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Lutein nanodisks protect human retinal pigment epithelial cells from UV light-induced damage
The hydrophobic carotenoid, lutein, was conferred with aqueous solubility upon formulation into reconstituted discoidal high density lipoprotein particles, termed lutein nanodisks (ND). When formulated with phosphatidylcholine (PC), apolipoprotein (apo) A-I and lutein (formulation ratio = 5 mg PC/2...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9851610/ https://www.ncbi.nlm.nih.gov/pubmed/36686279 http://dx.doi.org/10.3389/fnano.2022.955022 |
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author | Moschetti, Anthony Fox, Colin A. McGowen, Samuel Ryan, Robert O. |
author_facet | Moschetti, Anthony Fox, Colin A. McGowen, Samuel Ryan, Robert O. |
author_sort | Moschetti, Anthony |
collection | PubMed |
description | The hydrophobic carotenoid, lutein, was conferred with aqueous solubility upon formulation into reconstituted discoidal high density lipoprotein particles, termed lutein nanodisks (ND). When formulated with phosphatidylcholine (PC), apolipoprotein (apo) A-I and lutein (formulation ratio = 5 mg PC/2 mg apoA-I/1 mg lutein), lutein solubilization efficiency in phosphate buffered saline (PBS) was ~90%. The UV/Vis absorbance maxima for lutein ND in PBS were red shifted by 6–13 nm versus the corresponding lutein absorbance maxima in ethanol. FPLC gel filtration chromatography gave rise to a single major absorbance peak in the size range of ND. Incubation of cultured ARPE-19 cells with lutein ND resulted in lutein uptake, as determined by HPLC analysis of cell extracts. Compared to control incubations, ARPE-19 cells incubated with lutein ND were protected from UV light-induced loss of cell viability. Consistent with this, reactive oxygen species generation, induced by exposure to UV irradiation, was lower in lutein-enriched cells than in control cells. Thus, uptake of ND-associated lutein protects ARPE-19 cells from UV light-induced damage. Taken together, the data indicate ND provide an aqueous lutein delivery vehicle for biotechnological or therapeutic applications. |
format | Online Article Text |
id | pubmed-9851610 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-98516102023-01-19 Lutein nanodisks protect human retinal pigment epithelial cells from UV light-induced damage Moschetti, Anthony Fox, Colin A. McGowen, Samuel Ryan, Robert O. Front Nanotechnol Article The hydrophobic carotenoid, lutein, was conferred with aqueous solubility upon formulation into reconstituted discoidal high density lipoprotein particles, termed lutein nanodisks (ND). When formulated with phosphatidylcholine (PC), apolipoprotein (apo) A-I and lutein (formulation ratio = 5 mg PC/2 mg apoA-I/1 mg lutein), lutein solubilization efficiency in phosphate buffered saline (PBS) was ~90%. The UV/Vis absorbance maxima for lutein ND in PBS were red shifted by 6–13 nm versus the corresponding lutein absorbance maxima in ethanol. FPLC gel filtration chromatography gave rise to a single major absorbance peak in the size range of ND. Incubation of cultured ARPE-19 cells with lutein ND resulted in lutein uptake, as determined by HPLC analysis of cell extracts. Compared to control incubations, ARPE-19 cells incubated with lutein ND were protected from UV light-induced loss of cell viability. Consistent with this, reactive oxygen species generation, induced by exposure to UV irradiation, was lower in lutein-enriched cells than in control cells. Thus, uptake of ND-associated lutein protects ARPE-19 cells from UV light-induced damage. Taken together, the data indicate ND provide an aqueous lutein delivery vehicle for biotechnological or therapeutic applications. 2022 2022-08-15 /pmc/articles/PMC9851610/ /pubmed/36686279 http://dx.doi.org/10.3389/fnano.2022.955022 Text en https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Article Moschetti, Anthony Fox, Colin A. McGowen, Samuel Ryan, Robert O. Lutein nanodisks protect human retinal pigment epithelial cells from UV light-induced damage |
title | Lutein nanodisks protect human retinal pigment epithelial cells from UV light-induced damage |
title_full | Lutein nanodisks protect human retinal pigment epithelial cells from UV light-induced damage |
title_fullStr | Lutein nanodisks protect human retinal pigment epithelial cells from UV light-induced damage |
title_full_unstemmed | Lutein nanodisks protect human retinal pigment epithelial cells from UV light-induced damage |
title_short | Lutein nanodisks protect human retinal pigment epithelial cells from UV light-induced damage |
title_sort | lutein nanodisks protect human retinal pigment epithelial cells from uv light-induced damage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9851610/ https://www.ncbi.nlm.nih.gov/pubmed/36686279 http://dx.doi.org/10.3389/fnano.2022.955022 |
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