Investigation of dermal toxicity of ionic liquids in monolayer-cultured skin cells and 3D reconstructed human skin models

Jee hyun Hwang, Hyeonji Park, Dal Woong Choi, KiTaek Nam, Kyung Min Lim

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Ionic liquids have gained increasing attention in the chemical industry as potential green substitutes for traditional solvents. However, little is known about toxicity of ionic liquids on the skin, a major exposure portal to toxic substances. Here, we evaluated dermal toxicity of ionic liquids using human keratinocyte and fibroblast cell line, 3D reconstructed human epidermis, and full-thickness model to investigate underlying mechanisms. Cytotoxicity of ionic liquids was evaluated for representative anions, [TFSI], [PF6], [BF4], and [DCA], as well as for cations, [EMIM], [BMPY], [TBA] and [Zn], in human keratinocyte cell line, HaCaT, and human dermal fibroblasts. In our results, significant cytotoxicity was induced by ionic liquids with [TFSI] in both cell lines. Notably, cytotoxicity of [TFSI] containing ionic liquids was comparable to xylene, a toxic conventional organic solvent. Fluorescent and flow cytometric analysis revealed that [TFSI]-exposed cells underwent necrotic cell death. Reactive oxygen species (ROS) was increased while the amount of glutathione was decreased by [TFSI] in dose-dependent manner, which was reversed by antioxidant, N-acetylcysteine. In 3D reconstructed human epidermis and full-thickness model, a single application of [TFSI] induced toxicity although it was minimal and largely limited to epidermal layer. Collectively, these results demonstrated potential dermal toxicity of ionic liquids.

Original languageEnglish
Pages (from-to)194-202
Number of pages9
JournalToxicology in Vitro
Volume46
DOIs
Publication statusPublished - 2018 Feb 1

Fingerprint

Ionic Liquids
Toxicity
Cultured Cells
Monolayers
Skin
Cytotoxicity
Poisons
Cells
Fibroblasts
Keratinocytes
Epidermis
Cell Line
Chemical Industry
Xylenes
Acetylcysteine
Cell death
Chemical industry
Organic solvents
Anions
Glutathione

All Science Journal Classification (ASJC) codes

  • Toxicology

Cite this

Hwang, Jee hyun ; Park, Hyeonji ; Choi, Dal Woong ; Nam, KiTaek ; Lim, Kyung Min. / Investigation of dermal toxicity of ionic liquids in monolayer-cultured skin cells and 3D reconstructed human skin models. In: Toxicology in Vitro. 2018 ; Vol. 46. pp. 194-202.
@article{14ce35d8ab25418c9184f702775d14da,
title = "Investigation of dermal toxicity of ionic liquids in monolayer-cultured skin cells and 3D reconstructed human skin models",
abstract = "Ionic liquids have gained increasing attention in the chemical industry as potential green substitutes for traditional solvents. However, little is known about toxicity of ionic liquids on the skin, a major exposure portal to toxic substances. Here, we evaluated dermal toxicity of ionic liquids using human keratinocyte and fibroblast cell line, 3D reconstructed human epidermis, and full-thickness model to investigate underlying mechanisms. Cytotoxicity of ionic liquids was evaluated for representative anions, [TFSI], [PF6], [BF4], and [DCA], as well as for cations, [EMIM], [BMPY], [TBA] and [Zn], in human keratinocyte cell line, HaCaT, and human dermal fibroblasts. In our results, significant cytotoxicity was induced by ionic liquids with [TFSI] in both cell lines. Notably, cytotoxicity of [TFSI] containing ionic liquids was comparable to xylene, a toxic conventional organic solvent. Fluorescent and flow cytometric analysis revealed that [TFSI]-exposed cells underwent necrotic cell death. Reactive oxygen species (ROS) was increased while the amount of glutathione was decreased by [TFSI] in dose-dependent manner, which was reversed by antioxidant, N-acetylcysteine. In 3D reconstructed human epidermis and full-thickness model, a single application of [TFSI] induced toxicity although it was minimal and largely limited to epidermal layer. Collectively, these results demonstrated potential dermal toxicity of ionic liquids.",
author = "Hwang, {Jee hyun} and Hyeonji Park and Choi, {Dal Woong} and KiTaek Nam and Lim, {Kyung Min}",
year = "2018",
month = "2",
day = "1",
doi = "10.1016/j.tiv.2017.09.025",
language = "English",
volume = "46",
pages = "194--202",
journal = "Toxicology in Vitro",
issn = "0887-2333",
publisher = "Elsevier Limited",

}

Investigation of dermal toxicity of ionic liquids in monolayer-cultured skin cells and 3D reconstructed human skin models. / Hwang, Jee hyun; Park, Hyeonji; Choi, Dal Woong; Nam, KiTaek; Lim, Kyung Min.

