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Titlebook: Discovering and Developing Molecules with Optimal Drug-Like Properties; Allen C Templeton,Stephen R. Byrn,Thomas E. Prisin Book 2015 Ameri

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书目名称Discovering and Developing Molecules with Optimal Drug-Like Properties
编辑Allen C Templeton,Stephen R. Byrn,Thomas E. Prisin
视频video
概述Addresses the challenge to more efficiently select better molecules for drug development.Discusses how to expand the chemical space within which a pharmacological benefit can be found.Examines the rea
丛书名称AAPS Advances in the Pharmaceutical Sciences Series
图书封面Titlebook: Discovering and Developing Molecules with Optimal Drug-Like Properties;  Allen C Templeton,Stephen R. Byrn,Thomas E. Prisin Book 2015 Ameri
描述.This authoritative volume provides a contemporary view on the latest research in molecules with optimal drug-like properties. It is a valuable source to access current best practices as well as new research techniques and strategies. Written by leading scientists in their fields, the text consists of fourteen chapters with an underlying theme of early collaborative opportunities between pharmaceutical and discovery sciences. The book explores the practical realities of performing physical pharmaceutical and biopharmaceutical research in the context of drug discovery with short timelines and low compound availability. Chapters cover strategies and tactics to enable discovery as well as predictive approaches to establish, understand and communicate risks in early development. It also examines the detection, characterization, and assessment of risks on the solid state properties of advanced discovery and early development candidates, highlighting the link between solid state propertiesand critical development parameters such as solubility and stability. Final chapters center on techniques to improve molecular solubilization and prevent precipitation, with particularly emphasis on lin
出版日期Book 2015
关键词drug delivery; in silico; modeling; physicochemical
版次1
doihttps://doi.org/10.1007/978-1-4939-1399-2
isbn_softcover978-1-4939-4860-4
isbn_ebook978-1-4939-1399-2Series ISSN 2210-7371 Series E-ISSN 2210-738X
issn_series 2210-7371
copyrightAmerican Association of Pharmaceutical Scientists 2015
The information of publication is updating

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Enabling Discovery Through Leveraging and Miniaturizing Pharmaceutical Principles and Processesneed to execute in a parallel fashion. These realities in turn can place severe restrictions on the options available to the development and implementation of drug delivery strategies. While one would expect the contrary, these realities do not preclude the use of development-stage formulation techn
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Diagnosing Biopharmaceutical Limitationsands adequate exposure throughout the dosing interval and none of the compounds tested approaches the targeted exposure. Studying compounds to determine why exposure is poor may assist the structure–activity relationship (SAR) process, even if the compounds are not suitable for further development.
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Practical Considerations for Spray Dried Formulation and Process Developmentug to a high energy polymer stabilized amorphous state. Spray drying is a mature process with demonstrated production capability from lab to commercial scale for manufacturing amorphous solid dispersions. However, the impact of the drying process on the performance, manufacture, and stability of the
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