Nifedipine controlled delivery by sandwiched osmotic tablet system
The sandwiched osmotic tablet system (SOTS), which is composed of a sandwiched osmotic tablet core surrounded by a cellulose acetate membrane with two orifices on both side surfaces, has been successfully prepared with the purpose of delivering nifedipine. The sandwiched osmotic tablet core consists...
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Veröffentlicht in: | Journal of controlled release 2000-08, Vol.68 (2), p.145-156 |
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creator | Liu, Longxiao Ku, Jeong Khang, Gilson Lee, Bong Rhee, John M Lee, Hai Bang |
description | The sandwiched osmotic tablet system (SOTS), which is composed of a sandwiched osmotic tablet core surrounded by a cellulose acetate membrane with two orifices on both side surfaces, has been successfully prepared with the purpose of delivering nifedipine. The sandwiched osmotic tablet core consists of a middle push layer and two attached drug layers. Influences of tablet formulation variables, orifice size and membrane variables on nifedipine release of SOTS have been studied. It was found that potassium chloride amount of push layer and polyethylene oxide amount of drug layer had markedly positive effects on nifedipine release. A push layer/drug layer co-controlled osmotic delivery mechanism and the optimal core formulation have been proposed. The appropriate orifice size was observed in the range of 0.50–1.41 mm. It was also found that the drug release rate of SOTS could be increased by incorporating hydrophilic plasticizer in the membrane, whereas it decreased with hydrophobic plasticizer. It has been observed that the SOTS gives fairly comparable in vitro release features as that of commercialized push–pull osmotic tablet system, such as an approximately constant rate up to 24 h and independence of release media and agitation rate. Exempting side identification before drilling, it is easier to prepare the SOTS than the push–pull osmotic tablet system. |
doi_str_mv | 10.1016/S0168-3659(00)00243-1 |
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The sandwiched osmotic tablet core consists of a middle push layer and two attached drug layers. Influences of tablet formulation variables, orifice size and membrane variables on nifedipine release of SOTS have been studied. It was found that potassium chloride amount of push layer and polyethylene oxide amount of drug layer had markedly positive effects on nifedipine release. A push layer/drug layer co-controlled osmotic delivery mechanism and the optimal core formulation have been proposed. The appropriate orifice size was observed in the range of 0.50–1.41 mm. It was also found that the drug release rate of SOTS could be increased by incorporating hydrophilic plasticizer in the membrane, whereas it decreased with hydrophobic plasticizer. It has been observed that the SOTS gives fairly comparable in vitro release features as that of commercialized push–pull osmotic tablet system, such as an approximately constant rate up to 24 h and independence of release media and agitation rate. Exempting side identification before drilling, it is easier to prepare the SOTS than the push–pull osmotic tablet system.</description><identifier>ISSN: 0168-3659</identifier><identifier>EISSN: 1873-4995</identifier><identifier>DOI: 10.1016/S0168-3659(00)00243-1</identifier><identifier>PMID: 10925123</identifier><identifier>CODEN: JCREEC</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>24-Hour delivery ; Antihypertensive agents ; Biological and medical sciences ; Calcium Channel Blockers - administration & dosage ; Cardiovascular system ; Drug Delivery Systems ; General pharmacology ; Medical sciences ; Nifedipine ; Nifedipine - administration & dosage ; Nifedipine - chemistry ; Osmotic Pressure ; Osmotic pump ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Polyethylene Glycols - pharmacology ; Potassium Chloride - pharmacology ; Regression Analysis ; Sandwiched osmotic tablet system ; Tablets</subject><ispartof>Journal of controlled release, 2000-08, Vol.68 (2), p.145-156</ispartof><rights>2000 Elsevier Science B.V.