Macrophage membrane-biomimetic ROS-responsive platinum nanozyme clusters for acute kidney injury treatment
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Updated: Jul 21, 2026

Renal Ischaemia Reperfusion Injury: A Mouse Model of Injury and Regeneration
Published on: June 7, 2014
Hanzhi Deng1, Ying Qu1, Bingyang Chu1
1Department of Biotherapy and Department of Hematology, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, People's Republic of China.
Abstract:
Acute kidney injury (AKI) is a common clinical syndrome characterized by the rapid loss of renal filtration function. No standard therapeutic agent option is currently available. The development and progression of AKI is a continuous and dynamical pathological process. Oxidative stress and inflammatory responses are the primary influencing factors. Here, we developed a biomimetic nano-system (MM-PtNCs) with reactive oxygen species (ROS)-responsive platinum nanozyme clusters (PtNCs) wrapped in macrophage membrane (MM) to alleviate AKI by modulating oxidative stress and inflammation. The inflammatory cytokines receptors retained on MM surface allowed the biomimetic nano-system to target renal inflammation and neutralize these pro-inflammatory cytokines to ameliorate inflammation. PtNCs exhibit free radical scavenging-ability and catalase (CAT)-like activity to scavenge ROS and regulate the oxidative stress situations both in injured cells and tissues. Meanwhile, it could responsively dissociate into ultrasmall platinum nanoparticles under AKI-specific ROS conditions to eliminate ROS and eventually excreted through the renal filtration system. In a mouse model of ischemia/reperfusion-induced AKI, systemic injection of MM-PtNCs significantly reduced renal damage and restored kidney function. Additionally, MM-PtNCs effectively prevented the progression of AKI to chronic kidney disease. In conclusion, MM-PtNCs may propose a multi-faceted regulatory approach for clinical AKI treatment.
Insights
A novel biomimetic nano-system (MM-PtNCs) effectively treats acute kidney injury (AKI) by targeting inflammation and scavenging reactive oxygen species (ROS). This approach reduces kidney damage and prevents progression to chronic kidney disease.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Renal Physiology
Background:
- Acute kidney injury (AKI) is a prevalent condition with no effective treatments, characterized by rapid loss of kidney function.
- Oxidative stress and inflammation are key drivers in AKI development and progression.
- Current therapeutic options for AKI are limited.
Purpose of the Study:
- To develop and evaluate a novel biomimetic nano-system (MM-PtNCs) for alleviating AKI.
- To investigate the potential of MM-PtNCs in modulating oxidative stress and inflammation in AKI.
- To assess the efficacy of MM-PtNCs in preventing AKI progression to chronic kidney disease.
Main Methods:
- Development of a macrophage membrane (MM)-coated nano-system encapsulating reactive oxygen species (ROS)-responsive platinum nanozyme clusters (PtNCs).
- Utilizing the targeting and anti-inflammatory properties of macrophage membranes.
- Employing the ROS-scavenging and catalase-like activity of PtNCs for oxidative stress regulation.
- Evaluating MM-PtNCs in a mouse model of ischemia/reperfusion-induced AKI.
Main Results:
- Systemic injection of MM-PtNCs significantly reduced renal damage in a mouse AKI model.
- MM-PtNCs effectively restored kidney function.
- The nano-system demonstrated efficacy in preventing the progression of AKI to chronic kidney disease.
Conclusions:
- MM-PtNCs represent a promising multi-faceted therapeutic strategy for AKI.
- The biomimetic nano-system effectively targets renal inflammation and mitigates oxidative stress.
- This approach offers potential for clinical translation in AKI treatment.
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