Validation of a Static Franz Diffusion Cell System for In Vitro Permeation Studies
Over the years, in vitro Franz diffusion experiments have evolved into one of the most important methods for researching transdermal drug administration. Unfortunately, this type of testing often yields permeation data that suffer from poor reproducibility. Moreover, this feature frequently occurs w...
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creator | Ng, Shiow-Fern Rouse, Jennifer J. Sanderson, Francis D. Meidan, Victor Eccleston, Gillian M. |
description | Over the years,
in vitro
Franz diffusion experiments have evolved into one of the most important methods for researching transdermal drug administration. Unfortunately, this type of testing often yields permeation data that suffer from poor reproducibility. Moreover, this feature frequently occurs when synthetic membranes are used as barriers, in which case biological tissue-associated variability has been removed as an artefact of total variation. The objective of the current study was to evaluate the influence of a full-validation protocol on the performance of a tailor-made array of Franz diffusion cells (GlaxoSmithKline, Harlow, UK) available in our laboratory. To this end, ibuprofen was used as a model hydrophobic drug while synthetic membranes were used as barriers. The parameters investigated included Franz cell dimensions, stirring conditions, membrane type, membrane treatment, temperature regulation and sampling frequency. It was determined that validation dramatically reduced derived data variability as the coefficient of variation for steady-state ibuprofen permeation from a gel formulation was reduced from 25.7% to 5.3% (
n
= 6). Thus, validation and refinement of the protocol combined with improved operator training can greatly enhance reproducibility in Franz cell experimentation. |
doi_str_mv | 10.1208/s12249-010-9522-9 |
format | Article |
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in vitro
Franz diffusion experiments have evolved into one of the most important methods for researching transdermal drug administration. Unfortunately, this type of testing often yields permeation data that suffer from poor reproducibility. Moreover, this feature frequently occurs when synthetic membranes are used as barriers, in which case biological tissue-associated variability has been removed as an artefact of total variation. The objective of the current study was to evaluate the influence of a full-validation protocol on the performance of a tailor-made array of Franz diffusion cells (GlaxoSmithKline, Harlow, UK) available in our laboratory. To this end, ibuprofen was used as a model hydrophobic drug while synthetic membranes were used as barriers. The parameters investigated included Franz cell dimensions, stirring conditions, membrane type, membrane treatment, temperature regulation and sampling frequency. It was determined that validation dramatically reduced derived data variability as the coefficient of variation for steady-state ibuprofen permeation from a gel formulation was reduced from 25.7% to 5.3% (
n
= 6). Thus, validation and refinement of the protocol combined with improved operator training can greatly enhance reproducibility in Franz cell experimentation.</description><identifier>ISSN: 1530-9932</identifier><identifier>EISSN: 1530-9932</identifier><identifier>DOI: 10.1208/s12249-010-9522-9</identifier><identifier>PMID: 20842539</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Absorption ; Administration, Cutaneous ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Biotechnology ; Drug Evaluation, Preclinical - instrumentation ; Equipment Design ; Equipment Failure Analysis ; Humans ; Indexing in process ; Membranes, Artificial ; Pharmacokinetics ; Pharmacology/Toxicology ; Pharmacy ; Research Article ; Sensitivity and Specificity ; Skin - metabolism ; Skin Absorption - physiology ; Skin, Artificial ; Transdermal Patch</subject><ispartof>AAPS PharmSciTech, 2010-09, Vol.11 (3), p.1432-1441</ispartof><rights>American Association of Pharmaceutical Scientists 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-fab7efa33effca99f141267d1a0ba07b40be54634e34a5bb94662f6cb36bc0353</citedby><cites>FETCH-LOGICAL-c540t-fab7efa33effca99f141267d1a0ba07b40be54634e34a5bb94662f6cb36bc0353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974154/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974154/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20842539$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ng, Shiow-Fern</creatorcontrib><creatorcontrib>Rouse, Jennifer J.</creatorcontrib><creatorcontrib>Sanderson, Francis D.</creatorcontrib><creatorcontrib>Meidan, Victor</creatorcontrib><creatorcontrib>Eccleston, Gillian M.</creatorcontrib><title>Validation of a Static Franz Diffusion Cell System for In Vitro Permeation Studies</title><title>AAPS PharmSciTech</title><addtitle>AAPS PharmSciTech</addtitle><addtitle>AAPS PharmSciTech</addtitle><description>Over the years,
in vitro
Franz diffusion experiments have evolved into one of the most important methods for researching transdermal drug administration. Unfortunately, this type of testing often yields permeation data that suffer from poor reproducibility. Moreover, this feature frequently occurs when synthetic membranes are used as barriers, in which case biological tissue-associated variability has been removed as an artefact of total variation. The objective of the current study was to evaluate the influence of a full-validation protocol on the performance of a tailor-made array of Franz diffusion cells (GlaxoSmithKline, Harlow, UK) available in our laboratory. To this end, ibuprofen was used as a model hydrophobic drug while synthetic membranes were used as barriers. The parameters investigated included Franz cell dimensions, stirring conditions, membrane type, membrane treatment, temperature regulation and sampling frequency. It was determined that validation dramatically reduced derived data variability as the coefficient of variation for steady-state ibuprofen permeation from a gel formulation was reduced from 25.7% to 5.3% (
