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020 _a9781493913992
024 7 _a10.1007/978-1-4939-1399-2
_2doi
050 4 _aRM301.25
_bD573 2015
245 1 0 _aDiscovering and Developing Molecules with Optimal Drug-Like Properties
_cedited by Allen C Templeton, Stephen R. Byrn, Roy J Haskell, Thomas E. Prisinzano.
260 _aNew York
_bSpringer
_c2015
300 _a1 recurso en línea (XI, 511 páginas)
_b161 ilustraciones, 130 ilustraciones en color
336 _aTexto
_btxt
_2rdacontent
337 _aelectrónico
_bc
_2rdamedia
338 _arecurso electrónico
_bcr
_2rdacarrier
490 0 _aAAPS Advances in the Pharmaceutical Sciences Series
_x2210-7371
_v15
505 0 _a1 Developability Assessment and Risk Management During Drug Discovery -- 2 Discovery Formulations â€{u0070}proaches and Practices in Early Preclinical Development -- 3 Enabling Discovery Through Leveraging and Miniaturizing Pharmaceutical Principles and Processes -- 4 Diagnosing Biopharmaceutical Limitations -- 5 The Importance of Molecular Design Principles in Delivering High Quality Pharmaceutical Candidates -- 6 Predictive Approaches to Establishing, Understanding, and Communicating Risk with Emphasis on Early Development -- 7 Strategies and Methods for Drug Candidate Phase Optimization in Discovery Space -- 8 Efficient Laboratory Methods to Assess Risk and Design Formulations -- 9 Advanced X-ray Analytical Methods to Understand Structure, Properties and Risk -- 10 Performance and Characterization of Amorphous Solid Dispersions: An Overview -- 11 Hot-Melt Extrusion: The Process-Product-Performance Interplay -- 12 Practical Considerations for Spray Dried Formulation and Process Development -- 13 Nanosizing: “End-to-Endâ€Ưrmulation Strategy for Poorly-Water- Soluble Molecules -- 14 Leveraging Solid State Form and Physiochemical Properties for Early Clinical Formulation Efforts:Â{uFC30}portunities and Challenges during Telcagepant Liquid Capsule Development.
520 3 _aThis 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 properties and critical development parameters such as solubility and stability. Final chapters center on techniques to improve molecular solubilization and prevent precipitation, with particularly emphasis on linking physiochemical properties of molecules to formulation selection in preclinical and clinical settings.
710 2 _aSpringerLink (Online service)
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988 _aEBOOK, asignarmaterias, EBSPRINGER,
650 7 _aTecnología farmacéutica
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650 2 7 _aFarmacia
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700 1 _aTempleton, Allen C
_eeditor literario
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700 1 _aByrn, Stephen R.
_eeditor literario
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700 1 _aHaskell, Roy J.
_eeditor literario
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_993438
700 1 _aPrisinzano, Thomas E
_eeditor literario
_993439
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856 4 0 _uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/978-1-4939-1399-2
_zAcceso a este recurso digital (usuarios Universidad Europea de Madrid)
907 _a.b12897577
_b10-10-17
_c18-01-16
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