Analytical Profiles of Drug Substances and Excipients

Although the official compendia define a drug substance as to identity, purity, strength, and quality, they normally do not provide other physical or chemical data, nor do they list methods of synthesis or pathways of physical or biological degradation and metabolism. Such information is scattered throughout the scientific literature and the files of pharmaceutical laboratories. Analytical Profiles of Drug Substances and Excipients, brings the latest information together in one source.

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Excipient Development for Pharmaceutical, Biotechnology, and Drug Delivery Systems

Enhancing awareness to increase the development of excipients, this source

provides guidelines for testing new excipients - offers information to ensure that the product ingredients are in compliance with regulatory and quality requirements, and to guarantee the manufacturing and supply chain is in control

includes excipient harmonization activities -  features descriptions on the development and ways of optimal utilization of excipients for the pharmaceutical and biotechnology industries - presents multiple case studies for numerous 

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Handbook of Pharmaceutical Excipients 7th Edition

Uniquely, the Handbook of Pharmaceutical Excipients collects together the essential data on the physical properties of excipients, drug safety and potential drug toxicity. Information is presented in a structured and easy-to-use format.

 

Written concisely by leading international experts, the Handbook has become the best first drug reference point for users of excipients across many industries.

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Handbook of Cosmeceutical Excipients and their Safeties, 1st Edition

Handbook of Cosmeceutical Excipients summarises the current evidence relating to the side effects of cosmeceuticals and highlights the important information that practitioners and consumers need to know.

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Pharmaceutical Capsules 2nd Edition

Previously published as Hard Capsules, this updated and expanded second edition covers all aspects of capsule technology, including history, standards, methods and equipment used in manufacture, filling, printing, weighing, cleaning and inspecting of both hard and soft capsules.

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Pharmaceutical Excipients: Properties, Functionality, and Applications in Research and Industry

This book provides an overview of excipients, their functionalities in pharmaceutical dosage forms, regulation, and selection for pharmaceutical products formulation. It includes development, characterization methodology, applications, and up-to-date advances through the perspectives of excipients developers, users, and regulatory experts.

 

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Polyvinylpyrrolidone Excipients for Pharmaceuticals

The book describes the properties, analytical methods and the applications of different polyvinylpyrrolidone excipients (povidone, crospovidone, copovidone etc.) for use in pharmaceutical preparations. This group of excipients is one of the most important excipients used in modern technology to produce drugs. The book is intended for all persons working in the research, development and quality control of drugs. It gives a survey of all applications in solid, liquid and semisolid dosage forms including many drug formulation examples and more than 600 references to the literature.

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Profiles of Drug Substances, Excipients and Related Methodology

Although the official compendia define a drug substance as to identity, purity, strength, and quality, they normally do not provide other physical or chemical data, nor do they list methods of synthesis or pathways of physical or biological degradation and metabolism. Such information is scattered throughout the scientific literature and the files of pharmaceutical laboratories. Analytical Profiles of Drug Substances and Excipients, brings the latest information together in one source.

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Role of Lipid Excipients in Modifying Oral and Parenteral Drug Delivery: Basic Principles and Biological Examples

This comprehensive resource covers the fundamentals, formulation, and biopharmaceutical issues of lipid-based drug delivery. It presents the principles of lipid absorption and covers formulation issues, such as dissolution testing and stability testing, and physiological and biopharmaceutical issues, including the role of specific enzymes, the evaluation of transport systems in the body, and the mechanisms governing the transport of water-insoluble drugs.

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