Tabata Y, Lonikar S V, Horii F, Ikada Y
Biomaterials. 1986 May;7(3):234-8. doi: 10.1016/0142-9612(86)90110-9.
The cyanogen bromide (CNBr) activation method was adopted to link collagen molecules onto the surface of cellulose and poly(vinyl alcohol) (PVA) films via covalent bonding. The amount of bound protein was determined by the ninhydrin method and found to be 1.0 microgram/cm2 for the native collagen and 0.6 microgram/cm2 for the denatured collagen. The amount of bound protein was larger for cellulose than PVA. When p-toluene-sulphonyl chloride was used to activate the cellulose film, this activation method was found to be effective in grafting the collagen as well. The cellulose film was found to become brittle and weak after activation with CNBr, but the PVA films was not. This might be due to the difference in the extent of crosslinking between cellulose and PVA films, as demonstrated by the change in degree of swelling and solubility of both the activated films.
采用溴化氰(CNBr)活化法通过共价键将胶原蛋白分子连接到纤维素和聚乙烯醇(PVA)膜的表面。通过茚三酮法测定结合蛋白的量,发现天然胶原蛋白为1.0微克/平方厘米,变性胶原蛋白为0.6微克/平方厘米。纤维素结合的蛋白量比PVA的多。当用对甲苯磺酰氯活化纤维素膜时,发现这种活化方法对接枝胶原蛋白也有效。发现用CNBr活化后纤维素膜变脆且脆弱,但PVA膜没有。这可能是由于纤维素膜和PVA膜交联程度的差异,这通过两种活化膜的溶胀度和溶解度的变化得以证明。