» Articles » PMID: 36828424

Adsorption- and Displacement-Based Approaches for the Removal of Protein-Bound Uremic Toxins

Overview
Journal Toxins (Basel)
Publisher MDPI
Specialty Toxicology
Date 2023 Feb 24
PMID 36828424
Authors
Affiliations
Soon will be listed here.
Abstract

End-stage renal disease (ESRD) patients rely on renal replacement therapies to survive. Hemodialysis (HD), the most widely applied treatment, is responsible for the removal of excess fluid and uremic toxins (UTs) from blood, particularly those with low molecular weight (MW < 500 Da). The development of high-flux membranes and more efficient treatment modes, such as hemodiafiltration, have resulted in improved removal rates of UTs in the middle molecular weight range. However, the concentrations of protein-bound uremic toxins (PBUTs) remain essentially untouched. Due to the high binding affinity to large proteins, such as albumin, PBUTs form large complexes (MW > 66 kDa) which are not removed during HD and their accumulation has been strongly associated with the increased morbidity and mortality of patients with ESRD. In this review, we describe adsorption- and displacement-based approaches currently being studied to enhance the removal of PBUTs. The development of mixed matrix membranes (MMMs) with selective adsorption properties, infusion of compounds capable of displacing UTs from their binding site on albumin, and competitive binding membranes show promising results, but the road to clinical application is still long, and further investigation is required.

Citing Articles

The Choice of Anti-Inflammatory Influences the Elimination of Protein-Bound Uremic Toxins.

Escudero-Saiz V, Cuadrado-Payan E, Rodriguez-Garcia M, Casals G, Rodas L, Fontsere N Toxins (Basel). 2024; 16(12).

PMID: 39728803 PMC: 11679929. DOI: 10.3390/toxins16120545.


Analysis of research trends and hotspots in the primary treatment of end-stage renal disease.

Shi L, Wang J, Wei T, Liang Z, Zhang L, Li C Int Urol Nephrol. 2024; .

PMID: 39589637 DOI: 10.1007/s11255-024-04290-4.


Displacing the Burden: A Review of Protein-Bound Uremic Toxin Clearance Strategies in Chronic Kidney Disease.

Sanchez-Ospina D, Mas-Fontao S, Gracia-Iguacel C, Avello A, Gonzalez de Rivera M, Mujika-Marticorena M J Clin Med. 2024; 13(5).

PMID: 38592263 PMC: 10934686. DOI: 10.3390/jcm13051428.


Focus on Mitochondrial Respiratory Chain: Potential Therapeutic Target for Chronic Renal Failure.

Wang Y, Yang J, Zhang Y, Zhou J Int J Mol Sci. 2024; 25(2).

PMID: 38256023 PMC: 10815764. DOI: 10.3390/ijms25020949.


Improving Structural Homogeneity, Hydraulic Permeability, and Mechanical Performance of Asymmetric Monophasic Cellulose Acetate/Silica Membranes: Spinodal Decomposition Mix.

Zare F, Goncalves S, Faria M, Goncalves M Membranes (Basel). 2023; 13(3).

PMID: 36984734 PMC: 10059883. DOI: 10.3390/membranes13030346.


References
1.
Ficheux A, Kerr P, Brunet P, Argiles A . The ultrafiltration coefficient of a dialyser (KUF) is not a fixed value, and it follows a parabolic function: the new concept of KUF max. Nephrol Dial Transplant. 2010; 26(2):636-40. DOI: 10.1093/ndt/gfq510. View

2.
Tao X, Thijssen S, Levin N, Kotanko P, Handelman G . Enhanced Indoxyl Sulfate Dialyzer Clearance with the Use of Binding Competitors. Blood Purif. 2015; 39(4):323-30. DOI: 10.1159/000381008. View

3.
Maduell F . Hemodiafiltration versus conventional hemodialysis: Should "conventional" be redefined?. Semin Dial. 2018; 31(6):625-632. DOI: 10.1111/sdi.12715. View

4.
Fasano M, Curry S, Terreno E, Galliano M, Fanali G, Narciso P . The extraordinary ligand binding properties of human serum albumin. IUBMB Life. 2006; 57(12):787-96. DOI: 10.1080/15216540500404093. View

5.
Ronco C, Brendolan A, Crepaldi C, Rodighiero M, Scabardi M . Blood and dialysate flow distributions in hollow-fiber hemodialyzers analyzed by computerized helical scanning technique. J Am Soc Nephrol. 2002; 13 Suppl 1:S53-61. View