Profiling and Trend Analysis of Food Effects on Oral Drug Absorption Considering Micelle Interaction and Solubilization by Bile Micelles

Correlation analysis between food effects on oral drug absorption (food effect) and physicochemical properties is important for efficient drug discovery and contributes to drug design. This study focused on micelle binding and solubilization considering bile micelles in the intestinal fluid. Profili...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:DRUG METABOLISM AND PHARMACOKINETICS 2011-01, Vol.26 (2), p.180-191
Hauptverfasser: Kawai, Yukinori, Fujii, Yoshimine, Tabata, Fumiko, Ito, Junko, Metsugi, Yukiko, Kameda, Atsuko, Akimoto, Katsuya, Takahashi, Masayuki
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 191
container_issue 2
container_start_page 180
container_title DRUG METABOLISM AND PHARMACOKINETICS
container_volume 26
creator Kawai, Yukinori
Fujii, Yoshimine
Tabata, Fumiko
Ito, Junko
Metsugi, Yukiko
Kameda, Atsuko
Akimoto, Katsuya
Takahashi, Masayuki
description Correlation analysis between food effects on oral drug absorption (food effect) and physicochemical properties is important for efficient drug discovery and contributes to drug design. This study focused on micelle binding and solubilization considering bile micelles in the intestinal fluid. Profiling using about 40 launched drugs demonstrated that those in a high solubilization area (area 1) tended to have a positive food effect, and that drugs exhibiting negative/no food effect tended to coexist in a no/low solubilization area (area 2). In area 1, the solubilization effect by bile micelles was demonstrated quantitatively as an important factor that indicates a positive food effect. In area 2, the relative and quantitative relationships among the membrane permeation rate, dissolution rate, micelle binding and food effect could be clarified by simulation. The improvement of membrane permeability and the suppression of micelle binding are considered to be required to avoid a negative food effect. In conclusion, important factors contributing to the food effect were clarified relatively and quantitatively. Data generated from this profiling may be beneficial to find a solution for negative food effects. Furthermore, this risk assessment of food effects is considered to be a useful tool in rational drug design for drug discovery.
doi_str_mv 10.2133/dmpk.DMPK-10-RG-098
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_864779617</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1347436715306595</els_id><sourcerecordid>864779617</sourcerecordid><originalsourceid>FETCH-LOGICAL-c613t-98a5ceb36df3b98411ba4c1a05fc2e44044d9c77ed9dbe12dc602f611dc103d53</originalsourceid><addsrcrecordid>eNp9UU1v1DAQjRCIlsIvQEK-cUrx2M7XgcOybZeKVq1KOVuOPalcknixE6TlF_CzmXQXjlw845k3z-P3suwt8FMBUn5ww_b76dn17ZcceH63yXlTP8uOoa45pYI_p1yqKleyrI6yVyk9ci5locTL7EiA4CVIcZz9vo2h870fH5gZHbuPSOdqNP0u-cRCxy5CcOy869BOdB_ZTTQ9O4vzA1u1KcTt5Km4DmPyDuNCc-0t9j2yy3HCaOxTf6H-Gvq5pZd-madSu2OfPMEO8PQ6e9GZPuGbQzzJvl2c368_51c3m8v16iq3tPCUN7UpLLaydJ1sm1oBtEZZMLzorECluFKusVWFrnEtgnC25KIrAZwFLl0hT7L3e95tDD9mTJMefFpWMCOGOem6VFXVlFARUu6RNoaUInZ6G_1g4k4D14sDenFALw4slbuNJgdo6t2Bf24HdP9m_kpOgM0eQF1vTR9GUh_1Y5gjyZ60DTDgZFotOIDmXNAHKDSaQ83paABUWRcFJ6aPeyYkvX56jDpZj6Ml3kh2aRf8f1f9A52ssNY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>864779617</pqid></control><display><type>article</type><title>Profiling and Trend Analysis of Food Effects on Oral Drug Absorption Considering Micelle Interaction and Solubilization by Bile Micelles</title><source>MEDLINE</source><source>J-STAGE (Japan Science &amp; Technology Information Aggregator, Electronic) Freely Available Titles - Japanese</source><source>Alma/SFX Local Collection</source><source>Free Full-Text Journals in Chemistry</source><creator>Kawai, Yukinori ; Fujii, Yoshimine ; Tabata, Fumiko ; Ito, Junko ; Metsugi, Yukiko ; Kameda, Atsuko ; Akimoto, Katsuya ; Takahashi, Masayuki</creator><creatorcontrib>Kawai, Yukinori ; Fujii, Yoshimine ; Tabata, Fumiko ; Ito, Junko ; Metsugi, Yukiko ; Kameda, Atsuko ; Akimoto, Katsuya ; Takahashi, Masayuki ; Daiichi Sankyo Co ; Ltd ; Drug Metabolism &amp; Pharmacokinetics Research Laboratories</creatorcontrib><description>Correlation analysis between food effects on oral drug absorption (food effect) and physicochemical properties is important for efficient drug discovery and contributes to drug design. This study focused on micelle binding and solubilization considering bile micelles in the intestinal fluid. Profiling using about 40 launched drugs demonstrated that those in a high solubilization area (area 1) tended to have a positive food effect, and that drugs exhibiting negative/no food effect tended to coexist in a no/low solubilization area (area 2). In area 1, the solubilization effect by bile micelles was demonstrated quantitatively as an important factor that indicates a positive food effect. In area 2, the relative and quantitative relationships among the membrane permeation rate, dissolution rate, micelle binding and food effect could be clarified by simulation. The improvement of membrane permeability and the suppression of micelle binding are considered to be required to avoid a negative food effect. In conclusion, important factors contributing to the food effect were clarified relatively and quantitatively. Data generated from this profiling may be beneficial to find a solution for negative food effects. Furthermore, this risk assessment of food effects is considered to be a useful tool in rational drug design for drug discovery.</description><identifier>ISSN: 1347-4367</identifier><identifier>EISSN: 1880-0920</identifier><identifier>DOI: 10.2133/dmpk.DMPK-10-RG-098</identifier><identifier>PMID: 21206132</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Absorption ; Administration, Oral ; Animals ; Bile - chemistry ; Bile - metabolism ; Body Fluids - metabolism ; Cell Line ; Cell Membrane Permeability ; Chemistry, Pharmaceutical ; dissolution rate ; Drug Design ; Food ; food effect ; Humans ; Intestinal Absorption - drug effects ; membrane permeation rate ; micelle binding ; Micelles ; Models, Biological ; Pharmaceutical Preparations - analysis ; Pharmaceutical Preparations - chemistry ; Pharmaceutical Preparations - metabolism ; Pharmacokinetics ; physicochemical property ; Solubility ; solubilization</subject><ispartof>DRUG METABOLISM AND PHARMACOKINETICS, 2011-01, Vol.26 (2), p.180-191</ispartof><rights>2011 The Japanese Society for the Study of Xenobiotics</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c613t-98a5ceb36df3b98411ba4c1a05fc2e44044d9c77ed9dbe12dc602f611dc103d53</citedby><cites>FETCH-LOGICAL-c613t-98a5ceb36df3b98411ba4c1a05fc2e44044d9c77ed9dbe12dc602f611dc103d53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21206132$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kawai, Yukinori</creatorcontrib><creatorcontrib>Fujii, Yoshimine</creatorcontrib><creatorcontrib>Tabata, Fumiko</creatorcontrib><creatorcontrib>Ito, Junko</creatorcontrib><creatorcontrib>Metsugi, Yukiko</creatorcontrib><creatorcontrib>Kameda, Atsuko</creatorcontrib><creatorcontrib>Akimoto, Katsuya</creatorcontrib><creatorcontrib>Takahashi, Masayuki</creatorcontrib><creatorcontrib>Daiichi Sankyo Co</creatorcontrib><creatorcontrib>Ltd</creatorcontrib><creatorcontrib>Drug Metabolism &amp; Pharmacokinetics Research Laboratories</creatorcontrib><title>Profiling and Trend Analysis of Food Effects on Oral Drug Absorption Considering Micelle Interaction and Solubilization by Bile Micelles</title><title>DRUG METABOLISM AND PHARMACOKINETICS</title><addtitle>Drug Metab Pharmacokinet</addtitle><description>Correlation analysis between food effects on oral drug absorption (food effect) and physicochemical properties is important for efficient drug discovery and contributes to drug design. This study focused on micelle binding and solubilization considering bile micelles in the intestinal fluid. Profiling using about 40 launched drugs demonstrated that those in a high solubilization area (area 1) tended to have a positive food effect, and that drugs exhibiting negative/no food effect tended to coexist in a no/low solubilization area (area 2). In area 1, the solubilization effect by bile micelles was demonstrated quantitatively as an important factor that indicates a positive food effect. In area 2, the relative and quantitative relationships among the membrane permeation rate, dissolution rate, micelle binding and food effect could be clarified by simulation. The improvement of membrane permeability and the suppression of micelle binding are considered to be required to avoid a negative food effect. In conclusion, important factors contributing to the food effect were clarified relatively and quantitatively. Data generated from this profiling may be beneficial to find a solution for negative food effects. Furthermore, this risk assessment of food effects is considered to be a useful tool in rational drug design for drug discovery.