n
= 6). Thus, validation and refinement of the protocol combined with improved operator training can greatly enhance reproducibility in Franz cell experimentation.</description><subject>Absorption</subject><subject>Administration, Cutaneous</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Biotechnology</subject><subject>Drug Evaluation, Preclinical - instrumentation</subject><subject>Equipment Design</subject><subject>Equipment Failure Analysis</subject><subject>Humans</subject><subject>Indexing in process</subject><subject>Membranes, Artificial</subject><subject>Pharmacokinetics</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Research Article</subject><subject>Sensitivity and Specificity</subject><subject>Skin - metabolism</subject><subject>Skin Absorption - physiology</subject><subject>Skin, Artificial</subject><subject>Transdermal Patch</subject><issn>1530-9932</issn><issn>1530-9932</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UctOAyEUJUbj-wPcGJZuRnlOZWNiqtUmTTRWuyUwhYqZGRQYk_r10kw1deMKbs7jwjkAnGB0jgm6vIiYECYKhFEhOCGF2AL7mNM8CUq2N-574CDGN4QIxYLugr0sZoRTsQ-eZqp2c5Wcb6G3UMFpykMFR0G1X_DGWdvFFTY0dQ2ny5hMA60PcNzCmUvBw0cTGtPrp6mbOxOPwI5VdTTH6_MQvIxun4f3xeThbjy8nhQVZygVVumBsYpSY22lhLCYYVIO5lghrdBAM6QNZyVlhjLFtRasLIktK01LXSHK6SG46n3fO92YeWXaFFQt34NrVFhKr5z8i7TuVS78pyRiwDBn2eBsbRD8R2diko2LVf6oao3vosSY8JzYJSaZintqFXyMwdjfNRjJVRey70LmLuSqCymy5nTzfb-Kn_AzgfSEmKF2YYJ8811oc2b_uH4DLrOVvA</recordid><startdate>20100901</startdate><enddate>20100901</enddate><creator>Ng, Shiow-Fern</creator><creator>Rouse, Jennifer J.</creator><creator>Sanderson, Francis D.</creator><creator>Meidan, Victor</creator><creator>Eccleston, Gillian M.</creator><general>Springer US</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20100901</creationdate><title>Validation of a Static Franz Diffusion Cell System for In Vitro Permeation Studies</title><author>Ng, Shiow-Fern ; Rouse, Jennifer J. ; Sanderson, Francis D. ; Meidan, Victor ; Eccleston, Gillian M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c540t-fab7efa33effca99f141267d1a0ba07b40be54634e34a5bb94662f6cb36bc0353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Absorption</topic><topic>Administration, Cutaneous</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Biotechnology</topic><topic>Drug Evaluation, Preclinical - instrumentation</topic><topic>Equipment Design</topic><topic>Equipment Failure Analysis</topic><topic>Humans</topic><topic>Indexing in process</topic><topic>Membranes, Artificial</topic><topic>Pharmacokinetics</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>Research Article</topic><topic>Sensitivity and Specificity</topic><topic>Skin - metabolism</topic><topic>Skin Absorption - physiology</topic><topic>Skin, Artificial</topic><topic>Transdermal Patch</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ng, Shiow-Fern</creatorcontrib><creatorcontrib>Rouse, Jennifer J.</creatorcontrib><creatorcontrib>Sanderson, Francis D.</creatorcontrib><creatorcontrib>Meidan, Victor</creatorcontrib><creatorcontrib>Eccleston, Gillian 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>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>AAPS PharmSciTech</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ng, Shiow-Fern</au><au>Rouse, Jennifer J.</au><au>Sanderson, Francis D.</au><au>Meidan, Victor</au><au>Eccleston, Gillian M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Validation of a Static Franz Diffusion Cell System for In Vitro Permeation Studies</atitle><jtitle>AAPS PharmSciTech</jtitle><stitle>AAPS PharmSciTech</stitle><addtitle>AAPS PharmSciTech</addtitle><date>2010-09-01</date><risdate>2010</risdate><volume>11</volume><issue>3</issue><spage>1432</spage><epage>1441</epage><pages>1432-1441</pages><issn>1530-9932</issn><eissn>1530-9932</eissn><abstract>Over the years,
in vitro
Franz diffusion experiments have evolved into one of the most important methods for researching transdermal drug administration. Unfortunately, this type of testing often yields permeation data that suffer from poor reproducibility. Moreover, this feature frequently occurs when synthetic membranes are used as barriers, in which case biological tissue-associated variability has been removed as an artefact of total variation. The objective of the current study was to evaluate the influence of a full-validation protocol on the performance of a tailor-made array of Franz diffusion cells (GlaxoSmithKline, Harlow, UK) available in our laboratory. To this end, ibuprofen was used as a model hydrophobic drug while synthetic membranes were used as barriers. The parameters investigated included Franz cell dimensions, stirring conditions, membrane type, membrane treatment, temperature regulation and sampling frequency. It was determined that validation dramatically reduced derived data variability as the coefficient of variation for steady-state ibuprofen permeation from a gel formulation was reduced from 25.7% to 5.3% (
n
= 6). Thus, validation and refinement of the protocol combined with improved operator training can greatly enhance reproducibility in Franz cell experimentation.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>20842539</pmid><doi>10.1208/s12249-010-9522-9</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Absorption Administration, Cutaneous Biochemistry Biomedical and Life Sciences Biomedicine Biotechnology Drug Evaluation, Preclinical - instrumentation Equipment Design Equipment Failure Analysis Humans Indexing in process Membranes, Artificial Pharmacokinetics Pharmacology/Toxicology Pharmacy Research Article Sensitivity and Specificity Skin - metabolism Skin Absorption - physiology Skin, Artificial Transdermal Patch |
title | Validation of a Static Franz Diffusion Cell System for In Vitro Permeation Studies |
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