PP-016 Effect of tacrolimus eye drops on human primary corneal epithelial cells

BackgroundEnsuring the safety of products made in pharmacy departments is an essential parameter in the development of any ophthalmic formulation.PurposeThe aim of this study was to show the cytotoxic effect of tacrolimus 0.03 mg/mL eye drops on human primary corneal epithelial cells using real time...

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Veröffentlicht in:European journal of hospital pharmacy. Science and practice 2017-03, Vol.24 (Suppl 1), p.A208-A210
Hauptverfasser: Fernández-Ferreiro, A, González-Barcia, M, Garcia-Quintanilla, L, Luaces, A, Díaz-Tome, V, Alonso-Rodriguez, I, Garcia-Otero, X, Lamas, M, Otero-Espinar, FJ
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container_end_page A210
container_issue Suppl 1
container_start_page A208
container_title European journal of hospital pharmacy. Science and practice
container_volume 24
creator Fernández-Ferreiro, A
González-Barcia, M
Garcia-Quintanilla, L
Luaces, A
Díaz-Tome, V
Alonso-Rodriguez, I
Garcia-Otero, X
Lamas, M
Otero-Espinar, FJ
description BackgroundEnsuring the safety of products made in pharmacy departments is an essential parameter in the development of any ophthalmic formulation.PurposeThe aim of this study was to show the cytotoxic effect of tacrolimus 0.03 mg/mL eye drops on human primary corneal epithelial cells using real time monitoring of dynamic changes based on bioimpedance measurements induced by cell–toxicant interactions.Material and methodsInitially, tacrolimus 0.03 mg/mL eye drops (TED) were prepared as a pharmaceutical compound in the department of pharmacy. The effect of the TED on the viability of cells was studied on ATCC normal human primary corneal epithelial cells. We used the xCELLigence real time cell analyser system (ACEA Biosciences, San Diego, California, USA) for monitoring the growth of cell cultures in real time. The cell index, based on the measured electric impedance across the cell culture, was used to represent the number of cells. 3000 cells/well (16 wells E-plates) were incubated for 20 hours. Subsequently, the original culture medium was aspirated and different TED concentrations (7.5 µg/mL, 15 µg/mL, 22 µg/mL, 30 µg/mL, 37 µg/mL and 45 µg/mL) were added to different wells. The results are represented as dose response curves versus time, and IC50 was calculated in different times.ResultsSurviving rate kinetic curves showed that TED induced a gradual decline in the cell surviving rate over a 20 hour exposure period. This behaviour suggests that TED cause significant corneal cellular toxicity. An analysis of the kinetic curve of the cell surviving rate showed that these effects were time and dose dependent. The IC50 at 30 min was 0.0139 mg/mL, at 4 hours 0.0125 mg/mL and at 16 hours 0.00836 mg/mL.ConclusionThese results may be particularly relevant to estimate the optimal TED concentration in clinical situations to avoid a toxic effect.References and/or acknowledgementsAcknowledgements: Fundación Mutua Madrileña and Fundación Española Farmacia Hospitalaria.No conflict of interest
doi_str_mv 10.1136/ejhpharm-2017-000640.463
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The effect of the TED on the viability of cells was studied on ATCC normal human primary corneal epithelial cells. We used the xCELLigence real time cell analyser system (ACEA Biosciences, San Diego, California, USA) for monitoring the growth of cell cultures in real time. The cell index, based on the measured electric impedance across the cell culture, was used to represent the number of cells. 3000 cells/well (16 wells E-plates) were incubated for 20 hours. Subsequently, the original culture medium was aspirated and different TED concentrations (7.5 µg/mL, 15 µg/mL, 22 µg/mL, 30 µg/mL, 37 µg/mL and 45 µg/mL) were added to different wells. The results are represented as dose response curves versus time, and IC50 was calculated in different times.ResultsSurviving rate kinetic curves showed that TED induced a gradual decline in the cell surviving rate over a 20 hour exposure period. This behaviour suggests that TED cause significant corneal cellular toxicity. An analysis of the kinetic curve of the cell surviving rate showed that these effects were time and dose dependent. The IC50 at 30 min was 0.0139 mg/mL, at 4 hours 0.0125 mg/mL and at 16 