In: Toxicology in Vitro, Vol. 46, 01.02.2018, p. 194-202.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Investigation of dermal toxicity of ionic liquids in monolayer-cultured skin cells and 3D reconstructed human skin models

AU - Hwang, Jee hyun

AU - Park, Hyeonji

AU - Choi, Dal Woong

AU - Nam, KiTaek

AU - Lim, Kyung Min

PY - 2018/2/1

Y1 - 2018/2/1

N2 - Ionic liquids have gained increasing attention in the chemical industry as potential green substitutes for traditional solvents. However, little is known about toxicity of ionic liquids on the skin, a major exposure portal to toxic substances. Here, we evaluated dermal toxicity of ionic liquids using human keratinocyte and fibroblast cell line, 3D reconstructed human epidermis, and full-thickness model to investigate underlying mechanisms. Cytotoxicity of ionic liquids was evaluated for representative anions, [TFSI], [PF6], [BF4], and [DCA], as well as for cations, [EMIM], [BMPY], [TBA] and [Zn], in human keratinocyte cell line, HaCaT, and human dermal fibroblasts. In our results, significant cytotoxicity was induced by ionic liquids with [TFSI] in both cell lines. Notably, cytotoxicity of [TFSI] containing ionic liquids was comparable to xylene, a toxic conventional organic solvent. Fluorescent and flow cytometric analysis revealed that [TFSI]-exposed cells underwent necrotic cell death. Reactive oxygen species (ROS) was increased while the amount of glutathione was decreased by [TFSI] in dose-dependent manner, which was reversed by antioxidant, N-acetylcysteine. In 3D reconstructed human epidermis and full-thickness model, a single application of [TFSI] induced toxicity although it was minimal and largely limited to epidermal layer. Collectively, these results demonstrated potential dermal toxicity of ionic liquids.

AB - Ionic liquids have gained increasing attention in the chemical industry as potential green substitutes for traditional solvents. However, little is known about toxicity of ionic liquids on the skin, a major exposure portal to toxic substances. Here, we evaluated dermal toxicity of ionic liquids using human keratinocyte and fibroblast cell line, 3D reconstructed human epidermis, and full-thickness model to investigate underlying mechanisms. Cytotoxicity of ionic liquids was evaluated for representative anions, [TFSI], [PF6], [BF4], and [DCA], as well as for cations, [EMIM], [BMPY], [TBA] and [Zn], in human keratinocyte cell line, HaCaT, and human dermal fibroblasts. In our results, significant cytotoxicity was induced by ionic liquids with [TFSI] in both cell lines. Notably, cytotoxicity of [TFSI] containing ionic liquids was comparable to xylene, a toxic conventional organic solvent. Fluorescent and flow cytometric analysis revealed that [TFSI]-exposed cells underwent necrotic cell death. Reactive oxygen species (ROS) was increased while the amount of glutathione was decreased by [TFSI] in dose-dependent manner, which was reversed by antioxidant, N-acetylcysteine. In 3D reconstructed human epidermis and full-thickness model, a single application of [TFSI] induced toxicity although it was minimal and largely limited to epidermal layer. Collectively, these results demonstrated potential dermal toxicity of ionic liquids.

UR - http://www.scopus.com/inward/record.url?scp=85031099821&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85031099821&partnerID=8YFLogxK

U2 - 10.1016/j.tiv.2017.09.025

DO - 10.1016/j.tiv.2017.09.025

M3 - Article

VL - 46

SP - 194

EP - 202

JO - Toxicology in Vitro

JF - Toxicology in Vitro

SN - 0887-2333

ER -