A Comparison of Drug Transport in Pulmonary Absorption Models: Isolated Perfused rat Lungs, Respiratory Epithelial Cell Lines and Primary Cell Culture
Purpose To evaluate the ability of human airway epithelial cell layers and a simple rat isolated perfused lung (IPL) model to predict pulmonary drug absorption in rats in vivo . Method The permeability of seven compounds selected to possess a range of lipophilicity was measured in two airway cell li...
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creator | Bosquillon, Cynthia Madlova, Michaela Patel, Nilesh Clear, Nicola Forbes, Ben |
description | Purpose
To evaluate the ability of human airway epithelial cell layers and a simple rat isolated perfused lung (IPL) model to predict pulmonary drug absorption in rats
in vivo
.
Method
The permeability of seven compounds selected to possess a range of lipophilicity was measured in two airway cell lines (Calu-3 and 16HBE14o-), in normal human bronchial epithelial (NHBE) cells and using a simple isolated perfused lungs (IPL) technique. Data from the cell layers and
ex vivo
lungs were compared to published absorption rates from rat lungs measured
in vivo
.
Results
A strong relationship was observed between the logarithm of the
in vivo
absorption half-life and the absorption half-life in the IPL (
r
= 0.97; excluding formoterol). Good log-linear relationships were also found between the apparent first-order absorption rate
in vivo
and cell layer permeability with correlation coefficients of 0.92, 0.93, 0.91 in Calu-3, 16HBE14o- and NHBE cells, respectively.
Conclusion
The simple IPL technique provided a good prediction of drug absorption from the lungs, making it a useful method for empirical screening of drug absorption in the lungs. Permeability measurements were similar in all the respiratory epithelial cell models evaluated, with Calu-3 having the advantage for routine permeability screening purposes of being readily availability, robust and easy to culture. |
doi_str_mv | 10.1007/s11095-017-2251-y |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5736767</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A747438798</galeid><sourcerecordid>A747438798</sourcerecordid><originalsourceid>FETCH-LOGICAL-c603t-76459c552bb45b5cb2d02bf7aba6e0d9b1ef89fd8fd471afd03b7527ff14d8093</originalsourceid><addsrcrecordid>eNp1kl9v1SAYxhujccfpB_DGkHjjhZ1AoYAXJid16pJjXMxMvCO0hY6FQoXW5HwRP68cO-dmNFzw7_c88L55iuIpgicIQvYqIQQFLSFiJcYUlft7xQZRVpUCkq_3iw1kmJScEXRUPErpCkLIkSAPiyPMBSYci03xYwuaME4q2hQ8CAa8jcsALqLyaQpxBtaD88WNwau4B9s2hTjNNpMfQ69deg3OUnBq1j0419EsKS-imsFu8UN6CT7rNNm8D1l7Otn5UjurHGi0c2BnvU5A-ayMdjy4_zpuFjcvUT8uHhjlkn5yPR8XX96dXjQfyt2n92fNdld2NazmktWEio5S3LaEtrRrcQ9xa5hqVa1hL1qkDRem56YnDCnTw6plFDNjEOk5FNVx8Wb1nZZ21H2n_RyVk9P6JRmUlXdvvL2UQ_guc5drVrNs8OLaIIZvi06zHG3qciXK67AkmfsNqagxpxl9_hd6FZboc3mZYpxywgT8Qw3KaWm9Cfnd7mAqt4wwUnEmeKZO_kHl0evRdsFrY_P5HQFaBV0MKUVtbmpEUB7CJNcwyRwmeQiT3GfNs9vNuVH8Tk8G8AqkfOUHHW9V9F_Xn7sh12Q</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1978584790</pqid></control><display><type>article</type><title>A Comparison of Drug Transport in Pulmonary Absorption Models: Isolated Perfused rat Lungs, Respiratory Epithelial Cell Lines and Primary Cell Culture</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Bosquillon, Cynthia ; Madlova, Michaela ; Patel, Nilesh ; Clear, Nicola ; Forbes, Ben</creator><creatorcontrib>Bosquillon, Cynthia ; Madlova, Michaela ; Patel, Nilesh ; Clear, Nicola ; Forbes, Ben</creatorcontrib><description>Purpose
To evaluate the ability of human airway epithelial cell layers and a simple rat isolated perfused lung (IPL) model to predict pulmonary drug absorption in rats
in vivo
.
