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Book
Long Acting Animal Health Drug Products : Fundamentals and Applications
Authors: ---
ISSN: 21926204 ISBN: 1283697122 146144439X 1461444381 1489994106 Year: 2013 Publisher: New York, NY : Springer US : Imprint: Springer,

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Abstract

This authoritative book is a comprehensive guide on the theories, applications, and challenges associated with the design and development of long acting veterinary formulations.  The volume acts as a reference to the animal health formulation scientist and contains chapters written by some of the leading experts in the field.  In addition it offers additional details through a mixture of figures, tables, and references to provide information not found in other similar texts.   The book covers everything a student or a formulation scientist in industry or academia needs to know about this unique drug delivery field. It provides an overview of the fundamental science necessary for the rational design and development of veterinary animal health products, and provides in-depth descriptions of the technologies that are currently commercially available for the prolonged delivery of drugs to animals.   Long Acting Animal Health Drug Products: Fundamentals and Applications will be indispensable to scientists interested in the science and technology of drug delivery to animals and be essential for those developing long acting delivery systems for farmed and companion animals.


Book
Fundamentals and Applications of Controlled Release Drug Delivery
Authors: --- --- ---
ISBN: 1461408806 1489986464 9786613440990 1283440997 1461408814 Year: 2012 Publisher: New York, NY : Springer US : Imprint: Springer,

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This authoritative book covers the fundamentals relating to the science and technology of drug delivery.  The book is written at a level that is understandable to those entering the field and who are not familiar with its common phrases or complex terms.  It is a book that provides a simple encapsulation of concepts and expands on them using a building block approach to each subject, starting at a basic level and building to extend the readers knowledge and application of the subject.  In each chapter the basic concept is explained as simply and clearly as possible without a great deal of detail, then in subsequent sections additional material is introduced in order to build up the reader’s understanding and comprehension of the subject matter.   The book comprises several Parts.  The first part covers the fundamentals of drug delivery, the second covers delivery materials, the third deals with delivery systems (both temporal and spatial) and the fourth introduces the reader to some clinical applications of drug delivery. The book ends with a future outlook chapter in which prospects for the field are envisioned.   This book will be indispensable to scientists interested in the science and technology of drug delivery and be essential for those developing delivery systems designed to improve the clinical performance of a drug.   Professor Juergen Siepmann is Professor of Pharmaceutics at the College of Pharmacy, Université Lille Nord de France, Lille, France. He studied pharmacy and received his doctoral degree from the Freie Universitaet Berlin, Berlin, Germany, in 1999. His research focuses on the elucidation of the underlying mass transport phenomena in controlled drug delivery systems. Prof. Siepmann is reviews editor of the International Journal of Pharmaceutics and president of APGI (French Association of Pharmaceutical Technology). Since 2010 he is heading the INSERM (French National Institute of Health and Medical Research) research group “Controlled Drug Delivery Systems and Biomaterials”.     Ronald A. Siegel, Sc.D., is Professor of Pharmaceutics and Biomedical Engineering at the University of Minnesota.  He received his doctoral degree from MIT under the direction of Prof. Robert Langer in 1984, and taught at the University of California, San Francisco until 1998, when he moved to Minnesota.  Professor Siegel is Fellow of the Controlled Release Society (CRS), the American Association of Pharmaceutical Scientists, and the American Institute of Medical and Biological Engineering.  He was president of CRS from 1997-1998.  His present research interests include hydrogels, block polymers, microfabricated sensors and drug delivery systems, and mathematical modeling of transport.     Michael J. Rathbone is Associate Professor of Pharmaceutics at the School of Pharmacy, Griffith University, Australia.  Dr. Rathbone’s research interests are in the modified delivery of bioactives to the mouth, polymeric delivery systems and long acting veterinary drug delivery systems.  He is a Fellow of the Controlled Release Society (CRS) and received the CRS Distinguished Service Award in 2006.  He has edited or co-edited many books in the fields of modified release drug delivery, oral mucosal drug delivery and veterinary drug delivery.

