Preformulation in Solid Dosage Form Development (eBook, ePUB)

Redaktion: Adeyeye, Moji Christianah; Brittain, Harry G.

• Format: ePub

Produktbeschreibung

During the onset of any clinical trial there are many factors and variables to consider. Funding, time restraints, and regulatory agency guidelines are factors that often influence which variables will be studied, leaving other important information out of the study. Preformulation in Solid Dosage Form Development covers every topic of critical imp

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Produktdetails

• Verlag: Taylor & Francis eBooks
• Seitenzahl: 616
• Erscheinungstermin: 7. Januar 2008
• Englisch
• ISBN-13: 9781040170212
• Artikelnr.: 72583409

Autorenporträt

MOJI CHRISTIANAH ADEYEYE is currently a Professor of Pharmaceutics and Pharmaceutical Technology, a Fulbright Scholar, and a member of the graduate faculty at the School of Pharmacy, Duquesne University, Pittsburgh, Pennsylvania. She graduated from the University of Nigeria, Nsukka and the University of Georgia, Athens, where she earned her B.S., M.S., and Ph.D. respectively. Her research interests include, preformulation, drug/excipient characterization, delivery systems with a focus on bioavailability and bioequivalence of solid, semi-solid and liquid dosage forms (conventional, modified release). She has worked extensively on nonsteroidal anti-inflammatory drugs, steroids and excipients such as cyclodextrins, microcrystalline cellulose and silicified microcrystalline cellulose. She has published over 40 manuscripts and two patents and given over 100 scientific presentations. She was the past President of the Nigerian American Association of Pharmaceutical Scientists (NAAPS) and former Chair of the AAPS Preformulation Focus Group. She is the Founder and President of a non-profit organization-Drugs for AIDS and HIV Patients (DAHP) whose focus is to care and provide treatment for HIV/AIDS orphans and widows. She is a member of AAPS, APHA, CRS, AACP, AAUP and Christian Connections for International Health. HARRY G. BRITTAIN is Founder of the Center for Pharmaceutical Physics, Milford, New Jersey. Previously, Dr. Brittain was Vice President for Pharmaceutical Development at Discovery Laboratories, Inc. He also served as Director of Pharmaceutical Development at Ohmeda Inc., and led a variety of groups within the Analytical R&D Department at Bristol-Myers Squibb Co. Dr. Brittain has authored more than 275 research publications and book chapters and has presented numerous invited lectures and short courses in pharmaceutics. He is editor of several books including Physical Characterization of Pharmaceutical Solids, Polymorphism in Pharmaceutical Solids, and Spectroscopy of Pharmaceutical Solids (Taylor & Francis, Inc.). Dr. Brittain is an Associate Editor for the Journal of Pharmaceutical Sciences, and a member of the editorial boards of Pharmaceutical Development and Technology, AAPS PharmSciTech, and Chirality. Dr. Brittain is a Fellow of the American Association of Pharmaceutical Scientists and of the Royal Institute of Chemistry, and a recipient of the AAPS Research Achievement Award in Analysis and Pharmaceutical Quality.

Inhaltsangabe

1. Introduction and Overview. 2. Preliminary Preformulation. 2.1.
Accelerating the Course of Preliminary-Preformulation through Prediction of
Molecular Physical Properties and Integrated Analytical Data Management.
2.2. Prediction of Crystallographic Characteristics. 2.3. Salt Selection
for Pharmaceutical Compounds. 2.4. Intelligent Preformulation Design and
Predictions using Artificial Neural Networks. 3. Profiling the Drug
Substance. 3.1. Developing a Profile of the Active Pharmaceutical
Ingredient. 3.2. Particle Morphology and Characterization in
Preformulation. 3.3. Preparation and Identification of Polymorphs and
Solvatomorphs. 3.4. X-Ray Diffraction Methods for the Characterization of
Solid Pharmaceutical Materials. 3.5. Spectroscopic Methods for the
Characterization of Drug Substances. 3.6. Thermal Analysis and Calorimetric
Methods for the Characterization of New Crystal Forms. 3.7. Solubility
Methods for the Characterization of New Crystal Forms. 4. Development of
the Ideal Formulation. 4.1. Overview of the Solid Dosage Form
Preformulation Program . 4.2. Drug-Excipient Interactions Appropriate to
Solid Dosage Forms. 4.3. Methods for the Determination of the Physical and
Chemical Stability of a New Solid Dosage Form. 4.4. Dissolution Testing. 5.
Beyond Preformulation. 5.1. Structure, Content, and Format of the
Preformulation Report. 5.1. Significance of Drug Substance Physicochemical
Properties in Regulatory Quality by Design.