Grabenwöger M, Sider J, Fitzal F, Zelenka C, Windberger U, Grimm M, Moritz A, Böck P, Wolner E
Department of Cardio-Thoracic Surgery, University of Vienna, Austria.
Ann Thorac Surg. 1996 Sep;62(3):772-7.
This study was conducted to investigate the impact of the preservation method of bioprosthetic heart valve materials on calcification rates and biocompatibility of the biologic tissue.
In subcutaneous rat implants, conventionally preserved bioprosthetic heart valve material was compared with bovine pericardium that was treated with L-glutamic acid to reduce residual glutaraldehyde released from the fixed tissue. Both these methods were compared with bovine pericardium that was stabilized by a dye-mediated photooxidation reaction without glutaraldehyde. Biocompatibility of these biomaterials was tested in vitro using human endothelial cell cultures.
Conventionally preserved bovine pericardium with a high amount of glutaraldehyde incorporated into the tissue resulted in severe calcification 63 days after subcutaneous implantation in rats (165.4 +/- 20 mg Ca2+/g dry weight). Postfixation treatment with L-glutamic acid, which reduces free, unbound aldehyde groups, showed a significant decrease in calcification (89.6 +/- 14 mg Ca2+/g dry weight). Glutaraldehyde-free preservation by dye-mediated photooxidation showed no calcification after 63 days of subcutaneous implantation (1.0 +/- 0.4 mg Ca2+/g dry weight). Regular endothelial cell proliferation was observed on photooxidized and L-glutamic acid-treated tissue, whereas conventionally treated tissue caused endothelial cell death.
This study underlines the detrimental role of glutaraldehyde in the calcification process of bioprosthetic heart valve materials and emphasizes alternative preservation methods that reduce or avoid the use of glutaraldehyde.
本研究旨在调查生物人工心脏瓣膜材料的保存方法对生物组织钙化率和生物相容性的影响。
在大鼠皮下植入实验中,将传统保存的生物人工心脏瓣膜材料与经L-谷氨酸处理以减少固定组织中释放的残留戊二醛的牛心包进行比较。将这两种方法与通过无戊二醛的染料介导光氧化反应稳定化的牛心包进行比较。使用人内皮细胞培养物在体外测试这些生物材料的生物相容性。
传统保存的牛心包组织中掺入大量戊二醛,在大鼠皮下植入63天后导致严重钙化(165.4±20mg Ca2+/g干重)。用L-谷氨酸进行后固定处理可减少游离的、未结合的醛基,钙化显著减少(89.6±14mg Ca2+/g干重)。通过染料介导光氧化进行的无戊二醛保存,在皮下植入63天后未出现钙化(1.0±0.4mg Ca2+/g干重)。在光氧化和L-谷氨酸处理的组织上观察到内皮细胞正常增殖,而传统处理的组织导致内皮细胞死亡。
本研究强调了戊二醛在生物人工心脏瓣膜材料钙化过程中的有害作用,并强调了减少或避免使用戊二醛的替代保存方法。