Dergiler / Turkish Journal of Chemistry / 2021 / Cilt: 45 - Sayı: 2

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

Sayfa
436–451
Yayın Tarihi
2021-04-28
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The findings show that nanoformulations have promising in vitro hepatoprotective effects on the THLE-2 cell line against ethanol exposure.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:To improve bioavailability and stability of hydrophobic and hydrophilic compounds, nanoemulsions are good alternatives as delivery systems because of their nontoxic and nonirritant nature.
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Temel Bulgular & Veri:Glutathione (GSH) suffers from low stability in water, where its encapsulation in nanoemulsions is a powerful strategy to its stability in aqueous systems.
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Sonuç & Katkı:The findings show that nanoformulations have promising in vitro hepatoprotective effects on the THLE-2 cell line against ethanol exposure.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Ethanol · Nigella sativa · glutathione

Abstract

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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Bu Makaleye Atıf Yap

YESİLTEPE, O., CELİK, E. G., GEYİK, C., GUMUS, Z. P., DEMİRKOL, D. O., COSKUNOL, H., TİMUR, S. (2021). Preparation of glutathione loaded nanoemulsions and testing of hepatoprotective activity on THLE-2 cells. Turkish Journal of Chemistry, Cilt: 45 - Sayı: 2, 436–451. https://ajindex.com/articles/198094

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Kaynakça (4)

  1. Ahmad Aftab, 2013, Asian Pacific Journal of Tropical Biomedicine, V3, P337, DOI 10.1016/S2221-1691(13)60075-1 Ali BH, 2003, PHYTOTHER RES, V17, P299, DOI 10.1002/ptr.1309 Araujo FA, 2011, EUR J PHARM SCI, V42, P238, DOI 10.1016/j.ejps.2010.11.014 Atta MB, 2003, FOOD CHEM, V83, P63, DOI 10.1016/S0308-8146(03)00038-4 Biswas A, 2012, AM J PHYSIOL-CELL PH, V302, pC203, DOI 10.1152/ajpcell.00283.2011 BLOIS MS, 1958,
  2. NATURE, V181, P1199, DOI 10.1038/1811199a0 Bourgou S, 2008, CR BIOL, V331, P48, DOI 10.1016/j.crvi.2007.11.001 Cai YZ, 2004, LIFE SCI, V74, P2157, DOI 10.1016/j.lfs.2003.09.047 Cameron RG, 1998, TOXICOL IN VITRO, V12, P111, DOI 10.1016/S0887-2333(97)00095-7 Cheikh-Rouhou S, 2007, FOOD CHEM, V101, P673, DOI 10.1016/j.foodchem.2006.02.022 Chong WT, 2018, PLOS ONE, V13, DOI 10.1371/journal.pone.0202771 Coelho JP, 2012,
  3. MOLECULES, V17, P10550, DOI 10.3390/molecules170910550 Da Porto C, 2012, IND CROP PROD, V36, P401, DOI 10.1016/j.indcrop.2011.09.015 Daems N, 2019, INT J NANOMED, V14, P4991, DOI 10.2147/IJN.S203546 European Medicines Agency (EMA), 1996, ICH TOP Q 2 B VAL AN Forman HJ, 2009, MOL ASPECTS MED, V30, P1, DOI 10.1016/j.mam.2008.08.006 Gao F, 2011, J CONTROL RELEASE, V149, P168, DOI 10.1016/j.jconrel.2010.10.013 Guler B, 2016, APPL NANOBIOMATER, V8, P209, DOI 10.1016/B978-0-323-41736-5.00007-8 Guler E, 2017, NANO STR MED, P51. Guler E, 2014, COLLOID SURFACE B, V121, P299, DOI 10.1016/j.colsurfb.2014.05.026 Gumus ZP, 2018, J FOOD MEAS CHARACT, V12, P1325, DOI 10.1007/s11694-018-9746-z Gumus ZP, 2015, COLLOID SURFACE B, V133, P73, DOI 10.1016/j.colsurfb.2015.05.044 Gunes A, 2017, J DRUG DELIV SCI TEC, V37, P158, DOI 10.1016/j.jddst.2016.12.013 Iimuro Y, 2000,
  4. HEPATOLOGY, V31, P391, DOI 10.1002/hep.510310219 Kade S., 2016, J CELLULAR BIOTECHNO, V1, P183 Khalife KH, 2007, FREE RADICAL RES, V41, P153, DOI 10.1080/10715760600978815 Khan NU, 2018, J COSMET SCI, V69, P257. Kirbay FO, 2017, COLLOID SURFACE B, V152, P289, DOI 10.1016/j.colsurfb.2017.01.006 Kizil G, 2008, PHARM BIOL, V46, P231, DOI 10.1080/13880200701739363 Kyffin JA, 2018, TOXICOL IN VITRO, V48, P262, DOI 10.1016/j.tiv.2018.01.023 Leu JG, 2012, NANOMED-NANOTECHNOL, V8, P767, DOI 10.1016/j.nano.2011.08.013 Li Y, 2004, APPL MICROBIOL BIOT, V66, P233, DOI 10.1007/s00253-004-1751-y Loguercio C, 1996, SCAND J CLIN LAB INV, V56, P441, DOI 10.3109/00365519609088799 Lutterodt H, 2010, LWT-FOOD SCI TECHNOL, V43, P1409, DOI 10.1016/j.lwt.2010.04.009 MEISTER A, 1988, J BIOL CHEM, V263, P17205 Mo