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使用ARE-Nrf2荧光素酶角质形成细胞检测法评估金属氧化物纳米颗粒的皮肤致敏潜力。

Evaluation of the skin sensitization potential of metal oxide nanoparticles using the ARE-Nrf2 Luciferase KeratinoSens assay.

作者信息

Kim Sung-Hyun, Lee DongHan, Lee JinHee, Yang Jun-Young, Seok JiHyun, Jung Kikyung, Lee JongKwon

机构信息

Division of Toxicological Research, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Osong, Korea.

出版信息

Toxicol Res. 2021 Jan 1;37(2):277-284. doi: 10.1007/s43188-020-00071-0. eCollection 2021 Apr.


DOI:10.1007/s43188-020-00071-0
PMID:33868983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8007649/
Abstract

Numerous studies have reported the potential of chemicals for inducing skin sensitization; however, few studies have examined skin sensitization induced by nanomaterials. This study aimed to evaluate skin sensitization induced by metal oxide nanoparticles (NPs) using the ARE-Nrf2 Luciferase KeratinoSens™ assay. Seven different metal oxide NPs, including copper oxide, cobalt oxide, nickel oxide, titanium oxide, cerium oxide, iron oxide, and zinc oxide, were assessed on KeratinoSens™ cells. We selected an appropriate vehicle among three vehicles (DMSO, DW, and culture medium) by assessing the hydrodynamic size at vehicle selection process. Seven metal oxide NPs were analyzed, and their physicochemical properties, including hydrodynamic size, polydispersity, and zeta potential, were determined in the selected vehicle. Thereafter, we assessed the sensitization potential of the NPs using the ARE-Nrf2 Luciferase KeratinoSens™ assay. Copper oxide NPs induced a positive response, whereas cobalt oxide, nickel oxide, titanium oxide, cerium oxide, iron oxide, and zinc oxide NPs induced no response. These results suggest that the ARE-Nrf2 Luciferase KeratinoSens™ assay may be useful for evaluating the potential for skin sensitization induced by metal oxide NPs.

摘要

众多研究报告了化学物质诱导皮肤致敏的可能性;然而,很少有研究考察纳米材料诱导的皮肤致敏情况。本研究旨在使用ARE-Nrf2荧光素酶角质形成细胞敏感性检测法(ARE-Nrf2 Luciferase KeratinoSens™ assay)评估金属氧化物纳米颗粒(NPs)诱导的皮肤致敏情况。在KeratinoSens™细胞上评估了七种不同的金属氧化物纳米颗粒,包括氧化铜、氧化钴、氧化镍、氧化钛、氧化铈、氧化铁和氧化锌。在载体选择过程中,通过评估流体动力学尺寸,我们在三种载体(二甲基亚砜、去离子水和培养基)中选择了合适的载体。分析了七种金属氧化物纳米颗粒,并在所选载体中测定了它们的物理化学性质,包括流体动力学尺寸、多分散性和zeta电位。此后,我们使用ARE-Nrf2荧光素酶角质形成细胞敏感性检测法评估了纳米颗粒的致敏潜力。氧化铜纳米颗粒诱导了阳性反应,而氧化钴、氧化镍、氧化钛、氧化铈、氧化铁和氧化锌纳米颗粒未诱导反应。这些结果表明,ARE-Nrf2荧光素酶角质形成细胞敏感性检测法可能有助于评估金属氧化物纳米颗粒诱导皮肤致敏的潜力。

相似文献

[1]
Evaluation of the skin sensitization potential of metal oxide nanoparticles using the ARE-Nrf2 Luciferase KeratinoSens assay.

Toxicol Res. 2021-1-1

[2]
Flow cytometric evaluation of the potential of metal oxide nanoparticles for skin sensitization using 5-Bromo-2-deoxyuridine.

Toxicol Res. 2021-1-4

[3]
Copper and Cobalt Ions Released from Metal Oxide Nanoparticles Trigger Skin Sensitization.

Front Pharmacol. 2021-2-19

[4]
Evaluation of the Skin Sensitization Potential of Carbon Nanotubes Using Alternative In Vitro and In Vivo Assays.

