Effect of vehicle systems, pH and enhancers on the permeation of highly lipophilic aripiprazole from Carbopol 971P gel systems across human cadaver skin
The objective of this study was to investigate the effect of vehicle systems, pH and enhancers on the permeation of a highly lipophilic basic drug aripiprazole (ARPZ) through human cadaver skin. Solubility of ARPZ in single, binary, tertiary, and quaternary vehicle systems of N-methyl pyrrolidone (N...
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Veröffentlicht in: | Drug development and industrial pharmacy 2012-03, Vol.38 (3), p.323-330 |
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description | The objective of this study was to investigate the effect of vehicle systems, pH and enhancers on the permeation of a highly lipophilic basic drug aripiprazole (ARPZ) through human cadaver skin. Solubility of ARPZ in single, binary, tertiary, and quaternary vehicle systems of N-methyl pyrrolidone (NMP), dimethyl sulfoxide (DMSO), water, ethanol and isopropyl myristate (IPM) was studied. Gel formulations of 5% ARPZ were developed with 0.5% Carbopol 971P in quaternary vehicle systems consisting of NMP, DMSO, water and ethanol or IPM at optimum ratio of 40/40/5/15. The effect of pH of the gel formulations and fatty acids with different chain lengths on the permeation was studied. The flux of ARPZ from gel formulation with IPM and ethanol was comparable. A four fold increase in APRZ flux was observed when the pH of the gel systems was lowered from pH 8.2 to pH 6 or pH 7. For fatty acids, the order of flux is lauric acid > myristic acid > caprylic acid > oleic acid. In all the cases, in vitro permeation rate of ARPZ through human cadaver skin followed zero order kinetics. This study demonstrated that ARPZ in tertiary vehicle system of NMP/DMSO/water/IPM at ratio of 40/40/5/15 and gel system of Carbopol 971P with pH 7 is a promising candidate for transdermal delivery. |
doi_str_mv | 10.3109/03639045.2011.602978 |
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Solubility of ARPZ in single, binary, tertiary, and quaternary vehicle systems of N-methyl pyrrolidone (NMP), dimethyl sulfoxide (DMSO), water, ethanol and isopropyl myristate (IPM) was studied. Gel formulations of 5% ARPZ were developed with 0.5% Carbopol 971P in quaternary vehicle systems consisting of NMP, DMSO, water and ethanol or IPM at optimum ratio of 40/40/5/15. The effect of pH of the gel formulations and fatty acids with different chain lengths on the permeation was studied. The flux of ARPZ from gel formulation with IPM and ethanol was comparable. A four fold increase in APRZ flux was observed when the pH of the gel systems was lowered from pH 8.2 to pH 6 or pH 7. For fatty acids, the order of flux is lauric acid > myristic acid > caprylic acid > oleic acid. In all the cases, in vitro permeation rate of ARPZ through human cadaver skin followed zero order kinetics. This study demonstrated that ARPZ in tertiary vehicle system of NMP/DMSO/water/IPM at ratio of 40/40/5/15 and gel system of Carbopol 971P with pH 7 is a promising candidate for transdermal delivery.</description><identifier>ISSN: 0363-9045</identifier><identifier>EISSN: 1520-5762</identifier><identifier>DOI: 10.3109/03639045.2011.602978</identifier><identifier>PMID: 22067044</identifier><language>eng</language><publisher>England: Informa Healthcare</publisher><subject>Acrylates - chemistry ; Administration, Cutaneous ; Antipsychotic Agents - chemistry ; Antipsychotic Agents - pharmacokinetics ; Aripiprazole ; dimethyl sulfoxide ; Drug Delivery Systems ; fatty acids ; Fatty Acids - metabolism ; Gels - pharmacology ; Humans ; Hydrogen-Ion Concentration ; isopropyl myristate ; N-methyl pyrrolidone ; penetration enhancer ; Permeability ; Pharmaceutical Vehicles - pharmacology ; Piperazines - chemistry ; Piperazines - pharmacokinetics ; Psychotropic drug ; quaternary vehicle systems ; Quinolones - chemistry ; Quinolones - pharmacokinetics ; Skin - metabolism ; Skin Absorption ; stratum corneum ; transdermal delivery system</subject><ispartof>Drug development and industrial pharmacy, 2012-03, Vol.38 (3), p.323-330</ispartof><rights>2012 Informa Healthcare USA, Inc. 