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Handbook of modern pharmaceutical analysis[electronic resource] /

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
杜威分類號:	615.1901
書名/作者:	Handbook of modern pharmaceutical analysis/ edited by Satinder Ahuja, Stephen Scypinski.
其他作者:	Ahuja, Satinder,
出版者:	Amsterdam ; : Academic Press/Elsevier,, 2011.
面頁冊數:	1 online resource (xv, 582 p., [4] p. of plates) : : ill. (some col.)
附註:	Previous ed.: 2001.
標題:	Pharmaceutical chemistry
標題:	Drugs - Handbooks, manuals, etc. - Analysis
標題:	Drug development - Handbooks, manuals, etc.
標題:	Chemistry, Pharmaceutical - methods.
標題:	Pharmaceutical Preparations - analysis.
標題:	Technology, Pharmaceutical - methods.
標題:	Drug development.
標題:	Drugs - Analysis.
標題:	Medicine.
標題:	Pharmacy.
標題:	MEDICAL - Drug Guides.
標題:	MEDICAL - Pharmacology.
標題:	MEDICAL - Pharmacy.
標題:	MEDICAL - Nursing
ISBN:	9780123759818 (electronic bk.)
ISBN:	0123759811 (electronic bk.)
書目註:	Includes bibliographical references and index.
內容註:	Overview / (Satinder Ahuja) -- High Throughput Screening in Drug Discovery and Development / (Ken Apple) -- Solid-State Analysis / (Harry Brittain) -- Degradation Studies of Drug Candidates / (Karen Alsante) -- Analytical Considerations for Genotoxic and Other Impurities / (Scott Miller) -- Quality by Design / (James Drennen) -- Preformulation Studies -- Process Analytical Technology / (Christine Richardson) -- Solid Dosage-Form Analysis / (Joe Etse) -- Parenteral Dosage Form Analysis / (Greg Birrer) -- Analysis of Alternate Drug Delivery systems / (Ron Smith) -- Method Development for Chiral Compounds / (S. Ahuja) -- Method Development for Early Phase Drug Development / (Kevin Bynum) -- Method Development for Late Phase Drug Development / (Ilias Jimidar) -- Analysis of Biomolecules / (Ilias Jimidar) -- Setting Up Specifications / (Doug Raynie) -- Validation of Test Methods / (Jonathan Crowther) -- Stability Evaluations / (Jessica Cha) -- Transferring Analytical Methods / (Stephen Scypinski) -- Pharmaceutical Analysis Documentation / (H. Chokshi) -- Emerging Analytical Methodologies / (Jim Lander).
摘要、提要註:	Handbook of Modern Pharmaceutical Analysis, Second Edition, synthesizes the complex research and recent changes in the field, while covering the techniques and technology required for today's laboratories. The work integrates strategy, case studies, methodologies, and implications of new regulatory structures, providing complete coverage of quality assurance from the point of discovery to the point of use. Treats pharmaceutical analysis (PA) as an integral partner to the drug development process rather than as a service to it. Covers method development, validation, selection, testing, modeling, and simulation studies combined with advanced exploration of assays, impurity testing, biomolecules, and chiral separations. *Features detailed coverage of QA, ethics, and regulatory guidance and structures, as well as high-tech methodologies and technologies from "lab-on-a-chip" to LC-MS, LC-NMR, and LC-NMR-MS.
電子資源:	http://www.sciencedirect.com/science/book/9780123756800

Handbook of modern pharmaceutical analysis[electronic resource] /
Handbook of modern pharmaceutical analysis[electronic resource] /edited by Satinder Ahuja, Stephen Scypinski. - 2nd ed. - Amsterdam ;Academic Press/Elsevier,2011. - 1 online resource (xv, 582 p., [4] p. of plates) :ill. (some col.) - Separation science and technology ;v. 10. - Separation science and technology (San Diego, Calif.) ;v. 4..

Previous ed.: 2001.

Includes bibliographical references and index.

Overview / (Satinder Ahuja) -- High Throughput Screening in Drug Discovery and Development / (Ken Apple) -- Solid-State Analysis / (Harry Brittain) -- Degradation Studies of Drug Candidates / (Karen Alsante) -- Analytical Considerations for Genotoxic and Other Impurities / (Scott Miller) -- Quality by Design / (James Drennen) -- Preformulation Studies -- Process Analytical Technology / (Christine Richardson) -- Solid Dosage-Form Analysis / (Joe Etse) -- Parenteral Dosage Form Analysis / (Greg Birrer) -- Analysis of Alternate Drug Delivery systems / (Ron Smith) -- Method Development for Chiral Compounds / (S. Ahuja) -- Method Development for Early Phase Drug Development / (Kevin Bynum) -- Method Development for Late Phase Drug Development / (Ilias Jimidar) -- Analysis of Biomolecules / (Ilias Jimidar) -- Setting Up Specifications / (Doug Raynie) -- Validation of Test Methods / (Jonathan Crowther) -- Stability Evaluations / (Jessica Cha) -- Transferring Analytical Methods / (Stephen Scypinski) -- Pharmaceutical Analysis Documentation / (H. Chokshi) -- Emerging Analytical Methodologies / (Jim Lander).

