Ascherl R, Siebels W, Kobor B, Geissdörfer K, Schmeller M L, Lichti H, Fraefel W, Blümel G
Unfallchirurgie. 1985 Dec;11(6):278-88. doi: 10.1007/BF02587978.
Allogeneic and xenogeneic biological tendon and ligament materials for ligament replacement were tested in the knee of rabbits and sheep. In-vitro and ex-vivo biomechanical tests as well as micromorphological investigations following implantation were performed. The preparation procedure mainly consists in cross linking of collagen by dicarboxylic acids (DC). Modifications in the method induce changes in the biomechanical stability also after implantation. Sheep with autologous patellar tendons substitutions and glutaraldehyde (GA) fixed bovine tendons served as controls. Because of biocompatibility reasons the later seem to be not yet suitable for clinical applications. The DC-tendons need for improved midterm stability prior to clinical implantations; the biocompatibility appears to be excellent.
用于韧带替代的同种异体和异种生物肌腱及韧带材料在兔和羊的膝关节中进行了测试。进行了体外和离体生物力学测试以及植入后的微观形态学研究。制备过程主要包括通过二元羧酸(DC)交联胶原蛋白。该方法的改变在植入后也会引起生物力学稳定性的变化。自体髌腱替代和戊二醛(GA)固定的牛肌腱的羊作为对照。由于生物相容性原因,后者似乎仍不适合临床应用。DC肌腱在临床植入前需要提高中期稳定性;其生物相容性似乎极佳。