Biorelevant In Vitro Performance Testing of Orally Administered Dosage Forms—Workshop Report

Biorelevant in vitro performance testing of orally administered dosage forms has become an important tool for the assessment of drug product in vivo behavior. An in vitro performance test which mimics the intraluminal performance of an oral dosage form is termed biorelevant. Biorelevant tests have b...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Pharmaceutical research 2014-07, Vol.31 (7), p.1867-1876
Hauptverfasser: Reppas, Christos, Friedel, Horst-Dieter, Barker, Amy R., Buhse, Lucinda F., Cecil, Todd L., Keitel, Susanne, Kraemer, Johannes, Morris, J. Michael, Shah, Vinod P., Stickelmeyer, Mary P., Yomota, Chikako, Brown, Cynthia K.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1876
container_issue 7
container_start_page 1867
container_title Pharmaceutical research
container_volume 31
creator Reppas, Christos
Friedel, Horst-Dieter
Barker, Amy R.
Buhse, Lucinda F.
Cecil, Todd L.
Keitel, Susanne
Kraemer, Johannes
Morris, J. Michael
Shah, Vinod P.
Stickelmeyer, Mary P.
Yomota, Chikako
Brown, Cynthia K.
description Biorelevant in vitro performance testing of orally administered dosage forms has become an important tool for the assessment of drug product in vivo behavior. An in vitro performance test which mimics the intraluminal performance of an oral dosage form is termed biorelevant. Biorelevant tests have been utilized to decrease the number of in vivo studies required during the drug development process and to mitigate the risk related to in vivo bioequivalence studies. This report reviews the ability of current in vitro performance tests to predict in vivo performance and generate successful in vitro and in vivo correlations for oral dosage forms. It also summarizes efforts to improve the predictability of biorelevant tests. The report is based on the presentations at the 2013 workshop, Biorelevant In Vitro Performance Testing of Orally Administered Dosage Forms, in Washington, DC, sponsored by the FIP Dissolution/Drug Release Focus Group in partnership with the American Association of Pharmaceutical Scientists (AAPS) and a symposium at the AAPS 2012 Annual meeting on the same topic.
doi_str_mv 10.1007/s11095-014-1348-9
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1537160012</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3338702551</sourcerecordid><originalsourceid>FETCH-LOGICAL-c442t-257013e9dcc4ef6259762575bd89b28c522cf298df0fb2b1ee660c7af6befd503</originalsourceid><addsrcrecordid>eNp1kMlOwzAQhi0EgrI8ABdkiXNg7DhxfGQrVEIqQmU5YWUZl0ATBztF4sZD8IQ8CUYtiAuXmcN888_oI2SXwQEDkIeeMVBJBExELBZZpFbIgCUyjhSI-1UyAMlFlEnBNsim908AkDEl1skGF6mIVRwPyMNxbR3O8DVvezpq6W3dO0uv0BnrmrwtkU7Q93U7pdbQsctnszd6VDV1W_seHVb01Pp8inQYcP_5_nFn3bN_tB29xs66fpusmXzmcWfZt8jN8GxychFdjs9HJ0eXUSkE7yOeSGAxqqosBZqUJ0qGIpOiylTBszLhvDRcZZUBU_CCIaYplDI3aYGmSiDeIvuL3M7Zl3n4WD_ZuWvDSc2SWLIUgPFAsQVVOuu9Q6M7Vze5e9MM9LdRvTCqg1H9bVSrsLO3TJ4XDVa_Gz8KA8AXgA-jdoruz-l_U78A0GiCmA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1537160012</pqid></control><display><type>article</type><title>Biorelevant In Vitro Performance Testing of Orally Administered Dosage Forms—Workshop Report</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Reppas, Christos ; Friedel, Horst-Dieter ; Barker, Amy R. ; Buhse, Lucinda F. ; Cecil, Todd L. ; Keitel, Susanne ; Kraemer, Johannes ; Morris, J. Michael ; Shah, Vinod P. ; Stickelmeyer, Mary P. ; Yomota, Chikako ; Brown, Cynthia K.</creator><creatorcontrib>Reppas, Christos ; Friedel, Horst-Dieter ; Barker, Amy R. ; Buhse, Lucinda F. ; Cecil, Todd L. ; Keitel, Susanne ; Kraemer, Johannes ; Morris, J. Michael ; Shah, Vinod P. ; Stickelmeyer, Mary P. ; Yomota, Chikako ; Brown, Cynthia K.