Handbook of Downstream Processing

E. Goldberg

ISBN 10: 9401071985 / ISBN 13: 9789401071987

Published by Springer Netherlands, Springer Netherlands, 2011

About this Item

Druck auf Anfrage Neuware - Printed after ordering - The last two decades have seen a phenomenal growth of the field of genetic or biochemical engineering and have witnessed the development and ultimately marketing of a variety of products-typically through the manipulation and growth of different types of microorganisms, followed by the recovery and purification of the associated products. The engineers and biotechnologists who are involved in the full-scale process design of such facilities must be familiar with the variety of unit operations and equipment and the applicable regulatory requirements. This book describes current commercial practice and will be useful to those engineers working in this field in the design, construction and operation of pharmaceutical and biotechnology plants. It will be of help to the chemical or pharmaceutical engineer who is developing a plant design and who faces issues such as: Should the process be batch or continuous or a combination of batch and continuous How should the optimum process design be developed Should one employ a new revolutionary separation which could be potentially difficult to validate or use accepted technology which involves less risk Should the process be run with ingredients formulated from water for injection, deionized water, or even filtered tap water Should any of the separations be run in cold rooms or in glycol jacketed lines to minimize microbial growth where sterilization is not possible Should the process equipment and lines be designed to be sterilized in-place, cleaned-in-place, or should every piece be broken down, cleaned and autoclaved after every turn.

Seller Inventory # 9789401071987

Bibliographic Details

• Title: Handbook of Downstream Processing
• Publisher: Springer Netherlands, Springer Netherlands
• Publication Date: 2011
• Language: English
• ISBN 10: 9401071985
• ISBN 13: 9789401071987
• Binding: Taschenbuch
• Condition: Neu
• Dimensions: 235W x 155H x 41D millimeters 235 millimeters width by 155 millimeters height by 41 millimeters depth
• Weight: 1118 grams

About this title

Synopsis

The last two decades have seen a phenomenal growth of the field of genetic or biochemical engineering and have witnessed the development and ultimately marketing of a variety of products-typically through the manipulation and growth of different types of microorganisms, followed by the recovery and purification of the associated products. The engineers and biotechnologists who are involved in the full-scale process design of such facilities must be familiar with the variety of unit operations and equipment and the applicable regulatory requirements. This book describes current commercial practice and will be useful to those engineers working in this field in the design, construction and operation of pharmaceutical and biotechnology plants. It will be of help to the chemical or pharmaceutical engineer who is developing a plant design and who faces issues such as: Should the process be batch or continuous or a combination of batch and continuous? How should the optimum process design be developed? Should one employ a new revolutionary separation which could be potentially difficult to validate or use accepted technology which involves less risk? Should the process be run with ingredients formulated from water for injection, deionized water, or even filtered tap water? Should any of the separations be run in cold rooms or in glycol jacketed lines to minimize microbial growth where sterilization is not possible? Should the process equipment and lines be designed to be sterilized­ in-place, cleaned-in-place, or should every piece be broken down, cleaned and autoclaved after every turn?

Review

`... the book offers a great deal of useful information for readers.'
Angewandte Chemie