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核心技术专利:CN118964589B侵权必究
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Molecular mechanism of nanomaterials induced liver injury: A review.

作者信息

Das Sanjib Kumar, Sen Koushik, Ghosh Biswatosh, Ghosh Nabanita, Sinha Krishnendu, Sil Parames C

机构信息

Department of Zoology, Jhargram Raj College, Jhargram 721507, India.

Department of Zoology, Bidhannagar College, Kolkata 700064, India.

出版信息

World J Hepatol. 2024 Apr 27;16(4):566-600. doi: 10.4254/wjh.v16.i4.566.


DOI:10.4254/wjh.v16.i4.566
PMID:38689743
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11056894/
Abstract

The unique physicochemical properties inherent to nanoscale materials have unveiled numerous potential applications, spanning beyond the pharmaceutical and medical sectors into various consumer industries like food and cosmetics. Consequently, humans encounter nanomaterials through diverse exposure routes, giving rise to potential health considerations. Noteworthy among these materials are silica and specific metallic nanoparticles, extensively utilized in consumer products, which have garnered substantial attention due to their propensity to accumulate and induce adverse effects in the liver. This review paper aims to provide an exhaustive examination of the molecular mechanisms underpinning nanomaterial-induced hepatotoxicity, drawing insights from both and studies. Primarily, the most frequently observed manifestations of toxicity following the exposure of cells or animal models to various nanomaterials involve the initiation of oxidative stress and inflammation. Additionally, we delve into the existing models employed for evaluating the hepatotoxic effects of nanomaterials, emphasizing the persistent endeavors to advance and bolster the reliability of these models for nanotoxicology research.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c671/11056894/5359a608ab5b/WJH-16-566-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c671/11056894/8d4ebdaf6f96/WJH-16-566-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c671/11056894/57c72fa53e4e/WJH-16-566-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c671/11056894/5359a608ab5b/WJH-16-566-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c671/11056894/8d4ebdaf6f96/WJH-16-566-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c671/11056894/57c72fa53e4e/WJH-16-566-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c671/11056894/5359a608ab5b/WJH-16-566-g003.jpg

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Molecular mechanism of nanomaterials induced liver injury: A review.

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引用本文的文献

[1]
The Toxicological Profile of Active Pharmaceutical Ingredients-Containing Nanoparticles: Classification, Mechanistic Pathways, and Health Implications.

Pharmaceuticals (Basel). 2025-5-9

[2]
Nanoparticle Contrast Agents for Photon-Counting Computed Tomography: Recent Developments and Future Opportunities.

Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2025

[3]
Harnessing nanotechnology for cancer treatment.

Front Bioeng Biotechnol. 2025-1-20

[4]
Liver-targeting iron oxide nanoparticles and their complexes with plant extracts for biocompatibility.

Beilstein J Nanotechnol. 2024-12-11

[5]
Nanofillers in Novel Food Packaging Systems and Their Toxicity Issues.

Foods. 2024-6-26

本文引用的文献

[1]
Nickel Nanoparticles Induced Hepatotoxicity in Mice via Lipid-Metabolism-Dysfunction-Regulated Inflammatory Injury.

Molecules. 2023-7-30

[2]
Organic and inorganic nanomaterials: fabrication, properties and applications.

RSC Adv. 2023-5-5

[3]
Sustained oral intake of nano-iron oxide perturbs the gut-liver axis.

NanoImpact. 2023-4

[4]
Short term exposure to polystyrene nanoplastics in mice evokes self-regulation of glycolipid metabolism.

Ecotoxicol Environ Saf. 2023-5

[5]
Metal Oxides Nanoparticles: General Structural Description, Chemical, Physical, and Biological Synthesis Methods, Role in Pesticides and Heavy Metal Removal through Wastewater Treatment.

Molecules. 2023-3-30

[6]
Hepatic effect of subacute Fe O nanoparticles exposure in Sprague-Dawley rats by LC-MS/MS based lipidomics.

Biomed Chromatogr. 2023-6

[7]
TFEB coordinates autophagy and pyroptosis as hepatotoxicity responses to ZnO nanoparticles.

Sci Total Environ. 2023-3-20

[8]
Silica nanoparticles aggravated the metabolic associated fatty liver disease through disturbed amino acid and lipid metabolisms-mediated oxidative stress.

Redox Biol. 2023-2

[9]
Oxidative stress-related canonical pyroptosis pathway, as a target of liver toxicity triggered by zinc oxide nanoparticles.

J Hazard Mater. 2023-1-15

[10]
Hepatotoxicity and the role of the gut-liver axis in dogs after oral administration of zinc oxide nanoparticles.

Metallomics. 2022-11-1

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