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Basic fundamentals of drug delivery /

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 bo...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Tekade, Rakesh K. (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: London, United Kingdom ; San Diego, CA : Academic Press, an imprint of Elsevier, [2019]
Colección:Advances in pharmaceutical product development and research series.
Temas:
Acceso en línea:Texto completo

MARC

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245 0 0 |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). 
264 1 |a London, United Kingdom ;  |a San Diego, CA :  |b Academic Press, an imprint of Elsevier,  |c [2019] 
264 4 |c �2019 
300 |a 1 online resource :  |b color illustrations 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
490 1 |a Advances in pharmaceutical product development and research series 
520 |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. 
504 |a Includes bibliographical references and index. 
588 0 |a Online resource; title from PDF title page (EBSCO, viewed December 10, 2018). 
505 0 |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 
505 8 |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 
505 8 |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 
505 8 |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 
505 8 |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 
650 0 |a Drug delivery systems. 
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650 7 |a Drug delivery systems  |2 fast  |0 (OCoLC)fst00898667 
700 1 |a Tekade, Rakesh K.,  |e editor. 
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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