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Ditemukan 5530 dokumen yang sesuai dengan query
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"Explaining the assessment of potential drug compounds, this is an ideal introductory reference for those new to drug discovery. It includes sections on pharmacokinetics and drug metabolism, integration of pharmaceutical development, and predictive safety assessment. Topics include: cost analysis, drug transporters, cytochrome P-450 and drug-drug interactions, plasma protein binding, assessing stability, ways to optimize drug formulation, toxicology and toxicokinetics, and more. Readers will understand why absorption-distribution-metabolism-excretion-toxicology (ADMET) is key in drug development. "
Hoboken: John Wiley & Sons, 2010
e20393919
eBooks  Universitas Indonesia Library
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"The book serves as a basic,comprehensive reference to prioritizing and optimizing leads, toxicity, pharmacogenomics, modeling, and regulations. This single definitive, easy-to-use resource discusses all the issues that need consideration and provides detailed instructions for current methods and techniques. Each chapter was written by one or more leading experts in the field. These authors, representing the many disciplines involved in preclinical toxicology screening and testing, give you the tools needed to apply an effective multidisciplinary approach. The editor, with more than thirty years' experience working with pharmaceutical and biotechnology companies, carefully reviewed all the chapters to ensure that each one is thorough, accurate, and clear. Among the key topics covered are: In vitro mammalian cytogenetics tests Phototoxicity Carcinogenicity studies The pharmacogenomics of personalized medicine Bridging studies Toxicogenomics and toxicoproteomics Each chapter offers a full exploration of problems that may be encountered and their solutions. The authors also set forth the limitations of various methods and techniques used in determining the safety and efficacy of a drug during the preclinical stage. This is a hands-on guide for pharmaceutical scientists involved in preclinical testing,enabling them to perform and document preclinical safety tests to meet all FDA requirements before clinical trials may begin."
Hoboken, New Jersey: Wiley-VCH, 2008
e20394504
eBooks  Universitas Indonesia Library
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"The medical benefits of a drug are not only dependent on its biological effect, but also on its "life cycle" within the organism, from its absorption into the blood, distribution to tissue until its eventual breakdown or excretion by the liver and kidneys.
Here, the authors, all of them employed at Pfizer in the discovery and development of new active substances, discuss the significant parameters and processes important for the absorption, distribution and retention of drug compounds in the body, plus the potential problems created by their transformation into toxic byproducts. The authors cover everything from the fundamental principles right up to the latest developments using high throughput methods to analyze the pharmacokinetic properties of active substances.
Particular emphasis is placed on the impact of pharmacokinetic parameters on the discovery of new drugs, one of the most challenging tasks in global pharmaceutical research."
Weinheim, Germany: Wiley-VCH, 2001
e20394494
eBooks  Universitas Indonesia Library
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"Highlighting the extremely important preclinical aspects of flavonoids, including pharmacokinetics and analysis in biological samples, Flavonoid Pharmacokinetics covers the methods of analysis and pharmacokinetics (preclinical and clinical) of flavonoids to help readers comprehend pharmacokinetic terminology, understand the large number of compounds that encompass the flavonoid family, appreciate the multiple analytical methods available, and assess preclinical and clinical pharmacokinetics of flavonoids and similar chemical-derived compounds. The book uses applicable examples in differ."
Chicester : Wiley , 2013
615.7 FLA
Buku Teks  Universitas Indonesia Library
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Fox, Shelley Chambers
"This book provides comprehensive yet concise coverage of all aspects of pharmaceutics. The first part of the book covers physico-chemical principles and highlights the importance of designing dosage forms that contain the appropriate dose, are stable, palatable, easily used by the patient and release drugs in a predictable fashion for absorption. The second part applies these formulation principles to the design of dosage forms used by each route of administration. Each chapter advises on both the science of the delivery mechanism and appropriate use of that delivery system including patient counselling points. Written for students who aspire to be practicing pharmacists, this book includes numerous case studies and self assessment questions to enable the key concepts to be grasped more readily, while illustrating how the science can be applied to practice to make sure that drugs offer the intended benefit to the patient"
London : Pharmaceutical Press, 2014
615.1 FOX p (1)
Buku Teks SO  Universitas Indonesia Library
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Sadee, Wolfgang
New York: John Wiley & Sons, 1980
615.7 SAD d
Buku Teks  Universitas Indonesia Library
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Gibson, G. Gordon
Jakarta: Penerbit Universitas Indonesia (UI-Press), 2006
574.133 GIB p
Buku Teks  Universitas Indonesia Library
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"This book gives an updated and expert overview of nuclear hormone receptors in drug metabolism and drug development and equips you with the interdisciplinary understanding of these receptors and how they can be regulated. Pharmaceutical researchers will find this extremely useful in developing drugs for cancer, heart disease, and diabetes treatment. This comprehensive resource collects scattered materials into one handy, informative volume."
Hoboken, New Jersey: John Wiley & Sons, 2009
e20394374
eBooks  Universitas Indonesia Library
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"The essentials of drug metabolism vital to developing new therapeutic entities.
Information on the metabolism and disposition of candidate drugs is a critical part of all aspects of the drug discovery and development process. Drug metabolism, as practiced in the pharmaceutical industry today, is a complex, multidisciplinary field that requires knowledge of sophisticated analytical technologies and expertise in mechanistic and kinetic enzymology, organic reaction mechanism, pharmacokinetic analysis, animal physiology, basic chemical toxicology, preclinical pharmacology, and molecular biology. With chapters contributed by experts in their specific areas, this reference covers :
- Basic concepts of drug metabolism
- The role of drug metabolism in the pharmaceutical industry
- Analytical techniques in drug metabolism
- Common experimental approaches and protocols
Drug metabolism in drug design and development emphasizes practical considerations such as the data needed, the experiments and analytical methods typically employed, and the interpretation and application of data. Chapters highlight facts, common protocols, detailed experimental designs, applications, and limitations of techniques."
Hoboken, New Jersey: John Wiley & Sons, 2008
e20395867
eBooks  Universitas Indonesia Library
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New York: Informa Healthcare USA , 2009
615.1 MOD
Buku Teks SO  Universitas Indonesia Library
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