Influence of Kaolin–Pectin Suspension on Digoxin Bioavailability
The effect of a kaolin-pectin suspension on the bioavailability of orally administered digoxin was evaluated when both drugs were given concomitantly and when their time of administration was separated by 2 hr. Coadministration of the antidiarrheal with the cardiac glycoside delayed absorption of th...
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Veröffentlicht in: | Journal of pharmaceutical sciences 1978-11, Vol.67 (11), p.1582-1586 |
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creator | Albert, K.S. Ayres, J.W. DiSanto, A.R. Weidler, D.J. Sakmar, E. Hallmark, M.R. Stoll, R.G. DeSante, K.A. Wagner, J.G. |
description | The effect of a kaolin-pectin suspension on the bioavailability of orally administered digoxin was evaluated when both drugs were given concomitantly and when their time of administration was separated by 2 hr. Coadministration of the antidiarrheal with the cardiac glycoside delayed absorption of the latter and, at the same time, decreased by 62% the amount of drug absorbed. Intersubject variation in digoxin bioavailability also was increased more than twofold. When the kaolin- pectin suspension was given 2 hr before the cardiac glycoside, the digoxin absorption rate was not affected, although its relative extent of absorption was reduced by about 20%. In contrast, when the antidiarrheal was given 2 hr after digoxin, neither the rate nor the extent of absorption of the cardiac glycoside was perturbed. No change in the intersubject variability in digoxin bioavailability was noted whether the antidiarrheal was given 2 hr before or 2 hr after the cardiac glycoside. |
doi_str_mv | 10.1002/jps.2600671121 |
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Coadministration of the antidiarrheal with the cardiac glycoside delayed absorption of the latter and, at the same time, decreased by 62% the amount of drug absorbed. Intersubject variation in digoxin bioavailability also was increased more than twofold. When the kaolin- pectin suspension was given 2 hr before the cardiac glycoside, the digoxin absorption rate was not affected, although its relative extent of absorption was reduced by about 20%. In contrast, when the antidiarrheal was given 2 hr after digoxin, neither the rate nor the extent of absorption of the cardiac glycoside was perturbed. No change in the intersubject variability in digoxin bioavailability was noted whether the antidiarrheal was given 2 hr before or 2 hr after the cardiac glycoside.</description><identifier>ISSN: 0022-3549</identifier><identifier>EISSN: 1520-6017</identifier><identifier>DOI: 10.1002/jps.2600671121</identifier><identifier>PMID: 712596</identifier><language>eng</language><publisher>Washington: Elsevier Inc</publisher><subject>Absorption ; Absorption, GI—digoxin, effect of kaolin‐pectin suspension in humans ; Adult ; Antidiarrheals-kaolin-pectin suspension ; Antidiarrheals—kaolin‐pectin suspension, effect on GI absorption and bioavailability of digoxin in humans ; Bioavailability-digoxin ; Bioavailability—digoxin, effect of kaolin‐pectin suspension in humans ; Biological Availability ; Cardiotonic agents-digoxin ; Cardiotonic agents—digoxin, GI absorption and bioavailability, effect of kaolin‐pectin suspension in humans ; Digoxin - blood ; Digoxin - metabolism ; Digoxin-GI absorption and bioavailability ; Digoxin—GI absorption and bioavailability, effect of kaolin‐pectin suspension in humans ; Drug Combinations ; Drug Interactions ; effect of kaolin-pectin suspension in humans ; effect on GI absorption and bioavailability of digoxin in humans ; GI absorption and bioavailability ; GI-digoxin ; Humans ; Intestinal Absorption - drug effects ; Kaolin - administration & dosage ; Kaolin - pharmacology ; Kaolin-pectin suspension-effect on GI absorption and bioavailability of digoxin in humans ; Pectins - administration & dosage ; Pectins - pharmacology ; Suspensions ; Time Factors</subject><ispartof>Journal of pharmaceutical sciences, 1978-11, Vol.67 (11), p.1582-1586</ispartof><rights>1978 Wiley-Liss, Inc., A Wiley Company</rights><rights>Copyright © 1978 Wiley‐Liss, Inc., A Wiley Company</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4261-4249ae52d09591418d50e84f7d15a28854c6191a15495601cbc28156db3202053</citedby><cites>FETCH-LOGICAL-c4261-4249ae52d09591418d50e84f7d15a28854c6191a15495601cbc28156db3202053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjps.2600671121$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjps.2600671121$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/712596$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Albert, K.S.</creatorcontrib><creatorcontrib>Ayres, J.W.</creatorcontrib><creatorcontrib>DiSanto, A.R.