</creatorcontrib><description>Biorelevant in vitro performance testing of orally administered dosage forms has become an important tool for the assessment of drug product in vivo behavior. An in vitro performance test which mimics the intraluminal performance of an oral dosage form is termed biorelevant. Biorelevant tests have been utilized to decrease the number of in vivo studies required during the drug development process and to mitigate the risk related to in vivo bioequivalence studies. This report reviews the ability of current in vitro performance tests to predict in vivo performance and generate successful in vitro and in vivo correlations for oral dosage forms. It also summarizes efforts to improve the predictability of biorelevant tests. The report is based on the presentations at the 2013 workshop, Biorelevant In Vitro Performance Testing of Orally Administered Dosage Forms, in Washington, DC, sponsored by the FIP Dissolution/Drug Release Focus Group in partnership with the American Association of Pharmaceutical Scientists (AAPS) and a symposium at the AAPS 2012 Annual meeting on the same topic.</description><identifier>ISSN: 0724-8741</identifier><identifier>EISSN: 1573-904X</identifier><identifier>DOI: 10.1007/s11095-014-1348-9</identifier><identifier>PMID: 24643933</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Administration, Oral ; Biochemistry ; Biomedical and Life Sciences ; Biomedical Engineering and Bioengineering ; Biomedicine ; Chemistry, Pharmaceutical - education ; Chemistry, Pharmaceutical - methods ; Chemistry, Pharmaceutical - standards ; Delayed-Action Preparations - chemistry ; Delayed-Action Preparations - metabolism ; Dosage Forms ; Drug Evaluation, Preclinical - methods ; Drug Evaluation, Preclinical - standards ; Drug therapy ; Health risk assessment ; Humans ; Medical Law ; Meeting Report ; Pharmaceutical Preparations - administration &amp; dosage ; Pharmaceuticals ; Pharmacokinetics ; Pharmacology/Toxicology ; Pharmacy ; Quality Control ; Solubility</subject><ispartof>Pharmaceutical research, 2014-07, Vol.31 (7), p.1867-1876</ispartof><rights>Springer Science+Business Media New York 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-257013e9dcc4ef6259762575bd89b28c522cf298df0fb2b1ee660c7af6befd503</citedby><cites>FETCH-LOGICAL-c442t-257013e9dcc4ef6259762575bd89b28c522cf298df0fb2b1ee660c7af6befd503</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11095-014-1348-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11095-014-1348-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,777,781,27906,27907,41470,42539,51301</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24643933$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Reppas, Christos</creatorcontrib><creatorcontrib>Friedel, Horst-Dieter</creatorcontrib><creatorcontrib>Barker, Amy R.</creatorcontrib><creatorcontrib>Buhse, Lucinda F.</creatorcontrib><creatorcontrib>Cecil, Todd L.</creatorcontrib><creatorcontrib>Keitel, Susanne</creatorcontrib><creatorcontrib>Kraemer, Johannes</creatorcontrib><creatorcontrib>Morris, J. Michael</creatorcontrib><creatorcontrib>Shah, Vinod P.</creatorcontrib><creatorcontrib>Stickelmeyer, Mary P.</creatorcontrib><creatorcontrib>Yomota, Chikako</creatorcontrib><creatorcontrib>Brown, Cynthia K.</creatorcontrib><title>Biorelevant In Vitro Performance Testing of Orally Administered Dosage Forms—Workshop Report</title><title>Pharmaceutical research</title><addtitle>Pharm Res</addtitle><addtitle>Pharm Res</addtitle><description>Biorelevant in vitro performance testing of orally administered dosage forms has become an important tool for the assessment of drug product in vivo behavior. An in vitro performance test which mimics the intraluminal performance of an oral dosage form is termed biorelevant. Biorelevant tests have been utilized to decrease the number of in vivo studies required during the drug development process and to mitigate the risk related to in vivo bioequivalence studies. This report reviews the ability of current in vitro performance tests to predict in vivo performance and generate successful in vitro and in vivo correlations for oral dosage forms. It also summarizes efforts to improve the predictability of biorelevant tests. The report is based on the presentations at the 2013 workshop, Biorelevant In Vitro Performance Testing of Orally Administered Dosage Forms, in Washington, DC, sponsored by the FIP Dissolution/Drug Release Focus Group in partnership with the American Association of Pharmaceutical Scientists (AAPS) and a symposium at the AAPS 2012 Annual meeting on the same topic.</description><subject>Administration, Oral</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering and Bioengineering</subject><subject>Biomedicine</subject><subject>Chemistry, Pharmaceutical - education</subject><subject>Chemistry, Pharmaceutical - methods</subject><subject>Chemistry, Pharmaceutical - standards</subject><subject>Delayed-Action Preparations - chemistry</subject><subject>Delayed-Action Preparations - metabolism</subject><subject>Dosage Forms</subject><subject>Drug Evaluation, Preclinical - methods</subject><subject>Drug Evaluation, Preclinical - standards</subject><subject>Drug therapy</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Medical Law</subject><subject>Meeting Report</subject><subject>Pharmaceutical Preparations - administration &amp; dosage</subject><subject>Pharmaceuticals</subject><subject>Pharmacokinetics</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Quality Control</subject><subject>Solubility</subject><issn>0724-8741</issn><issn>1573-904X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp1kMlOwzAQhi0EgrI8ABdkiXNg7DhxfGQrVEIqQmU5YWUZl0ATBztF4sZD8IQ8CUYtiAuXmcN888_oI2SXwQEDkIeeMVBJBExELBZZpFbIgCUyjhSI-1UyAMlFlEnBNsim908AkDEl1skGF6mIVRwPyMNxbR3O8DVvezpq6W3dO0uv0BnrmrwtkU7Q93U7pdbQsctnszd6VDV1W_seHVb01Pp8inQYcP_5_nFn3bN_tB29xs66fpusmXzmcWfZt8jN8GxychFdjs9HJ0eXUSkE7yOeSGAxqqosBZqUJ0qGIpOiylTBszLhvDRcZZUBU_CCIaYplDI3aYGmSiDeIvuL3M7Zl3n4WD_ZuWvDSc2SWLIUgPFAsQVVOuu9Q6M7Vze5e9MM9LdRvTCqg1H9bVSrsLO3TJ4XDVa_Gz8KA8AXgA-jdoruz-l_U78A0GiCmA</recordid><startdate>20140701</startdate><enddate>20140701</enddate><creator>Reppas, Christos</creator><creator>Friedel, Horst-Dieter</creator><creator>Barker, Amy R.</creator><creator>Buhse, Lucinda F.</creator><creator>Cecil, Todd L.</creator><creator>Keitel, Susanne</creator><creator>Kraemer, Johannes</creator><creator>Morris, J. Michael</creator><creator>Shah, Vinod P.</creator><creator>Stickelmeyer, Mary P.</creator><creator>Yomota, Chikako</creator><creator>Brown, Cynthia K.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20140701</creationdate><title>Biorelevant In Vitro Performance Testing of Orally Administered Dosage Forms—Workshop Report</title><author>Reppas, Christos ; Friedel, Horst-Dieter ; Barker, Amy R. ; Buhse, Lucinda F. ; Cecil, Todd L. ; Keitel, Susanne ; Kraemer, Johannes ; Morris, J. Michael ; Shah, Vinod P. ; Stickelmeyer, Mary P. ; Yomota, Chikako ; Brown, Cynthia K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-257013e9dcc4ef6259762575bd89b28c522cf298df0fb2b1ee660c7af6befd503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Administration, Oral</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedical Engineering and Bioengineering</topic><topic>Biomedicine</topic><topic>Chemistry, Pharmaceutical - education</topic><topic>Chemistry, Pharmaceutical - methods</topic><topic>Chemistry, Pharmaceutical - standards</topic><topic>Delayed-Action Preparations - chemistry</topic><topic>Delayed-Action Preparations - metabolism</topic><topic>Dosage Forms</topic><topic>Drug Evaluation, Preclinical - methods</topic><topic>Drug Evaluation, Preclinical - standards</topic><topic>Drug therapy</topic><topic>Health risk assessment</topic><topic>Humans</topic><topic>Medical Law</topic><topic>Meeting Report</topic><topic>Pharmaceutical Preparations - administration &amp; dosage</topic><topic>Pharmaceuticals</topic><topic>Pharmacokinetics</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>Quality Control</topic><topic>Solubility</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reppas, Christos</creatorcontrib><creatorcontrib>Friedel, Horst-Dieter</creatorcontrib><creatorcontrib>Barker, Amy R.