Handbook of Modern Pharmaceutical Analysis, Second Edition, synthesizes the complex research and recent changes in the field, while covering the techniques and technology required for today's laboratories. The work integrates strategy, case studies, methodologies, and implications of new regulatory structures, providing complete coverage of quality assurance from the point of discovery to the point of use. *Treats pharmaceutical analysis (PA) as an integral partner to the drug development process rather than as a service to it. *Covers method development, validation, selection, testing, modeling, and simulation studies combined with advanced exploration of assays, impurity testing, biomolecules, and chiral separations. *Features detailed coverage of QA, ethics, and regulatory guidance and structures, as well as high-tech methodologies and technologies from "lab-on-a-chip" to LC-MS, LC-NMR, and LC-NMR-MS.

ISBN: 9780123759818 (electronic bk.)

Source: 1047444:10475732Elsevier Science & Technologyhttp://www.sciencedirect.comSubjects--Topical Terms:

197116
Pharmaceutical chemistry
Index Terms--Genre/Form:

336502
Electronic books.

LC Class. No.: RS404.5 / .H36 2011eb

Dewey Class. No.: 615.1901

National Library of Medicine Call No.: 2010 M-158

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245 0 0 $a Handbook of modern pharmaceutical analysis $h [electronic resource] / $c edited by Satinder Ahuja, Stephen Scypinski.
250 $a 2nd ed.
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300 $a 1 online resource (xv, 582 p., [4] p. of plates) : $b ill. (some col.)
490 1 $a Separation science and technology ; $v v. 10
500 $a Previous ed.: 2001.
504 $a Includes bibliographical references and index.
505 0 $a Overview / (Satinder Ahuja) -- High Throughput Screening in Drug Discovery and Development / (Ken Apple) -- Solid-State Analysis / (Harry Brittain) -- Degradation Studies of Drug Candidates / (Karen Alsante) -- Analytical Considerations for Genotoxic and Other Impurities / (Scott Miller) -- Quality by Design / (James Drennen) -- Preformulation Studies -- Process Analytical Technology / (Christine Richardson) -- Solid Dosage-Form Analysis / (Joe Etse) -- Parenteral Dosage Form Analysis / (Greg Birrer) -- Analysis of Alternate Drug Delivery systems / (Ron Smith) -- Method Development for Chiral Compounds / (S. Ahuja) -- Method Development for Early Phase Drug Development / (Kevin Bynum) -- Method Development for Late Phase Drug Development / (Ilias Jimidar) -- Analysis of Biomolecules / (Ilias Jimidar) -- Setting Up Specifications / (Doug Raynie) -- Validation of Test Methods / (Jonathan Crowther) -- Stability Evaluations / (Jessica Cha) -- Transferring Analytical Methods / (Stephen Scypinski) -- Pharmaceutical Analysis Documentation / (H. Chokshi) -- Emerging Analytical Methodologies / (Jim Lander).
520 $a Handbook of Modern Pharmaceutical Analysis, Second Edition, synthesizes the complex research and recent changes in the field, while covering the techniques and technology required for today's laboratories. The work integrates strategy, case studies, methodologies, and implications of new regulatory structures, providing complete coverage of quality assurance from the point of discovery to the point of use. *Treats pharmaceutical analysis (PA) as an integral partner to the drug development process rather than as a service to it. *Covers method development, validation, selection, testing, modeling, and simulation studies combined with advanced exploration of assays, impurity testing, biomolecules, and chiral separations. *Features detailed coverage of QA, ethics, and regulatory guidance and structures, as well as high-tech methodologies and technologies from "lab-on-a-chip" to LC-MS, LC-NMR, and LC-NMR-MS.
588 $a Description based on print version record.
650 0 $a Pharmaceutical chemistry $3 197116
650 0 $a Drugs $x Analysis $v Handbooks, manuals, etc. $3 431531
650 0 $a Drug development $v Handbooks, manuals, etc. $3 438126
650 1 2 $a Chemistry, Pharmaceutical $x methods. $3 431435
650 2 2 $a Pharmaceutical Preparations $x analysis. $3 431434
650 2 2 $a Technology, Pharmaceutical $x methods. $3 445981
650 4 $a Drug development. $3 339189
650 4 $a Drugs $x Analysis. $3 431431
650 4 $a Medicine. $3 373206
650 4 $a Pharmacy. $3 343916
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650 7 $a MEDICAL $x Pharmacology. $2 bisacsh $3 431471
650 7 $a MEDICAL $x Pharmacy. $2 bisacsh $3 445650
650 7 $a MEDICAL $x Nursing $x Pharmacology. $2 bisacsh $3 445651
655 4 $a Electronic books. $2 local $3 336502
700 1 $a Ahuja, Satinder, $d 1933- $3 404741
700 1 $a Scypinski, Stephen. $3 431530
776 0 8 $i Print version: $t Handbook of modern pharmaceutical analysis. $b 2nd ed. $d Amsterdam ; Boston : Academic Press/Elsevier, 2011 $z 9780123756800 $w (OCoLC)646393823
830 0 $a Separation science and technology (San Diego, Calif.) ; $v v. 4. $3 431386
856 4 0 $3 ScienceDirect $u http://www.sciencedirect.com/science/book/9780123756800