Method
The permeability of seven compounds selected to possess a range of lipophilicity was measured in two airway cell lines (Calu-3 and 16HBE14o-), in normal human bronchial epithelial (NHBE) cells and using a simple isolated perfused lungs (IPL) technique. Data from the cell layers and
ex vivo
lungs were compared to published absorption rates from rat lungs measured
in vivo
.
Results
A strong relationship was observed between the logarithm of the
in vivo
absorption half-life and the absorption half-life in the IPL (
r
= 0.97; excluding formoterol). Good log-linear relationships were also found between the apparent first-order absorption rate
in vivo
and cell layer permeability with correlation coefficients of 0.92, 0.93, 0.91 in Calu-3, 16HBE14o- and NHBE cells, respectively.
Conclusion
The simple IPL technique provided a good prediction of drug absorption from the lungs, making it a useful method for empirical screening of drug absorption in the lungs. Permeability measurements were similar in all the respiratory epithelial cell models evaluated, with Calu-3 having the advantage for routine permeability screening purposes of being readily availability, robust and easy to culture.</description><identifier>ISSN: 0724-8741</identifier><identifier>EISSN: 1573-904X</identifier><identifier>DOI: 10.1007/s11095-017-2251-y</identifier><identifier>PMID: 28924829</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Absorption ; Alveolar Epithelial Cells - metabolism ; Animal models ; Animals ; Biochemistry ; Biomedical and Life Sciences ; Biomedical Engineering and Bioengineering ; Biomedicine ; Cell culture ; Cell Line ; Cell lines ; Cells, Cultured ; Comparative analysis ; Correlation coefficients ; Epithelial cells ; Flight corridors ; Formoterol ; Humans ; Lipophilicity ; Lung - metabolism ; Lungs ; Male ; Medical Law ; Models, Biological ; Permeability ; Pharmacology/Toxicology ; Pharmacy ; Primary Cell Culture ; Radioactive half-life ; Rats ; Rats, Wistar ; Research Paper ; Respiratory tract ; Respiratory Tract Absorption ; Terbutaline</subject><ispartof>Pharmaceutical research, 2017-12, Vol.34 (12), p.2532-2540</ispartof><rights>The Author(s) 2017</rights><rights>COPYRIGHT 2017 Springer</rights><rights>Pharmaceutical Research is a copyright of Springer, (2017). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c603t-76459c552bb45b5cb2d02bf7aba6e0d9b1ef89fd8fd471afd03b7527ff14d8093</citedby><cites>FETCH-LOGICAL-c603t-76459c552bb45b5cb2d02bf7aba6e0d9b1ef89fd8fd471afd03b7527ff14d8093</cites><orcidid>0000-0001-8193-6107</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11095-017-2251-y$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11095-017-2251-y$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28924829$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bosquillon, Cynthia</creatorcontrib><creatorcontrib>Madlova, Michaela</creatorcontrib><creatorcontrib>Patel, Nilesh</creatorcontrib><creatorcontrib>Clear, Nicola</creatorcontrib><creatorcontrib>Forbes, Ben</creatorcontrib><title>A Comparison of Drug Transport in Pulmonary Absorption Models: Isolated Perfused rat Lungs, Respiratory Epithelial Cell Lines and Primary Cell Culture</title><title>Pharmaceutical research</title><addtitle>Pharm Res</addtitle><addtitle>Pharm Res</addtitle><description>Purpose
To evaluate the ability of human airway epithelial cell layers and a simple rat isolated perfused lung (IPL) model to predict pulmonary drug absorption in rats
in vivo
.
