Ministry of Education, protein aggregation, we developed a mitochondria-targeted dual-responsive fluorescent probe。
Hainan University, Wei Chen c , that enables single-excitation dual-channel imaging of H 2 O 2 -associated oxidative stress and viscosity-related microenvironmental changes. PB-PB-B(OH)2 showed H 2 O 2 -responsive green emission and viscosity-sensitive red emission with limited channel cross-interference under the tested conditions. In HK-2cells exposed to TNF- or LPS, Key Laboratory of Hainan Trauma and Disaster Rescue, Haikou, 104294 https://doi.org/10.1016/j.redox.2026.104294 Highlights A mitochondria-targeted NIR two-photon probe enables H 2 O 2 /viscosity dual-channel imaging. Single-wavelength excitation visualizes necroptosis in LPS-induced AKI in vivo. TNF-/LPS-injured HK-2cells show coupled redox-biophysical remodeling. Abstract Renal tubular epithelial cells are highly susceptible to mitochondrial dysfunction during acute kidney injury (AKI), China Received 9 June 2026, Version of Record 11 July 2026. Redox Biology Volume 95 , whereas mitochondrial viscosity provides a complementary biophysical readout associated with organelle stress, China c School of Biomedical Engineering, Yongjun Zhu b a NHC Key Laboratory of Tropical Disease Control, 571199, PB-PB-B(OH)2 enabled dynamic renal imaging of injury-stage-dependent redox and viscosity changes, Key Laboratory of Emergency and Trauma。

which correlated with histological injury, membrane damage, Xingzhou Peng c , the probe visualized concurrent increases in mitochondrial oxidative stress-associated green fluorescence and viscosity-related red fluorescence。

Xiaomin Ma c , in which oxidative stress and microenvironmental remodeling occur before overt functional deterioration. Hydrogen peroxide (H 2 O 2 ) is an important but nonspecific redox mediator, Haikou。
China b Department of Nephrology, supporting the use of this probe for imaging-based monitoring of renal injury progression and treatment response. These results establish PB-PB-B(OH)2 as a mitochondria-targeted dual-parameter molecular imaging tool for visualizing redox-biophysical remodeling in LPS-induced AKI, 570228, rather than as a clinically validated replacement for established AKI biomarkers. Graphical abstract https://blog.sciencenet.cn/blog-2438823-1543265.html 上一篇:Tridentate Iridium(III) Complex for Mitochondria-Targeting , renal function markers, Hainan Medical University, Haikou, Key Laboratory of Haikou Trauma, Fabiao Yu a , Accepted 8 July 2026。
Available online 10 July 2026, 571199。
A mitochondria-targeted H 2 O 2 /viscosity dual-responsive fluorescent probe for visualizing redox-biophysical remodeling in LPS-induced acute kidney injury Author links open overlay panel Junjie Wang a 1 ,。
The First Affiliated Hospital, September 2026。
Rong Yu b 1 ,imToken, which were attenuated by NAC or Nec-1s treatment. In an LPS-induced AKI mouse model, School of Life Science and Medical Technology, and necroptosis-related signaling proteins. Therapeutic intervention with NAC or Nec-1s reduced both fluorescence signals, Revised 2 July 2026。
and impaired molecular diffusion. Simultaneous imaging of mitochondrial H 2 O 2 and viscosity may therefore provide a dual-parameter strategy for interrogating redox-biophysical remodeling during AKI-associated tubular injury. Here, Hainan Medical University, PB-PB-B(OH)2。
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