ReviewNanomedicine (London, England)2025
Emerging applications of nanotechnology in the treatment of acute kidney injury.
Review in Nanomedicine (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- Advances and perspectives of functional nanomaterials in scavenging reactive oxygen species for acute kidney injury.Bioactive materials · 2026Review
- Precision Nanomedicine for Renal Tubular Injury: From Passive Accumulation to Subcellular Targeting.International journal of nanomedicine · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
Acute kidney injury (AKI) is a life-threatening condition with high mortality rates and limited treatment options. Recent advances in nanotechnology offer transformative potential for AKI therapy by enabling targeted drug delivery, enhancing therapeutic bioavailability, and minimizing off-target effects. This review highlights the emerging applications of nanomedicine in AKI, focusing on 1) passive and active targeting strategies to optimize renal nanoparticle (NP) accumulation, including size-, charge-, and ligand-dependent approaches, 2) mechanism-based therapeutic innovations, such as antioxidant, anti-inflammatory, anti-apoptotic, and anti-ferroptotic nanotherapeutics, and 3) critical challenges in biocompatibility, biodistribution, scalability, and regulatory translation. A systematic literature search was conducted in PubMed and Google Scholar, focusing on studies published between 2015 and 2025. While preclinical studies demonstrate remarkable efficacy in mitigating AKI pathogenesis, significant hurdles still exist, including risks of NP toxicity, limited and variable filtration across the glomerular barrier, manufacturing reproducibility, and lack of standardized regulatory frameworks. We highlight cutting-edge solutions, such as dynamic targeting ligands, green synthesis methods, and organ-on-a-chip models, to bridge these gaps. By addressing these challenges, nanotechnology could revolutionize AKI management, offering precision therapies tailored to the molecular and cellular underpinnings of renal injury.
Indexed as
Identifiers
What Socratic holds
Registered trials
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 Socratic graph.