</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-2e06fb1fed060ef166ceacd76847dfa0067d85110ec554b39960d5e590dd86413</citedby><cites>FETCH-LOGICAL-c390t-2e06fb1fed060ef166ceacd76847dfa0067d85110ec554b39960d5e590dd86413</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0168-3659(00)00243-1$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1438083$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10925123$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Longxiao</creatorcontrib><creatorcontrib>Ku, Jeong</creatorcontrib><creatorcontrib>Khang, Gilson</creatorcontrib><creatorcontrib>Lee, Bong</creatorcontrib><creatorcontrib>Rhee, John M</creatorcontrib><creatorcontrib>Lee, Hai Bang</creatorcontrib><title>Nifedipine controlled delivery by sandwiched osmotic tablet system</title><title>Journal of controlled release</title><addtitle>J Control Release</addtitle><description>The sandwiched osmotic tablet system (SOTS), which is composed of a sandwiched osmotic tablet core surrounded by a cellulose acetate membrane with two orifices on both side surfaces, has been successfully prepared with the purpose of delivering nifedipine. The sandwiched osmotic tablet core consists of a middle push layer and two attached drug layers. Influences of tablet formulation variables, orifice size and membrane variables on nifedipine release of SOTS have been studied. It was found that potassium chloride amount of push layer and polyethylene oxide amount of drug layer had markedly positive effects on nifedipine release. A push layer/drug layer co-controlled osmotic delivery mechanism and the optimal core formulation have been proposed. The appropriate orifice size was observed in the range of 0.50–1.41 mm. It was also found that the drug release rate of SOTS could be increased by incorporating hydrophilic plasticizer in the membrane, whereas it decreased with hydrophobic plasticizer. It has been observed that the SOTS gives fairly comparable in vitro release features as that of commercialized push–pull osmotic tablet system, such as an approximately constant rate up to 24 h and independence of release media and agitation rate. Exempting side identification before drilling, it is easier to prepare the SOTS than the push–pull osmotic tablet system.</description><subject>24-Hour delivery</subject><subject>Antihypertensive agents</subject><subject>Biological and medical sciences</subject><subject>Calcium Channel Blockers - administration & dosage</subject><subject>Cardiovascular system</subject><subject>Drug Delivery Systems</subject><subject>General pharmacology</subject><subject>Medical sciences</subject><subject>Nifedipine</subject><subject>Nifedipine - administration & dosage</subject><subject>Nifedipine - chemistry</subject><subject>Osmotic Pressure</subject><subject>Osmotic pump</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Polyethylene Glycols - pharmacology</subject><subject>Potassium Chloride - pharmacology</subject><subject>Regression Analysis</subject><subject>Sandwiched osmotic tablet system</subject><subject>Tablets</subject><issn>0168-3659</issn><issn>1873-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLxDAQx4Mo7vr4CEoPInqoTpomaU-iiy9Y9KCeQ5pMMdLHmnRX-u3tPlBvXmZg-M38hx8hRxQuKFBx-TKULGaC52cA5wBJymK6RcY0kyxO85xvk_EPMiJ7IXwAAGep3CUjCnnCacLG5ObJlWjdzDUYmbbpfFtVaCOLlVug76Oij4Ju7Jcz78O4DXXbORN1uqiwi0IfOqwPyE6pq4CHm75P3u5uXycP8fT5_nFyPY0Ny6GLEwRRFnRIAwFYUiEMamOlyFJpSw0gpM04pYCG87RgeS7AcuQ5WJuJlLJ9crq-O_Pt5xxDp2oXDFaVbrCdByWpTCVP5ADyNWh8G4LHUs28q7XvFQW1lKdW8tTSjAJQK3lqGXC8CZgXNdo_W2tbA3CyAXQwuiq9bowLv1zKMsiW2NUaw8HGwqFXwThszODZo-mUbd0_n3wDoCWLSw</recordid><startdate>20000810</startdate><enddate>20000810</enddate><creator>Liu, Longxiao</creator><creator>Ku, Jeong</creator><creator>Khang, Gilson</creator><creator>Lee, Bong</creator><creator>Rhee, John M</creator><creator>Lee, Hai Bang</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</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><scope>7X8</scope></search><sort><creationdate>20000810</creationdate><title>Nifedipine controlled delivery by sandwiched osmotic tablet system</title><author>Liu, Longxiao ; Ku, Jeong ; Khang, Gilson ; Lee, Bong ; Rhee, John M ; Lee, Hai Bang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-2e06fb1fed060ef166ceacd76847dfa0067d85110ec554b39960d5e590dd86413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>24-Hour delivery</topic><topic>Antihypertensive agents</topic><topic>Biological and medical sciences</topic><topic>Calcium Channel Blockers - administration & dosage</topic><topic>Cardiovascular system</topic><topic>Drug Delivery Systems</topic><topic>General pharmacology</topic><topic>Medical sciences</topic><topic>Nifedipine</topic><topic>Nifedipine - administration & dosage</topic><topic>Nifedipine - chemistry</topic><topic>Osmotic Pressure</topic><topic>Osmotic pump</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Polyethylene Glycols - pharmacology</topic><topic>Potassium Chloride - pharmacology</topic><topic>Regression Analysis</topic><topic>Sandwiched osmotic tablet system</topic><topic>Tablets</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Longxiao</creatorcontrib><creatorcontrib>Ku, Jeong</creatorcontrib><creatorcontrib>Khang, Gilson</creatorcontrib><creatorcontrib>Lee, Bong</creatorcontrib><creatorcontrib>Rhee, John M</creatorcontrib><creatorcontrib>Lee, Hai Bang</creatorcontrib><collection>Pascal-Francis</collection><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>Journal of controlled release</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Longxiao</au><au>Ku, Jeong</au><au>Khang, Gilson</au><au>Lee, Bong</au><au>Rhee, John M</au><au>Lee, Hai Bang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nifedipine controlled delivery by sandwiched osmotic tablet system</atitle><jtitle>Journal of controlled release</jtitle><addtitle>J Control Release</addtitle><date>2000-08-10</date><risdate>2000</risdate><volume>68</volume><issue>2</issue><spage>145</spage><epage>156</epage><pages>145-156</pages><issn>0168-3659</issn><eissn>1873-4995</eissn><coden>JCREEC</coden><abstract>The sandwiched osmotic tablet system (SOTS), which is composed of a sandwiched osmotic tablet core surrounded by a cellulose acetate membrane with two orifices on both side surfaces, has been successfully prepared with the purpose of delivering nifedipine. The sandwiched osmotic tablet core consists of a middle push layer and two attached drug layers. Influences of tablet formulation variables, orifice size and membrane variables on nifedipine release of SOTS have been studied. It was found that potassium chloride amount of push layer and polyethylene oxide amount of drug layer had markedly positive effects on nifedipine release. A push layer/drug layer co-controlled osmotic delivery mechanism and the optimal core formulation have been proposed. The appropriate orifice size was observed in the range of 0.50–1.41 mm. It was also found that the drug release rate of SOTS could be increased by incorporating hydrophilic plasticizer in the membrane, whereas it decreased with hydrophobic plasticizer. It has been observed that the SOTS gives fairly comparable in vitro release features as that of commercialized push–pull osmotic tablet system, such as an approximately constant rate up to 24 h and independence of release media and agitation rate. Exempting side identification before drilling, it is easier to prepare the SOTS than the push–pull osmotic tablet system.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>10925123</pmid><doi>10.1016/S0168-3659(00)00243-1</doi><tpages>12</tpages></addata></record> |
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subjects | 24-Hour delivery Antihypertensive agents Biological and medical sciences Calcium Channel Blockers - administration & dosage Cardiovascular system Drug Delivery Systems General pharmacology Medical sciences Nifedipine Nifedipine - administration & dosage Nifedipine - chemistry Osmotic Pressure Osmotic pump Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Polyethylene Glycols - pharmacology Potassium Chloride - pharmacology Regression Analysis Sandwiched osmotic tablet system Tablets |
title | Nifedipine controlled delivery by sandwiched osmotic tablet system |
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