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Small molecule absorption by PDMS in the context of drug response bioassays
The polymer polydimethylsiloxane (PDMS) is widely used to build microfluidic devices compatible with cell culture. Whilst convenient in manufacture, PDMS has the disadvantage that it can absorb small molecules such as drugs. In microfluidic devices like “Organs-on-Chip”, designed to examine cell beh...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240851/ https://www.ncbi.nlm.nih.gov/pubmed/27856254 http://dx.doi.org/10.1016/j.bbrc.2016.11.062 |
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author | van Meer, B.J. de Vries, H. Firth, K.S.A. van Weerd, J. Tertoolen, L.G.J. Karperien, H.B.J. Jonkheijm, P. Denning, C. IJzerman, A.P. Mummery, C.L. |
author_facet | van Meer, B.J. de Vries, H. Firth, K.S.A. van Weerd, J. Tertoolen, L.G.J. Karperien, H.B.J. Jonkheijm, P. Denning, C. IJzerman, A.P. Mummery, C.L. |
author_sort | van Meer, B.J. |
collection | PubMed |
description | The polymer polydimethylsiloxane (PDMS) is widely used to build microfluidic devices compatible with cell culture. Whilst convenient in manufacture, PDMS has the disadvantage that it can absorb small molecules such as drugs. In microfluidic devices like “Organs-on-Chip”, designed to examine cell behavior and test the effects of drugs, this might impact drug bioavailability. Here we developed an assay to compare the absorption of a test set of four cardiac drugs by PDMS based on measuring the residual non-absorbed compound by High Pressure Liquid Chromatography (HPLC). We showed that absorption was variable and time dependent and not determined exclusively by hydrophobicity as claimed previously. We demonstrated that two commercially available lipophilic coatings and the presence of cells affected absorption. The use of lipophilic coatings may be useful in preventing small molecule absorption by PDMS. |
format | Online Article Text |
id | pubmed-5240851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-52408512017-01-25 Small molecule absorption by PDMS in the context of drug response bioassays van Meer, B.J. de Vries, H. Firth, K.S.A. van Weerd, J. Tertoolen, L.G.J. Karperien, H.B.J. Jonkheijm, P. Denning, C. IJzerman, A.P. Mummery, C.L. Biochem Biophys Res Commun Article The polymer polydimethylsiloxane (PDMS) is widely used to build microfluidic devices compatible with cell culture. Whilst convenient in manufacture, PDMS has the disadvantage that it can absorb small molecules such as drugs. In microfluidic devices like “Organs-on-Chip”, designed to examine cell behavior and test the effects of drugs, this might impact drug bioavailability. Here we developed an assay to compare the absorption of a test set of four cardiac drugs by PDMS based on measuring the residual non-absorbed compound by High Pressure Liquid Chromatography (HPLC). We showed that absorption was variable and time dependent and not determined exclusively by hydrophobicity as claimed previously. We demonstrated that two commercially available lipophilic coatings and the presence of cells affected absorption. The use of lipophilic coatings may be useful in preventing small molecule absorption by PDMS. Elsevier 2017-01-08 /pmc/articles/PMC5240851/ /pubmed/27856254 http://dx.doi.org/10.1016/j.bbrc.2016.11.062 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article van Meer, B.J. de Vries, H. Firth, K.S.A. van Weerd, J. Tertoolen, L.G.J. Karperien, H.B.J. Jonkheijm, P. Denning, C. IJzerman, A.P. Mummery, C.L. Small molecule absorption by PDMS in the context of drug response bioassays |
title | Small molecule absorption by PDMS in the context of drug response bioassays |
title_full | Small molecule absorption by PDMS in the context of drug response bioassays |
title_fullStr | Small molecule absorption by PDMS in the context of drug response bioassays |
title_full_unstemmed | Small molecule absorption by PDMS in the context of drug response bioassays |
title_short | Small molecule absorption by PDMS in the context of drug response bioassays |
title_sort | small molecule absorption by pdms in the context of drug response bioassays |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240851/ https://www.ncbi.nlm.nih.gov/pubmed/27856254 http://dx.doi.org/10.1016/j.bbrc.2016.11.062 |
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