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Sorption of Cationic Surfactants to Artificial Cell Membranes: Comparing Phospholipid Bilayers with Monolayer Coatings and Molecular Simulations
[Image: see text] This study reports the distribution coefficient between phospholipid bilayer membranes and phosphate buffered saline (PBS) medium (D(MW,PBS)) for 19 cationic surfactants. The method used a sorbent dilution series with solid supported lipid membranes (SSLMs). The existing SSLM proto...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343551/ https://www.ncbi.nlm.nih.gov/pubmed/28187261 http://dx.doi.org/10.1021/acs.est.6b05662 |
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author | Timmer, Niels Droge, Steven T. J. |
author_facet | Timmer, Niels Droge, Steven T. J. |
author_sort | Timmer, Niels |
collection | PubMed |
description | [Image: see text] This study reports the distribution coefficient between phospholipid bilayer membranes and phosphate buffered saline (PBS) medium (D(MW,PBS)) for 19 cationic surfactants. The method used a sorbent dilution series with solid supported lipid membranes (SSLMs). The existing SSLM protocol, applying a 96 well plate setup, was adapted to use 1.5 mL glass autosampler vials instead, which facilitated sampling and circumvented several confounding loss processes for some of the cationic surfactants. About 1% of the phospholipids were found to be detached from the SSLM beads, resulting in nonlinear sorption isotherms for compounds with log D(MW) values above 4. Renewal of the medium resulted in linear sorption isotherms. D(MW) values determined at pH 5.4 demonstrated that cationic surfactant species account for the observed D(MW,PBS). Log D(MW,PBS) values above 5.5 are only experimentally feasible with lower LC-MS/MS detection limits and/or concentrated extracts of the aqueous samples. Based on the number of carbon atoms, dialkylamines showed a considerably lower sorption affinity than linear alkylamine analogues. These SSLM results closely overlapped with measurements on a chromatographic tool based on immobilized artificial membranes (IAM-HPLC) and with quantum-chemistry based calculations with COSMOmic. The SSLM data suggest that IAM-HPLC underestimates the D(MW) of ionized primary and secondary alkylamines by 0.8 and 0.5 log units, respectively. |
format | Online Article Text |
id | pubmed-5343551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-53435512017-03-10 Sorption of Cationic Surfactants to Artificial Cell Membranes: Comparing Phospholipid Bilayers with Monolayer Coatings and Molecular Simulations Timmer, Niels Droge, Steven T. J. Environ Sci Technol [Image: see text] This study reports the distribution coefficient between phospholipid bilayer membranes and phosphate buffered saline (PBS) medium (D(MW,PBS)) for 19 cationic surfactants. The method used a sorbent dilution series with solid supported lipid membranes (SSLMs). The existing SSLM protocol, applying a 96 well plate setup, was adapted to use 1.5 mL glass autosampler vials instead, which facilitated sampling and circumvented several confounding loss processes for some of the cationic surfactants. About 1% of the phospholipids were found to be detached from the SSLM beads, resulting in nonlinear sorption isotherms for compounds with log D(MW) values above 4. Renewal of the medium resulted in linear sorption isotherms. D(MW) values determined at pH 5.4 demonstrated that cationic surfactant species account for the observed D(MW,PBS). Log D(MW,PBS) values above 5.5 are only experimentally feasible with lower LC-MS/MS detection limits and/or concentrated extracts of the aqueous samples. Based on the number of carbon atoms, dialkylamines showed a considerably lower sorption affinity than linear alkylamine analogues. These SSLM results closely overlapped with measurements on a chromatographic tool based on immobilized artificial membranes (IAM-HPLC) and with quantum-chemistry based calculations with COSMOmic. The SSLM data suggest that IAM-HPLC underestimates the D(MW) of ionized primary and secondary alkylamines by 0.8 and 0.5 log units, respectively. American Chemical Society 2017-02-10 2017-03-07 /pmc/articles/PMC5343551/ /pubmed/28187261 http://dx.doi.org/10.1021/acs.est.6b05662 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Timmer, Niels Droge, Steven T. J. Sorption of Cationic Surfactants to Artificial Cell Membranes: Comparing Phospholipid Bilayers with Monolayer Coatings and Molecular Simulations |
title | Sorption
of Cationic Surfactants to Artificial Cell Membranes: Comparing Phospholipid
Bilayers with Monolayer Coatings and Molecular Simulations |
title_full | Sorption
of Cationic Surfactants to Artificial Cell Membranes: Comparing Phospholipid
Bilayers with Monolayer Coatings and Molecular Simulations |
title_fullStr | Sorption
of Cationic Surfactants to Artificial Cell Membranes: Comparing Phospholipid
Bilayers with Monolayer Coatings and Molecular Simulations |
title_full_unstemmed | Sorption
of Cationic Surfactants to Artificial Cell Membranes: Comparing Phospholipid
Bilayers with Monolayer Coatings and Molecular Simulations |
title_short | Sorption
of Cationic Surfactants to Artificial Cell Membranes: Comparing Phospholipid
Bilayers with Monolayer Coatings and Molecular Simulations |
title_sort | sorption
of cationic surfactants to artificial cell membranes: comparing phospholipid
bilayers with monolayer coatings and molecular simulations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343551/ https://www.ncbi.nlm.nih.gov/pubmed/28187261 http://dx.doi.org/10.1021/acs.est.6b05662 |
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