Software Supported Modelling in Pharmacokinetics
A powerful new software concept to physiologically based pharmacokinetic (PBPK) modelling of drug disposition is presented. It links the inherent modular understanding in pharmacology with orthogonal design principles from software engineering. This concept allows for flexible and user-friendly desi...
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creator | Telgmann, Regina von Kleist, Max Huisinga, Wilhelm |
description | A powerful new software concept to physiologically based pharmacokinetic (PBPK) modelling of drug disposition is presented. It links the inherent modular understanding in pharmacology with orthogonal design principles from software engineering. This concept allows for flexible and user-friendly design of pharmacokinetic whole body models, data analysis, hypotheses testing or extrapolation. The typical structure of physiologically-based pharmacokinetic models is introduced. The resulting requirements from a modelling and software engineering point of view and its realizations in the software tool MEDICI-PK [9] are described. Finally, an example in the context of drug-drug interaction studies is given that demonstrates the advantage of defining a whole-body pharmacokinetic model in terms of the underlying physiological processes quite impressively: A system of 162 ODEs is automatically compiled based on the specification of 7 local physiological processes only. |
doi_str_mv | 10.1007/11875741_21 |
format | Book Chapter |
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Berthold, Michael</contributor><creatorcontrib>Telgmann, Regina ; von Kleist, Max ; Huisinga, Wilhelm ; Glen, Robert C. ; Fischer, Ingrid ; R. Berthold, Michael</creatorcontrib><description>A powerful new software concept to physiologically based pharmacokinetic (PBPK) modelling of drug disposition is presented. It links the inherent modular understanding in pharmacology with orthogonal design principles from software engineering. This concept allows for flexible and user-friendly design of pharmacokinetic whole body models, data analysis, hypotheses testing or extrapolation. The typical structure of physiologically-based pharmacokinetic models is introduced. The resulting requirements from a modelling and software engineering point of view and its realizations in the software tool MEDICI-PK [9] are described. Finally, an example in the context of drug-drug interaction studies is given that demonstrates the advantage of defining a whole-body pharmacokinetic model in terms of the underlying physiological processes quite impressively: A system of 162 ODEs is automatically compiled based on the specification of 7 local physiological processes only.</description><identifier>ISSN: 0302-9743</identifier><identifier>ISBN: 9783540457671</identifier><identifier>ISBN: 3540457674</identifier><identifier>EISSN: 1611-3349</identifier><identifier>EISBN: 3540457682</identifier><identifier>EISBN: 9783540457688</identifier><identifier>DOI: 10.1007/11875741_21</identifier><language>eng</language><publisher>Berlin, Heidelberg: Springer Berlin Heidelberg</publisher><subject>Imulation Object ; Metabolism Model ; PBPK Model ; Saturable Metabolism ; Software Concept</subject><ispartof>Computational Life Sciences II, 2006, p.216-225</ispartof><rights>Springer-Verlag Berlin Heidelberg 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><relation>Lecture Notes in Computer Science</relation></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/11875741_21$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/11875741_21$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>779,780,784,793,27925,38255,41442,42511</link.rule.ids></links><search><contributor>Glen, Robert C.</contributor><contributor>Fischer, Ingrid</contributor><contributor>R. Berthold, Michael</contributor><creatorcontrib>Telgmann, Regina</creatorcontrib><creatorcontrib>von Kleist, Max</creatorcontrib><creatorcontrib>Huisinga, Wilhelm</creatorcontrib><title>Software Supported Modelling in Pharmacokinetics</title><title>Computational Life Sciences II</title><description>A powerful new software concept to physiologically based pharmacokinetic (PBPK) modelling of drug disposition is presented. It links the inherent modular understanding in pharmacology with orthogonal design principles from software engineering. This concept allows for flexible and user-friendly design of pharmacokinetic whole body models, data analysis, hypotheses testing or extrapolation. The typical structure of physiologically-based pharmacokinetic models is introduced. The resulting requirements from a modelling and software engineering point of view and its realizations in the software tool MEDICI-PK [9] are described. Finally, an example in the context of drug-drug interaction studies is given that demonstrates the advantage of defining a whole-body pharmacokinetic model in terms of the underlying physiological processes quite impressively: A system of 162 ODEs is automatically compiled based on the specification of 7 local physiological processes only.