• Modern pharmaceutical analysis : an overview / S. Ahuja
• Combinatorial chemistry and high-throughput screening in drug discovery and development / Ken Appell, John J. Baldwin and William J. Egan
• Solid-state analysis / Harry G. Brittain
• Degradation and impurity analysis for pharmaceutical drug candidates / Karen M. Alsante, Robert C. Friedmann, Todd D. Hatajik, Linda L. Lohr, Thomas R. Sharp, Kimberly D. Snyder and Edward J. Szczesny
• Preformulation studies / Edward Lau
• Solid dosage-form analysis / Philip J. Palermo
• Parenteral dosage forms / Gregory A. Birrer, Satya S. Murthy, Jie Liu and Judy Estrada
• New drug delivery systems / David C. Pang
• Compendial testing / Christine F. Richardson
• Method development / Henrik T. Rasmussen
• Setting up specifications / Ian E. Davidson
• Validation of pharmaceutical test methods / Jonathan B. Crowther
• Stability studies / Jessica Cha, Joseph S. Ranweiler and Philip A. Lane
• Analytical methodology transfer / Stephen Scypinski
• Pharmaceutical analysis documentation / Hitesh Chokshi and Kathleen Schostack
• An innovative separation platform : electrophoretic microchip technology / Lian Ji Jin, Jerome Ferrance, Zhili Huang and James P. Landers.

• Modern Pharmaceutical Analysis: An Overview (S. AHUJA) Combinatorial Chemistry and High-Throughput Screening in Drug Discovery and Development (KEN APPELL, JOHN J. BALDWIN, AND WILLIAM J. EGAN) Solid-State Analysis (HARRY G. BRITTAIN) Degradation and Impurity Analysis for Pharmaceutical Drug Candidates (KAREN M. ALSANTE, ROBERT C. FRIEDMANN, TODD D. HATAJIK, LINDA L. LOHR, THOMAS R. SHARP, KIMBERLY D. SNYDER, AND EDWARD J. SZCZESNY) Preformulation Studies (EDWARD LAU (deceased)) Solid Dosage-Form Analysis (PHILIP J. PALERMO) Parenteral Dosage Forms (GREGORY A. BIRRER, SATYA S. MURTHY, AND JIE LIU) New Drug Delivery Systems (DAVID C. PANG) Compendial Testing (CHRISTINE F. RICHARDSON) Method Development (HENRIK T. RASMUSSEN) Setting Up Specifications (IAN E. DAVIDSON) Validation of Pharmaceutical Test Methods (JONATHAN B. CROWTHER) Stability Studies (JESSICA CHA, JOSEPH S. RANWEILER, PHILIP A. LANE) Analytical Methodology Transfer (STEPHEN SCYPINSKI) Pharmaceutical Analysis Documentation (HITESH CHOKSHI AND KATHLEEN SCHOSTACK) An Innovative Separation Platform: Electrophoretic Microchip Technology (LIAN JI JIN, JEROME FERRANCE, ZHILI HUANG, AND JAMES P. LANDERS) Index.
• (source: Nielsen Book Data)

This book describes the role modern pharmaceutical analysis plays in the development of new drugs. Detailed information is provided as to how the quality of drug products is assured from the point of discovery until the patient uses the drug. Coverage includes state-of-the-art topics such as analytics for combinatorial chemistry and high-throughput screening, formulation development, stability studies, international regulatory aspects and documentation, and future technologies that are likely to impact the field. Emphasis is placed on current, easy-to-follow methods that readers can apply in their laboratories. No book has effectively replaced the very popular text, Pharmaceutical Analysis, that was edited in the 1960s by Tak Higuchi. This book will fill that gap with an up-to-date treatment that is both handy and authoritative.
(source: Nielsen Book Data)

• Chromatography and Pharmaceutical Analysis-- Chromatography and New Drug Development-- Alternate Strategies for Analysis of Pharmaceuticals-- Ruggedness of Impurity Determinations in Pharmaceuticals: High-Performance Liquid Chromatography Analysis with Ultraviolet Detection-- High-Performance Liquid Chromatography in Pharmaceutical Development of Antibiotic Products-- Gas Chromatography and Pharmaceutical Analyses-- Gas Chromatography and Mass Spectrometry of Erythrina Alkaloids from the Foliage of Genetic Clones of Three Erythrina Species-- Developing Stereoselective High-Performance Liquid Chromatographic Assays for Pharmacokinetic Studies-- Direct Enantiomeric Separation and Analysis of Some Aromatase Inhibitors on Cellulose-Based Chiral Stationary Phases-- Chromatographic Analysis of Host-Cell Protein Impurities in Pharmaceuticals Derived from Recombinant DNA-- Binding Proteins in Development of Online Postcolumn Reaction Detection Systems for Liquid Chromatography-- Determination of a New Oral Cephalosporin in Biological Fluids: Liquid Chromatographic, Ultraviolet, and Mass Spectrometric Methods-- Drugs and Metabolites in Biological Fluids: Automated Analysis by Laboratory Robotics-- Preparative Separations of Glycerophospholipids by High-Performance Liquid Chromatography-- Small-Molecule Pharmaceutical Separations by Capillary Electrophoresis: Method Development and Manipulation of Selectivity.
• (source: Nielsen Book Data)

Describes the role of chromatography in the development of new drugs. Features chapters on the analysis of natural and recombinant pharmaceutical products. Covers new techniques such as capillary electrophoresis and a number of hyphenated techniques that combine liquid chromatography or gas chromatography with mass spectrometry. Describes such applications as impurity analysis, chiral separations, metabolic studies, robotics, and support of biotechnology products. Also describes trace and ultratrace analyses in a variety of matrices.
(source: Nielsen Book Data)