</description><subject>Absorption</subject><subject>Administration, Oral</subject><subject>Animals</subject><subject>Bile - chemistry</subject><subject>Bile - metabolism</subject><subject>Body Fluids - metabolism</subject><subject>Cell Line</subject><subject>Cell Membrane Permeability</subject><subject>Chemistry, Pharmaceutical</subject><subject>dissolution rate</subject><subject>Drug Design</subject><subject>Food</subject><subject>food effect</subject><subject>Humans</subject><subject>Intestinal Absorption - drug effects</subject><subject>membrane permeation rate</subject><subject>micelle binding</subject><subject>Micelles</subject><subject>Models, Biological</subject><subject>Pharmaceutical Preparations - analysis</subject><subject>Pharmaceutical Preparations - chemistry</subject><subject>Pharmaceutical Preparations - metabolism</subject><subject>Pharmacokinetics</subject><subject>physicochemical property</subject><subject>Solubility</subject><subject>solubilization</subject><issn>1347-4367</issn><issn>1880-0920</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UU1v1DAQjRCIlsIvQEK-cUrx2M7XgcOybZeKVq1KOVuOPalcknixE6TlF_CzmXQXjlw845k3z-P3suwt8FMBUn5ww_b76dn17ZcceH63yXlTP8uOoa45pYI_p1yqKleyrI6yVyk9ci5locTL7EiA4CVIcZz9vo2h870fH5gZHbuPSOdqNP0u-cRCxy5CcOy869BOdB_ZTTQ9O4vzA1u1KcTt5Km4DmPyDuNCc-0t9j2yy3HCaOxTf6H-Gvq5pZd-madSu2OfPMEO8PQ6e9GZPuGbQzzJvl2c368_51c3m8v16iq3tPCUN7UpLLaydJ1sm1oBtEZZMLzorECluFKusVWFrnEtgnC25KIrAZwFLl0hT7L3e95tDD9mTJMefFpWMCOGOem6VFXVlFARUu6RNoaUInZ6G_1g4k4D14sDenFALw4slbuNJgdo6t2Bf24HdP9m_kpOgM0eQF1vTR9GUh_1Y5gjyZ60DTDgZFotOIDmXNAHKDSaQ83paABUWRcFJ6aPeyYkvX56jDpZj6Ml3kh2aRf8f1f9A52ssNY</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Kawai, Yukinori</creator><creator>Fujii, Yoshimine</creator><creator>Tabata, Fumiko</creator><creator>Ito, Junko</creator><creator>Metsugi, Yukiko</creator><creator>Kameda, Atsuko</creator><creator>Akimoto, Katsuya</creator><creator>Takahashi, Masayuki</creator><general>Elsevier Ltd</general><general>Japanese Society for the Study of Xenobiotics</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>7X8</scope></search><sort><creationdate>20110101</creationdate><title>Profiling and Trend Analysis of Food Effects on Oral Drug Absorption Considering Micelle Interaction and Solubilization by Bile Micelles</title><author>Kawai, Yukinori ; Fujii, Yoshimine ; Tabata, Fumiko ; Ito, Junko ; Metsugi, Yukiko ; Kameda, Atsuko ; Akimoto, Katsuya ; Takahashi, Masayuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c613t-98a5ceb36df3b98411ba4c1a05fc2e44044d9c77ed9dbe12dc602f611dc103d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Absorption</topic><topic>Administration, Oral</topic><topic>Animals</topic><topic>Bile - chemistry</topic><topic>Bile - metabolism</topic><topic>Body Fluids - metabolism</topic><topic>Cell Line</topic><topic>Cell Membrane Permeability</topic><topic>Chemistry, Pharmaceutical</topic><topic>dissolution rate</topic><topic>Drug Design</topic><topic>Food</topic><topic>food effect</topic><topic>Humans</topic><topic>Intestinal Absorption - drug effects</topic><topic>membrane permeation rate</topic><topic>micelle binding</topic><topic>Micelles</topic><topic>Models, Biological</topic><topic>Pharmaceutical Preparations - analysis</topic><topic>Pharmaceutical Preparations - chemistry</topic><topic>Pharmaceutical Preparations - metabolism</topic><topic>Pharmacokinetics</topic><topic>physicochemical property</topic><topic>Solubility</topic><topic>solubilization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kawai, Yukinori</creatorcontrib><creatorcontrib>Fujii, Yoshimine</creatorcontrib><creatorcontrib>Tabata, Fumiko</creatorcontrib><creatorcontrib>Ito, Junko</creatorcontrib><creatorcontrib>Metsugi, Yukiko</creatorcontrib><creatorcontrib>Kameda, Atsuko</creatorcontrib><creatorcontrib>Akimoto, Katsuya</creatorcontrib><creatorcontrib>Takahashi, Masayuki</creatorcontrib><creatorcontrib>Daiichi