Formulation and Process Development Strategies for Manufacturing Biopharmaceuticals

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Format: eBook
Pub. Date: 2010-07-01
Publisher(s): Wiley
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Summary

A real-world guide to the production and manufacturing of biopharmaceuticalsWhile much has been written about the science of biopharmaceuticals, there is a need for practical, up-to-date information on key issues at all stages of developing and manufacturing commercially viable biopharmaceutical drug products. This book helps fill the gap in the field, examining all areas of biopharmaceuticals manufacturing, from development and formulation to production and packaging.Written by a group of experts from industry and academia, the book focuses on real-world methods for maintaining product integrity throughout the commercialization process, clearly explaining the fundamentals and essential pathways for all development stages. Coverage includes:Research and early development phase-appropriate approaches for ensuring product stabilityDevelopment of commercially viable formulations for liquid and lyophilized dosage formsOptimal storage, packaging, and shipping methodsCase studies relating to therapeutic monoclonal antibodies, recombinant proteins, and plasma fractionsUseful analysis of successful and failed productsFormulation and Process Development Strategies for Manufacturing Biopharma-ceuticals is an essential resource for scientists and engineers in the pharmaceutical and biotech industries, for government and regulatory agencies, and for anyone with an interest in the latest developments in the field.

Table of Contents

Introduction
Preformulation and Development of Stability Indicating Assays: Biophysical Characterization Techniques
The Structure of Biological Therapeutics
Chemical Instability in Peptide and Protein Pharmaceuticals
Physical Instability in Peptide and Protein Pharmaceuticals
Immunogenicity of Therapeutic Proteins
Preformulation Research: Assessing Protein Solution Behavior Early During Therapeutic Development
Formulation Development of Phase I/II Biopharmaceuticals: An Efficient and Timely Approach
Late Stage Formulation Development and Characterization of Biopharmaceuticals
An Empirical Phase Diagram/ High Throughput Screening Approach to the Characterization and Formulation of Biopharmaceuticals
Fluorescence and Phosphorescence Methods to Probe Protein Structure and Stability in Ice: the Case of Azurin
Applications of Sedimentation Velocity Analytical Ultracentrifugation
Field Flow Fractionation with Multi-angle Light Scattering for Measuring Particle Size of Virus-like Particles
Light Scattering Techniques and their Application to Formulation and Aggregation Concerns
Development of a Formulation for Liquid Dosage Form
Efficient Approaches to Formulation Development of Biopharmaceuticals
Prediction of Protein Aggregation Propensities from Primary Sequence Information
High Concentration Antibody Formulations
Development of Formulations for Therapeutic Monoclonal Antibodies and Fc Fusion Proteins
Reversible Self-Association of Pharmaceutical Proteins: Characterization and Case Studies
Development of Formulation for Lyophilized Dosage Form
Design of a Formulation for Freeze Drying
Protein Conformation and Reactivity in Amorphous Solids
The Impact of Buffer on Solid-State Properties and Stability of Freeze-Dried Dosage Forms
Stabilization of Lyophilized Pharmaceuticals by Control of Molecular Mobility: Impact of Thermal History
Structural Analysis of Proteins in Dried Matrices
The Impact of Formulation and Drying Processes on the Characteristics and Performance of Biopharmaceutical Powders
Manufacturing Sciences
Manufacturing Fundamentals for Biopharmaceuticals
Protein Stability during Bioprocessing
Freezing and Thawing of Protein Solutions
Strategies for Bulk Storage and Shipment of Proteins
Drying Process Methods for Biopharmaceutical Products: An Overview
Spray Drying of Biopharmaceuticals and Vaccines
Development and Optimization of Freeze Drying Process
Considerations for Successful Lyophilization Process Scale-up, Technology Transfer and Routine Production
Process Robustness in Freeze-Drying of Biopharmaceuticals
Filling Processes and Technologies for Liquid Biopharmaceuticals
Leachables and Extractables
Primary Container/Closure Selection for Biopharmaceuticals
Pre-filled Syringes for Biopharmaceuticals
Impact of Manufacturing Processes on the Drug Product Stability and Quality
Index
Table of Contents provided by Publisher. All Rights Reserved.

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