Lee W K, Park K D, Kim Y H, Suh H, Park J C, Lee J E, Sun K, Baek M J, Kim H M, Kim S H
Korea Institute of Science and Technology, Biomaterials Research Center, P.O. Box 131, Cheongnyang, Seoul 130-650, Korea.
J Biomed Mater Res. 2001;58(1):27-35. doi: 10.1002/1097-4636(2001)58:1<27::aid-jbm40>3.0.co;2-2.
A novel chemical modification of biological tissues was developed aimed at improving biocompatibility and calcification resistance. This method involved the additional grafting of sulfonated PEO (PEO-SO(3)) or heparin after conventional glutaraldehyde (GA) fixation of bovine pericardium (BP). The amino groups of PEO-SO(3) or heparin were utilized to react to the GA residues to block them. The PEO-SO(3) or heparin grafted tissues demonstrated a slightly higher shrinkage temperature and tensile strength, but greater resistance to collagenase digestion, than GA treated ones. These results suggest that modified tissues have improved durability due to the grafting and filling effect of PEO-SO(3) or heparin in addition to the GA cross-linking. At the direct contact cytotoxicity test in vitro, PEO-SO(3) or heparin grafted tissue was shown to be nontoxic, while relatively significant cytotoxicity was observed for the GA treated tissues, possibly due to the release of GA. From the in vivo calcification study, calcium contents deposited on the modified tissues were much less than those on GA treated tissues. Such a decreased calcification might be explained by the decrease of residual GA groups during the additional treatment, and the space-filling effect and the nonadhesive property and/or the blood compatibility of PEO-SO(3) or heparin grafted covalently. The newly modified tissue patch was observed to show improved pathological assessibility including less inflammation and tissue reactions. This simple modification method may be useful for calcification-resistant and blood-compatible tissue patches for cardiovascular implants.
为了提高生物相容性和抗钙化性能,开发了一种新型的生物组织化学修饰方法。该方法包括在牛心包(BP)经传统戊二醛(GA)固定后,额外接枝磺化聚环氧乙烷(PEO-SO(3))或肝素。利用PEO-SO(3)或肝素的氨基与GA残基反应以阻断它们。与GA处理的组织相比,接枝了PEO-SO(3)或肝素的组织表现出略高的收缩温度和拉伸强度,但对胶原酶消化的抵抗力更强。这些结果表明,除了GA交联外,由于PEO-SO(3)或肝素的接枝和填充作用,修饰后的组织具有更好的耐久性。在体外直接接触细胞毒性试验中,接枝了PEO-SO(3)或肝素的组织显示无毒性,而GA处理的组织观察到相对显著的细胞毒性,这可能是由于GA的释放。从体内钙化研究来看,沉积在修饰组织上的钙含量远低于GA处理的组织。这种钙化的减少可能是由于额外处理过程中残留GA基团的减少,以及PEO-SO(3)或肝素共价接枝的空间填充效应、非粘附特性和/或血液相容性。观察到新修饰的组织贴片在病理可评估性方面有所改善,包括炎症和组织反应减少。这种简单的修饰方法可能对用于心血管植入物的抗钙化和血液相容性组织贴片有用。