Bowry S K, Rintelen T H
Akzo Nobel Central Research, GmBH, Obernburg, Germany.
ASAIO J. 1998 Sep-Oct;44(5):M579-83. doi: 10.1097/00002480-199809000-00054.
More dialysis treatments have been performed with cellulose based membranes than with any other material. As unmodified cellulose membranes activate the complement system, much effort has been directed toward the development of noncomplement activating cellulose membranes. One successful approach was the substitution of -OH groups in the cellobiose units of the cellulose molecule with tertiary amino groups, which resulted in a membrane called Hemophan. Synthetically modified cellulose (SMC) is a new hemodialysis membrane made by specific chemical modification whereby aromatic benzyl groups are covalently introduced into the cellulosic structure by ether bonds, creating hydrophobic domains within the overall hydrophilic cellulose surface: basic research investigations have shown that a characteristic hydrophobic-hydrophilic balance of surfaces is a prerequisite for improved hemocompatibility. Several cellulose modifications with aliphatic and aromatic groups were performed to achieve a membrane with the desired hemocompatibility profile; 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 synthetic hemodialysis membrane). Activation of coagulation (formation of the thrombin-antithrombin III complex [TAT]) in a clinical study showed that SMC caused 16 ng/ml TAT generation compared with 36 ng/ml for polysulphone. SMC, a low-flux cellulosic dialysis membrane, thus combines the typically high diffusive performance characteristics of cellulosic membranes with excellent hemocompatibility, matching synthetic dialysis membranes.
与其他任何材料相比,基于纤维素的膜进行的透析治疗更多。由于未改性的纤维素膜会激活补体系统,因此人们致力于开发不激活补体的纤维素膜。一种成功的方法是用叔氨基取代纤维素分子中纤维二糖单元的 -OH 基团,从而得到一种名为 Hemophan 的膜。合成改性纤维素(SMC)是一种新型血液透析膜,通过特定的化学改性制成,即通过醚键将芳香苄基共价引入纤维素结构中,在整体亲水性纤维素表面形成疏水区域:基础研究表明,表面具有特征性的疏水 - 亲水平衡是改善血液相容性的先决条件。人们进行了几种用脂肪族和芳香族基团对纤维素的改性,以获得具有所需血液相容性特征的膜;具有疏水苄基的 SMC 对血液补体、凝血和细胞激活系统的激活作用最小。血液的体外实验表明,与铜仿膜相比,SMC 的 C5a 生成量减少了 94%(而合成血液透析膜聚砜为 96%)。一项临床研究中凝血的激活(凝血酶 - 抗凝血酶 III 复合物 [TAT] 的形成)表明,与聚砜的 36 ng/ml 相比,SMC 导致 TAT 生成量为 16 ng/ml。因此,SMC 这种低通量纤维素透析膜将纤维素膜通常具有的高扩散性能特征与优异的血液相容性相结合,可与合成透析膜相媲美。