Drug Stability for Pharmaceutical Scientists

Drug Stability for Pharmaceutical Scientists

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Description

Drug Stability for Pharmaceutical Scientists is a clear and easy-to-follow guide on drug degradation in pharmaceutical formulation. This book features valuable content on both aqueous and solid drug solutions, the stability of proteins and peptides, acid-base catalyzed and solvent catalyzed reactions, how drug formulation can influence drug stability, the influence of external factors on reaction rates and much more. Full of examples of real-life formulation problems and step-by-step calculations, this book is the ideal resource for graduate students, as well as scientists in the pharmaceutical and related industries.
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Product details

  • Paperback | 170 pages
  • 150 x 228 x 12mm | 240g
  • Academic Press Inc
  • San Diego, United States
  • English
  • Illustrated; Illustrations, unspecified
  • 0124115489
  • 9780124115484
  • 1,087,006

Table of contents

I. Principles of drug degradation (the solution kinetics and mathematical treatment): 1. Zero, first, second and third order reactions 2. Complex reactions (e.g. reversible reactions, parallel reactions, consecutive reactions, steady state, enzyme kinetics etc.) 3. Effect of temperature (e.g. Arrhenius, Q10-values, Collision theory, Transition state theory, Eyring equation etc.) 4. Effect of pH (Specific acid/base catalysis, pH-rate profiles) 5. Effect of buffer salts (General acid/base catalysis or buffer catalysis) 6. Ionic strength 7. Solvent effects (e.g. dielectric constant) 8. Surface active compounds (micelle effect) 9. Effect of complexation (e.g. cyclodextrins, metal ions and carbohydrates) 10. Effect of light, oxygen and other catalytic compounds. II. Degradation pathways Selected examples of drug degradation with examples and mathematical calculations. 1. Hydrolysis (aspirin, procaine, procainamide, acetaminophen, ss-lactam antibiotics, nitrogen mustards etc.) 2. Oxidation (morphine, epinephrine, vitamin C, vitamin A, hydrocortisone, polyunsaturated fatty acids (autoxidation) etc.; antioxidants) 3. Isomerization and racemization (ephedrine, tetracyclines, pilocarpine, vitamin A, thalidomide, etc.) 4. Photodegradation 5. Polymerization (ss-lactam antibiotics etc.) 6. Decarboxylation and elimination (p-aminosalicylic acid) 7. Dehydration (prostaglandins etc.) III. Drug degradation in semi-solid state 1. Ointments 2. Creams (o/w and w/o emulsions) 3. Gels IV. Drug degradation in solid state 1. Physical stability of drugs (crystallization of amorphous drugs, polymorph transitions, crystal growth, moisture absorption and vapor absorption, nitroglycerine) 2. Chemical stability (hydrolysis (aspirin), etc.) V. Stability of peptide and proteins VI. Stability testing 1. Stability testing during preformulation studies. 2. Stability testing of the final product 3. Regulations of stability testing (including ICH guidelines) Appendix
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Review Text

".a good foundation in chemistry is assumed, making this text most useful for science graduate students and scientists in the pharmaceutical industry. Students or newcomers to the field of drug stability should find the 'problem' section useful, with questions and answers based on real data provided."-- PharmaceuticalJournal.com, July 18, 2014 ".describes the stability of pharmaceutical products as the capacity of the product or a given drug substance to remain within established specifications of identity, potency, and purity during a specified time period.topics are principles of drug degradation, degradation pathways, drug degradation in semi-solid dosage forms."-- ProtoView.com, April 2014
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Review quote

"...a good foundation in chemistry is assumed, making this text most useful for science graduate students and scientists in the pharmaceutical industry. Students or newcomers to the field of drug stability should find the `problem' section useful, with questions and answers based on real data provided."--PharmaceuticalJournal.com, July 18, 2014 "...describes the stability of pharmaceutical products as the capacity of the product or a given drug substance to remain within established specifications of identity, potency, and purity during a specified time period...topics are principles of drug degradation, degradation pathways, drug degradation in semi-solid dosage forms..."--ProtoView.com, April 2014
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About Thorsteinn Loftsson

Dr. Thorsteinn Loftsson is a Professor of Physical Pharmacy at the University of Iceland in Reykjavik. He received his MS Pharm degree from University of Copenhagen and his MS and PhD degrees from the Department of Pharmaceutical Chemistry at the University of Kansas. Dr. Loftsson has authored or co-authors over 200 papers in peer-reviewed journals, numerous book chapters and 20 patents and patent applications. His main research areas include the pharmaceutical applications of cyclodextrins, marine lipids, prodrugs and soft drugs. He has conducted over 100 lectures and is a Fellow of the American Association of Pharmaceutical Scientists (AAPS). Dr. Loftsson is also a member for the editorial board of Journal of Pharmaceutical Sciences, International Journal of Pharmaceutics, Journal of Pharmacy and Pharmacology, die Pharmazie and Journal of Drug Delivery Science and Technology (formerly STP Pharma Sciences).
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