Drug and enzyme targeting. 149 : Part B
Authors: ---
ISBN: 0121820491 9780121820497 9780121820121 0121820122 Year: 1987 Volume: 112 Publisher: New York, NY ; London : Academic Press,


Book
Formes Pharmaceutiques Nouvelles. Aspects technologique, biopharmaceutique et médical
Authors: --- --- ---
ISBN: 2852063093 9782852063099 Year: 1985 Publisher: Paris : Technique & Documentation - Lavoisier,


Book
Controlled Release in Oral Drug Delivery
Authors: ---
ISBN: 1461410037 9786613353511 1283353512 1461410045 Year: 2011 Publisher: New York, NY : Springer US : Imprint: Springer,

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Abstract

Controlling the rate, extent and time of a drug’s delivery can optimize its performance in many ways, relative to “immediate release” delivery. Such optimized design requires a broad knowledge base of topics such as gastro intestinal tract physiology, polymer science, and the mechanisms by which drugs are released from the formulated units. Technologies to “reduce to practice” also need to be carefully considered. Such knowledge must be allied to the physico chemical properties of the drug, its pharmacokinetic behaviors, enzyme susceptibility and other factors that can affect absorption or timecourse in the biosystem.   Traditionally, controlled release systems tended to be “second-generation products, building on accumulated clinical experience.  However, better awareness of the molecular biology of drug action and the promise of biomarkers and personalized medicine may mean that optimizing performance by controlling release may become a first option in new product development. Such optimization may well help reduce the alarming attrition rates that are now prevalent in new drug development.   Controlled Release in Oral Drug Delivery provides chapters, dealing with all facets of the above subject matter, and its challenges. Authors have been drawn from academia, providers of excipients and from those designing controlled release systems in industrial R&D and manufacture. The contents provide a unique blend of cutting edge knowledge, data on materials and practical experiences.  It is essential text for students, researchers and industrial engineering, formulation and manufacturing technologists as well as quality testing and control functions.   Clive Wilson is the J. P. Todd Professor of Pharmaceutics at Strathclyde University in Glasgow, Scotland and the current president of the European Union Federation for Pharmaceutical Sciences. He is the Chief Scientist of Bio-Images Research Group, a Phase II imaging specialist clinical unit in Glasgow Royal Infirmary. Major areas of research have been the study of the behaviour of drug formulations in man.  With colleagues at Nottingham, he pioneered applications of scintigraphy in the study of physiological and patho-physiological effects of transit on drug absorption and began the investigations into regional drug absorption in man.  This was later applied to the design and optimisation of oral dosage forms, in silico modelling of formulations in man and  studies on IVIVR. He has published more than 150 papers, six books and over 130 reviews and book chapters. He was made a fellow of the Controlled Release Society in June 2010 and a Fellow of the Academy of Pharmaceutical Sciences in September 2010.   Patrick Crowley has over 40 years’ experience in dosage form development in the pharmaceutical industry, in both the UK and USA.  He has played key roles in the development of 16 commercial products, including fermentation products, semi synthetics, synthetic structures and a biopharmaceutical product and holds several formulation-related Patents. His interests and publications include drug and product stability, enhancing performance by dosage form design and the application of Quality by Design principles and practices in dosage form development, manufacture and control.


Book
Current Antipsychotics
Authors: ---
ISSN: 01712004 ISBN: 3642445470 3642257607 3642257615 1283849402 Year: 2012 Volume: v. 212 Publisher: Berlin, Heidelberg : Springer Berlin Heidelberg : Imprint: Springer,