</creatorcontrib><creatorcontrib>Weidler, D.J.</creatorcontrib><creatorcontrib>Sakmar, E.</creatorcontrib><creatorcontrib>Hallmark, M.R.</creatorcontrib><creatorcontrib>Stoll, R.G.</creatorcontrib><creatorcontrib>DeSante, K.A.</creatorcontrib><creatorcontrib>Wagner, J.G.</creatorcontrib><title>Influence of Kaolin–Pectin Suspension on Digoxin Bioavailability</title><title>Journal of pharmaceutical sciences</title><addtitle>J. Pharm. Sci</addtitle><description>The effect of a kaolin-pectin suspension on the bioavailability of orally administered digoxin was evaluated when both drugs were given concomitantly and when their time of administration was separated by 2 hr. Coadministration of the antidiarrheal with the cardiac glycoside delayed absorption of the latter and, at the same time, decreased by 62% the amount of drug absorbed. Intersubject variation in digoxin bioavailability also was increased more than twofold. When the kaolin- pectin suspension was given 2 hr before the cardiac glycoside, the digoxin absorption rate was not affected, although its relative extent of absorption was reduced by about 20%. In contrast, when the antidiarrheal was given 2 hr after digoxin, neither the rate nor the extent of absorption of the cardiac glycoside was perturbed. No change in the intersubject variability in digoxin bioavailability was noted whether the antidiarrheal was given 2 hr before or 2 hr after the cardiac glycoside.</description><subject>Absorption</subject><subject>Absorption, GI—digoxin, effect of kaolin‐pectin suspension in humans</subject><subject>Adult</subject><subject>Antidiarrheals-kaolin-pectin suspension</subject><subject>Antidiarrheals—kaolin‐pectin suspension, effect on GI absorption and bioavailability of digoxin in humans</subject><subject>Bioavailability-digoxin</subject><subject>Bioavailability—digoxin, effect of kaolin‐pectin suspension in humans</subject><subject>Biological Availability</subject><subject>Cardiotonic agents-digoxin</subject><subject>Cardiotonic agents—digoxin, GI absorption and bioavailability, effect of kaolin‐pectin suspension in humans</subject><subject>Digoxin - blood</subject><subject>Digoxin - metabolism</subject><subject>Digoxin-GI absorption and bioavailability</subject><subject>Digoxin—GI absorption and bioavailability, effect of kaolin‐pectin suspension in humans</subject><subject>Drug Combinations</subject><subject>Drug Interactions</subject><subject>effect of kaolin-pectin suspension in humans</subject><subject>effect on GI absorption and bioavailability of digoxin in humans</subject><subject>GI absorption and bioavailability</subject><subject>GI-digoxin</subject><subject>Humans</subject><subject>Intestinal Absorption - drug effects</subject><subject>Kaolin - administration & dosage</subject><subject>Kaolin - pharmacology</subject><subject>Kaolin-pectin suspension-effect on GI absorption and bioavailability of digoxin in humans</subject><subject>Pectins - administration & dosage</subject><subject>Pectins - pharmacology</subject><subject>Suspensions</subject><subject>Time Factors</subject><issn>0022-3549</issn><issn>1520-6017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1978</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1OwzAQhS3EXylsWbHIBVI8TuwkSxqgPxSoKIil5TgOckmTKG5Lu-MO3JCT4CqoiAVCGmmkmfeeZj6ETgF3AGNyPq1MhzCMWQBAYAe1gBLsMgzBLmpZAXE96keH6MiYKbYyTOkB2g-A0Ii1UHdQZPlCFVI5ZebciDLXxef7x1jJuS6cycJUqjC6LBxbl_qlXNlpV5diKXQuEp3r-foY7WUiN-rku7fR0_XVY9x3R_e9QXwxcqVPGLg-8SOhKElxRCPwIUwpVqGfBSlQQcKQ-pJBBALstdSeLxNJQqAsTTyCCaZeG3WaXFmXxtQq41WtZ6Jec8B8g4JbFPwHhTWcNYZqkcxUupU3v9t11KzfdK7W_4Tx4XjyK9ptvNrM1WrrFfUrZ4EXUP581-OT_gMexr1bHlt92OiVBbTUquZG6g31VNcWNU9L_dcXXxIvi0c</recordid><startdate>197811</startdate><enddate>197811</enddate><creator>Albert, K.S.</creator><creator>Ayres, J.W.</creator><creator>DiSanto, A.R.</creator><creator>Weidler, D.J.</creator><creator>Sakmar, E.</creator><creator>Hallmark, M.R.</creator><creator>Stoll, R.G.</creator><creator>DeSante, K.A.</creator><creator>Wagner, J.G.</creator><general>Elsevier Inc</general><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>197811</creationdate><title>Influence of Kaolin–Pectin Suspension on Digoxin Bioavailability</title><author>Albert, K.S. ; Ayres, J.W. ; DiSanto, A.R. ; Weidler, D.J. ; Sakmar, E. ; Hallmark, M.R. ; Stoll, R.G. ; DeSante, K.A. ; Wagner, J.G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4261-4249ae52d09591418d50e84f7d15a28854c6191a15495601cbc28156db3202053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1978</creationdate><topic>Absorption</topic><topic>Absorption, GI—digoxin, effect of kaolin‐pectin suspension in humans</topic><topic>Adult</topic><topic>Antidiarrheals-kaolin-pectin suspension</topic><topic>Antidiarrheals—kaolin‐pectin