Evidence map›Paper›PMID 42559358›Full record

ArticleTheranostics2026

Surface-cleaned black phosphorus nanosheets chelate iron and rebalance the ferroptosis-immune axis in acute kidney injury.

Wan-Lin Tan, Jin-Ming Zhu, Xiao-Xiao Xu, Jing Jia, Rong-Yu Chen, Xiong Yu, Lu-Qun Liang, Yuan-Yuan Ruan, Fang-Fang Wang, Yu-Ting Chen and 8 more

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Article in Theranostics, 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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

18 authors.

Wan-Lin TanState Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Guizhou Medical University.
Jin-Ming ZhuSchool of Basic Medical Sciences, Guizhou Medical University, Guiyang 561113, China.
Xiao-Xiao XuDepartment of Pathophysiology, School of Basic Medical Sciences, Guizhou Medical University, Anshun, Guizhou 561113, China.
Jing JiaDepartment of Pathophysiology, School of Basic Medical Sciences, Guizhou Medical University, Anshun, Guizhou 561113, China.
Rong-Yu ChenDepartment of Pathophysiology, School of Basic Medical Sciences, Guizhou Medical University, Anshun, Guizhou 561113, China.
Xiong YuDepartment of Pathophysiology, School of Basic Medical Sciences, Guizhou Medical University, Anshun, Guizhou 561113, China.
Lu-Qun LiangDepartment of Pathophysiology, School of Basic Medical Sciences, Guizhou Medical University, Anshun, Guizhou 561113, China.
Yuan-Yuan RuanDepartment of Pathophysiology, School of Basic Medical Sciences, Guizhou Medical University, Anshun, Guizhou 561113, China.
Fang-Fang WangDepartment of Pathophysiology, School of Basic Medical Sciences, Guizhou Medical University, Anshun, Guizhou 561113, China.
Yu-Ting ChenDepartment of Pathophysiology, School of Basic Medical Sciences, Guizhou Medical University, Anshun, Guizhou 561113, China.
Yu-Lin PengDepartment of Pathophysiology, School of Basic Medical Sciences, Guizhou Medical University, Anshun, Guizhou 561113, China.
Jin PengDepartment of Pathophysiology, School of Basic Medical Sciences, Guizhou Medical University, Anshun, Guizhou 561113, China.
Dan WangDepartment of Pathophysiology, School of Basic Medical Sciences, Guizhou Medical University, Anshun, Guizhou 561113, China.
Ling-Ling LiuDepartment of Pathophysiology, School of Basic Medical Sciences, Guizhou Medical University, Anshun, Guizhou 561113, China.
Yao RanDepartment of Pathophysiology, School of Basic Medical Sciences, Guizhou Medical University, Anshun, Guizhou 561113, China.
Bing GuoState Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Guizhou Medical University.
Jian FengSchool of Basic Medical Sciences, Guizhou Medical University, Guiyang 561113, China.
Yuan-Yuan WangState Key Laboratory of Discovery and Utilization of Functional Components in Traditional Chinese Medicine, Guizhou Medical University.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rationale: Nanomaterials have been explored for acute kidney injury (AKI) therapy because of their ability to scavenge reactive oxygen species (ROS) and reduce oxidative stress. Black phosphorus nanosheets (BPNSs) show renoprotective potential, but spontaneous surface oxidation may weaken their redox activity and therapeutic efficacy. It remains unclear whether surface engineering can improve the biological activity of BPNSs and modulate ferroptosis and immune activation during AKI. Methods: Surface-cleaned BPNSs (sc-BPNSs) were prepared by hydrogen reduction and characterized. Fluorescence-labeled sc-BPNSs were used to examine biodistribution, and therapeutic efficacy was evaluated in mice with AKI. Results: Hydrogen reduction produced sc-BPNSs with reduced surface oxidation, stronger antioxidant activity, and improved renal accumulation. After intravenous administration, sc-BPNSs preferentially accumulated in injured kidneys, reduced ROS accumulation and lipid peroxidation, alleviated tubular injury, and improved renal function. Transcriptomic analysis showed that sc-BPNSs affected pathways related to oxidative stress, iron metabolism, and immune regulation. Mechanistically, sc-BPNSs restored iron homeostasis by sequestering labile iron and regulating transferrin receptor 1/2 (TFR1/TFR2) and ferroportin (FPN1), thereby suppressing ferroptosis Conclusions: sc-BPNSs protect against AKI by reducing oxidative stress, restoring iron homeostasis, suppressing ferroptosis, and modulating macrophage activation. These findings suggest that surface-cleaned BPNSs may provide a therapeutic approach for AKI by targeting both tubular ferroptosis and inflammatory amplification.

Indexed as

Acute Kidney InjuryFerroptosisIronIron Chelating AgentsNanostructuresPhosphorusAnimalsEpithelial CellsMacrophagesMaleMiceMice, Inbred C57BLOxidative StressReactive Oxygen SpeciesIronIron Chelating AgentsPhosphorusReactive Oxygen SpeciesAcute kidney injuryferroptosisiron homeostasismacrophage polarizationsurface-cleaned black phosphorus nanosheets

Identifiers

PMID42559358
PMCPMC13440469

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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.