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Strategies for Removal of Protein-Bound Uremic Toxins in Hemodialysis

  • Joost C. de Vries
  • , Joao G. Bras
  • , Geert M. de Vries
  • , Jeroen C. Vollenbroek
  • , Fokko P. Wieringa
  • , Joachim Jankowski
  • , Marianne C. Verhaar
  • , Dimitrios Stamatialis
  • , Rosalinde Masereeuw
  • , Karin G. F. Gerritsen*
  • *Corresponding author for this work

Research output: Contribution to journal(Systematic) Review articlepeer-review

Abstract

The removal of protein-bound uremic toxins (PBUTs) from the blood of kidney failure patients with conventional dialysis is limited. However, as their harmful effects and association with morbidity and mortality in dialysis patients are increasingly recognized, PBUTs have become important therapeutic targets. In this review, PBUT removal with current state-of-the-art dialysis technologies and future perspectives are discussed. Strategies to enhance PBUT clearance include methods that interfere with PBUT-albumin binding, such as chemical displacers, high ionic strength, pH changes, or electromagnetic fields, thereby increasing the free fraction available for dialysis. While these methods have shown promise in vitro, and some also in vivo, long-term safety data are lacking. PBUT removal can also be increased by adsorption, either directly via hemoperfusion, or indirectly, e.g., via sorbents incorporated in a mixed-matrix membrane or dissolved in the dialysate. In the kidney, PBUTs are secreted in the proximal tubules; hence, a cell-based bioartificial kidney (BAK) that secretes PBUTs is proposed as an add-on to current dialysis. Yet both PBUT adsorption strategies and, in particular, BAKs face considerable challenges in upscaling and mass production at acceptable costs. In conclusion, many novel technologies are under development, all requiring further (pre)clinical testing and upscaling before these strategies can be applied in the clinic.
Original languageEnglish
Article number57
Number of pages22
JournalToxins
Volume18
Issue number1
DOIs
Publication statusPublished - 22 Jan 2026

Keywords

  • protein-bound uremic toxins
  • renal replacement therapy
  • hemodialysis
  • adsorption
  • bioartificial kidney
  • tissue engineering
  • CHRONIC KIDNEY-DISEASE
  • HUMAN SERUM-ALBUMIN
  • FRACTIONATED PLASMA SEPARATION
  • RAPID EQUILIBRIUM DIALYSIS
  • P-CRESOL SULFATE
  • INDOXYL SULFATE
  • BIOARTIFICIAL KIDNEY
  • IONIC-STRENGTH
  • FATTY-ACIDS
  • IN-VITRO

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