Sankyo Co</creatorcontrib><creatorcontrib>Ltd</creatorcontrib><creatorcontrib>Drug Metabolism &amp; Pharmacokinetics Research Laboratories</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>DRUG METABOLISM AND PHARMACOKINETICS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kawai, Yukinori</au><au>Fujii, Yoshimine</au><au>Tabata, Fumiko</au><au>Ito, Junko</au><au>Metsugi, Yukiko</au><au>Kameda, Atsuko</au><au>Akimoto, Katsuya</au><au>Takahashi, Masayuki</au><aucorp>Daiichi Sankyo Co</aucorp><aucorp>Ltd</aucorp><aucorp>Drug Metabolism &amp; Pharmacokinetics Research Laboratories</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Profiling and Trend Analysis of Food Effects on Oral Drug Absorption Considering Micelle Interaction and Solubilization by Bile Micelles</atitle><jtitle>DRUG METABOLISM AND PHARMACOKINETICS</jtitle><addtitle>Drug Metab Pharmacokinet</addtitle><date>2011-01-01</date><risdate>2011</risdate><volume>26</volume><issue>2</issue><spage>180</spage><epage>191</epage><pages>180-191</pages><issn>1347-4367</issn><eissn>1880-0920</eissn><abstract>Correlation analysis between food effects on oral drug absorption (food effect) and physicochemical properties is important for efficient drug discovery and contributes to drug design. This study focused on micelle binding and solubilization considering bile micelles in the intestinal fluid. Profiling using about 40 launched drugs demonstrated that those in a high solubilization area (area 1) tended to have a positive food effect, and that drugs exhibiting negative/no food effect tended to coexist in a no/low solubilization area (area 2). In area 1, the solubilization effect by bile micelles was demonstrated quantitatively as an important factor that indicates a positive food effect. In area 2, the relative and quantitative relationships among the membrane permeation rate, dissolution rate, micelle binding and food effect could be clarified by simulation. The improvement of membrane permeability and the suppression of micelle binding are considered to be required to avoid a negative food effect. In conclusion, important factors contributing to the food effect were clarified relatively and quantitatively. Data generated from this profiling may be beneficial to find a solution for negative food effects. Furthermore, this risk assessment of food effects is considered to be a useful tool in rational drug design for drug discovery.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>21206132</pmid><doi>10.2133/dmpk.DMPK-10-RG-098</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1347-4367
ispartof DRUG METABOLISM AND PHARMACOKINETICS, 2011-01, Vol.26 (2), p.180-191
issn 1347-4367
1880-0920
language eng
recordid cdi_proquest_miscellaneous_864779617
source MEDLINE; J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry
subjects Absorption
Administration, Oral
Animals
Bile - chemistry
Bile - metabolism
Body Fluids - metabolism
Cell Line
Cell Membrane Permeability
Chemistry, Pharmaceutical
dissolution rate
Drug Design
Food
food effect
Humans
Intestinal Absorption - drug effects
membrane permeation rate
micelle binding
Micelles
Models, Biological
Pharmaceutical Preparations - analysis
Pharmaceutical Preparations - chemistry
Pharmaceutical Preparations - metabolism
Pharmacokinetics
physicochemical property
Solubility
solubilization
title Profiling and Trend Analysis of Food Effects on Oral Drug Absorption Considering Micelle Interaction and Solubilization by Bile Micelles
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T17%3A04%3A43IST&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=Profiling%20and%20Trend%20Analysis%20of%20Food%20Effects%20on%20Oral%20Drug%20Absorption%20Considering%20Micelle%20Interaction%20and%20Solubilization%20by%20Bile%20Micelles&rft.jtitle=DRUG%20METABOLISM%20AND%20PHARMACOKINETICS&rft.au=Kawai,%20Yukinori&rft.aucorp=Daiichi%20Sankyo%20Co&rft.date=2011-01-01&rft.volume=26&rft.issue=2&rft.spage=180&rft.epage=191&rft.pages=180-191&rft.issn=1347-4367&rft.eissn=1880-0920&rft_id=info:doi/10.2133/dmpk.DMPK-10-RG-098&rft_dat=%3Cproquest_cross%3E864779617%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=864779617&rft_id=info:pmid/21206132&rft_els_id=S1347436715306595&rfr_iscdi=true