In Vitro Experimental Pharmacology

In Vitro Experimental Pharmacology
Author: Asmita Gajbhiye Patil
Publisher: CBS Publishers & Distributors Pvt Limited, India
Total Pages:
Release: 2019-04-30
Genre: Medical
ISBN: 9789388178938
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In the context of drug discovery and development, in vivo experimentation should be performed only if is necessary and well-conceived. From both an ethical and practical perspective, in vitro bioassays are more viable and efficacious in the preliminary pharmacological screening of a newly-discovered drug molecule. This book will be of immense value to both the experienced as well as new researchers in biomedicine. It discusses anti-inflammatory, antioxidant, antidiabetic, antimicrobial, antimalarial, antileshmanial and anticancer bioassays. Additionally the book discusses the basic concepts governing experimental pharmacology and a chapter dealing with enzyme-based bioassays has also been incorporated. The assays described in the book include step-by-step experimental procedures preceded with an explanation of the principal and theory governing the procedure.

Drugs on Trial

Drugs on Trial
Author: Andreas-Holger Maehle
Publisher: BRILL
Total Pages: 362
Release: 2016-08-29
Genre: Medical
ISBN: 9004333290
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This book describes the main issues of eighteenth-century pharmacology and therapeutics and provides detailed case studies of three key areas: lithontriptics (remedies against urinary stones), opium, and Peruvian bark (quinine).

Good Research Practice in Non-Clinical Pharmacology and Biomedicine

Good Research Practice in Non-Clinical Pharmacology and Biomedicine
Author: Anton Bespalov
Publisher: Springer Nature
Total Pages: 424
Release: 2020-01-01
Genre: Cardiology
ISBN: 3030336565
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This open access book, published under a CC BY 4.0 license in the Pubmed indexed book series Handbook of Experimental Pharmacology, provides up-to-date information on best practice to improve experimental design and quality of research in non-clinical pharmacology and biomedicine.

Experimental Design and Statistical Analysis for Pharmacology and the Biomedical Sciences

Experimental Design and Statistical Analysis for Pharmacology and the Biomedical Sciences
Author: Paul J. Mitchell
Publisher: John Wiley & Sons
Total Pages: 260
Release: 2022-04-06
Genre: Medical
ISBN: 1119437660
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Experimental Design and Statistical Analysis for Pharmacology and the Biomedical Sciences A practical guide to the use of basic principles of experimental design and statistical analysis in pharmacology Experimental Design and Statistical Analysis for Pharmacology and the Biomedical Sciences provides clear instructions on applying statistical analysis techniques to pharmacological data. Written by an experimental pharmacologist with decades of experience teaching statistics and designing preclinical experiments, this reader-friendly volume explains the variety of statistical tests that researchers require to analyze data and draw correct conclusions. Detailed, yet accessible, chapters explain how to determine the appropriate statistical tool for a particular type of data, run the statistical test, and analyze and interpret the results. By first introducing basic principles of experimental design and statistical analysis, the author then guides readers through descriptive and inferential statistics, analysis of variance, correlation and regression analysis, general linear modelling, and more. Lastly, throughout the textbook are numerous examples from molecular, cellular, in vitro, and in vivo pharmacology which highlight the importance of rigorous statistical analysis in real-world pharmacological and biomedical research. This textbook also: Describes the rigorous statistical approach needed for publication in scientific journals Covers a wide range of statistical concepts and methods, such as standard normal distribution, data confidence intervals, and post hoc and a priori analysis Discusses practical aspects of data collection, identification, and presentation Features images of the output from common statistical packages, including GraphPad Prism, Invivo Stat, MiniTab and SPSS Experimental Design and Statistical Analysis for Pharmacology and the Biomedical Sciences is an invaluable reference and guide for undergraduate and graduate students, post-doctoral researchers, and lecturers in pharmacology and allied subjects in the life sciences.

Experimental in Vitro Pharmacology

Experimental in Vitro Pharmacology
Author: University of Copenhagen. Faculty of Pharmaceutical Sciences. Department of Pharmacology and Pharmacotherapy
Publisher:
Total Pages:
Release: 2007
Genre:
ISBN:
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Pharmacology in Drug Discovery and Development