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c417t-fdcafcf85293687e3ec78e2f4db13025f5e65594db50bfe17e13fad9545d86ce3</citedby><cites>FETCH-LOGICAL-c417t-fdcafcf85293687e3ec78e2f4db13025f5e65594db50bfe17e13fad9545d86ce3</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/22067044$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hossain, Muhammed Anwar</creatorcontrib><creatorcontrib>Ahmed, Salah U.</creatorcontrib><creatorcontrib>Plakogiannis, Fotios M.</creatorcontrib><title>Effect of vehicle systems, pH and enhancers on the permeation of highly lipophilic aripiprazole from Carbopol 971P gel systems across human cadaver skin</title><title>Drug development and industrial pharmacy</title><addtitle>Drug Dev Ind Pharm</addtitle><description>The objective of this study was to investigate the effect of vehicle systems, pH and enhancers on the permeation of a highly lipophilic basic drug aripiprazole (ARPZ) through human cadaver skin. Solubility of ARPZ in single, binary, tertiary, and quaternary vehicle systems of N-methyl pyrrolidone (NMP), dimethyl sulfoxide (DMSO), water, ethanol and isopropyl myristate (IPM) was studied. Gel formulations of 5% ARPZ were developed with 0.5% Carbopol 971P in quaternary vehicle systems consisting of NMP, DMSO, water and ethanol or IPM at optimum ratio of 40/40/5/15. The effect of pH of the gel formulations and fatty acids with different chain lengths on the permeation was studied. The flux of ARPZ from gel formulation with IPM and ethanol was comparable. A four fold increase in APRZ flux was observed when the pH of the gel systems was lowered from pH 8.2 to pH 6 or pH 7. For fatty acids, the order of flux is lauric acid > myristic acid > caprylic acid > oleic acid. In all the cases, in vitro permeation rate of ARPZ through human cadaver skin followed zero order kinetics. This study demonstrated that ARPZ in tertiary vehicle system of NMP/DMSO/water/IPM at ratio of 40/40/5/15 and gel system of Carbopol 971P with pH 7 is a promising candidate for transdermal delivery.</description><subject>Acrylates - chemistry</subject><subject>Administration, Cutaneous</subject><subject>Antipsychotic Agents - chemistry</subject><subject>Antipsychotic Agents - pharmacokinetics</subject><subject>Aripiprazole</subject><subject>dimethyl sulfoxide</subject><subject>Drug Delivery Systems</subject><subject>fatty acids</subject><subject>Fatty Acids - metabolism</subject><subject>Gels - pharmacology</subject><subject>Humans</subject><subject>Hydrogen-Ion Concentration</subject><subject>isopropyl myristate</subject><subject>N-methyl pyrrolidone</subject><subject>penetration enhancer</subject><subject>Permeability</subject><subject>Pharmaceutical Vehicles - pharmacology</subject><subject>Piperazines - chemistry</subject><subject>Piperazines - pharmacokinetics</subject><subject>Psychotropic drug</subject><subject>quaternary vehicle systems</subject><subject>Quinolones - chemistry</subject><subject>Quinolones - pharmacokinetics</subject><subject>Skin - metabolism</subject><subject>Skin Absorption</subject><subject>stratum corneum</subject><subject>transdermal delivery system</subject><issn>0363-9045</issn><issn>1520-5762</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFv1DAQhS0EokvhHyDkGxey2E4cJxdQtSoUqRIc4GzNOuPGxYmDnRQtv4Sfi8N2kbj0NBrpe--N5hHykrNtyVn7lpV12bJKbgXjfFsz0armEdlwKVghVS0ek82KFCtzRp6ldMsYF62UT8mZEKxWrKo25PeltWhmGiy9w94ZjzQd0oxDekOnKwpjR3HsYTQYEw0jnXukE8YBYXZ5zbLe3fT-QL2bwtQ77wyF6CY3RfgVspuNYaA7iPswBU9bxb_QG_SnEAomhpRovwwwUgMd3GGk6bsbn5MnFnzCF_fznHz7cPl1d1Vcf_74aXdxXZiKq7mwnQFrbCNFW9aNwhKNalDYqtvzkglpJdZStnmVbG-RK-Slha6Vleya2mB5Tl4ffacYfiyYZj24ZNB7GDEsSbe8kapSSmSyOpJ_T45o9RTdAPGgOdNrJfpUiV4r0cdKsuzVfcCyH7D7Jzp1kIH3R8CNNsQBfoboOz3DwYdoY369S6v9gxHv_nPoEfzcG4iob8MSx_y_h2_8AzuKsSE</recordid><startdate>201203</startdate><enddate>201203</enddate><creator>Hossain, Muhammed Anwar</creator><creator>Ahmed, Salah U.</creator><creator>Plakogiannis, Fotios M.