Toxics. 2020-12-16

[5]
Gene expression changes induced by skin sensitizers in the KeratinoSens™ cell line: Discriminating Nrf2-dependent and Nrf2-independent events.

Toxicol In Vitro. 2013-9-20

[6]
Application of the KeratinoSens™ assay for assessing the skin sensitization potential of agrochemical active ingredients and formulations.

Regul Toxicol Pharmacol. 2015-7

[7]
A dataset on 145 chemicals tested in alternative assays for skin sensitization undergoing prevalidation.

J Appl Toxicol. 2013-11

[8]
Binary test battery with KeratinoSens™ and h-CLAT as part of a bottom-up approach for skin sensitization hazard prediction.

Regul Toxicol Pharmacol. 2017-8

[9]
Development of an artificial neural network model for risk assessment of skin sensitization using human cell line activation test, direct peptide reactivity assay, KeratinoSens™ and in silico structure alert parameter.

J Appl Toxicol. 2017-12-10

[10]
α-Sens: The improved ARE-Nrf2-based sensitization screening assay using normalized transcriptional activity.

Toxicology. 2020-4-23

引用本文的文献

[1]
Wisdom of Crowds for Supporting the Safety Evaluation of Nanomaterials.

Environ Sci Technol. 2025-7-29

[2]
Limitations and Modifications of Skin Sensitization NAMs for Testing Inorganic Nanomaterials.

Toxics. 2024-8-21

[3]
A convenient spectrophotometric test for screening skin-sensitizing chemicals using reactivity with glutathione .

Toxicol Res. 2023-12-13

[4]
Association of NRF2 with HIF-2α-induced cancer stem cell phenotypes in chronic hypoxic condition.

Redox Biol. 2023-4

[5]
Pre-validation of a reporter gene assay for oxidative stress for the rapid screening of nanobiomaterials.

Front Toxicol. 2022-9-5

[6]
Prediction of Skin Sensitization Potential of Silver and Zinc Oxide Nanoparticles Through the Human Cell Line Activation Test.

Front Toxicol. 2021-5-28

[7]
Copper and Cobalt Ions Released from Metal Oxide Nanoparticles Trigger Skin Sensitization.

Front Pharmacol. 2021-2-19

[8]
Evaluation of the Skin Sensitization Potential of Carbon Nanotubes Using Alternative In Vitro and In Vivo Assays.

Toxics. 2020-12-16

本文引用的文献

[1]
Evaluation of skin sensitization potential of chemicals by local lymph node assay using 5-bromo-2-deoxyuridine with flow cytometry.

Regul Toxicol Pharmacol. 2019-5-31

[2]
Surface Charge-Dependent Cellular Uptake of Polystyrene Nanoparticles.

Nanomaterials (Basel). 2018-12-10

[3]
Evaluation of immunoresponses and cytotoxicity from skin exposure to metallic nanoparticles.

Int J Nanomedicine. 2018-8-1

[4]
Differential Contribution of Constituent Metal Ions to the Cytotoxic Effects of Fast-Dissolving Metal-Oxide Nanoparticles.

Front Pharmacol. 2018-1-22

[5]
Immunological properties of gold nanoparticles.

Chem Sci. 2017-3-1

[6]
Allergic Responses Induced by the Immunomodulatory Effects of Nanomaterials upon Skin Exposure.

Front Immunol. 2017-2-16

[7]
Biopersistence and translocation to extrapulmonary organs of titanium dioxide nanoparticles after subacute inhalation exposure to aerosol in adult and elderly rats.

Toxicol Lett. 2017-1-4

[8]
Evaluation of the dose metric for acute lung inflammogenicity of fast-dissolving metal oxide nanoparticles.

Nanotoxicology. 2016-9-9

[9]
Application of the KeratinoSens™ assay for assessing the skin sensitization potential of agrochemical active ingredients and formulations.

Regul Toxicol Pharmacol. 2015-7

[10]
Nanoparticles skin absorption: New aspects for a safety profile evaluation.

Regul Toxicol Pharmacol. 2015-7

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