東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

Discovering and developing molecules...

Templeton, Allen C.

FindBook

Google Book

Amazon

博客來

Discovering and developing molecules with optimal drug-like properties

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Discovering and developing molecules with optimal drug-like properties/ edited by Allen C Templeton ... [et al.].
其他作者:	Templeton, Allen C.
出版者:	New York, NY :Springer New York : : 2015.,
面頁冊數:	xi, 511 p. :ill. (some col.), digital ;24 cm.
內容註:	1 Developability Assessment and Risk Management During Drug Discovery -- 2 Discovery Formulations Approaches 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-End Formulation Strategy for Poorly-Water- Soluble Molecules -- 14 Leveraging Solid State Form and Physiochemical Properties for Early Clinical Formulation Efforts: Opportunities and Challenges during Telcagepant Liquid Capsule Development.
Contained By:	Springer eBooks
標題:	Drugs - Research. -
電子資源:	http://dx.doi.org/10.1007/978-1-4939-1399-2
ISBN:	9781493913992 (electronic bk.)

Discovering and developing molecules with optimal drug-like properties
Discovering and developing molecules with optimal drug-like properties[electronic resource] /edited by Allen C Templeton ... [et al.]. - New York, NY :Springer New York :2015. - xi, 511 p. :ill. (some col.), digital ;24 cm. - AAPS advances in the pharmaceutical sciences series,152210-7371 ;. - AAPS advances in the pharmaceutical sciences series ;3..

1 Developability Assessment and Risk Management During Drug Discovery -- 2 Discovery Formulations Approaches 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-End Formulation Strategy for Poorly-Water- Soluble Molecules -- 14 Leveraging Solid State Form and Physiochemical Properties for Early Clinical Formulation Efforts: Opportunities and Challenges during Telcagepant Liquid Capsule Development.

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 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.

ISBN: 9781493913992 (electronic bk.)

Standard No.: 10.1007/978-1-4939-1399-2doiSubjects--Topical Terms:

685164
Drugs
--Research.

LC Class. No.: RM301.25

Dewey Class. No.: 615.19

Discovering and developing molecules with optimal drug-like properties
LDR:03653nmm a2200325 a 4500 001 1992964
003 DE-He213
005 20150609132619.0
006 m d
007 cr nn 008maaau
008 151019s2015 nyu s 0 eng d
020 $a 9781493913992 (electronic bk.)
020 $a 9781493913985 (paper)
024 7 $a 10.1007/978-1-4939-1399-2 $2 doi
035 $a 978-1-4939-1399-2
040 $a GP $c GP
041 0 $a eng
050 4 $a RM301.25
072 7 $a TDCW $2 bicssc
072 7 $a MED072000 $2 bisacsh
082 0 4 $a 615.19 $2 23
090 $a RM301.25 $b .D611 2015
245 0 0 $a Discovering and developing molecules with optimal drug-like properties $h [electronic resource] / $c edited by Allen C Templeton ... [et al.].
260 $a New York, NY : $b Springer New York : $b Imprint: Springer, $c 2015.
300 $a xi, 511 p. : $b ill. (some col.), digital ; $c 24 cm.
490 1 $a AAPS advances in the pharmaceutical sciences series, $x 2210-7371 ; $v 15
505 0 $a 1 Developability Assessment and Risk Management During Drug Discovery -- 2 Discovery Formulations Approaches 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-End Formulation Strategy for Poorly-Water- Soluble Molecules -- 14 Leveraging Solid State Form and Physiochemical Properties for Early Clinical Formulation Efforts: Opportunities and Challenges during Telcagepant Liquid Capsule Development.
520 $a 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 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.
650 0 $a Drugs $x Research. $3 685164
650 0 $a Drugs $x Design. $3 664528
650 1 4 $a Biomedicine. $3 890831
650 2 4 $a Pharmaceutical Sciences/Technology. $3 1001579
700 1 $a Templeton, Allen C. $3 2130864
710 2 $a SpringerLink (Online service) $3 836513
773 0 $t Springer eBooks
830 0 $a AAPS advances in the pharmaceutical sciences series ; $v 3. $3 1566956
856 4 0 $u http://dx.doi.org/10.1007/978-1-4939-1399-2
950 $a Biomedical and Life Sciences (Springer-11642)