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Preparation of glutathione loaded nanoemulsions and testing of hepatoprotective activity on THLE-2 cells

To improve bioavailability and stability of hydrophobic and hydrophilic compounds, nanoemulsions are good alternatives as delivery systems because of their nontoxic and nonirritant nature. Glutathione (GSH) suffers from low stability in water, where its encapsulation in nanoemulsions is a powerful s...

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Autores principales: YEŞİLTEPE, Ozan, GÜLER ÇELİK, Emine, GEYİK, Caner, GÜMÜŞ, Zinar Pınar, ODACI DEMİRKOL, Dilek, COŞKUNOL, Hakan, TİMUR, Suna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164205/
https://www.ncbi.nlm.nih.gov/pubmed/34104055
http://dx.doi.org/10.3906/kim-2007-54
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author YEŞİLTEPE, Ozan
GÜLER ÇELİK, Emine
GEYİK, Caner
GÜMÜŞ, Zinar Pınar
ODACI DEMİRKOL, Dilek
COŞKUNOL, Hakan
TİMUR, Suna
author_facet YEŞİLTEPE, Ozan
GÜLER ÇELİK, Emine
GEYİK, Caner
GÜMÜŞ, Zinar Pınar
ODACI DEMİRKOL, Dilek
COŞKUNOL, Hakan
TİMUR, Suna
author_sort YEŞİLTEPE, Ozan
collection PubMed
description To improve bioavailability and stability of hydrophobic and hydrophilic compounds, nanoemulsions are good alternatives as delivery systems because of their nontoxic and nonirritant nature. Glutathione (GSH) suffers from low stability in water, where its encapsulation in nanoemulsions is a powerful strategy to its stability in aqueous systems. The aim of this study was to obtain nanoemulsions from the hydrophobic/hydrophilic contents of N. sativa seed oil so as to improve GSH stability along with bioavailability of N. sativa seed oil. Then, the prepared nanoemulsions were tested for in vitro hepatoprotective activity against ethanol toxicity. To the best of our knowledge, there is no study on the test of nanoemulsions by the combination of Nigella sativa seed oils and GSH in hepatoprotective activity. Here, nanoemulsions with different contents were prepared using Nigella sativa seed oils. Content analyses and characterisation studies of prepared nanoemulsions were carried out. In order to investigate the protective effects against to ethanol exposure, THLE-2 cells were pretreated with nanoemulsions for 2 h with the maximum benign dose (0.5 mg/mL of nanoemulsions). Ethanol (400 mM) was introduced to pretreated cells and nontreated cells for 48- or 72-h periods, followed by cell viability assay was carried out. Fluorescence microscopy tests revealed the introduction of the nanoemulsions into THLE-2 cells. The findings show that nanoformulations have promising in vitro hepatoprotective effects on the THLE-2 cell line against ethanol exposure.
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spelling pubmed-81642052021-06-07 Preparation of glutathione loaded nanoemulsions and testing of hepatoprotective activity on THLE-2 cells YEŞİLTEPE, Ozan GÜLER ÇELİK, Emine GEYİK, Caner GÜMÜŞ, Zinar Pınar ODACI DEMİRKOL, Dilek COŞKUNOL, Hakan TİMUR, Suna Turk J Chem Article To improve bioavailability and stability of hydrophobic and hydrophilic compounds, nanoemulsions are good alternatives as delivery systems because of their nontoxic and nonirritant nature. Glutathione (GSH) suffers from low stability in water, where its encapsulation in nanoemulsions is a powerful strategy to its stability in aqueous systems. The aim of this study was to obtain nanoemulsions from the hydrophobic/hydrophilic contents of N. sativa seed oil so as to improve GSH stability along with bioavailability of N. sativa seed oil. Then, the prepared nanoemulsions were tested for in vitro hepatoprotective activity against ethanol toxicity. To the best of our knowledge, there is no study on the test of nanoemulsions by the combination of Nigella sativa seed oils and GSH in hepatoprotective activity. Here, nanoemulsions with different contents were prepared using Nigella sativa seed oils. Content analyses and characterisation studies of prepared nanoemulsions were carried out. In order to investigate the protective effects against to ethanol exposure, THLE-2 cells were pretreated with nanoemulsions for 2 h with the maximum benign dose (0.5 mg/mL of nanoemulsions). Ethanol (400 mM) was introduced to pretreated cells and nontreated cells for 48- or 72-h periods, followed by cell viability assay was carried out. Fluorescence microscopy tests revealed the introduction of the nanoemulsions into THLE-2 cells. The findings show that nanoformulations have promising in vitro hepatoprotective effects on the THLE-2 cell line against ethanol exposure. The Scientific and Technological Research Council of Turkey 2021-04-28 /pmc/articles/PMC8164205/ /pubmed/34104055 http://dx.doi.org/10.3906/kim-2007-54 Text en Copyright © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Article
YEŞİLTEPE, Ozan
GÜLER ÇELİK, Emine
GEYİK, Caner
GÜMÜŞ, Zinar Pınar
ODACI DEMİRKOL, Dilek
COŞKUNOL, Hakan
TİMUR, Suna
Preparation of glutathione loaded nanoemulsions and testing of hepatoprotective activity on THLE-2 cells
title Preparation of glutathione loaded nanoemulsions and testing of hepatoprotective activity on THLE-2 cells
title_full Preparation of glutathione loaded nanoemulsions and testing of hepatoprotective activity on THLE-2 cells
title_fullStr Preparation of glutathione loaded nanoemulsions and testing of hepatoprotective activity on THLE-2 cells
title_full_unstemmed Preparation of glutathione loaded nanoemulsions and testing of hepatoprotective activity on THLE-2 cells
title_short Preparation of glutathione loaded nanoemulsions and testing of hepatoprotective activity on THLE-2 cells
title_sort preparation of glutathione loaded nanoemulsions and testing of hepatoprotective activity on thle-2 cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164205/
https://www.ncbi.nlm.nih.gov/pubmed/34104055
http://dx.doi.org/10.3906/kim-2007-54
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