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Six decades after the serendipitous discovery of chlorpromazine as an antipsychotic and four decades after the launch of clozapine, the first atypical or second generation antipsychotic, psychopharmacology has arrived at an important crossroad. It is clear that pharmacological research and pharmaceutical development must now focus on complementary or even alternative mechanisms of action to address unmet medical  needs, i.e. poorly treated domains of schizophrenia, improved acceptance by patients, better adherence to medication, safety in psychoses in demented patients, and avoiding cardiac and metabolic adverse effects. The first completely novel mechanisms evolving from our insights into the pathophysiology of psychotic disorders, especially the role of glutamatergic mechanisms in schizophrenia, are now under development, and further principles are on the horizon. This situation, in many respects similar to that when the initial second-generation antipsychotics became available, can be rewarding for all.  Preclinical and clinical researchers now have the opportunity to confirm their hypotheses and the pharmaceutical industry may be able to develop really novel classes of therapeutics. When we were approached by the publishers of the Handbook of Experimental Pharmacology to prepare a new volume on antipsychotics, our intention was to capture both, the accumulated preclinical and clinical knowledge about current antipsychotics as well as prospects for new and potentially more specific antischizophrenia principles. These efforts should be based on the pathophysiology of the diseases and the affected neurotransmitter systems. Since preclinical research on antipsychotic compounds is only reliable when intimately linked through translational aspects to clinical results, we decided to include clinical science as well. It turned out that that this endeavor could not be covered by a single volume. We thank the editorial board and the publishers for supporting our decision to prepare two volumes: Current Antipsychotics and Novel Antischizophrenia Treatments. These topics cannot really be separated from one another and should be seen as a composite entity despite the somewhat arbitrary separation of contributions into two volumes. The continuing challenges of developing improved and safer antipsychotic medications remain of concern and are discussed in the first volume. The new opportunities for the field to develop and license adjunctive treatments for the negative symptoms and cognitive deficits that are treated inadequately by existing compounds have been incentivized recently and provide the focus for the second volume. We hope these collective contributions will facilitate the development of improved treatments for the full range of symptomatology seen in the group of schizophrenias and other major psychotic disorders. Gerhard Gross, Ludwigshafen, Germany Mark A. Geyer, La Jolla, CA This volume will try to put current therapy - achievements, shortcomings, remaining medical needs - and emerging new targets into the context of increasing knowledge regarding the genetic and neurodevelopmental contributions to the pathophysiology of schizophrenia. Some of the chapters will also deal with respective experimental and clinical methodology, biomarkers, and translational aspects of drug development. Non-schizophrenia indications will be covered to some extent, but not exhaustively.

Keywords

Antipsychotic agents -- Therapeutic use. --- Antipsychotic drugs -- Controlled release. --- Injections. --- Antipsychotic drugs --- Tranquilizing Agents --- Schizophrenia and Disorders with Psychotic Features --- Therapeutics --- Psychotropic Drugs --- Central Nervous System Depressants --- Mental Disorders --- Analytical, Diagnostic and Therapeutic Techniques and Equipment --- Central Nervous System Agents --- Physiological Effects of Drugs --- Psychiatry and Psychology --- Pharmacologic Actions --- Therapeutic Uses --- Chemical Actions and Uses --- Chemicals and Drugs --- Antipsychotic Agents --- Drug Therapy --- Psychotic Disorders --- Health & Biological Sciences --- Pharmacy, Therapeutics, & Pharmacology --- Antipsychotic drugs. --- Antipsychotic agents --- Antipsychotics --- Major tranquilizers --- Major tranquilizing agents --- Major tranquilizing drugs --- Neuroleptic agents --- Neuroleptic drugs --- Neuroleptics --- Neurolepts --- Tranquilizing drugs, Major --- Medicine. --- Pharmacy. --- Neurosciences. --- Pharmacology. --- Behavioral sciences. --- Proteins. --- Neurobiology. --- Biomedicine. --- Pharmacology/Toxicology. --- Receptors. --- Behavioral Sciences. --- Psychotropic drugs --- Psychoses --- Chemotherapy --- Toxicology. --- Cell receptors. --- Animal behavior. --- Chemistry --- Medicine --- Drugs --- Materia medica --- Pharmacology --- Animals --- Animals, Habits and behavior of --- Behavior, Animal --- Ethology --- Animal psychology --- Zoology --- Ethologists --- Psychology, Comparative --- Neurosciences --- Cell membrane receptors --- Cell surface receptors --- Receptors, Cell --- Binding sites (Biochemistry) --- Cell membranes --- Proteins --- Neural sciences --- Neurological sciences --- Neuroscience --- Medical sciences --- Nervous system --- Chemicals --- Poisoning --- Poisons --- Behavior --- Toxicology --- Proteins . --- Proteids --- Biomolecules --- Polypeptides --- Proteomics --- Drug effects --- Medical pharmacology --- Pharmacy --- Physiological effect

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