More dialysis treatments have been performed with cellulose based memb
ranes than with any other material. As unmodified cellulose membranes
activate the complement system, much effort has been directed toward t
he development of noncomplement activating cellulose membranes. One su
ccessful approach was the substitution of -OH groups in the cellobiose
units of the cellulose molecule with tertiary amino groups, which res
ulted in a membrane called Hemophan. Synthetically modified cellulose
(SMC) is a new hemodialysis membrane made by specific chemical modific
ation whereby aromatic benzyl groups are covalently introduced into th
e cellulosic structure by ether bonds, creating hydrophobic domains wi
thin the overall hydrophilic cellulose surface: basic research investi
gations have shown that a characteristic hydrophobic-hydrophilic balan
ce of surfaces is a prerequisite for improved hemocompatibility. Sever
al cellulose modifications with aliphatic and aromatic groups were per
formed to achieve a membrane with the desired hemocompatibility profil
e; SMC, having hydrophobic benzyl groups, causes minimal activation of
blood complement, coagulation, and cell activation systems. In vitro
experiments with blood showed that C5a generation for SMC was reduced
by 94% relative to Cuprophan (compared with 96% for polysulphone, a sy
nthetic hemodialysis membrane). Activation of coagulation (formation o
f the thrombin-antithrombin III complex [TATI) in a clinical study sho
wed that SMC caused 16 ng/ml TAT generation compared with 36 ng/ml for
polysulphone. SMC, a low-flux cellulosic dialysis membrane, thus comb
ines the typically high diffusive performance characteristics of cellu
losic membranes with excellent hemocompatibility, matching synthetic d
ialysis membranes.