes, such as potency, purity, content uniformity, and dissolution, that are addressed with consideration of the applied statistics, process analytical technology, and process control. The 2nd Edition is divided into two separate books: 1) Active Pharmaceutical Ingredients (API's) and 2) Drug Product Design, Development and Modeling.

      The contributors explore technology transfer and scale-up of batch processes th

      Table of Contents

      List of Contributors ix

      Preface xv

      Unit Conversions xvii

      Part I Introduction 1

      1 Chemical Engineering in the Pharmaceutical Industry: An Introduction 3
      David J. am Ende and Mary T. am Ende

      Part II Drug Product Design, Development, and Modeling 19

      2 Design of Solid Dosage Formulations 21
      Kevin J. Bittorf, Tapan Sanghvi, and Jeffrey P. Katstra

      3 Powder Process Challenges and Solutions 53
      Thomas Baxter and James Prescott

      4 Design and Scale-up of Dry Granulation Processes 81
      Howard J. Stamato and Omar L. Sprockel

      5 Model-based Development of Roller Compaction Processes 119
      Gavin Reynolds

      6 Wet Granulation Processes 147
      Karen P. Hapgood and James D. Litster

      7 Toward a Generic Model for Twin-screw Wet Granulation 173
      Daan Van Hauwermeiren, Maxim Verstraeten, Michaël Ghijs, Kai Lee, Neil Turnbull, Mary T. am Ende, Pankaj Doshi, David Wilsdon, Thomas De Beer, and Ingmar Nopens

      8 Modeling a Dosator Capsule Filling Process for Hard-shell Capsules 187
      Peter Loidolt, Eva Faulhammer, and Johannes G. Khinast

      9 Powder Compaction: Process Design and Understanding 203
      David Wilson, Ron Roberts, and John Blyth

      10 Punch Sticking: Factors and Solutions 227
      Daryl M. Simmons

      11 Spray Atomization Modeling for Tablet Film Coating Processes 245
      Alfred Berchielli, Pankaj Doshi, Alberto Aliseda, and Juan C. Lasheras

      12 Spray Drying and Amorphous Dispersions 267
      Kristin J.M. Ploeger, Pavithra Sundararajan, Pedro C. Valente, Kenneth J. Rosenberg, João G. Henriques, and Paige Adack

      13 The Freeze Drying Process: The Use of Mathematical Modeling in Process Design, Understanding, and Scale-up 293
      Venkat Koganti, Sumit Luthra, and Michael J. Pikal

      14 Sterilization Processes in the Pharmaceutical Industry 311
      Piero M. Armenante and Otute Akiti

      15 Controlled Release Technology and Design of Oral Controlled Release Dosage Forms 381
      Avinash G. Thombre, Xiao Yu (Shirley) Wu, and Mary T. am Ende

      16 Process Design and Development for Novel Pharmaceutical Dosage Forms 409
      Leah Appel, Joshua Shockey, Matthew Shaffer, and Jennifer Chu

      17 Multiscale Modeling of a Pharmaceutical Fluid Bed Coating Process Using CFD/DEM and Population Balance Models to Predict Coating Uniformity 419
      Avik Sarkar, Dalibor Jajcevic, Peter Böhling, Peter Toson, Matej Zadravec, Brian Shoemaker, Pankaj Doshi, Johannes Khinast, and Mary T. am Ende

      18 Process Design of Topical Semisolids: Application of Fundamental Concepts in Pharmaceutical Engineering to PEG Ointment Development 451
      Amanda Samuel, Thean Yeoh, Rolf Larsen, and Avik Sarkar

      19 Achieving a Hot Melt Extrusion Design Space for the Production of Solid Solutions 469
      Luke Schenck, Gregory M. Troup, Mike Lowinger, Li Li, and Craig Mckelvey

      20 Drug Product Process Modeling 489
      Mary T. am Ende, William Ketterhagen, Andrew Prpich, Pankaj Doshi, Salvador García-Muñoz, and Rahul Bharadwajh

      Part III Continuous Manufacturing 527

      21 Continuous Manufacturing in Secondary Production 529
      Martin Warman

      22 Continuous Direct Compression Using Portable Continuous Miniature Modular & Manufacturing (PCM&M) 547
      Daniel O. Blackwood, Alexandre Bonnassieux, and Giuseppe Cogoni

      23 Process Control Levels for Continuous Pharmaceutical Tablet Manufacturing 561
      Niels Nicolaï, Ingmar Nopens, Maxim Verstraeten, and Thomas De Beer

      Part IV Applied Statistics and Regulatory Environment 585

      24 Multivariate Analysis for Pharmaceutical and Medical Device Development 587
      Frederick H. Long

      25 Pharmaceutical Manufacturing: The Role of Multivariate Analysis in Design Space, Control Strategy, Process Understanding, Troubleshooting, and Optimization 601
      Theodora Kourti

      26 Quality by Design: Pilot to Reality-The Honeymoon Phase to the Stormy Years 631
      Mary T. am Ende and Christine B. Seymour

      Index 645

      Recently viewed products

      © 2026 Book Curl

        • American Express
        • Apple Pay
        • Diners Club
        • Discover
        • Google Pay
        • Maestro
        • Mastercard
        • PayPal
        • Shop Pay
        • Union Pay
        • Visa

        Login

        Forgot your password?

        Don't have an account yet?
        Create account