Hemodialysis is a critical life-sustaining therapy for patients with end-stage renal disease (ESRD). However, its long-term efficacy is fundamentally constrained by the performance of dialysis membranes. Conventional polymeric membranes, primarily optimized for removing small solutes, are inadequate for clearing middle-molecular-weight and protein-bound uremic toxins (PBUTs), which drive chronic inflammation, cardiovascular dysfunction, and dialysis-related amyloidosis. Moreover, the hydrophobic nature and limited hemocompatibility of existing membranes often trigger immune activation, thrombogenesis, and fouling, compromising both treatment safety and patient comfort. This review provides a critical and integrative assessment of hemodialysis membrane technologies, bridging mechanistic transport theory with recent progress in advanced functional materials. Polymeric, inorganic, biomimetic, and mixed-matrix systems are systematically analyzed to elucidate how structure, surface chemistry, and nanostructure govern toxin selectivity, biostability, and blood compatibility. Emerging strategies, such as zwitterionic and heparin-mimetic coatings, nanomaterial-enabled hybrid architectures, and adsorption-diffusion coupling, are evaluated in relation to clinical scalability and regulatory readiness. Particular emphasis is placed on AI-assisted and data-driven membrane design, sustainable fabrication, and translational engineering as converging directions shaping next-generation dialysis materials. These perspectives collectively outline a roadmap toward safer, smarter, and more durable hemodialysis systems, advancing personalized and environmentally responsible renal replacement therapies.
Advanced Functional Materials in Kidney Dialysis: Progress, Challenges, and Clinical Prospects.
Brahim El Allaoui,Xinyun Wu,Tao Wu,C. Pang
Published 2025 in Advanced Healthcare Materials
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- Publication year
2025
- Venue
Advanced Healthcare Materials
- Publication date
2025-12-30
- Fields of study
Medicine, Materials Science
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Semantic Scholar, PubMed
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