Effect of Pulmonary Inflammation by Surface Functionalization of Zinc Oxide Nanoparticles

Zinc oxide nanoparticles (ZnO NPs) are used in various industries such as food additives, cosmetics, and biomedical applications. In this study, we evaluated lung damage over time by three types of ZnO NPs (L-serine, citrate, and pristine) following the regulation of functional groups after a single...

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Main Authors: Ayoung Jung, Sung-Hyun Kim, Jun-Young Yang, Jayoung Jeong, Jong Kwon Lee, Jae-Ho Oh, Jin Hee Lee
Format: Article
Language:English
Published: MDPI AG 2021-12-01
Series:Toxics
Subjects:
Online Access:https://www.mdpi.com/2305-6304/9/12/336
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author Ayoung Jung
Sung-Hyun Kim
Jun-Young Yang
Jayoung Jeong
Jong Kwon Lee
Jae-Ho Oh
Jin Hee Lee
author_facet Ayoung Jung
Sung-Hyun Kim
Jun-Young Yang
Jayoung Jeong
Jong Kwon Lee
Jae-Ho Oh
Jin Hee Lee
author_sort Ayoung Jung
collection DOAJ
description Zinc oxide nanoparticles (ZnO NPs) are used in various industries such as food additives, cosmetics, and biomedical applications. In this study, we evaluated lung damage over time by three types of ZnO NPs (L-serine, citrate, and pristine) following the regulation of functional groups after a single intratracheal instillation to rats. The three types of ZnO NPs showed an acute inflammatory reaction with increased LDH and inflammatory cell infiltration in the alveoli 24 h after administration. Especially in treatment with L-serine, citrate ZnO NPs showed higher acute granulocytic inflammation and total protein induction than the pristine ZnO NPs at 24 h. The acute inflammatory reaction of the lungs recovered on day 30 with bronchoalveolar fibrosis. The concentrations of IL-4, 6, TNF-α, and eotaxin in the bronchoalveolar lavage fluid (BALF) decreased over time, and the levels of these inflammation indicators are consistent with the following inflammatory cell data and acute lung inflammation by ZnO NP. This study suggests that single inhalation exposure to functionalized ZnO NPs may cause acute lung injury with granulocytic inflammation. Although it can recover 30 days after exposure, acute pulmonary inflammation in surface functionalization means that additional studies of exposure limits are needed to protect the workers that produce it.
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spelling doaj.art-676f0cc803f64051a8bcd4aee8abd14b2023-11-23T10:49:48ZengMDPI AGToxics2305-63042021-12-0191233610.3390/toxics9120336Effect of Pulmonary Inflammation by Surface Functionalization of Zinc Oxide NanoparticlesAyoung Jung0Sung-Hyun Kim1Jun-Young Yang2Jayoung Jeong3Jong Kwon Lee4Jae-Ho Oh5Jin Hee Lee6Division of Toxicological Research, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Osong, Cheongju 28159, KoreaDivision of Toxicological Research, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Osong, Cheongju 28159, KoreaDivision of Toxicological Research, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Osong, Cheongju 28159, KoreaDivision of Toxicological Research, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Osong, Cheongju 28159, KoreaDivision of Toxicological Research, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Osong, Cheongju 28159, KoreaDivision of Toxicological Research, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Osong, Cheongju 28159, KoreaDivision of Toxicological Research, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety, Osong, Cheongju 28159, KoreaZinc oxide nanoparticles (ZnO NPs) are used in various industries such as food additives, cosmetics, and biomedical applications. In this study, we evaluated lung damage over time by three types of ZnO NPs (L-serine, citrate, and pristine) following the regulation of functional groups after a single intratracheal instillation to rats. The three types of ZnO NPs showed an acute inflammatory reaction with increased LDH and inflammatory cell infiltration in the alveoli 24 h after administration. Especially in treatment with L-serine, citrate ZnO NPs showed higher acute granulocytic inflammation and total protein induction than the pristine ZnO NPs at 24 h. The acute inflammatory reaction of the lungs recovered on day 30 with bronchoalveolar fibrosis. The concentrations of IL-4, 6, TNF-α, and eotaxin in the bronchoalveolar lavage fluid (BALF) decreased over time, and the levels of these inflammation indicators are consistent with the following inflammatory cell data and acute lung inflammation by ZnO NP. This study suggests that single inhalation exposure to functionalized ZnO NPs may cause acute lung injury with granulocytic inflammation. Although it can recover 30 days after exposure, acute pulmonary inflammation in surface functionalization means that additional studies of exposure limits are needed to protect the workers that produce it.https://www.mdpi.com/2305-6304/9/12/336nanoparticleszinc oxideintratracheal instillationbronchoalveolar lavageacute inflammation
spellingShingle Ayoung Jung
Sung-Hyun Kim
Jun-Young Yang
Jayoung Jeong
Jong Kwon Lee
Jae-Ho Oh
Jin Hee Lee
Effect of Pulmonary Inflammation by Surface Functionalization of Zinc Oxide Nanoparticles
Toxics
nanoparticles
zinc oxide
intratracheal instillation
bronchoalveolar lavage
acute inflammation
title Effect of Pulmonary Inflammation by Surface Functionalization of Zinc Oxide Nanoparticles
title_full Effect of Pulmonary Inflammation by Surface Functionalization of Zinc Oxide Nanoparticles
title_fullStr Effect of Pulmonary Inflammation by Surface Functionalization of Zinc Oxide Nanoparticles
title_full_unstemmed Effect of Pulmonary Inflammation by Surface Functionalization of Zinc Oxide Nanoparticles
title_short Effect of Pulmonary Inflammation by Surface Functionalization of Zinc Oxide Nanoparticles
title_sort effect of pulmonary inflammation by surface functionalization of zinc oxide nanoparticles
topic nanoparticles
zinc oxide
intratracheal instillation
bronchoalveolar lavage
acute inflammation
url https://www.mdpi.com/2305-6304/9/12/336
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