</creatorcontrib><creatorcontrib>Buhse, Lucinda F.</creatorcontrib><creatorcontrib>Cecil, Todd L.</creatorcontrib><creatorcontrib>Keitel, Susanne</creatorcontrib><creatorcontrib>Kraemer, Johannes</creatorcontrib><creatorcontrib>Morris, J. Michael</creatorcontrib><creatorcontrib>Shah, Vinod P.</creatorcontrib><creatorcontrib>Stickelmeyer, Mary P.</creatorcontrib><creatorcontrib>Yomota, Chikako</creatorcontrib><creatorcontrib>Brown, Cynthia K.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reppas, Christos</au><au>Friedel, Horst-Dieter</au><au>Barker, Amy R.</au><au>Buhse, Lucinda F.</au><au>Cecil, Todd L.</au><au>Keitel, Susanne</au><au>Kraemer, Johannes</au><au>Morris, J. Michael</au><au>Shah, Vinod P.</au><au>Stickelmeyer, Mary P.</au><au>Yomota, Chikako</au><au>Brown, Cynthia K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biorelevant In Vitro Performance Testing of Orally Administered Dosage Forms—Workshop Report</atitle><jtitle>Pharmaceutical research</jtitle><stitle>Pharm Res</stitle><addtitle>Pharm Res</addtitle><date>2014-07-01</date><risdate>2014</risdate><volume>31</volume><issue>7</issue><spage>1867</spage><epage>1876</epage><pages>1867-1876</pages><issn>0724-8741</issn><eissn>1573-904X</eissn><abstract>Biorelevant in vitro performance testing of orally administered dosage forms has become an important tool for the assessment of drug product in vivo behavior. An in vitro performance test which mimics the intraluminal performance of an oral dosage form is termed biorelevant. Biorelevant tests have been utilized to decrease the number of in vivo studies required during the drug development process and to mitigate the risk related to in vivo bioequivalence studies. This report reviews the ability of current in vitro performance tests to predict in vivo performance and generate successful in vitro and in vivo correlations for oral dosage forms. It also summarizes efforts to improve the predictability of biorelevant tests. The report is based on the presentations at the 2013 workshop, Biorelevant In Vitro Performance Testing of Orally Administered Dosage Forms, in Washington, DC, sponsored by the FIP Dissolution/Drug Release Focus Group in partnership with the American Association of Pharmaceutical Scientists (AAPS) and a symposium at the AAPS 2012 Annual meeting on the same topic.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>24643933</pmid><doi>10.1007/s11095-014-1348-9</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0724-8741
ispartof Pharmaceutical research, 2014-07, Vol.31 (7), p.1867-1876
issn 0724-8741
1573-904X
language eng
recordid cdi_proquest_journals_1537160012
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Administration, Oral
Biochemistry
Biomedical and Life Sciences
Biomedical Engineering and Bioengineering
Biomedicine
Chemistry, Pharmaceutical - education
Chemistry, Pharmaceutical - methods
Chemistry, Pharmaceutical - standards
Delayed-Action Preparations - chemistry
Delayed-Action Preparations - metabolism
Dosage Forms
Drug Evaluation, Preclinical - methods
Drug Evaluation, Preclinical - standards
Drug therapy
Health risk assessment
Humans
Medical Law
Meeting Report
Pharmaceutical Preparations - administration & dosage
Pharmaceuticals
Pharmacokinetics
Pharmacology/Toxicology
Pharmacy
Quality Control
Solubility
title Biorelevant In Vitro Performance Testing of Orally Administered Dosage Forms—Workshop Report
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T08%3A59%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Biorelevant%20In%20Vitro%20Performance%20Testing%20of%20Orally%20Administered%20Dosage%20Forms%E2%80%94Workshop%20Report&rft.jtitle=Pharmaceutical%20research&rft.au=Reppas,%20Christos&rft.date=2014-07-01&rft.volume=31&rft.issue=7&rft.spage=1867&rft.epage=1876&rft.pages=1867-1876&rft.issn=0724-8741&rft.eissn=1573-904X&rft_id=info:doi/10.1007/s11095-014-1348-9&rft_dat=%3Cproquest_cross%3E3338702551%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1537160012&rft_id=info:pmid/24643933&rfr_iscdi=true