ArticleJournal of nanobiotechnology2025
Injured renal cell membrane encapsulated ICG/CORM-401 for homologous targeted NIR theranostics of acute kidney injury.
Article in Journal of nanobiotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Advances in Biomimetic Cell Membrane Nanoplatforms for Renal-Targeted Theranostics: From Pathophysiological Basis to Membrane-Stratified Design.International journal of nanomedicine · 2026Review
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Authors and funding
12 authors.
Funding
Abstract
Acute kidney injury (AKI) is frequently attributed to the lack of effective early diagnosis and incorrect timing for treatment, resulting in a high incidence rate and mortality. Currently, there is no precise clinical treatment available for AKI. In this study, we developed a good approach utilizing injured renal cell membrane-coated ICG/CORM-401 nanosystem (IRICP), which can specifically target to the injured kidney site through homologous targeting of the injured renal cell membrane. Through in vivo experiments, we demonstrated that indocyanine green (ICG), acting as a near-infrared (NIR) contrast agent, enables clear visualization of its distribution using fluorescence imaging and photoacoustic imaging (PAI) techniques. The addition of CORM-401 effectively mitigates AKI-induced oxidative stress by consuming reactive oxygen species and generating carbon monoxide for anti-inflammatory, anti-apoptotic, and anti-oxidative effects, thereby effectively inhibiting the progression of AKI and facilitating its recovery. In conclusion, this targeted theranostic strategy presents high efficiency and promise potential for the future clinical treatment of AKI.
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