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020 _a9781118838419 (pdf)
020 _a1118838416 (pdf)
020 _a9781118838327 (epub)
020 _a1118838327 (epub)
020 _z9781118838273 (cloth)
020 _a9781118838440
020 _a1118838440
028 0 2 _aEB00665390
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029 1 _aAU@
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029 1 _aDEBBG
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035 _a(OCoLC)905450321
_z(OCoLC)934935697
_z(OCoLC)966176713
035 _a(OCoLC)ocn905450321
037 _a9781118838327
_bWiley
039 9 _a201911051411
_bmurni
_y09-18-2019
_zhafiz
_wUKM UBCM Wiley MARC (363 titles).mrc
_x308
040 _aDLC
_beng
_erda
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082 0 0 _a615.7
_223
100 1 _aYanni, Souzan,
_eauthor.
245 1 0 _aTranslational ADMET for drug therapy :
_bprinciples, methods, and pharmaceutical applications /
_cSouzan Yanni.
264 1 _aHoboken, New Jersey :
_bJohn Wiley & Sons, Inc.,
_c[2015]
300 _a1 online resource.
336 _atext
_2rdacontent
337 _acomputer
_2rdamedia
338 _aonline resource
_2rdacarrier
504 _aIncludes bibliographical references and index.
505 0 _aTranslational Concept and Determination of Drug Absorption -- Distribution: Principle, Methods, and Applications -- Metabolism: Principle, Methods, and Applications -- Excretion: Principle, Methods, and Applications for Better Therapy -- Drug-Drug Interaction: From Bench to Drug Label -- General Toxicology: Principle, Methods, and Applications -- Toxicokinetics and Toxicity Testing in Drug Development -- PBPK Modeling and In Silico Prediction for ADME and Drug-Drug Interaction -- Translational Tools toward Better Drug Therapy in Human Populations -- Phase 1-Phase 3 Clinical Studies, Procedures, Responsibilities, and Documentation -- Regulatory Submission: MIST and Drug Safety Assessment.
506 _aOwing to Legal Deposit regulations this resource may only be accessed from within National Library of Scotland. For more information contact enquiries@nls.uk.
_5StEdNL
520 _aServing as a practical handbook about ADMET for drug therapy, this book presents effective technologies, methods, applications, data interpretation, and decision-making tactics for pharmaceutical and preclinical scientists. Chapters cover case studies and in vivo, in vitro, and computational tools for drug discovery and development, with new translational approaches to clinical drug investigations in various human populations. -Illustrates ADME properties, from bedside to bench and bench to bedside, for the design of safe and effective medicine in human populations -Provides examples that demonstrate the integration of in vitro, in vivo, and in silico data to address human PKPD and TKTD and help determine the proper therapeutic dosage -Presents successful tools for evaluating drugs and covers current translational ADMET with regulatory guidelines -Offers a hands-on manual for researchers and scientists to design and execute in vitro, in silico, preclinical, and clinical studies -Includes discussion of IND / NDA filing and drug labeling to support drug registration and approval.
588 _aDescription based on print version record and CIP data provided by publisher.
650 0 _aPharmacokinetics.
650 0 _aDrugs
_xMetabolism
_xPharmacokinetics.
650 2 _aDrug Evaluation, Preclinical.
650 2 _aPharmacokinetics.
650 2 _aDrug-Related Side Effects and Adverse Reactions.
650 2 _aPharmaceutical Preparations
_xmetabolism.
650 4 _aMedical.
655 4 _aElectronic books.
773 0 _tWiley e-books
776 0 8 _iPrint version:
_aYanni, Souzan, author.
_tTranslational ADMET for drug therapy
_dHoboken, New Jersey : John Wiley & Sons, Inc., [2015]
_z9781118838273
_w(DLC) 2015010195
856 4 0 _uhttps://eresourcesptsl.ukm.remotexs.co/user/login?url=https://doi.org/10.1002/9781118838440
_zWiley Online Library
907 _a.b16758067
_b2022-09-26
_c2019-11-12
942 _n0
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998 _ae
_b2019-05-09
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