Larionova N I, Kazanskaia N F, Mitiushina G V
Vopr Med Khim. 1985 Jul-Aug;31(4):25-30.
Several procedures for immobilization of basic polyvalent inhibitor of proteases on soluble and insoluble matrices of various chemical nature were studied. Water-soluble high molecular derivatives of the proteases inhibitor were produced, which exhibited the unaltered constants of trypsin inhibition, slower rate of elimination from circulation and the hepatotropism as compared with the native inhibitor. The higher therapeutic efficiency of the high molecular derivative of the proteases inhibitor and of the affinity sorbent, produced on its basis, as compared with the conventional methods of the experimental acute pancreatitis treatment, were confirmed by a number of biochemical data.
研究了几种将碱性多价蛋白酶抑制剂固定在各种化学性质的可溶和不溶基质上的方法。制备了蛋白酶抑制剂的水溶性高分子衍生物,与天然抑制剂相比,其胰蛋白酶抑制常数未改变,从循环中消除的速率较慢且具有亲肝性。一些生化数据证实,与实验性急性胰腺炎的传统治疗方法相比,蛋白酶抑制剂的高分子衍生物及其在此基础上制备的亲和吸附剂具有更高的治疗效率。