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. 2023 Apr 3:1–43. Online ahead of print. doi: 10.1007/s42765-023-00277-5

Table 1.

Basic membrane structure characteristics, main strengths and limitations of commercially available hemodialysis hollow-fiber membranes

Category Membrane name Basic membrane structure characteristics Main strengths and limitations References
Composition Structure Pore radius (Å) Wwall thickness (μm) Ultrafiltration coefficient (ml/hr/mmHg)
Cellulosic membrane (Unmodified) cuprophane membrane Cellulose Symmetric 21 5–17 Low-flux (3.8 -8.4) Negligible middle molecule removal, significant complement activation and leukopenia, only for standard hemodialysis [5658]
Cellulose triacetate membrane Cellulose triacetate Symmetric 58 ~ 78 15 Low- to high-flux (9.5–85.6) Minimal protein adsorption, attenuated complement activation, high antithrombotic performance, high phosphorus clearance, improved lipid metabolism [25, 5962]
Cellulose (di) acetate membrane Cellulose diacetate Symmetric NA 14–30 Low- to high-flux Improved biocompatibility and hydrophobicity vs cuprophane membrane, low middle molecule removal [24, 63]
Hemophan membrane Cellulose and diethylaminoethyl Symmetric 21 5–20 Low-flux Negligible middle molecule removal, improved biocompatibility and hydrophobicity vs cuprophane membrane, higher pro-inflammatory cytokine production than polyamide membrane, only for standard hemodialysis [24]
Cuprammonium rayon membrane Polyethylene and cellulose Asymmetric NA 9–26 Low- to high-flux (9–19) Improved biocompatibility and hydrophobicity vs cuprophane membrane, less platelet activation and higher albumin loss vs polysulfone membrane [15, 24, 64, 65]
Synthetic membrane AN69 membrane Copolymer of acrylonitrile and sodium methallyl sulfonate Symmetric 25–55 30 High-flux (19.42) With a specific hydrogel structure on its surface; bulk adsorption of low-molecular-weight proteins such as cytokines; decreased complement activation, platelet adhesion and activation; increased activation of kallikrein-kinase system, production of bradykinin, available for high-flux hemodialysis, hemodiafiltration, and hemofiltration [24, 66]
PAN membrane Copolymer of acrylonitrile, methacrylate and acrylic acid Asymmetric NA 19–55 High-flux (45–54) Yield of bradykinin, risk of allergic reactions higher than other synthesis membranes, sustained mild complement activation [15, 67]
PSF membrane Polysulfone, blending with polyvinylpyrrolidone or polyethylene glycol in most occasions Asymmetric NA 30–104 Low- to high-flux Meets solute and fluid removal needs in all therapy modalities (low and high throughput dialysis, in-line hemofiltration and hemofiltration), efficient endotoxin retaining capacity, significant intrinsic biocompatibility, low cytotoxicity, the most widely used dialysis membrane in routine hemodialysis, Optimal chemical and thermal stability for steam sterilization, Increased β2 macroglobulin clearance through advanced PSF-based Helixone® without any albumin loss [6, 24, 26]
PMMA membrane Isotactic and syndiotactic polymethylmethacrylate Asymmetric NA 20–40 Low- to high-flux Reduced complement activation compared to cuprophane membranes with increased removal of β2 microglobulin by adsorption, sustained mild complement activation, and unexpected slight leukopenia [10, 15, 24, 28]
PES membrane Polyethersulfone, blending with polyvinylpyrrolidone in most occasions Asymmetric NA 30–104 Low- to high-flux Meets solute and fluid removal needs in all therapy modalities (low and high throughput dialysis, in-line hemofiltration and hemofiltration), provides significant intrinsic biocompatibility, favorable chemical and thermal stability, allows for steam sterilization, and delivers dialysate uniformly through Diapes® [24, 30]
EVOH membrane Copolymer of ethylene and vinyl alcohol Symmetric NA 25–32 Low-flux (5.8–11.1) Smooth inner surface; few plasma protein adsorption; weak interactions with blood cells [24, 68]
MCO membrane Polyethersulfone, blending with polyvinylpyrrolidone Asymmetric 50 35 High-flux (48–59) Medium apertures, uniform distribution of pores, steep sieve curve and internal filtration–backfiltration mechanism, greater removal of middle-molecule toxins than conventional high-flux dialysis, insufficient removal of protein-bound and large-molecule uremic toxins and unwanted albumin loss [31, 33]
Bioactive membrane AN69ST membrane Copolymer of acrylonitrile and methallylsulfonate (AN69) coated with polyethyleneimine Symmetric NA 45 High-flux Lower surface charge, kallikrein-kinase system activation and high-molecular weight protein adsorption than AN69 membrane due to surface treatment technique with cationic polyethyleneimine, specific antithrombin III adsorption by binding to heparin coating, unique self-anticoagulant membrane for heparin-free dialysis [27, 69, 70]
HeprAN membrane Copolymer of acrylonitrile and methallylsulfonate (AN69) coated with polyethyleneimine and heparin Symmetric NA 45 High-flux Further superficial treatment by cationic polyethyleneimine polymer and grafting of heparin on the inner surface, specific antithrombin III adsorption by binding to heparin coating, unique self-anticoagulant membrane for heparin-free dialysis, effective endotoxin retention capacity [27, 69]
Vitamin-E coated membrane Cellulose-based or polysulfone-based membrane coated with vitamin-E NA NA NA Low- to high-flux Decreased oxidative stress, improved inflammation status and anemia, persistence of complement activation [15, 52, 55, 71, 72]