suspension, effect on GI absorption and bioavailability of digoxin in humans</topic><topic>Bioavailability-digoxin</topic><topic>Bioavailability—digoxin, effect of kaolin‐pectin suspension in humans</topic><topic>Biological Availability</topic><topic>Cardiotonic agents-digoxin</topic><topic>Cardiotonic agents—digoxin, GI absorption and bioavailability, effect of kaolin‐pectin suspension in humans</topic><topic>Digoxin - blood</topic><topic>Digoxin - metabolism</topic><topic>Digoxin-GI absorption and bioavailability</topic><topic>Digoxin—GI absorption and bioavailability, effect of kaolin‐pectin suspension in humans</topic><topic>Drug Combinations</topic><topic>Drug Interactions</topic><topic>effect of kaolin-pectin suspension in humans</topic><topic>effect on GI absorption and bioavailability of digoxin in humans</topic><topic>GI absorption and bioavailability</topic><topic>GI-digoxin</topic><topic>Humans</topic><topic>Intestinal Absorption - drug effects</topic><topic>Kaolin - administration & dosage</topic><topic>Kaolin - pharmacology</topic><topic>Kaolin-pectin suspension-effect on GI absorption and bioavailability of digoxin in humans</topic><topic>Pectins - administration & dosage</topic><topic>Pectins - pharmacology</topic><topic>Suspensions</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Albert, K.S.</creatorcontrib><creatorcontrib>Ayres, J.W.</creatorcontrib><creatorcontrib>DiSanto, A.R.</creatorcontrib><creatorcontrib>Weidler, D.J.</creatorcontrib><creatorcontrib>Sakmar, E.</creatorcontrib><creatorcontrib>Hallmark, M.R.</creatorcontrib><creatorcontrib>Stoll, R.G.</creatorcontrib><creatorcontrib>DeSante, K.A.</creatorcontrib><creatorcontrib>Wagner, J.G.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Albert, K.S.</au><au>Ayres, J.W.</au><au>DiSanto, A.R.</au><au>Weidler, D.J.</au><au>Sakmar, E.</au><au>Hallmark, M.R.</au><au>Stoll, R.G.</au><au>DeSante, K.A.</au><au>Wagner, J.G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of Kaolin–Pectin Suspension on Digoxin Bioavailability</atitle><jtitle>Journal of pharmaceutical sciences</jtitle><addtitle>J. Pharm. Sci</addtitle><date>1978-11</date><risdate>1978</risdate><volume>67</volume><issue>11</issue><spage>1582</spage><epage>1586</epage><pages>1582-1586</pages><issn>0022-3549</issn><eissn>1520-6017</eissn><abstract>The effect of a kaolin-pectin suspension on the bioavailability of orally administered digoxin was evaluated when both drugs were given concomitantly and when their time of administration was separated by 2 hr. Coadministration of the antidiarrheal with the cardiac glycoside delayed absorption of the latter and, at the same time, decreased by 62% the amount of drug absorbed. Intersubject variation in digoxin bioavailability also was increased more than twofold. When the kaolin- pectin suspension was given 2 hr before the cardiac glycoside, the digoxin absorption rate was not affected, although its relative extent of absorption was reduced by about 20%. In contrast, when the antidiarrheal was given 2 hr after digoxin, neither the rate nor the extent of absorption of the cardiac glycoside was perturbed. No change in the intersubject variability in digoxin bioavailability was noted whether the antidiarrheal was given 2 hr before or 2 hr after the cardiac glycoside.</abstract><cop>Washington</cop><pub>Elsevier Inc</pub><pmid>712596</pmid><doi>10.1002/jps.2600671121</doi><tpages>5</tpages></addata></record> |
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subjects | Absorption Absorption, GI—digoxin, effect of kaolin‐pectin suspension in humans Adult Antidiarrheals-kaolin-pectin suspension Antidiarrheals—kaolin‐pectin suspension, effect on GI absorption and bioavailability of digoxin in humans Bioavailability-digoxin Bioavailability—digoxin, effect of kaolin‐pectin suspension in humans Biological Availability Cardiotonic agents-digoxin Cardiotonic agents—digoxin, GI absorption and bioavailability, effect of kaolin‐pectin suspension in humans Digoxin - blood Digoxin - metabolism Digoxin-GI absorption and bioavailability Digoxin—GI absorption and bioavailability, effect of kaolin‐pectin suspension in humans Drug Combinations Drug Interactions effect of kaolin-pectin suspension in humans effect on GI absorption and bioavailability of digoxin in humans GI absorption and bioavailability GI-digoxin Humans Intestinal Absorption - drug effects Kaolin - administration & dosage Kaolin - pharmacology Kaolin-pectin suspension-effect on GI absorption and bioavailability of digoxin in humans Pectins - administration & dosage Pectins - pharmacology Suspensions Time Factors |
title | Influence of Kaolin–Pectin Suspension on Digoxin Bioavailability |
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