Development of Biopharmaceutical Parenteral Dosage Forms

Langue : Anglais

Coordonnateurs : Prantera Cosimo, Korelitz Burton I.

Couverture de l’ouvrage Development of Biopharmaceutical Parenteral Dosage Forms

Résumé
Sommaire
Lectorat
Biographie
Commentaire

This up-to-the-minute reference delineates-in a systematic fashion-the appropriate, sequential steps for the formulation of safe, effective, stable, and marketable liquid parenteral biopharmaceutical products-covering fundamentals and essential pathways for each phase as well as its purpose, function, and relation to other stages in the product development process.
Written by experts currently involved in state-of-the-art advances in the pharmaceutical drug industry, Development of Biopharmaceutical Parenteral Dosage Forms

details biopharmaceuticals that are licensed or undergoing clinical development, including genetically engineered cell and engineered vectors in the fermentation process

describes purification and characterization techniques for rDNA therapeutics, discussing several types of unit operations for isolation, purification, and characterization

considers preformulation and formulation requirements, such as physicochemical properties, drug delivery, stability studies programs, deactivation/denaturation routes, selection of compatible excipients, and regulatory compliance

elucidates basics of analytical techniques, methods development, separation methods using chromatographic and electrophoretic techniques, and bioactivity methods covering bioassays and immunoassays for quantifying the stability of biological activity

shows how to select the appropriate filter for maximizing compatibility and minimizing adsorption and inactivation, examining topics from basic filtration theories to future trends

reviews the selection process for compatible elastomeric closures, analyzing physical, chemical, toxicological properties, protein adsorption on elastomeric surfaces, strategies to reduce/eliminate adsorption, and specialized containers for biotechnological applications

and more!
Furnished with helpful references, tables, and drawings, this practical guide is indispensable

Introduction to the Development of Biopharmaceutical Parenteral Dosage Forms, John A. Bontempo
Fermentation Process Events Affecting Biopharmaceutical Quality, Anthony S. Lubiniecki
Development of Recovery Processes for Recombinant Proteins and Peptides, Paula J. Shadle
Preformulations Development of Parenteral Biopharmaceuticals, John A. Bontempo
Formulations Development, John A. Bontempo
The Analytical Techniques, Basant G. Sharma
Membrane Filtration Technology, Forrest Badmington
Considerations for Elastomeric Closures for Parenteral Biopharmaceutical Drugs, John A. Bontempo

Academic and Professional Practice & Development

John A. Bontempo

Delineates the appropriate, sequential steps for the formulation of safe, effective, stable, and marketable liquid parenteral biopharmaceutical products--covering fundamentals and essential pathways for each phase as well as its purpose, function, and relation to other stages in the product development process. Written by experts currently involved in state-of-the-art advances in the pharmaceutical drug industry.