Method
The permeability of seven compounds selected to possess a range of lipophilicity was measured in two airway cell lines (Calu-3 and 16HBE14o-), in normal human bronchial epithelial (NHBE) cells and using a simple isolated perfused lungs (IPL) technique. Data from the cell layers and
ex vivo
lungs were compared to published absorption rates from rat lungs measured
in vivo
.
Results
A strong relationship was observed between the logarithm of the
in vivo
absorption half-life and the absorption half-life in the IPL (
r
= 0.97; excluding formoterol). Good log-linear relationships were also found between the apparent first-order absorption rate
in vivo
and cell layer permeability with correlation coefficients of 0.92, 0.93, 0.91 in Calu-3, 16HBE14o- and NHBE cells, respectively.
Conclusion
The simple IPL technique provided a good prediction of drug absorption from the lungs, making it a useful method for empirical screening of drug absorption in the lungs. Permeability measurements were similar in all the respiratory epithelial cell models evaluated, with Calu-3 having the advantage for routine permeability screening purposes of being readily availability, robust and easy to culture.</description><subject>Absorption</subject><subject>Alveolar Epithelial Cells - metabolism</subject><subject>Animal models</subject><subject>Animals</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering and Bioengineering</subject><subject>Biomedicine</subject><subject>Cell culture</subject><subject>Cell Line</subject><subject>Cell lines</subject><subject>Cells, Cultured</subject><subject>Comparative analysis</subject><subject>Correlation coefficients</subject><subject>Epithelial cells</subject><subject>Flight corridors</subject><subject>Formoterol</subject><subject>Humans</subject><subject>Lipophilicity</subject><subject>Lung - metabolism</subject><subject>Lungs</subject><subject>Male</subject><subject>Medical Law</subject><subject>Models, Biological</subject><subject>Permeability</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Primary Cell Culture</subject><subject>Radioactive half-life</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Research Paper</subject><subject>Respiratory tract</subject><subject>Respiratory Tract Absorption</subject><subject>Terbutaline</subject><issn>0724-8741</issn><issn>1573-904X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kl9v1SAYxhujccfpB_DGkHjjhZ1AoYAXJid16pJjXMxMvCO0hY6FQoXW5HwRP68cO-dmNFzw7_c88L55iuIpgicIQvYqIQQFLSFiJcYUlft7xQZRVpUCkq_3iw1kmJScEXRUPErpCkLIkSAPiyPMBSYci03xYwuaME4q2hQ8CAa8jcsALqLyaQpxBtaD88WNwau4B9s2hTjNNpMfQ69deg3OUnBq1j0419EsKS-imsFu8UN6CT7rNNm8D1l7Otn5UjurHGi0c2BnvU5A-ayMdjy4_zpuFjcvUT8uHhjlkn5yPR8XX96dXjQfyt2n92fNdld2NazmktWEio5S3LaEtrRrcQ9xa5hqVa1hL1qkDRem56YnDCnTw6plFDNjEOk5FNVx8Wb1nZZ21H2n_RyVk9P6JRmUlXdvvL2UQ_guc5drVrNs8OLaIIZvi06zHG3qciXK67AkmfsNqagxpxl9_hd6FZboc3mZYpxywgT8Qw3KaWm9Cfnd7mAqt4wwUnEmeKZO_kHl0evRdsFrY_P5HQFaBV0MKUVtbmpEUB7CJNcwyRwmeQiT3GfNs9vNuVH8Tk8G8AqkfOUHHW9V9F_Xn7sh12Q</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Bosquillon, Cynthia</creator><creator>Madlova, Michaela</creator><creator>Patel, Nilesh</creator><creator>Clear, Nicola</creator><creator>Forbes, Ben</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>C6C</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>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8193-6107</orcidid></search><sort><creationdate>20171201</creationdate><title>A Comparison of Drug Transport in Pulmonary Absorption Models: Isolated Perfused rat Lungs, Respiratory Epithelial Cell Lines and Primary Cell Culture</title><author>Bosquillon, Cynthia ; Madlova, Michaela ; Patel, Nilesh ; Clear, Nicola ; Forbes, Ben</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c603t-76459c552bb45b5cb2d02bf7aba6e0d9b1ef89fd8fd471afd03b7527ff14d8093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Absorption</topic><topic>Alveolar Epithelial Cells - metabolism</topic><topic>Animal models</topic><topic>Animals</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedical Engineering and