Kindly note that we have put a lot of effort into researching the best books on Biopharmaceutical Technology subject and came out with a recommended list of top 10 best books. The table below contains the Name of these best books, their authors, publishers and an unbiased review of books on "Biopharmaceutical Technology" as well as links to the Amazon website to directly purchase these books. As an Amazon Associate, we earn from qualifying purchases, but this does not impact our reviews, comparisons, and listing of these top books; the table serves as a ready reckoner list of these best books.
|1. “Biopharmaceutical Technology” by Yu Qiong|
|2. “Biotechnology and Biopharmaceutical Manufacturing, Processing, and Preservation (Drug Manufacturing Technology Series)” by Kenneth E Avis and Vincent L Wu
“Biotechnology and Biopharmaceutical Manufacturing, Processing, and Preservation (Drug Manufacturing Technology Series)” Book Review: the volume explains practices implied to the large-scale processing of biotechnological produce. It covers processing and bulk storage preservation methodologies. It also presents plans for enhancing efficiency of process strategies of numerous products and manufacturing facilities for such processing methods. It explains large-scale chromatography for the distillation of biomolecules in manufacturing and lyophilization of protein pharmaceuticals. It inculcates case study on blow-fill-seal processing mechanics and explains economic and cost factors for bioprocess engineering.
|3. “GFP Whole Cell Microbial Biosensors: Scale-up and scale-down effects on biopharmaceutical processes” by Frank Delvigne
“GFP Whole Cell Microbial Biosensors: Scale-up and scale-down effects on biopharmaceutical processes” Book Review: the text encompasses new developments in bioreactor machinery following the scaling-out principle which is carrying out various cultures in parallel with controlled surroundings for screening purposes. It includes various mini-bioreactor concepts which are developed using the scaling-out principle like bioreactor with working volume of 1 to 100 mL with controlling devices. The work includes proper characterization of chemical engineering similarities between conventional stirred bioreactors and their miniature equivalent.
|4. “Delivery Technologies for Biopharmaceuticals: Peptides, Proteins, Nucleic Acids and Vaccines” by Lene Jorgensen and Hanne Morck Nielson
“Delivery Technologies for Biopharmaceuticals: Peptides, Proteins, Nucleic Acids and Vaccines” Book Review: The book explains plans to overcome the key barriers for successful delivery of therapeutic peptides, proteins and nucleic acid-based drugs or vaccines related to the site of administration and the target site. It contains concepts like problems in delivery of biopharmaceuticals, immune response, adjuvants and delivery systems for vaccines, several examples of delivery systems for various biopharmaceuticals and others. Further it covers novel formulation approaches for peptide and protein injectables and a critical assessment of delivery technologies for biopharmaceuticals. It presents the methods applied by researchers to make sure efficient delivery of this exciting new class of drugs.
|5. “Biopharmaceuticals: Biochemistry and Biotechnology” by Gary Walsh
“Biopharmaceuticals: Biochemistry and Biotechnology” Book Review: the book presents an accessible and recent outline of the science and medical uses of biopharmaceutical products. It explains therapeutic substances like interferons, interleukins and growth factors along with hormones, antibodies and vaccines. It focuses on polypeptide-based therapeutic agents, the possible uses of nucleic acids related to gene therapy and antisense methods. The book is designed for advanced undergraduate or postgraduate students in biotechnology, biochemistry, pharmaceutical science or medicine.
|6. “Quality by Design for Biopharmaceutical Drug Product Development” by Feroz Jameel and Susan Hershenson
“Quality by Design for Biopharmaceutical Drug Product Development” Book Review: the text describes the implementation of Quality by Design (QbD) to biopharmaceutical drug product development. The text includes dosage forms, liquid and lyophilized drug products. It describes essential elements of QbD and analyses how these elements are integrated into drug product development. It illustrates how QbD is applied for formulation development scoping from screening of formulations to developability assessment to development of lyophilized and liquid formats. It contains the use of small-scale and surrogate models along with QbD implementation to drug product processes such as drug substance freezing and thawing, lyophilization, inspection and shipping and handling.
|7. “Pharmaceutical Engineering Guides for New and Renovated Facilities: Biopharmaceutical Manufacturing Facilities” by ISPE
“Pharmaceutical Engineering Guides for New and Renovated Facilities: Biopharmaceutical Manufacturing Facilities” Book Review: the book will be appropriate for reference by industry for the design, construction, commissioning, and qualification of new facilities for the manufacture of biopharmaceutical Active Pharmaceutical Ingredients (APIs). The volume takes into consideration non-U.S. regulatory differences along with input by ISPE Members from both Europe and Asia – particularly Japan.
We have created a collection of best reference books on "Biopharmaceutical Technology" so that one can readily see the list of top books on "Biopharmaceutical Technology" and buy the books either online or offline.
If any more book needs to be added to the list of best books on Biopharmaceutical Technology subject, please let us know.
Sanfoundry Global Education & Learning Series – Best Reference Books!