hours 0.00836 mg/mL.ConclusionThese results may be particularly relevant to estimate the optimal TED concentration in clinical situations to avoid a toxic effect.References and/or acknowledgementsAcknowledgements: Fundación Mutua Madrileña and Fundación Española Farmacia Hospitalaria.No conflict of interest</description><identifier>ISSN: 2047-9956</identifier><identifier>EISSN: 2047-9964</identifier><identifier>DOI: 10.1136/ejhpharm-2017-000640.463</identifier><language>eng</language><publisher>London: BMJ Publishing Group LTD</publisher><subject>Cornea ; Pharmacy ; Real time</subject><ispartof>European journal of hospital pharmacy. Science and practice, 2017-03, Vol.24 (Suppl 1), p.A208-A210</ispartof><rights>2017, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>Copyright: 2017 (c) 2017, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>2017 2017, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Fernández-Ferreiro, A</creatorcontrib><creatorcontrib>González-Barcia, M</creatorcontrib><creatorcontrib>Garcia-Quintanilla, L</creatorcontrib><creatorcontrib>Luaces, A</creatorcontrib><creatorcontrib>Díaz-Tome, V</creatorcontrib><creatorcontrib>Alonso-Rodriguez, I</creatorcontrib><creatorcontrib>Garcia-Otero, X</creatorcontrib><creatorcontrib>Lamas, M</creatorcontrib><creatorcontrib>Otero-Espinar, FJ</creatorcontrib><title>PP-016 Effect of tacrolimus eye drops on human primary corneal epithelial cells</title><title>European journal of hospital pharmacy. Science and practice</title><description>BackgroundEnsuring the safety of products made in pharmacy departments is an essential parameter in the development of any ophthalmic formulation.PurposeThe aim of this study was to show the cytotoxic effect of tacrolimus 0.03 mg/mL eye drops on human primary corneal epithelial cells using real time monitoring of dynamic changes based on bioimpedance measurements induced by cell–toxicant interactions.Material and methodsInitially, tacrolimus 0.03 mg/mL eye drops (TED) were prepared as a pharmaceutical compound in the department of pharmacy. The effect of the TED on the viability of cells was studied on ATCC normal human primary corneal epithelial cells. We used the xCELLigence real time cell analyser system (ACEA Biosciences, San Diego, California, USA) for monitoring the growth of cell cultures in real time. The cell index, based on the measured electric impedance across the cell culture, was used to represent the number of cells. 3000 cells/well (16 wells E-plates) were incubated for 20 hours. Subsequently, the original culture medium was aspirated and different TED concentrations (7.5 µg/mL, 15 µg/mL, 22 µg/mL, 30 µg/mL, 37 µg/mL and 45 µg/mL) were added to different wells. The results are represented as dose response curves versus time, and IC50 was calculated in different times.ResultsSurviving rate kinetic curves showed that TED induced a gradual decline in the cell surviving rate over a 20 hour exposure period. This behaviour suggests that TED cause significant corneal cellular toxicity. An analysis of the kinetic curve of the cell surviving rate showed that these effects were time and dose dependent. The IC50 at 30 min was 0.0139 mg/mL, at 4 hours 0.0125 mg/mL and at 16 hours 0.00836 mg/mL.ConclusionThese results may be particularly relevant to estimate the optimal TED concentration in clinical situations to avoid a toxic effect.References and/or acknowledgementsAcknowledgements: Fundación Mutua Madrileña and Fundación Española Farmacia Hospitalaria.No conflict of interest</description><subject>Cornea</subject><subject>Pharmacy</subject><subject>Real time</subject><issn>2047-9956</issn><issn>2047-9964</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kM1Kw0AUhQdRsNS-w4Dr1DtzkzuZpZT6AwUr6HqYTCYkJX9O0kV3bnxRn8SUVpeu7ll8nMP9GOMClkIg3fld2Zc2NJEEoSIAoBiWMeEFm0mIVaQ1xZd_OaFrthiGKoMEMdUx6hl73W4jEPT9-bUuCu9G3hV8tC50ddXsB-4Pnueh6wfetbzcN7blfagaGw7cdaH1tua-r8bS19UUna_r4YZdFbYe_OJ85-z9Yf22eoo2L4_Pq_tNlAkAGcnUClvkaSEs5Q5tprTwnqQC7aVyYEWqSGuVeyQil8oCUGFKOktSckrinN2eevvQfez9MJpdtw_tNGlkkkhFUuO_1DSAiFIpPVF4orJmZ84PGgHmKNn8SjZHyeYk2UyS8QcQq3CG</recordid><startdate>201703</startdate><enddate>201703</enddate><creator>Fernández-Ferreiro, A</creator><creator>González-Barcia, M</creator><creator>Garcia-Quintanilla, L</creator><creator>Luaces, A</creator><creator>Díaz-Tome, V</creator><creator>Alonso-Rodriguez, I</creator><creator>Garcia-Otero, X</creator><creator>Lamas, M</creator><creator>Otero-Espinar, FJ</creator><general>BMJ Publishing Group LTD</general><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>201703</creationdate><title>PP-016 Effect of tacrolimus eye drops on human primary corneal epithelial cells</title><author>Fernández-Ferreiro, A ; González-Barcia, M ; Garcia-Quintanilla, L ; Luaces, A ; Díaz-Tome, V ; Alonso-Rodriguez, I ; Garcia-Otero, X ; Lamas, M ; Otero-Espinar, FJ</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b1002-28a1afd8f1a6dc3ab791ee62709e27c0a1876997de3666c82f0373869b586c723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Cornea</topic><topic>Pharmacy</topic><topic>Real time</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fernández-Ferreiro, A</creatorcontrib><creatorcontrib>González-Barcia, M</creatorcontrib><creatorcontrib>Garcia-Quintanilla, L</creatorcontrib><creatorcontrib>Luaces, A</creatorcontrib><creatorcontrib>Díaz-Tome, V</creatorcontrib><creatorcontrib>Alonso-Rodriguez, I</creatorcontrib><creatorcontrib>Garcia-Otero, X</creatorcontrib><creatorcontrib>Lamas, M</creatorcontrib><creatorcontrib>Otero-Espinar, FJ</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</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><jtitle>European journal of hospital pharmacy. Science and practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fernández-Ferreiro, A</au><au>González-Barcia, M</au><au>Garcia-Quintanilla, L</au><au>Luaces, A</au><au>Díaz-Tome, V</au><au>Alonso-Rodriguez, I</au><au>Garcia-Otero, X</au><au>Lamas, M</au><au>Otero-Espinar, FJ</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PP-016 Effect of tacrolimus eye drops on human primary corneal epithelial cells</atitle><jtitle>European journal of hospital pharmacy. Science and practice</jtitle><date>2017-03</date><risdate>2017</risdate><volume>24</volume><issue>Suppl 1</issue><spage>A208</spage><epage>A210</epage><pages>A208-A210</pages><issn>2047-9956</issn><eissn>2047-9964</eissn><abstract>BackgroundEnsuring the safety of products made in pharmacy departments is an essential parameter in the development of any ophthalmic formulation.PurposeThe aim of this study was to show the cytotoxic effect of tacrolimus 0.03 mg/mL eye drops on human primary corneal epithelial cells using real time monitoring of dynamic changes based on bioimpedance measurements induced by cell–toxicant interactions.Material and methodsInitially, tacrolimus 0.03 mg/mL eye drops (TED) were prepared as a pharmaceutical compound in the department of pharmacy. The effect of the TED on the viability of cells was studied on ATCC normal human primary corneal epithelial cells. We used the xCELLigence real time cell analyser system (ACEA Biosciences, San Diego, California, USA) for monitoring the growth of cell cultures in real time. The cell index, based on the measured electric impedance across the cell culture, was used to represent the number of cells. 3000 cells/well (16 wells E-plates) were incubated for 20 hours. Subsequently, the original culture medium was aspirated and different TED concentrations (7.5 µg/mL, 15 µg/mL, 22 µg/mL, 30 µg/mL, 37 µg/mL and 45 µg/mL) were added to different wells. The results are represented as dose response curves versus time, and IC50 was calculated in different times.ResultsSurviving rate kinetic curves showed that TED induced a gradual decline in the cell surviving rate over a 20 hour exposure period. This behaviour suggests that TED cause significant corneal cellular toxicity. An analysis of the kinetic curve of the cell surviving rate showed that these effects were time and dose dependent. The IC50 at 30 min was 0.0139 mg/mL, at 4 hours 0.0125 mg/mL and at 16 hours 0.00836 mg/mL.ConclusionThese results may be particularly relevant to estimate the optimal TED concentration in clinical situations to avoid a toxic effect.References and/or acknowledgementsAcknowledgements: Fundación Mutua Madrileña and Fundación Española Farmacia Hospitalaria.No conflict of interest</abstract><cop>London</cop><pub>BMJ Publishing Group LTD</pub><doi>10.1136/ejhpharm-2017-000640.463</doi></addata></record>
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subjects Cornea
Pharmacy
Real time
title PP-016 Effect of tacrolimus eye drops on human primary corneal epithelial cells
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