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Influence of PEGylation of Vitamin-K-Loaded Mixed Micelles on the Uptake by and Transport through Caco-2 Cells
[Image: see text] The aim of the study is to investigate the uptake by and transport through Caco-2 cells of two mixed micelle formulations (based on egg phosphatidylcholine and glycocholic acid) of vitamin K, i.e., with and without DSPE-PEG2000. The uptake of vitamin K and fluorescently labeled mix...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical
Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150738/ https://www.ncbi.nlm.nih.gov/pubmed/30063364 http://dx.doi.org/10.1021/acs.molpharmaceut.8b00258 |
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author | Sun, Feilong Adrian, Max Beztsinna, Nataliia van den Dikkenberg, Joep B. Maas-Bakker, Roel F. van Hasselt, Peter M. van Steenbergen, Mies J. Su, Xiangjie Kapitein, Lukas C. Hennink, Wim E. van Nostrum, Cornelus F. |
author_facet | Sun, Feilong Adrian, Max Beztsinna, Nataliia van den Dikkenberg, Joep B. Maas-Bakker, Roel F. van Hasselt, Peter M. van Steenbergen, Mies J. Su, Xiangjie Kapitein, Lukas C. Hennink, Wim E. van Nostrum, Cornelus F. |
author_sort | Sun, Feilong |
collection | PubMed |
description | [Image: see text] The aim of the study is to investigate the uptake by and transport through Caco-2 cells of two mixed micelle formulations (based on egg phosphatidylcholine and glycocholic acid) of vitamin K, i.e., with and without DSPE-PEG2000. The uptake of vitamin K and fluorescently labeled mixed micelles with and without PEG coating showed similar kinetics and their uptake ratio remained constant over time. Together with the fact that an inhibitor of scavenger receptor B1 (BLT-1) decreased cellular uptake of vitamin K by ∼80% compared to the uptake in the absence of this inhibitor, we conclude that both types of micelles loaded with vitamin K can be taken up intactly by Caco-2 cells via this scavenger receptor. The amount of vitamin K in chylomicrons fraction from Caco-2 cell monolayers further indicates that mixed micelles (with or without PEGylation) are likely packed into chylomicrons after internalization by Caco-2 cells. Uptake of vitamin K from PEGylated mixed micelles increased four- to five-fold at simulated gastrointestinal conditions. In conclusion, PEGylated mixed micelles are stable upon exposure to simulated gastric conditions, and as a result, they do show overall a higher cellular uptake efficiency of vitamin K as compared to mixed micelles without PEG coating. |
format | Online Article Text |
id | pubmed-6150738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American
Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-61507382018-09-24 Influence of PEGylation of Vitamin-K-Loaded Mixed Micelles on the Uptake by and Transport through Caco-2 Cells Sun, Feilong Adrian, Max Beztsinna, Nataliia van den Dikkenberg, Joep B. Maas-Bakker, Roel F. van Hasselt, Peter M. van Steenbergen, Mies J. Su, Xiangjie Kapitein, Lukas C. Hennink, Wim E. van Nostrum, Cornelus F. Mol Pharm [Image: see text] The aim of the study is to investigate the uptake by and transport through Caco-2 cells of two mixed micelle formulations (based on egg phosphatidylcholine and glycocholic acid) of vitamin K, i.e., with and without DSPE-PEG2000. The uptake of vitamin K and fluorescently labeled mixed micelles with and without PEG coating showed similar kinetics and their uptake ratio remained constant over time. Together with the fact that an inhibitor of scavenger receptor B1 (BLT-1) decreased cellular uptake of vitamin K by ∼80% compared to the uptake in the absence of this inhibitor, we conclude that both types of micelles loaded with vitamin K can be taken up intactly by Caco-2 cells via this scavenger receptor. The amount of vitamin K in chylomicrons fraction from Caco-2 cell monolayers further indicates that mixed micelles (with or without PEGylation) are likely packed into chylomicrons after internalization by Caco-2 cells. Uptake of vitamin K from PEGylated mixed micelles increased four- to five-fold at simulated gastrointestinal conditions. In conclusion, PEGylated mixed micelles are stable upon exposure to simulated gastric conditions, and as a result, they do show overall a higher cellular uptake efficiency of vitamin K as compared to mixed micelles without PEG coating. American Chemical Society 2018-07-31 2018-09-04 /pmc/articles/PMC6150738/ /pubmed/30063364 http://dx.doi.org/10.1021/acs.molpharmaceut.8b00258 Text en Copyright © 2018 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 | Sun, Feilong Adrian, Max Beztsinna, Nataliia van den Dikkenberg, Joep B. Maas-Bakker, Roel F. van Hasselt, Peter M. van Steenbergen, Mies J. Su, Xiangjie Kapitein, Lukas C. Hennink, Wim E. van Nostrum, Cornelus F. Influence of PEGylation of Vitamin-K-Loaded Mixed Micelles on the Uptake by and Transport through Caco-2 Cells |
title | Influence of PEGylation of Vitamin-K-Loaded Mixed
Micelles on the Uptake by and Transport through Caco-2 Cells |
title_full | Influence of PEGylation of Vitamin-K-Loaded Mixed
Micelles on the Uptake by and Transport through Caco-2 Cells |
title_fullStr | Influence of PEGylation of Vitamin-K-Loaded Mixed
Micelles on the Uptake by and Transport through Caco-2 Cells |
title_full_unstemmed | Influence of PEGylation of Vitamin-K-Loaded Mixed
Micelles on the Uptake by and Transport through Caco-2 Cells |
title_short | Influence of PEGylation of Vitamin-K-Loaded Mixed
Micelles on the Uptake by and Transport through Caco-2 Cells |
title_sort | influence of pegylation of vitamin-k-loaded mixed
micelles on the uptake by and transport through caco-2 cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150738/ https://www.ncbi.nlm.nih.gov/pubmed/30063364 http://dx.doi.org/10.1021/acs.molpharmaceut.8b00258 |
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