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|a Basic fundamentals of drug delivery /
|c edited by Rakesh K. Tekade (National Institute of Pharmaceutical Education and Research (NIPER)-Ahmedabad, Gandhinagar, Gujarat, India, formerly with the Department of Pharmaceutical Technology, School of Pharmacy, International Medical University, Kuala Lumpur, Malaysia).
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|a London, United Kingdom ;
|a San Diego, CA :
|b Academic Press, an imprint of Elsevier,
|c [2019]
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|c �2019
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|a 1 online resource :
|b color illustrations
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|a text
|b txt
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|a Advances in pharmaceutical product development and research series
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|a Basic Fundamentals of Drug Delivery covers the fundamental principles, advanced methodologies and technologies employed by pharmaceutical scientists, researchers and pharmaceutical industries to transform a drug candidate or new chemical entity into a final administrable drug delivery system. The book also covers various approaches involved in optimizing the therapeutic performance of a biomolecule while designing its appropriate advanced formulation.
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|a Includes bibliographical references and index.
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|a Online resource; title from PDF title page (EBSCO, viewed December 10, 2018).
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|a Front Cover; Basic Fundamentals of Drug Delivery; Copyright Page; Dedication; Contents; List of Contributors; About the Editor; 1 Scientific Rationale for Designing Controlled Drug Delivery Systems; 1.1 Conventional Drug Delivery Systems and Limitations; 1.2 Controlled Release Drug Delivery System; 1.2.1 Historical Perspective; 1.2.2 Concept and Understanding; 1.2.3 Advantages of CRDDS Over Conventional Delivery Systems; 1.2.4 Compounds That Are Unsuitable for CRDDS; 1.3 Design of CRDDS: Understanding of Factors; 1.3.1 Physicochemical Properties of Drug and Design Considerations
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|a 1.3.2 Pharmacokinetic/Dynamic Considerations1.3.3 Polymers for CRDDS; 1.3.3.1 Synthetic Polymers; 1.3.3.2 Natural Polymers; 1.3.3.3 Smart Polymers; 1.3.3.3.1 pH-sensitive Polymers; 1.3.3.3.2 Temperature Sensitive Polymers; 1.3.3.3.3 Ion Exchange Polymers; 1.4 Approaches for the Design of CRDDS; 1.4.1 Chemical Approach; 1.4.2 Biological Approach; 1.4.3 Pharmaceutical Approach; 1.5 Medical Rationale of CRDDS; 1.5.1 Reduction in Dosing Frequency; 1.5.2 Lesser Drug Exposure to the Biological Environment; 1.5.3 Minimization of Plasma Concentration Fluctuations; 1.5.4 Better Patient Compliance
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|a 1.5.5 Lower Adverse/Side Effects1.5.6 Augmented Efficacy; 1.6 The Biological Rationale for CRDDS; 1.6.1 Absorption; 1.6.2 Drug-Protein Binding; 1.6.3 Distribution; 1.6.4 Elimination; 1.6.5 Dose-Dependent Bioavailability; 1.6.6 Duration of Drug Residence Within the Therapeutic Window; 1.6.7 Better Safety Margin; 1.6.8 Individualization in a Diseased Condition; 1.7 Conclusion; Acknowledgment; Abbreviations; References; 2 Current Developments in Excipient Science: Implication of Quantitative Selection of Each Excipient in Product Development; 2.1 An Introduction to Excipient Science
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|a 2.1.1 History of Use of Excipients in Pharmaceutical Formulations2.1.2 Need and Rationale Behind the Use of Excipients; 2.1.3 Why Is the Pharma Industry Not Taking Interest to Develop and Use Novel Excipients?; 2.1.4 Role of Excipients in Pharmaceutical Formulations; 2.1.5 Criteria for Selection of Excipients; 2.1.6 Coprocessed Excipients; 2.1.7 Ideal Properties of Excipients; 2.2 Excipients Used in Different Dosage Formulations: Role in Product Development; 2.2.1 Excipients Used in the Solid Dosage Form; 2.2.1.1 Antiadherent and Lubricants; 2.2.1.2 Binders; 2.2.1.3 Disintegrants
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|a 2.2.1.3.1 Characteristics of Disintegrants2.2.1.3.2 Factors Affecting the Action of Disintegrants; 2.2.1.4 Fillers; 2.2.1.4.1 Sugars; 2.2.1.4.2 Lactose; 2.2.1.4.3 Dextrose; 2.2.1.4.4 Sucrose; 2.2.1.4.5 Mannitol; 2.2.1.4.6 Starch and Its Derivatives; 2.2.1.4.7 Celluloses; 2.2.1.4.8 Inorganic Compounds; 2.2.1.5 Flavoring Agents; 2.2.1.6 Sweeteners; 2.2.1.7 Coloring Agent; 2.2.1.8 Glidants; 2.2.1.9 Sorbents; 2.2.1.10 Preservatives; 2.2.2 Excipients Used in the Liquid Dosage Form; 2.2.2.1 Solvents; 2.2.2.2 Cosolvents; 2.2.2.3 Sequestering Agents; 2.2.2.4 Buffers and Buffering Agents; 2.2.2.5 Flavoring Agents
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650 |
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|a Drug delivery systems.
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|a Drug Delivery Systems
|0 (DNLM)D016503
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|a Syst�emes d'administration de m�edicaments.
|0 (CaQQLa)000260397
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|a MEDICAL
|x Pharmacology.
|2 bisacsh
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|a Drug delivery systems
|2 fast
|0 (OCoLC)fst00898667
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700 |
1 |
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|a Tekade, Rakesh K.,
|e editor.
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776 |
0 |
8 |
|i Print version:
|t Basic fundamentals of drug delivery.
|d London, United Kingdom ; San Diego, CA : Academic Press, an imprint of Elsevier, [2019]
|z 0128179090
|z 9780128179093
|w (OCoLC)1050607822
|
830 |
|
0 |
|a Advances in pharmaceutical product development and research series.
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856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/book/9780128179093
|z Texto completo
|