Evidence map›Paper›PMID 42458570›Full record

ArticleParticle and fibre toxicology2026

Black phosphorus nanomaterials induce hepatic lipid metabolism disorders by triggering oxidative stress and mitochondrial dysfunction.

Sihao Zhu, Fengkai Ruan, Yan Zhang, Yucheng Leng, You Wu, Yuchen Sun, Chunyan Yang, Zhenghong Zuo, Shuzhen Chen

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In one paragraph

Article in Particle and fibre toxicology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Sihao Zhu *State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Endocrinology, Faculty of Medicine and Life Sciences, Xiang'an Hospital of Xiamen University, Xiamen University, Xiamen, 361102, China.
Fengkai Ruan *State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Endocrinology, Faculty of Medicine and Life Sciences, Xiang'an Hospital of Xiamen University, Xiamen University, Xiamen, 361102, China.
Yan ZhangState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Endocrinology, Faculty of Medicine and Life Sciences, Xiang'an Hospital of Xiamen University, Xiamen University, Xiamen, 361102, China.
Yucheng LengState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Endocrinology, Faculty of Medicine and Life Sciences, Xiang'an Hospital of Xiamen University, Xiamen University, Xiamen, 361102, China.
You WuState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Endocrinology, Faculty of Medicine and Life Sciences, Xiang'an Hospital of Xiamen University, Xiamen University, Xiamen, 361102, China.
Yuchen SunState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Endocrinology, Faculty of Medicine and Life Sciences, Xiang'an Hospital of Xiamen University, Xiamen University, Xiamen, 361102, China.
Chunyan YangState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Endocrinology, Faculty of Medicine and Life Sciences, Xiang'an Hospital of Xiamen University, Xiamen University, Xiamen, 361102, China.
Zhenghong ZuoState Key Laboratory of Cellular Stress Biology, School of Life Sciences, Department of Endocrinology, Faculty of Medicine and Life Sciences, Xiang'an Hospital of Xiamen University, Xiamen University, Xiamen, 361102, China. zuozhenghong@xmu.edu.cn.
Shuzhen ChenFujian Provincial Key Laboratory of Functional and Clinical Translational Medicine, School of Basic Medicine, Xiamen Medical College, Xiamen, 361023, China. csz@xmmc.edu.cn.

Funding

National Natural Science Foundation of China 32571506Natural Science Foundation of Xiamen Municipality 3502Z202573350
6 · The paper itself

Abstract

backgroundBlack phosphorus is the most stable allotrope of phosphorus and possesses a unique layered structure. Black phosphorus nanosheets and black phosphorus quantum dots are the two main forms of black phosphorus nanomaterials (BPNM). BPNM hold significant application potential across various fields, yet a comprehensive evaluation of their biosafety, particularly the impact on hepatic metabolism, remains insufficient. This study investigates the hepatotoxic effects and mechanisms induced by BPNM, with a focus on lipid metabolic disorders.

resultsFollowing a 28-day daily oral administration of black phosphorus quantum dots or black phosphorus nanosheets at doses of 0.1 and 1 mg/kg, mice exhibited reduced insulin sensitivity, increased inflammatory responses, decreased serum levels of triglycerides and very-low-density lipoprotein (VLDL), and exacerbated hepatic lipid accumulation. RNA-sequencing revealed that oxidative stress is a key contributor to BPNM-induced metabolic disruption, accompanied by severe mitochondrial dysfunction. Similarly, BPNM exposure also elevated intracellular reactive oxygen species (ROS), impaired mitochondrial respiratory function and ATP production, consequently disrupted VLDL assembly and secretion in AML12 hepatocyte line. Moreover, ROS scavenger and ATP supplementation restored mitochondrial function and triglycerides transport in vitro.

conclusionsFindings demonstrate that BPNM promote hepatic lipid accumulation possibly by triggering oxidative stress and impairing mitochondrial function, thereby interfering with lipid transport, and resulting in hepatic lipid accumulation. This study highlights the potential metabolic disruption risks of BPNM and provides critical insights for their biosafety assessment and sustainable application.

Indexed as

Lipid MetabolismLipid Metabolism DisordersLiverMitochondria, LiverNanostructuresOxidative StressPhosphorusQuantum DotsAnimalsCell LineHepatocytesMaleMiceMice, Inbred C57BLReactive Oxygen SpeciesPhosphorusReactive Oxygen SpeciesBlack phosphorusLipid metabolismLiverMitochondriaOxidative stress

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.