Bioengineering</topic><topic>Biomedicine</topic><topic>Cell culture</topic><topic>Cell Line</topic><topic>Cell lines</topic><topic>Cells, Cultured</topic><topic>Comparative analysis</topic><topic>Correlation coefficients</topic><topic>Epithelial cells</topic><topic>Flight corridors</topic><topic>Formoterol</topic><topic>Humans</topic><topic>Lipophilicity</topic><topic>Lung - metabolism</topic><topic>Lungs</topic><topic>Male</topic><topic>Medical Law</topic><topic>Models, Biological</topic><topic>Permeability</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>Primary Cell Culture</topic><topic>Radioactive half-life</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Research Paper</topic><topic>Respiratory tract</topic><topic>Respiratory Tract Absorption</topic><topic>Terbutaline</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bosquillon, Cynthia</creatorcontrib><creatorcontrib>Madlova, Michaela</creatorcontrib><creatorcontrib>Patel, Nilesh</creatorcontrib><creatorcontrib>Clear, Nicola</creatorcontrib><creatorcontrib>Forbes, Ben</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bosquillon, Cynthia</au><au>Madlova, Michaela</au><au>Patel, Nilesh</au><au>Clear, Nicola</au><au>Forbes, Ben</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Comparison of Drug Transport in Pulmonary Absorption Models: Isolated Perfused rat Lungs, Respiratory Epithelial Cell Lines and Primary Cell Culture</atitle><jtitle>Pharmaceutical research</jtitle><stitle>Pharm Res</stitle><addtitle>Pharm Res</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>34</volume><issue>12</issue><spage>2532</spage><epage>2540</epage><pages>2532-2540</pages><issn>0724-8741</issn><eissn>1573-904X</eissn><abstract>Purpose
To evaluate the ability of human airway epithelial cell layers and a simple rat isolated perfused lung (IPL) model to predict pulmonary drug absorption in rats
in vivo
.
Method
The permeability of seven compounds selected to possess a range of lipophilicity was measured in two airway cell lines (Calu-3 and 16HBE14o-), in normal human bronchial epithelial (NHBE) cells and using a simple isolated perfused lungs (IPL) technique. Data from the cell layers and
ex vivo
lungs were compared to published absorption rates from rat lungs measured
in vivo
.
Results
A strong relationship was observed between the logarithm of the
in vivo
absorption half-life and the absorption half-life in the IPL (
r
= 0.97; excluding formoterol). Good log-linear relationships were also found between the apparent first-order absorption rate
in vivo
and cell layer permeability with correlation coefficients of 0.92, 0.93, 0.91 in Calu-3, 16HBE14o- and NHBE cells, respectively.
Conclusion
The simple IPL technique provided a good prediction of drug absorption from the lungs, making it a useful method for empirical screening of drug absorption in the lungs. Permeability measurements were similar in all the respiratory epithelial cell models evaluated, with Calu-3 having the advantage for routine permeability screening purposes of being readily availability, robust and easy to culture.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>28924829</pmid><doi>10.1007/s11095-017-2251-y</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-8193-6107</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Absorption Alveolar Epithelial Cells - metabolism Animal models Animals Biochemistry Biomedical and Life Sciences Biomedical Engineering and Bioengineering Biomedicine Cell culture Cell Line Cell lines Cells, Cultured Comparative analysis Correlation coefficients Epithelial cells Flight corridors Formoterol Humans Lipophilicity Lung - metabolism Lungs Male Medical Law Models, Biological Permeability Pharmacology/Toxicology Pharmacy Primary Cell Culture Radioactive half-life Rats Rats, Wistar Research Paper Respiratory tract Respiratory Tract Absorption Terbutaline |
title | A Comparison of Drug Transport in Pulmonary Absorption Models: Isolated Perfused rat Lungs, Respiratory Epithelial Cell Lines and Primary Cell Culture |
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