</creator><general>Informa Healthcare</general><general>Taylor & Francis</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>201203</creationdate><title>Effect of vehicle systems, pH and enhancers on the permeation of highly lipophilic aripiprazole from Carbopol 971P gel systems across human cadaver skin</title><author>Hossain, Muhammed Anwar ; Ahmed, Salah U. ; Plakogiannis, Fotios M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c417t-fdcafcf85293687e3ec78e2f4db13025f5e65594db50bfe17e13fad9545d86ce3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Acrylates - chemistry</topic><topic>Administration, Cutaneous</topic><topic>Antipsychotic Agents - chemistry</topic><topic>Antipsychotic Agents - pharmacokinetics</topic><topic>Aripiprazole</topic><topic>dimethyl sulfoxide</topic><topic>Drug Delivery Systems</topic><topic>fatty acids</topic><topic>Fatty Acids - metabolism</topic><topic>Gels - pharmacology</topic><topic>Humans</topic><topic>Hydrogen-Ion Concentration</topic><topic>isopropyl myristate</topic><topic>N-methyl pyrrolidone</topic><topic>penetration enhancer</topic><topic>Permeability</topic><topic>Pharmaceutical Vehicles - pharmacology</topic><topic>Piperazines - chemistry</topic><topic>Piperazines - pharmacokinetics</topic><topic>Psychotropic drug</topic><topic>quaternary vehicle systems</topic><topic>Quinolones - chemistry</topic><topic>Quinolones - pharmacokinetics</topic><topic>Skin - metabolism</topic><topic>Skin Absorption</topic><topic>stratum corneum</topic><topic>transdermal delivery system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hossain, Muhammed Anwar</creatorcontrib><creatorcontrib>Ahmed, Salah U.</creatorcontrib><creatorcontrib>Plakogiannis, Fotios M.</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 development and industrial pharmacy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hossain, Muhammed Anwar</au><au>Ahmed, Salah U.</au><au>Plakogiannis, Fotios M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of vehicle systems, pH and enhancers on the permeation of highly lipophilic aripiprazole from Carbopol 971P gel systems across human cadaver skin</atitle><jtitle>Drug development and industrial pharmacy</jtitle><addtitle>Drug Dev Ind Pharm</addtitle><date>2012-03</date><risdate>2012</risdate><volume>38</volume><issue>3</issue><spage>323</spage><epage>330</epage><pages>323-330</pages><issn>0363-9045</issn><eissn>1520-5762</eissn><abstract>The objective of this study was to investigate the effect of vehicle systems, pH and enhancers on the permeation of a highly lipophilic basic drug aripiprazole (ARPZ) through human cadaver skin. Solubility of ARPZ in single, binary, tertiary, and quaternary vehicle systems of N-methyl pyrrolidone (NMP), dimethyl sulfoxide (DMSO), water, ethanol and isopropyl myristate (IPM) was studied. Gel formulations of 5% ARPZ were developed with 0.5% Carbopol 971P in quaternary vehicle systems consisting of NMP, DMSO, water and ethanol or IPM at optimum ratio of 40/40/5/15. The effect of pH of the gel formulations and fatty acids with different chain lengths on the permeation was studied. The flux of ARPZ from gel formulation with IPM and ethanol was comparable. A four fold increase in APRZ flux was observed when the pH of the gel systems was lowered from pH 8.2 to pH 6 or pH 7. For fatty acids, the order of flux is lauric acid > myristic acid > caprylic acid > oleic acid. In all the cases, in vitro permeation rate of ARPZ through human cadaver skin followed zero order kinetics. This study demonstrated that ARPZ in tertiary vehicle system of NMP/DMSO/water/IPM at ratio of 40/40/5/15 and gel system of Carbopol 971P with pH 7 is a promising candidate for transdermal delivery.</abstract><cop>England</cop><pub>Informa Healthcare</pub><pmid>22067044</pmid><doi>10.3109/03639045.2011.602978</doi><tpages>8</tpages></addata></record> |
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subjects | Acrylates - chemistry Administration, Cutaneous Antipsychotic Agents - chemistry Antipsychotic Agents - pharmacokinetics Aripiprazole dimethyl sulfoxide Drug Delivery Systems fatty acids Fatty Acids - metabolism Gels - pharmacology Humans Hydrogen-Ion Concentration isopropyl myristate N-methyl pyrrolidone penetration enhancer Permeability Pharmaceutical Vehicles - pharmacology Piperazines - chemistry Piperazines - pharmacokinetics Psychotropic drug quaternary vehicle systems Quinolones - chemistry Quinolones - pharmacokinetics Skin - metabolism Skin Absorption stratum corneum transdermal delivery system |
title | Effect of vehicle systems, pH and enhancers on the permeation of highly lipophilic aripiprazole from Carbopol 971P gel systems across human cadaver skin |
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