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different techniques required for each one. In Vitro Drug Release Testing of Special Dosage Forms covers the in vitro release testing of: lipid;
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to develop prolonged release dosage forms for many drugs. Correspondingly, a growing number of new prolonged release dosage forms have been;
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controlled drug release and oral dosage forms. This book provides clear and straightforward information enabling the reader to carry out numerical;
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An expertly written source on the devices, systems, and technologies used in the dissolution testing of oral pharmaceutical dosage forms;
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of superdisintegrants and evaluated for general appearance and physical parameters, drug content, in vitro disintegration, in vitro dispersion, in vitro drug;
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Pharmaceutical manufacturers are constantly facing quality crises of drug products, leading to an escalating number of product recalls and;
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Introduction, Historical Highlights, and the Need for Dissolution Testing Theories of Dissolution Dissolution Testing Devices Automation;
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Oral drug delivery has been an important part of drug delivery and was often linked with tablets, capsules, syrups etc during the;
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Nicotinic acid (NA) as lipid lowering agent drug has not become a first-line treatment due to the strong side effect called flushing occurs;
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This is an essential resource for all those involved in the formulation, development, manufacture and testing of suppositories.The;
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The ultimate goal of drug product development is to design a system that maximizes the therapeutic potential of the drug substance and;
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Teaches future and current drug developers the latest innovations in drug formulation design and optimization This highly accessible;
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Since the earliest dosage forms to modern drug delivery systems, came a great development and growth of knowledge with respect to drug;
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testing, formulation, and clinical evaluation of intraoral drug delivery products-summarizing intraoral dosage forms in various stages of research;
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Considered the most comprehensive source of drug dosage forms and delivery systems, Ansel's Pharmaceutical Dosage Forms and Drug Delivery;
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of swelling, gelling and erosion, is what accounts for the rate of drug release. When the tablet is first swallowed, the drug concentration is high;
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Formulation is a key step in the drug design process, where the active drug is combined with other substances that maximise the therapeutic;
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In drug delivery, active pharmaceutical ingredient (API) is delivered to the patient through different methods and shapes which are called;
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in vitro percutaneous absorption, this reference provides comprehensive coverage of the development, preparation, and application of topical and;
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Clinical Challenges in Therapeutic Drug Monitoring: Special Populations, Physiological Conditions and Pharmacogenomics focuses on;
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activities in providing accurate and reliable data throughout the lifecycle of a drug product. This book is divided into four parts;
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complex into fast-Dispersible tablets (FDT) for the treatment of allergic rhinitis & chronic idiopathic urticaria. Drug release from FDT;
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Generic Drug Product Development: Specialty Dosage Forms explores the issues related to providing evidence of pharmaceutical equivalence;
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Completely revised and updated, this third edition of Pharmaceutical Dosage Forms and Drug Delivery elucidates the basic principles;
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Completely revised and updated, this third edition of Pharmaceutical Dosage Forms and Drug Delivery elucidates the basic principles;
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on current findings. Modern Pharmaceutics helps you stay current with the basic sciences, systems, applications, and advances in drug;
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of the tablet dosage form. The ultimate goal of drug product development is to design a system that maximizes the therapeutic potential of the;
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