Vasudev S C, Chandy T, Sharma C P
Sree Chitra Tirunal Institute for Medical Sciences and Technology, Poojappura, Trivandrum, India.
Artif Cells Blood Substit Immobil Biotechnol. 2000 Jan;28(1):79-94. doi: 10.3109/10731190009119787.
Pathologic calcification is thought to be the main cause of failure in the present generation tissue valves fabricated from glutaraldehyde pretreated bovine pericardium (BP). The present investigation describes the in vitro calcification and enzymatic degradation of bovine pericardia after hexamethylene diisocyanate (HMDIC) crosslinking and subsequent modification with polyethylene glycol. The enzymatic degradation of these treated surfaces were monitored by scanning electron micrography and tensile strength measurements. Various proteases, such as alpha-chymotrypsin, bromelain, esterase, trypsin and collagenase were investigated for tissue stability. Incubation of these enzymes with crosslinked pericardia had variably reduced their tensile strength. Among these treated surfaces, polyethylene glycol (PEG) grafted BP via isocyanate functionalities had retained maximum strength. The PEG modified tissues had also indicated a substantial reduction in calcification, when compared to other treated tissues. Further, the biocompatibility of various pericardial tissues were established by platelet adhesion and octane contact angle measurements. It is assumed that the PEG modification of pericardium may interfere with the cellular activation of injury (platelets) to reduce tissue associated calcification. In conclusion, it seems the PEG modification of bovine pericardium via HMDIC may provide new ways of controlling tissue biodegradation and calcification. However, more in vivo studies are needed to develop applications.
病理性钙化被认为是目前由戊二醛预处理牛心包(BP)制成的组织瓣膜失效的主要原因。本研究描述了六亚甲基二异氰酸酯(HMDIC)交联并随后用聚乙二醇改性后牛心包的体外钙化和酶促降解。通过扫描电子显微镜和拉伸强度测量来监测这些处理过的表面的酶促降解。研究了各种蛋白酶,如α-胰凝乳蛋白酶、菠萝蛋白酶、酯酶、胰蛋白酶和胶原酶对组织稳定性的影响。将这些酶与交联心包一起孵育会不同程度地降低其拉伸强度。在这些处理过的表面中,通过异氰酸酯官能团接枝聚乙二醇(PEG)的BP保留了最大强度。与其他处理过的组织相比,PEG改性的组织也显示出钙化显著减少。此外,通过血小板粘附和辛烷接触角测量确定了各种心包组织的生物相容性。据推测,心包的PEG改性可能会干扰损伤细胞(血小板)的激活,从而减少组织相关的钙化。总之,通过HMDIC对牛心包进行PEG改性似乎可以提供控制组织生物降解和钙化的新方法。然而,需要更多的体内研究来开发应用。