Pharmacology in Drug Discovery and Development
Author: Terry P. Kenakin
Publisher: Academic Press
Total Pages: 340
Release: 2016-10-21
Genre: Medical
ISBN: 0128037539
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Pharmacology in Drug Discovery and Development: Understanding Drug Response, Second Edition, is an introductory resource illustrating how pharmacology can be used to furnish the tools necessary to analyze different drug behavior and trace this behavior to its root cause or molecular mechanism of action. The concepts discussed in this book allow for the application of more predictive pharmacological procedures aimed at increasing therapeutic efficacy that will lead to more successful drug development. Chapters logically build upon one another to show how to characterize the pharmacology of any given molecule and allow for more informed predictions of drug effects in all biological systems. New chapters are dedicated to the interdisciplinary drug discovery environment in both industry and academia, and special techniques involved in new drug screening and lead optimization. This edition has been fully revised to address the latest advances and research related to real time kinetic assays, pluridimensional efficacy, signaling bias, irreversible and chemical antagonism, allosterically-induced bias, pharmacokinetics and safety, target and pathway validation, and much more. With numerous valuable chapter summaries, detailed references, practical examples and case studies throughout, Dr. Kenakin successfully navigates a highly complex subject, making it accessible for students, professors, and new researchers working in pharmacology and drug discovery. Includes example-based cases that illustrate how the pharmacological concepts discussed in this book lead to practical outcomes for further research Provides vignettes on those researchers and scientists who have contributed significantly to the fields of pharmacology and drug discovery throughout history Offers sample questions throughout the book and an appendix containing answers for self-testing and retention

Evaluating Chemical and Other Agent Exposures for Reproductive and Developmental Toxicity

Evaluating Chemical and Other Agent Exposures for Reproductive and Developmental Toxicity
Author: National Research Council
Publisher: National Academies Press
Total Pages: 261
Release: 2001-04-13
Genre: Nature
ISBN: 0309073162
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The United States Navy has been concerned for some time with protecting its military and civilian personnel from reproductive and developmental hazards in the workplace. As part of its efforts to reduce or eliminate exposure of Naval personnel and their families to reproductive and developmental toxicants, the Navy requested that the National Research Council (NRC) recommend an approach that can be used to evaluate chemicals and physical agents for their potential to cause reproductive and developmental toxicity. The NRC assigned this project to the Committee on Toxicology, which convened the Subcommittee on Reproductive and Developmental Toxicology, to prepare this report. In this report, the subcommittee recommends an approach for evaluating agents for potential reproductive and developmental toxicity and demonstrates how that approach can be used by the Navy. This report has been reviewed in draft form by individuals chosen for their diverse perspectives and technical expertise, in accordance with procedures approved by the NRC's Report Review Committee. The purpose of this independent review is to provide candid and critical comments that will assist the institution in making its published report as sound as possible and to ensure that the report meets institutional standards for objectivity, evidence, and responsiveness to the study charge. The review comments and draft manuscript remain confidential to protect the integrity of the deliberative process. We wish to thank the following individuals for their review of this report: James Chen (National Center for Toxicological Research), George Daston (Procter and Gamble Company), Jerry Heindel (National Institute of Environmental Health Sciences), Grace Lemasters (University of Cincinnati), and John Young (National Center for Toxicological Research).

Mechanisms of Drug Interactions

Mechanisms of Drug Interactions
Author: Patrick F. D'Arcy
Publisher: Springer Science & Business Media
Total Pages: 373
Release: 2012-12-06
Genre: Medical
ISBN: 3642610153
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Over the years a number of excellent books have classified and detailed drug drug interactions into their respective categories, e.g. interactions at plasma protein binding sites; those altering intestinal absorption or bioavailability; those involving hepatic metabolising enzymes; those involving competition or antagonism for receptor sites, and drug interactions modifying excretory mechanisms. Such books have presented extensive tables of interactions and their management. Although of considerable value to clinicians, such publica tions have not, however, been so expressive about the individual mechanisms that underlie these interactions. It is within this sphere of "mechanisms" that this present volume specialises. It deals with mechanisms of in vitro and in vivo, drug-drug, drug food and drug-herbals interactions and those that cause drugs to interfere with diagnostic laboratory tests. We believe that an explanation of the mechanisms of such interactions will enable practitioners to understand more fully the nature of the interactions and thus enable them to manage better their clinical outcome. If mechanisms of interactions are better understood, then it may be pos sible for the researcher to develop meaningful animal/biochemical/tissue cul ture or physicochemical models to which new molecules could be exposed during their development stages. The present position, which largely relies on patients experiencing adverse interactions before they can be established or documented, can hardly be regarded as satisfactory. This present volume is classified into two major parts; firstly, pharmacoki netic drug interactions and, secondly, pharmacodynamic drug interactions.

Bioassays in Experimental and Preclinical Pharmacology

Bioassays in Experimental and Preclinical Pharmacology
Author: Karuppusamy Arunachalam
Publisher:
Total Pages: 271
Release: 2021
Genre: Biological assay
ISBN: 9781071612330
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This detailed book explores protocols for a wide array of preclinical pharmacology and toxicology evaluations to be applied to chemical drugs and their development through in vitro, involving tissues and cell lines, and in vivo models, using animals as experimental systems, utilized to conduct pharmacological research. Written for the Springer Protocols Handbooks series, the methodologies included in this collection have been standardized by the authors through extensive use in the lab so that they are ready to be applied in the labs of readers around the world. Authoritative and practical, Bioassays in Experimental and Preclinical Pharmacology aims to assist undergraduate and postgraduate students, research scholars, scientists, and other academicians performing research in the vital field of drug discovery.