Hsu Shan-hui, Tsai I-jine, Lin Da-jun, Chen David C
Department of Chemical Engineering, National Chung Hsing University, 250 Kuo Kuang Road, Taichung, Taiwan 40227, ROC.
Med Eng Phys. 2005 Apr;27(3):267-72. doi: 10.1016/j.medengphy.2004.10.008.
Due to the limited number of cells available in endothelial cell (EC) seeding of small diameter vascular grafts, high seeding rate and ideal proliferation are normally required and can be achieved by optimizing the EC seeding and culture procedures. In this study, by using rotational seeding at 0.16 rpm for 12 h in an incubator, 90% cells were successfully seeded on the polyurethane vascular grafts. Following a period of 72 h of static culture, the cell retention after 6 h of flushing could reach 90%. The retention was further enhanced after perfuse culture (9 cm/s). The optimal procedures to prepare a polyurethane vascular graft (4-mm i.d., 4 cm long) populated with firmly attached EC were therefore: (1) seeding the graft with 0.5 ml of cell suspension containing approximately 10(5) cells rotated at 0.16 rpm for 12 h; (2) culturing the seeded graft in static for 72 h; and (3) culturing the graft by perfusion (9 cm/s) for another 72 h to 7 days. These procedures consistently resulted in a graft covered with confluent vein EC that fully retained on the surface after 6 h of in vitro flushing.
由于小口径血管移植物内皮细胞(EC)接种时可用细胞数量有限,通常需要高接种率和理想的增殖,这可通过优化EC接种和培养程序来实现。在本研究中,通过在培养箱中以0.16 rpm转速旋转接种12小时,90%的细胞成功接种到聚氨酯血管移植物上。经过72小时的静态培养后,冲洗6小时后的细胞保留率可达90%。灌注培养(9 cm/s)后保留率进一步提高。因此,制备充满牢固附着EC的聚氨酯血管移植物(内径4 mm,长4 cm)的最佳程序为:(1)用0.5 ml含有约10⁵个细胞的细胞悬液接种移植物,以0.16 rpm转速旋转12小时;(2)将接种后的移植物静态培养72小时;(3)将移植物再灌注培养(9 cm/s)72小时至7天。这些程序始终能使移植物表面覆盖汇合的静脉EC,体外冲洗6小时后EC完全保留在表面。