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...
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Veröffentlicht in: | DRUG METABOLISM AND PHARMACOKINETICS 2011-01, Vol.26 (2), p.180-191 |
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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 |
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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 & 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 & 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 & 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> |
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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 |
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