It is evident even to the casual observer that the vast majority of pharmaceutical products are administered as solid dosage forms, which are in turn produced by the formulation and processing of powdered solids. All too often characterization of raw materials and products has centered on aspects of
Physical Methods to Characterize Pharmaceutical Proteins
β Scribed by Wim Jiskoot, Vladimir Hlady, John J. Naleway (auth.), James N. Herron, Wim Jiskoot, Daan J. A. Crommelin (eds.)
- Publisher
- Springer US
- Year
- 1995
- Tongue
- English
- Leaves
- 374
- Series
- Pharmaceutical Biotechnology 7
- Edition
- 1
- Category
- Library
No coin nor oath required. For personal study only.
β¦ Synopsis
Proteins are still gaining importance in the pharmaceutical world, where they are used to improve our arsenal of therapeutic drugs and vaccines and as diagnostic tools. Proteins are different from "traditional" low-molecular-weight drugs. As a group, they exhibit a number of biopharmaceutical and formulation problems. These problems have drawn considerable interest from both industrial and acaΒ demic environments, forcing pharmaceutical scientists to explore a domain previΒ ously examined only by peptide and protein chemists. Biopharmaceutical aspects of proteins, e.g., low oral bioavailability, have been extensively investigated. Although all possible conventional routes of adΒ ministration have been examined for proteins, no real, generally applicable alterΒ native to parenteral administration in order to achieve systemic effects has yet been discovered. Several of these biopharmaceutical options have been discussed in Volume 4 of this series, Biological Barriers to Protein Delivery. Proteins are composed of many amino acids, several of which are notorious for their chemical instability. Rational design of formulations that optimize the native structure and/or bioactivity of a protein is therefore of great importance when long shelf life is required, as it is for pharmaceutical products. This issue has also been examined in two prior volumes of this series: Volume 2: Stability of Protein Pharmaceuticals (Part A) and Volume 5: Stability and Characterization of Protein and Peptide Drugs.
β¦ Table of Contents
Front Matter....Pages i-xvii
Application of Fluorescence Spectroscopy for Determining the Structure and Function of Proteins....Pages 1-63
Structural Information on Proteins from Circular Dichroism Spectroscopy Possibilities and Limitations....Pages 65-100
Fourier Transform Infrared Spectroscopy Investigations of Protein Structure....Pages 101-143
Mass Spectrometry in Protein Structural Analysis....Pages 145-177
Two-, Three-, and Four-Dimensional Nuclear Magnetic Resonance Spectroscopy of Protein Pharmaceuticals....Pages 179-218
Thermodynamic Strategies for Rational Protein and Drug Design....Pages 219-241
Chromatographic Techniques for the Characterization of Proteins....Pages 243-299
Capillary Electrophoresis of Proteins....Pages 301-327
Applying Genetic Engineering to the Structural Analysis of Proteins....Pages 329-350
Back Matter....Pages 351-362
β¦ Subjects
Pharmacy; Animal Physiology; Biophysics and Biological Physics
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