</description><subject>Imulation Object</subject><subject>Metabolism Model</subject><subject>PBPK Model</subject><subject>Saturable Metabolism</subject><subject>Software Concept</subject><issn>0302-9743</issn><issn>1611-3349</issn><isbn>9783540457671</isbn><isbn>3540457674</isbn><isbn>3540457682</isbn><isbn>9783540457688</isbn><fulltext>true</fulltext><rsrctype>book_chapter</rsrctype><creationdate>2006</creationdate><recordtype>book_chapter</recordtype><sourceid/><recordid>eNpNkE1LxDAUReMXWMeu_APduqi-5KV5yVIGR4URhdF1SZNU69SmNBX_viMqeDd3ceFwOYydcbjgAHTJuaaKJK8F32MnWEmQFSkt9lnGFeclojQHLDek_zbihywDBFEaknjM8pTeYBfkSgNkDDaxnT_tFIrNxzjGaQ6-uI8-9H03vBTdUDy-2undurjthjB3Lp2yo9b2KeS_vWDPq-un5W25fri5W16tyySEmksDnhorgzSIWoUWK4PaCUG-Ur5yjQiN9tJrB44asgq0llI653TrFBnCBTv_4aZx2l0JU93EuE01h_pbRf1PBX4BOJFLCQ</recordid><startdate>2006</startdate><enddate>2006</enddate><creator>Telgmann, Regina</creator><creator>von Kleist, Max</creator><creator>Huisinga, Wilhelm</creator><general>Springer Berlin Heidelberg</general><scope/></search><sort><creationdate>2006</creationdate><title>Software Supported Modelling in Pharmacokinetics</title><author>Telgmann, Regina ; von Kleist, Max ; Huisinga, Wilhelm</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-s226t-90d7ba4e493386ef35938c227d56d5cb2eb8d4d8c0c7b7a6088444ccc8fc67973</frbrgroupid><rsrctype>book_chapters</rsrctype><prefilter>book_chapters</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Imulation Object</topic><topic>Metabolism Model</topic><topic>PBPK Model</topic><topic>Saturable Metabolism</topic><topic>Software Concept</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Telgmann, Regina</creatorcontrib><creatorcontrib>von Kleist, Max</creatorcontrib><creatorcontrib>Huisinga, Wilhelm</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Telgmann, Regina</au><au>von Kleist, Max</au><au>Huisinga, Wilhelm</au><au>Glen, Robert C.</au><au>Fischer, Ingrid</au><au>R. Berthold, Michael</au><format>book</format><genre>bookitem</genre><ristype>CHAP</ristype><atitle>Software Supported Modelling in Pharmacokinetics</atitle><btitle>Computational Life Sciences II</btitle><seriestitle>Lecture Notes in Computer Science</seriestitle><date>2006</date><risdate>2006</risdate><spage>216</spage><epage>225</epage><pages>216-225</pages><issn>0302-9743</issn><eissn>1611-3349</eissn><isbn>9783540457671</isbn><isbn>3540457674</isbn><eisbn>3540457682</eisbn><eisbn>9783540457688</eisbn><abstract>A powerful new software concept to physiologically based pharmacokinetic (PBPK) modelling of drug disposition is presented. It links the inherent modular understanding in pharmacology with orthogonal design principles from software engineering. This concept allows for flexible and user-friendly design of pharmacokinetic whole body models, data analysis, hypotheses testing or extrapolation. The typical structure of physiologically-based pharmacokinetic models is introduced. The resulting requirements from a modelling and software engineering point of view and its realizations in the software tool MEDICI-PK [9] are described. Finally, an example in the context of drug-drug interaction studies is given that demonstrates the advantage of defining a whole-body pharmacokinetic model in terms of the underlying physiological processes quite impressively: A system of 162 ODEs is automatically compiled based on the specification of 7 local physiological processes only.</abstract><cop>Berlin, Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/11875741_21</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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identifier | ISSN: 0302-9743 |
ispartof | Computational Life Sciences II, 2006, p.216-225 |
issn | 0302-9743 1611-3349 |
language | eng |
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source | Springer Books |
subjects | Imulation Object Metabolism Model PBPK Model Saturable Metabolism Software Concept |
title | Software Supported Modelling in Pharmacokinetics |
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