Na. Hoenich et S. Stamp, Clinical investigation of the role of membrane structure on blood contact and solute transport characteristics of a cellulose membrane, BIOMATERIAL, 21(3), 2000, pp. 317-324
Regenerated cellulose membranes contain cellulose chains with crystalline a
nd amorphous regions in the direction of extrusion. A study was undertaken
to investigate if reduced contact surface arising from alteration of pore s
ize alters biocompatibility (complement activation (C3a and C5a) and neutro
penia) and solute transport. The average pore size for the membrane studied
(RC HP400A) was 7.23 compared to 2.76 nm for the standard membrane (Cuprop
han(R)). C3a levels rose to 6861 +/- 1595 compared to 2723 +/- 1228 ng/ml f
or Cuprophan(R) at 15 min after initial blood contact(P < 0.0001). C5a leve
ls also rose to 30.1 +/- 11.9 compared to 21.3 +/- 6.6 ng/ml for Cuprophan(
R) (P = 0.18). Both fractions gradually returned to baseline levels thereaf
ter. Circulating white cell count fell rapidly over the same time period to
39 +/- 17% of the baseline value by 15 min and was similar to Cuprophan(R)
(27.5 +/- 11.2%) (P = 0.25). A small (<10%) change in platelet numbers was
noted for both membranes. Removal of urea (60 Da) was independent of pore
size; however, the RC HP400A removed beta(2) microglobulin (11 818 Da). The
se findings indicate that pore distribution fails to influence material-ind
uced complement activation but influences large solute transport. (C) 1999
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