DEVELOPMENT OF BIOPHARMACEUTICAL PARENTERAL DOSAGE FORMS, DPSS VOL 85. Dieser Artikel ist nicht verfügbar.
Sprache: Englisch
Verlag: CRC Press, 1997
- Softcover
- Neu
Anbieter: Romtrade Corp., STERLING HEIGHTS, MI, USARomtrade Corp.
Verkäufer/-in mit 5 Sternen
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Internationale Ausgabe
Nicht verfügbar
Softcover
Zustand: Neu
EUR 44,94
Artikelbeschreibung vom Verkäufer
Brand New. Soft Cover International Edition. Different ISBN and Cover Image. Priced lower than the standard editions which is usually intended to make them more affordable for students abroad. The core content of the book is generally the same as the standard edition. The country selling restrictions may be printed on the book but is no problem for the self-use. This Item maybe shipped from US or any other country as we have multiple locations worldwide.
Bestandsnummer des Verkäufers ABBB-205765
- Titel
- DEVELOPMENT OF BIOPHARMACEUTICAL PARENTERAL DOSAGE FORMS, DPSS VOL 85
- Verlag
- CRC Press
- Veröffentlichungsjahr
- 1997
- Zustand
- New
- Einband
- Softcover
- Sprache
- Englisch
- ISBN-10
- 082479981X
- ISBN-13
- 9780824799816
- Ausgabe
- Internationale Ausgabe
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
Written by experts currently involved in state-of-the-art advances in the pharmaceutical drug industry, Development of Biopharmaceutical Parenteral Dosage Forms
Furnished with helpful references, tables, and drawings, this practical guide is indispensable
„Inhaltsangabe“ gehört möglicherweise zu einer anderen Auflage dieses Titels.
Über die Autorin bzw. den Autor
John A. Bontempo
„Über diesen Titel“ gehört möglicherweise zu einer anderen Auflage dieses Titels.